Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.81305928T>GCA7695661IL16c.3582T>G (p.Asn1194Lys)
c.3441T>G (p.Asn1147Lys)
c.*2618T>G (n.*2618T>G)
c.1338T>G (p.Asn446Lys)
c.1352T>G
c.1555T>G (n.1555T>G)
n.285T>G
n.183T>G
c.3411T>G
c.3303T>G (p.Asn1101Lys)
n.3618T>G
c.1611T>G (p.Asn537Lys)
c.2931T>G (p.Asn977Lys)
c.3594T>G (p.Asn1198Lys)
n.3653T>G
n.3652T>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.81305928T=CA2190829844IL16c.3582T= (p.Asn1194=)
c.3441T= (p.Asn1147=)
c.*2618T= (n.*2618T=)
c.1338T= (p.Asn446=)
c.1352T=
c.1555T= (n.1555T=)
n.285T=
n.183T=
c.3411T=
c.3303T= (p.Asn1101=)
n.3618T=
c.1611T= (p.Asn537=)
c.2931T= (p.Asn977=)
c.3594T= (p.Asn1198=)
n.3653T=
n.3652T=
dbSNP
15g.81305928T>CCA491994805IL16c.3582T>C (p.Asn1194=)
c.3441T>C (p.Asn1147=)
c.*2618T>C (n.*2618T>C)
c.1338T>C (p.Asn446=)
c.1352T>C
c.1555T>C (n.1555T>C)
n.285T>C
n.183T>C
c.3411T>C
c.3303T>C (p.Asn1101=)
n.3618T>C
c.1611T>C (p.Asn537=)
c.2931T>C (p.Asn977=)
c.3594T>C (p.Asn1198=)
n.3653T>C
n.3652T>C
dbSNP gnomAD v4
15g.81305928T>ACA393250917IL16c.3582T>A (p.Asn1194Lys)
c.3441T>A (p.Asn1147Lys)
c.*2618T>A (n.*2618T>A)
c.1338T>A (p.Asn446Lys)
c.1352T>A
c.1555T>A (n.1555T>A)
n.285T>A
n.183T>A
c.3411T>A
c.3303T>A (p.Asn1101Lys)
n.3618T>A
c.1611T>A (p.Asn537Lys)
c.2931T>A (p.Asn977Lys)
c.3594T>A (p.Asn1198Lys)
n.3653T>A
n.3652T>A
dbSNP

Number of alleles fetched