Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.46011595A=CA2366478862MMP9c.845A= (p.Asn282=)
20g.46011595A>CCA409214567MMP9c.845A>C (p.Asn282Thr)
20g.46011595A>GCA409214569MMP9c.845A>G (p.Asn282Ser)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.46011595A>TCA409214572MMP9c.845A>T (p.Asn282Ile)
20g.46011596T>ACA409214576MMP9c.846T>A (p.Asn282Lys)
dbSNP gnomAD v2 gnomAD v4
20g.46011596T>CCA510642515MMP9c.846T>C (p.Asn282=)
ClinVar dbSNP gnomAD v2 gnomAD v4
20g.46011596T>GCA409214578MMP9c.846T>G (p.Asn282Lys)
20g.46011596T=CA2366478863MMP9c.846T= (p.Asn282=)
20g.46011597G>ACA9886548MMP9c.847G>A (p.Ala283Thr)
dbSNP ExAC gnomAD v2
20g.46011597G>CCA409214589MMP9c.847G>C (p.Ala283Pro)
20g.46011597G=CA2366478864MMP9c.847G= (p.Ala283=)
20g.46011597G>TCA409214587MMP9c.847G>T (p.Ala283Ser)
20g.46011598C>ACA409214591MMP9c.848C>A (p.Ala283Asp)
dbSNP
20g.46011598C>GCA409214596MMP9c.848C>G (p.Ala283Gly)
20g.46011598C>TCA409214601MMP9c.848C>T (p.Ala283Val)
20g.46011599T>ACA510642518MMP9c.849T>A (p.Ala283=)
20g.46011599T>CCA510642519MMP9c.849T>C (p.Ala283=)
20g.46011599T>GCA510642520MMP9c.849T>G (p.Ala283=)
20g.46011600G>ACA409214604MMP9c.850G>A (p.Asp284Asn)
dbSNP gnomAD v3 gnomAD v4
20g.46011600G>CCA409214608MMP9c.850G>C (p.Asp284His)
20g.46011600G=CA2366478865MMP9c.850G= (p.Asp284=)
20g.46011600G>TCA409214611MMP9c.850G>T (p.Asp284Tyr)
COSMIC
20g.46011601A=CA2366478866MMP9c.851A= (p.Asp284=)
20g.46011601A>CCA409214614MMP9c.851A>C (p.Asp284Ala)
20g.46011601A>GCA409214615MMP9c.851A>G (p.Asp284Gly)
gnomAD v4
20g.46011601A>TCA409214616MMP9c.851A>T (p.Asp284Val)
ClinVar dbSNP gnomAD v2
20g.46011602T>ACA409214617MMP9c.852T>A (p.Asp284Glu)
20g.46011602T>CCA510642523MMP9c.852T>C (p.Asp284=)
gnomAD v4
20g.46011602T>GCA409214619MMP9c.852T>G (p.Asp284Glu)
20g.46011603G>ACA409214625MMP9c.853G>A (p.Gly285Arg)
20g.46011603G>CCA409214628MMP9c.853G>C (p.Gly285Arg)
20g.46011603G>TCA409214622MMP9c.853G>T (p.Gly285Trp)
20g.46011604G>ACA409214631MMP9c.854G>A (p.Gly285Glu)
gnomAD v4
20g.46011604G>CCA409214636MMP9c.854G>C (p.Gly285Ala)
20g.46011604G>TCA409214634MMP9c.854G>T (p.Gly285Val)
20g.46011605G>ACA9886549MMP9c.855G>A (p.Gly285=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46011605G>CCA510642528MMP9c.855G>C (p.Gly285=)
20g.46011605G=CA2366478867MMP9c.855G= (p.Gly285=)
20g.46011605G>TCA510642527MMP9c.855G>T (p.Gly285=)
20g.46011606A>CCA409214650MMP9c.856A>C (p.Lys286Gln)
20g.46011606A>GCA409214645MMP9c.856A>G (p.Lys286Glu)
20g.46011606A>TCA409214647MMP9c.856A>T (p.Lys286Ter)
20g.46011607A>CCA409214654MMP9c.857A>C (p.Lys286Thr)
20g.46011607A>GCA409214656MMP9c.857A>G (p.Lys286Arg)
20g.46011607A>TCA409214660MMP9c.857A>T (p.Lys286Ile)
ClinVar gnomAD v4
20g.46011608A=CA2366478868MMP9c.858A= (p.Lys286=)
20g.46011608A>CCA9886550MMP9c.858A>C (p.Lys286Asn)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
20g.46011608A>GCA510642529MMP9c.858A>G (p.Lys286=)
20g.46011608A>TCA409214678MMP9c.858A>T (p.Lys286Asn)
20g.46011609C>ACA409214682MMP9c.859C>A (p.Pro287Thr)

Number of alleles fetched