Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.67754206A>CCA357056311GNRHRc.130T>G (p.Phe44Val)
4g.67754206A>GCA357056313GNRHRc.130T>C (p.Phe44Leu)
4g.67754206A>TCA357056315GNRHRc.130T>A (p.Phe44Ile)
4g.67754207G>ACA2938992GNRHRc.129C>T (p.Phe43=)
dbSNP ExAC gnomAD v2
4g.67754207G>CCA357056319GNRHRc.129C>G (p.Phe43Leu)
4g.67754207G=CA1465420967GNRHRc.129C= (p.Phe43=)
4g.67754207G>TCA357056321GNRHRc.129C>A (p.Phe43Leu)
4g.67754208A>CCA357056325GNRHRc.128T>G (p.Phe43Cys)
4g.67754208A>GCA357056327GNRHRc.128T>C (p.Phe43Ser)
COSMIC
4g.67754208A>TCA357056323GNRHRc.128T>A (p.Phe43Tyr)
4g.67754209A=CA1465420968GNRHRc.127T= (p.Phe43=)
4g.67754209A>CCA357056328GNRHRc.127T>G (p.Phe43Val)
4g.67754209A>GCA2938993GNRHRc.127T>C (p.Phe43Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.67754209A>TCA357056329GNRHRc.127T>A (p.Phe43Ile)
4g.67754210A>CCA439933867GNRHRc.126T>G (p.Thr42=)
4g.67754210A>GCA439933868GNRHRc.126T>C (p.Thr42=)
COSMIC
4g.67754210A>TCA439933869GNRHRc.126T>A (p.Thr42=)
4g.67754211G>ACA357056331GNRHRc.125C>T (p.Thr42Ile)
gnomAD v4
4g.67754211G>CCA357056333GNRHRc.125C>G (p.Thr42Ser)
4g.67754211G>TCA357056335GNRHRc.125C>A (p.Thr42Asn)
4g.67754212T>ACA357056338GNRHRc.124A>T (p.Thr42Ser)
4g.67754212T>CCA357056339GNRHRc.124A>G (p.Thr42Ala)
4g.67754212T>GCA357056342GNRHRc.124A>C (p.Thr42Pro)
gnomAD v4
4g.67754213A>CCA439933870GNRHRc.123T>G (p.Val41=)
4g.67754213A>GCA439933871GNRHRc.123T>C (p.Val41=)
gnomAD v4
4g.67754213A>TCA439933872GNRHRc.123T>A (p.Val41=)
4g.67754214A>CCA357056345GNRHRc.122T>G (p.Val41Gly)
4g.67754214A>GCA357056347GNRHRc.122T>C (p.Val41Ala)
4g.67754214A>TCA357056350GNRHRc.122T>A (p.Val41Asp)
4g.67754215C>ACA357056353GNRHRc.121G>T (p.Val41Phe)
4g.67754215C>GCA357056356GNRHRc.121G>C (p.Val41Leu)
4g.67754215C>TCA357056352GNRHRc.121G>A (p.Val41Ile)
4g.67754216C>ACA439933874GNRHRc.120G>T (p.Thr40=)
COSMIC
4g.67754216C=CA1465420969GNRHRc.120G= (p.Thr40=)
4g.67754216C>GCA439933873GNRHRc.120G>C (p.Thr40=)
dbSNP gnomAD v3 gnomAD v4
4g.67754216C>TCA2938994GNRHRc.120G>A (p.Thr40=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67754217G>ACA2938995GNRHRc.119C>T (p.Thr40Met)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.67754217G>CCA357056358GNRHRc.119C>G (p.Thr40Arg)
dbSNP gnomAD v2 gnomAD v4
4g.67754217G=CA1465420970GNRHRc.119C= (p.Thr40=)
4g.67754217G>TCA357056359GNRHRc.119C>A (p.Thr40Lys)
4g.67754218T>ACA357056364GNRHRc.118A>T (p.Thr40Ser)
4g.67754218T>CCA357056363GNRHRc.118A>G (p.Thr40Ala)
4g.67754218T>GCA357056361GNRHRc.118A>C (p.Thr40Pro)
4g.67754219C>ACA439933875GNRHRc.117G>T (p.Val39=)
4g.67754219C>GCA439933876GNRHRc.117G>C (p.Val39=)
4g.67754219C>TCA439933877GNRHRc.117G>A (p.Val39=)
4g.67754220A>CCA357056365GNRHRc.116T>G (p.Val39Gly)
4g.67754220A>GCA357056366GNRHRc.116T>C (p.Val39Ala)
4g.67754220A>TCA357056368GNRHRc.116T>A (p.Val39Glu)
4g.67754221C>ACA357056370GNRHRc.115G>T (p.Val39Leu)

Number of alleles fetched