Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.67753832A=CA1465420468GNRHRc.504T= (p.Ser168=)
4g.67753832A>CCA357054310GNRHRc.504T>G (p.Ser168Arg)
4g.67753832A>GCA439928918GNRHRc.504T>C (p.Ser168=)
4g.67753832A>TCA130205GNRHRc.504T>A (p.Ser168Arg)
ClinVar dbSNP
4g.67753833C>ACA357054312GNRHRc.503G>T (p.Ser168Ile)
4g.67753833C=CA1465420472GNRHRc.503G= (p.Ser168=)
4g.67753833C>GCA357054313GNRHRc.503G>C (p.Ser168Thr)
4g.67753833C>TCA357054311GNRHRc.503G>A (p.Ser168Asn)
dbSNP gnomAD v4
4g.67753834T>ACA357054314GNRHRc.502A>T (p.Ser168Cys)
4g.67753834T>CCA357054315GNRHRc.502A>G (p.Ser168Gly)
4g.67753834T>GCA357054316GNRHRc.502A>C (p.Ser168Arg)
4g.67753835A=CA1465420477GNRHRc.501T= (p.Ser167=)
4g.67753835A>CCA98671910GNRHRc.501T>G (p.Ser167Arg)
dbSNP
4g.67753835A>GCA439928941GNRHRc.501T>C (p.Ser167=)
gnomAD v4
4g.67753835A>TCA357054317GNRHRc.501T>A (p.Ser167Arg)
dbSNP
4g.67753836C>ACA357054318GNRHRc.500G>T (p.Ser167Ile)
4g.67753836C=CA1465420479GNRHRc.500G= (p.Ser167=)
4g.67753836C>GCA357054319GNRHRc.500G>C (p.Ser167Thr)
4g.67753836C>TCA357054320GNRHRc.500G>A (p.Ser167Asn)
dbSNP gnomAD v2 gnomAD v4
4g.67753837T>ACA357054321GNRHRc.499A>T (p.Ser167Cys)
4g.67753837T>CCA357054322GNRHRc.499A>G (p.Ser167Gly)
4g.67753837T>GCA357054323GNRHRc.499A>C (p.Ser167Arg)
4g.67753838G>ACA439928968GNRHRc.498C>T (p.Leu166=)
4g.67753838G>CCA439928971GNRHRc.498C>G (p.Leu166=)
dbSNP gnomAD v2
4g.67753838G=CA1465420482GNRHRc.498C= (p.Leu166=)
4g.67753838G>TCA439928973GNRHRc.498C>A (p.Leu166=)
COSMIC
4g.67753839A>CCA357054326GNRHRc.497T>G (p.Leu166Arg)
4g.67753839A>GCA357054325GNRHRc.497T>C (p.Leu166Pro)
gnomAD v4
4g.67753839A>TCA357054324GNRHRc.497T>A (p.Leu166His)
4g.67753840G>ACA2938928GNRHRc.496C>T (p.Leu166Phe)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.67753840G>CCA357054327GNRHRc.496C>G (p.Leu166Val)
4g.67753840G=CA1465420486GNRHRc.496C= (p.Leu166=)
4g.67753840G>TCA357054328GNRHRc.496C>A (p.Leu166Ile)
4g.67753841G>ACA439928993GNRHRc.495C>T (p.Ile165=)
4g.67753841G>CCA357054329GNRHRc.495C>G (p.Ile165Met)
4g.67753841G>TCA439928996GNRHRc.495C>A (p.Ile165=)
gnomAD v4
4g.67753842A>CCA357054330GNRHRc.494T>G (p.Ile165Ser)
4g.67753842A>GCA357054331GNRHRc.494T>C (p.Ile165Thr)
4g.67753842A>TCA357054332GNRHRc.494T>A (p.Ile165Asn)
4g.67753843T>ACA357054333GNRHRc.493A>T (p.Ile165Phe)
4g.67753843T>CCA357054334GNRHRc.493A>G (p.Ile165Val)
4g.67753843T>GCA357054335GNRHRc.493A>C (p.Ile165Leu)
4g.67753844C>ACA357054336GNRHRc.492G>T (p.Trp164Cys)
4g.67753844C>GCA357054337GNRHRc.492G>C (p.Trp164Cys)
4g.67753844C>TCA357054338GNRHRc.492G>A (p.Trp164Ter)
4g.67753845C>ACA357054340GNRHRc.491G>T (p.Trp164Leu)
dbSNP
4g.67753845C=CA1465420489GNRHRc.491G= (p.Trp164=)
4g.67753845C>GCA357054341GNRHRc.491G>C (p.Trp164Ser)
4g.67753845C>TCA357054339GNRHRc.491G>A (p.Trp164Ter)
4g.67753846A=CA1465420493GNRHRc.490T= (p.Trp164=)

Number of alleles fetched