Cannot find gene class

R

rhubarb

New member
hello,

i am 15 weeks pregnant with identical twins and have just learned that both my husband and i are CF carriers. we are awaiting counseling and an amnio, but in the meantime i am trying to do some research. i believe that DF508 is a class 1 or 2 mutation, but i can't find anything on V520f...does anyone know anything about this mutation or know where i can find out which class it is in? i understand that we cannot predict the severity of the disease based on the mutation combination...i'm just grasping at straws here to understand a little more.

thank you!
jackie
 
R

rhubarb

New member
hello,

i am 15 weeks pregnant with identical twins and have just learned that both my husband and i are CF carriers. we are awaiting counseling and an amnio, but in the meantime i am trying to do some research. i believe that DF508 is a class 1 or 2 mutation, but i can't find anything on V520f...does anyone know anything about this mutation or know where i can find out which class it is in? i understand that we cannot predict the severity of the disease based on the mutation combination...i'm just grasping at straws here to understand a little more.

thank you!
jackie
 
R

rhubarb

New member
hello,

i am 15 weeks pregnant with identical twins and have just learned that both my husband and i are CF carriers. we are awaiting counseling and an amnio, but in the meantime i am trying to do some research. i believe that DF508 is a class 1 or 2 mutation, but i can't find anything on V520f...does anyone know anything about this mutation or know where i can find out which class it is in? i understand that we cannot predict the severity of the disease based on the mutation combination...i'm just grasping at straws here to understand a little more.

thank you!
jackie
 
R

rhubarb

New member
hello,

i am 15 weeks pregnant with identical twins and have just learned that both my husband and i are CF carriers. we are awaiting counseling and an amnio, but in the meantime i am trying to do some research. i believe that DF508 is a class 1 or 2 mutation, but i can't find anything on V520f...does anyone know anything about this mutation or know where i can find out which class it is in? i understand that we cannot predict the severity of the disease based on the mutation combination...i'm just grasping at straws here to understand a little more.

thank you!
jackie
 
R

rhubarb

New member
hello,
<br />
<br />i am 15 weeks pregnant with identical twins and have just learned that both my husband and i are CF carriers. we are awaiting counseling and an amnio, but in the meantime i am trying to do some research. i believe that DF508 is a class 1 or 2 mutation, but i can't find anything on V520f...does anyone know anything about this mutation or know where i can find out which class it is in? i understand that we cannot predict the severity of the disease based on the mutation combination...i'm just grasping at straws here to understand a little more.
<br />
<br />thank you!
<br />jackie
 
C

chrissyd

New member
Jackie,
First of all welcome to the site. Sorry that it's under these circumstances...I really hope the amnio comes back showing no CF. I've been looking around for the mutation you listed v520f, and all I was able to find was:
<a target=_blank class=ftalternatingbarlinklarge href="http://hmg.oxfordjournals.org/cgi/content/abstract/1/1/11">article</a>

That however doesn't tate a class or really anything useful. You could always ask Steve, he knows his stuff...see if he can help. The thread of posts you want are on the families forum uner "welcome ambry genetics"

<a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=6&threadid=12677&enterthread=y">Ambry thread</a>

I myself have DF508 but don't know anything about v520f; I hope you find answers!!

<img src="i/expressions/rose.gif" border="0">

Chrissy
31 W/ CF
 
C

chrissyd

New member
Jackie,
First of all welcome to the site. Sorry that it's under these circumstances...I really hope the amnio comes back showing no CF. I've been looking around for the mutation you listed v520f, and all I was able to find was:
<a target=_blank class=ftalternatingbarlinklarge href="http://hmg.oxfordjournals.org/cgi/content/abstract/1/1/11">article</a>

That however doesn't tate a class or really anything useful. You could always ask Steve, he knows his stuff...see if he can help. The thread of posts you want are on the families forum uner "welcome ambry genetics"

<a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=6&threadid=12677&enterthread=y">Ambry thread</a>

I myself have DF508 but don't know anything about v520f; I hope you find answers!!

<img src="i/expressions/rose.gif" border="0">

Chrissy
31 W/ CF
 
C

chrissyd

New member
Jackie,
First of all welcome to the site. Sorry that it's under these circumstances...I really hope the amnio comes back showing no CF. I've been looking around for the mutation you listed v520f, and all I was able to find was:
<a target=_blank class=ftalternatingbarlinklarge href="http://hmg.oxfordjournals.org/cgi/content/abstract/1/1/11">article</a>

That however doesn't tate a class or really anything useful. You could always ask Steve, he knows his stuff...see if he can help. The thread of posts you want are on the families forum uner "welcome ambry genetics"

<a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=6&threadid=12677&enterthread=y">Ambry thread</a>

I myself have DF508 but don't know anything about v520f; I hope you find answers!!

<img src="i/expressions/rose.gif" border="0">

Chrissy
31 W/ CF
 
C

chrissyd

New member
Jackie,
First of all welcome to the site. Sorry that it's under these circumstances...I really hope the amnio comes back showing no CF. I've been looking around for the mutation you listed v520f, and all I was able to find was:
<a target=_blank class=ftalternatingbarlinklarge href="http://hmg.oxfordjournals.org/cgi/content/abstract/1/1/11">article</a>

That however doesn't tate a class or really anything useful. You could always ask Steve, he knows his stuff...see if he can help. The thread of posts you want are on the families forum uner "welcome ambry genetics"

<a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=6&threadid=12677&enterthread=y">Ambry thread</a>

I myself have DF508 but don't know anything about v520f; I hope you find answers!!

<img src="i/expressions/rose.gif" border="0">

Chrissy
31 W/ CF
 
C

chrissyd

New member
Jackie,
<br />First of all welcome to the site. Sorry that it's under these circumstances...I really hope the amnio comes back showing no CF. I've been looking around for the mutation you listed v520f, and all I was able to find was:
<br /><a target=_blank class=ftalternatingbarlinklarge href="http://hmg.oxfordjournals.org/cgi/content/abstract/1/1/11">article</a>
<br />
<br />That however doesn't tate a class or really anything useful. You could always ask Steve, he knows his stuff...see if he can help. The thread of posts you want are on the families forum uner "welcome ambry genetics"
<br />
<br /><a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=6&threadid=12677&enterthread=y">Ambry thread</a>
<br />
<br />I myself have DF508 but don't know anything about v520f; I hope you find answers!!
<br />
<br /><img src="i/expressions/rose.gif" border="0">
<br />
<br />Chrissy
<br />31 W/ CF
 
N

NoExcuses

New member
best preparation you can do is get in touch with parents of CF kids so you know how to best prepare for CF children.

preventative care will be as important, if not more, than the class of mutations that the children will have.

all the best.
 
N

NoExcuses

New member
best preparation you can do is get in touch with parents of CF kids so you know how to best prepare for CF children.

preventative care will be as important, if not more, than the class of mutations that the children will have.

all the best.
 
N

NoExcuses

New member
best preparation you can do is get in touch with parents of CF kids so you know how to best prepare for CF children.

preventative care will be as important, if not more, than the class of mutations that the children will have.

all the best.
 
N

NoExcuses

New member
best preparation you can do is get in touch with parents of CF kids so you know how to best prepare for CF children.

preventative care will be as important, if not more, than the class of mutations that the children will have.

all the best.
 
N

NoExcuses

New member
best preparation you can do is get in touch with parents of CF kids so you know how to best prepare for CF children.
<br />
<br />preventative care will be as important, if not more, than the class of mutations that the children will have.
<br />
<br />all the best.
 
R

rhubarb

New member
thank you both! i have posted on the ambry thread. if anyone else has this mutation (v520f), please let me know!

jackie
 
R

rhubarb

New member
thank you both! i have posted on the ambry thread. if anyone else has this mutation (v520f), please let me know!

jackie
 
R

rhubarb

New member
thank you both! i have posted on the ambry thread. if anyone else has this mutation (v520f), please let me know!

jackie
 
R

rhubarb

New member
thank you both! i have posted on the ambry thread. if anyone else has this mutation (v520f), please let me know!

jackie
 
R

rhubarb

New member
thank you both! i have posted on the ambry thread. if anyone else has this mutation (v520f), please let me know!
<br />
<br />jackie
 
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