Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.27750957G>ACA322870762MN1n.446C>T
c.3921C>T (p.Asp1307=)
c.274C>T
n.277C>T
 dbSNP
22g.27750957G>CCA411032908MN1n.446C>G
c.3921C>G (p.Asp1307Glu)
c.274C>G
n.277C>G
22g.27750957G=CA2399818108MN1n.446C=
c.3921C= (p.Asp1307=)
c.274C=
n.277C=
22g.27750957G>TCA411032910MN1n.446C>A
c.3921C>A (p.Asp1307Glu)
c.274C>A
n.277C>A
22g.27750958T>ACA411032914MN1n.445A>T
c.3920A>T (p.Asp1307Val)
c.273A>T
n.276A>T
22g.27750958T>CCA411032917MN1n.445A>G
c.3920A>G (p.Asp1307Gly)
c.273A>G
n.276A>G
22g.27750958T>GCA411032919MN1n.445A>C
c.3920A>C (p.Asp1307Ala)
c.273A>C
n.276A>C
22g.27750959C>ACA411032921MN1n.444G>T
c.3919G>T (p.Asp1307Tyr)
c.272G>T
n.275G>T
22g.27750959C=CA2399818109MN1n.444G=
c.3919G= (p.Asp1307=)
c.272G=
n.275G=
22g.27750959C>GCA411032924MN1n.444G>C
c.3919G>C (p.Asp1307His)
c.272G>C
n.275G>C
22g.27750959C>TCA10165935MN1n.444G>A
c.3919G>A (p.Asp1307Asn)
c.272G>A
n.275G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
22g.27750960A>CCA513939247MN1n.443T>G
c.3918T>G (p.Ser1306=)
c.271T>G
n.274T>G
22g.27750960A>GCA513939248MN1n.443T>C
c.3918T>C (p.Ser1306=)
c.271T>C
n.274T>C
22g.27750960A>TCA513939249MN1n.443T>A
c.3918T>A (p.Ser1306=)
c.271T>A
n.274T>A
22g.27750961G>ACA411032927MN1n.442C>T
c.3917C>T (p.Ser1306Phe)
c.270C>T
n.273C>T
 dbSNP gnomAD v2
22g.27750961G>CCA411032928MN1n.442C>G
c.3917C>G (p.Ser1306Cys)
c.270C>G
n.273C>G
22g.27750961G=CA2399818110MN1n.442C=
c.3917C= (p.Ser1306=)
c.270C=
n.273C=
22g.27750961G>TCA411032929MN1n.442C>A
c.3917C>A (p.Ser1306Tyr)
c.270C>A
n.273C>A
22g.27750962A>CCA411032930MN1n.441T>G
c.3916T>G (p.Ser1306Ala)
c.269T>G
n.272T>G
22g.27750962A>GCA411032932MN1n.441T>C
c.3916T>C (p.Ser1306Pro)
c.269T>C
n.272T>C
 gnomAD v4
22g.27750962A>TCA411032933MN1n.441T>A
c.3916T>A (p.Ser1306Thr)
c.269T>A
n.272T>A
22g.27750963A>CCA411032934MN1n.440T>G
c.3915T>G (p.His1305Gln)
c.268T>G
n.271T>G
22g.27750963A>GCA513939250MN1n.440T>C
c.3915T>C (p.His1305=)
c.268T>C
n.271T>C
22g.27750963A>TCA411032936MN1n.440T>A
c.3915T>A (p.His1305Gln)
c.268T>A
n.271T>A
22g.27750964T>ACA411032939MN1n.439A>T
c.3914A>T (p.His1305Leu)
c.267A>T
n.270A>T
22g.27750964T>CCA411032940MN1n.439A>G
c.3914A>G (p.His1305Arg)
c.267A>G
n.270A>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
22g.27750964T>GCA411032943MN1n.439A>C
c.3914A>C (p.His1305Pro)
c.267A>C
n.270A>C
22g.27750964T=CA2399818111MN1n.439A=
c.3914A= (p.His1305=)
c.267A=
n.270A=
22g.27750965G>ACA411032949MN1n.438C>T
c.3913C>T (p.His1305Tyr)
c.266C>T
n.269C>T
 gnomAD v4
22g.27750965G>CCA411032947MN1n.438C>G
c.3913C>G (p.His1305Asp)
c.266C>G
n.269C>G
22g.27750965G>TCA411032945MN1n.438C>A
c.3913C>A (p.His1305Asn)
c.266C>A
n.269C>A
22g.27750966C>ACA513939251MN1n.437G>T
c.3912G>T (p.Leu1304=)
c.265G>T
n.268G>T
22g.27750966C>GCA513939252MN1n.437G>C
c.3912G>C (p.Leu1304=)
c.265G>C
n.268G>C
22g.27750966C>TCA513939253MN1n.437G>A
c.3912G>A (p.Leu1304=)
c.265G>A
n.268G>A
22g.27750967A>CCA411032952MN1n.436T>G
c.3911T>G (p.Leu1304Arg)
c.264T>G
n.267T>G
22g.27750967A>GCA411032953MN1n.436T>C
c.3911T>C (p.Leu1304Pro)
c.264T>C
n.267T>C
22g.27750967A>TCA411032955MN1n.436T>A
c.3911T>A (p.Leu1304Gln)
c.264T>A
n.267T>A
22g.27750968G>ACA322870779MN1n.435C>T
c.3910C>T (p.Leu1304=)
c.263C>T
n.266C>T
 dbSNP gnomAD v2 gnomAD v4
22g.27750968G>CCA411032958MN1n.435C>G
c.3910C>G (p.Leu1304Val)
c.263C>G
n.266C>G
22g.27750968G=CA2399818112MN1n.435C=
c.3910C= (p.Leu1304=)
c.263C=
n.266C=
22g.27750968G>TCA411032960MN1n.435C>A
c.3910C>A (p.Leu1304Met)
c.263C>A
n.266C>A
22g.27750969G>ACA513939255MN1n.434C>T
c.3909C>T (p.Ser1303=)
c.262C>T
n.265C>T
22g.27750969G>CCA10165936MN1n.434C>G
c.3909C>G (p.Ser1303=)
c.262C>G
n.265C>G
 dbSNP ExAC gnomAD v2 gnomAD v4
22g.27750969G=CA2399818113MN1n.434C=
c.3909C= (p.Ser1303=)
c.262C=
n.265C=
22g.27750969G>TCA513939254MN1n.434C>A
c.3909C>A (p.Ser1303=)
c.262C>A
n.265C>A
22g.27750970G>ACA411032963MN1n.433C>T
c.3908C>T (p.Ser1303Phe)
c.261C>T
n.264C>T
22g.27750970G>CCA411032965MN1n.433C>G
c.3908C>G (p.Ser1303Cys)
c.261C>G
n.264C>G
22g.27750970G>TCA411032967MN1n.433C>A
c.3908C>A (p.Ser1303Tyr)
c.261C>A
n.264C>A
22g.27750971A>CCA411033102MN1n.432T>G
c.3907T>G (p.Ser1303Ala)
c.260T>G
n.263T>G
22g.27750971A>GCA411033105MN1n.432T>C
c.3907T>C (p.Ser1303Pro)
c.260T>C
n.263T>C

Number of alleles fetched