Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.122257249C>ACA119487CASRc.354C>A (p.Asn118Lys)
c.9+2875C>A (p.=)
n.213C>A
ClinVar dbSNP
3g.122257249C>GCA354362715CASRc.354C>G (p.Asn118Lys)
c.9+2875C>G (p.=)
n.213C>G
3g.122257249C>TCA435404086CASRc.354C>T (p.Asn118=)
c.9+2875C>T (p.=)
n.213C>T
3g.122257250A>CCA354362716CASRc.355A>C (p.Lys119Gln)
c.9+2876A>C (p.=)
n.214A>C
3g.122257250A>GCA354362717CASRc.355A>G (p.Lys119Glu)
c.9+2876A>G (p.=)
n.214A>G
3g.122257250A>TCA354362718CASRc.355A>T (p.Lys119Ter)
c.9+2876A>T (p.=)
n.214A>T
3g.122257251A>CCA354362719CASRc.356A>C (p.Lys119Thr)
c.9+2877A>C (p.=)
n.215A>C
3g.122257251A>GCA354362720CASRc.356A>G (p.Lys119Arg)
c.9+2877A>G (p.=)
n.215A>G
3g.122257251A>TCA354362721CASRc.356A>T (p.Lys119Ile)
c.9+2877A>T (p.=)
n.215A>T
3g.122257252A>CCA354362722CASRc.357A>C (p.Lys119Asn)
c.9+2878A>C (p.=)
n.216A>C
3g.122257252A>GCA435404087CASRc.357A>G (p.Lys119=)
c.9+2878A>G (p.=)
n.216A>G
3g.122257252A>TCA354362723CASRc.357A>T (p.Lys119Asn)
c.9+2878A>T (p.=)
n.216A>T
3g.122257253A>CCA354362724CASRc.358A>C (p.Ile120Leu)
c.9+2879A>C (p.=)
n.217A>C
3g.122257253A>GCA354362725CASRc.358A>G (p.Ile120Val)
c.9+2879A>G (p.=)
n.217A>G
3g.122257253A>TCA354362726CASRc.358A>T (p.Ile120Phe)
c.9+2879A>T (p.=)
n.217A>T
3g.122257254T>ACA354362727CASRc.359T>A (p.Ile120Asn)
c.9+2880T>A (p.=)
n.218T>A
3g.122257254T>CCA354362728CASRc.359T>C (p.Ile120Thr)
c.9+2880T>C (p.=)
n.218T>C
3g.122257254T>GCA354362729CASRc.359T>G (p.Ile120Ser)
c.9+2880T>G (p.=)
n.218T>G
3g.122257255T>ACA435404088CASRc.360T>A (p.Ile120=)
c.9+2881T>A (p.=)
n.219T>A
3g.122257255T>CCA435404089CASRc.360T>C (p.Ile120=)
c.9+2881T>C (p.=)
n.219T>C
3g.122257255T>GCA354362730CASRc.360T>G (p.Ile120Met)
c.9+2881T>G (p.=)
n.219T>G
ClinVar COSMIC
3g.122257256G>ACA354362731CASRc.361G>A (p.Asp121Asn)
c.9+2882G>A (p.=)
n.220G>A
3g.122257256G>CCA354362732CASRc.361G>C (p.Asp121His)
c.9+2882G>C (p.=)
n.220G>C
3g.122257256G>TCA354362733CASRc.361G>T (p.Asp121Tyr)
c.9+2882G>T (p.=)
n.220G>T
3g.122257257A>CCA354362734CASRc.362A>C (p.Asp121Ala)
c.9+2883A>C (p.=)
n.221A>C
3g.122257257A>GCA354362735CASRc.362A>G (p.Asp121Gly)
c.9+2883A>G (p.=)
n.221A>G
3g.122257257A>TCA354362736CASRc.362A>T (p.Asp121Val)
c.9+2883A>T (p.=)
n.221A>T
3g.122257258T>ACA82610017CASRc.363T>A (p.Asp121Glu)
c.9+2884T>A (p.=)
n.222T>A
ClinVar dbSNP
3g.122257258T>CCA435404090CASRc.363T>C (p.Asp121=)
c.9+2884T>C (p.=)
n.222T>C
3g.122257258T>GCA354362737CASRc.363T>G (p.Asp121Glu)
c.9+2884T>G (p.=)
n.222T>G
gnomAD
3g.122257259T>ACA354362739CASRc.364T>A (p.Ser122Thr)
c.9+2885T>A (p.=)
n.223T>A
3g.122257259T>CCA354362741CASRc.364T>C (p.Ser122Pro)
c.9+2885T>C (p.=)
n.223T>C
3g.122257259T>GCA354362742CASRc.364T>G (p.Ser122Ala)
c.9+2885T>G (p.=)
n.223T>G
3g.122257260C>ACA2569462CASRc.365C>A (p.Ser122Tyr)
c.9+2886C>A (p.=)
n.224C>A
ClinVar dbSNP ExAC gnomAD COSMIC
3g.122257260C>GCA354362743CASRc.365C>G (p.Ser122Cys)
c.9+2886C>G (p.=)
n.224C>G
3g.122257260C>TCA354362744CASRc.365C>T (p.Ser122Phe)
c.9+2886C>T (p.=)
n.224C>T
3g.122257261T>ACA435404091CASRc.366T>A (p.Ser122=)
c.9+2887T>A (p.=)
n.225T>A
3g.122257261T>CCA435404092CASRc.366T>C (p.Ser122=)
c.9+2887T>C (p.=)
n.225T>C
3g.122257261T>GCA2569463CASRc.366T>G (p.Ser122=)
c.9+2887T>G (p.=)
n.225T>G
dbSNP ExAC gnomAD
3g.122257262T>ACA354362745CASRc.367T>A (p.Leu123Met)
c.9+2888T>A (p.=)
n.226T>A
3g.122257262T>CCA435404093CASRc.367T>C (p.Leu123=)
c.9+2888T>C (p.=)
n.226T>C
3g.122257262T>GCA354362746CASRc.367T>G (p.Leu123Val)
c.9+2888T>G (p.=)
n.226T>G
3g.122257263T>ACA354362747CASRc.368T>A (p.Leu123Ter)
c.9+2889T>A (p.=)
n.227T>A
3g.122257263T>CCA354362748CASRc.368T>C (p.Leu123Ser)
c.9+2889T>C (p.=)
n.227T>C
3g.122257263T>GCA354362749CASRc.368T>G (p.Leu123Trp)
c.9+2889T>G (p.=)
n.227T>G
3g.122257264G>ACA435404095CASRc.369G>A (p.Leu123=)
c.9+2890G>A (p.=)
n.228G>A
3g.122257264G>CCA354362751CASRc.369G>C (p.Leu123Phe)
c.9+2890G>C (p.=)
n.228G>C
3g.122257264G>TCA354362750CASRc.369G>T (p.Leu123Phe)
c.9+2890G>T (p.=)
n.228G>T
3g.122257265A>CCA354362752CASRc.370A>C (p.Asn124His)
c.9+2891A>C (p.=)
n.229A>C
3g.122257265A>GCA354362754CASRc.370A>G (p.Asn124Asp)
c.9+2891A>G (p.=)
n.229A>G

Number of alleles fetched