Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.79599040C>ACA396535070MAFc.863G>T (p.Arg288Leu)
n.2913G>T
16g.79599040C=CA2235930976MAFc.863G= (p.Arg288=)
n.2913G=
16g.79599040C>GCA122972MAFc.863G>C (p.Arg288Pro)
n.2913G>C
ClinVar dbSNP
16g.79599040C>TCA8184015MAFc.863G>A (p.Arg288Gln)
n.2913G>A
dbSNP ExAC gnomAD v2 gnomAD v4
16g.79599041G>ACA396535071MAFc.862C>T (p.Arg288Trp)
n.2912C>T
dbSNP gnomAD v4
16g.79599041G>CCA396535072MAFc.862C>G (p.Arg288Gly)
n.2912C>G
ClinVar
16g.79599041G=CA2235930985MAFc.862C= (p.Arg288=)
n.2912C=
16g.79599041G>TCA8184016MAFc.862C>A (p.Arg288=)
n.2912C>A
dbSNP ExAC gnomAD v2 gnomAD v4
16g.79599042G>ACA8184017MAFc.861C>T (p.Ile287=)
n.2911C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.79599042G>CCA8184018MAFc.861C>G (p.Ile287Met)
n.2911C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.79599042G=CA2235930994MAFc.861C= (p.Ile287=)
n.2911C=
16g.79599042G>TCA496509092MAFc.861C>A (p.Ile287=)
n.2911C>A
gnomAD v4
16g.79599043A=CA2235930997MAFc.860T= (p.Ile287=)
n.2910T=
16g.79599043A>CCA8184019MAFc.860T>G (p.Ile287Ser)
n.2910T>G
ClinVar dbSNP ExAC gnomAD v2
16g.79599043A>GCA396535073MAFc.860T>C (p.Ile287Thr)
n.2910T>C
gnomAD v4
16g.79599043A>TCA396535074MAFc.860T>A (p.Ile287Asn)
n.2910T>A
16g.79599044T>ACA396535075MAFc.859A>T (p.Ile287Phe)
n.2909A>T
16g.79599044T>CCA396535076MAFc.859A>G (p.Ile287Val)
n.2909A>G
gnomAD v4
16g.79599044T>GCA396535077MAFc.859A>C (p.Ile287Leu)
n.2909A>C
16g.79599045C>ACA496509099MAFc.858G>T (p.Val286=)
n.2908G>T
16g.79599045C>GCA496509104MAFc.858G>C (p.Val286=)
n.2908G>C
16g.79599045C>TCA496509105MAFc.858G>A (p.Val286=)
n.2908G>A
gnomAD v4
16g.79599046A=CA2235931000MAFc.857T= (p.Val286=)
n.2907T=
16g.79599046A>CCA396535078MAFc.857T>G (p.Val286Gly)
n.2907T>G
dbSNP
16g.79599046A>GCA396535079MAFc.857T>C (p.Val286Ala)
n.2907T>C
16g.79599046A>TCA396535080MAFc.857T>A (p.Val286Glu)
n.2907T>A
dbSNP
16g.79599047C>ACA396535081MAFc.856G>T (p.Val286Leu)
n.2906G>T
16g.79599047C>GCA396535082MAFc.856G>C (p.Val286Leu)
n.2906G>C
16g.79599047C>TCA396535083MAFc.856G>A (p.Val286Met)
n.2906G>A
16g.79599053_79599055delCA2695197684MAFc.854_856del (p.Glu285del)
n.2904_2906del
ClinVar
16g.79599048C>ACA396535084MAFc.855G>T (p.Glu285Asp)
n.2905G>T
16g.79599048C>GCA396535085MAFc.855G>C (p.Glu285Asp)
n.2905G>C
16g.79599048C>TCA496509112MAFc.855G>A (p.Glu285=)
n.2905G>A
gnomAD v4
16g.79599049T>ACA396535086MAFc.854A>T (p.Glu285Val)
n.2904A>T
16g.79599049T>CCA396535087MAFc.854A>G (p.Glu285Gly)
n.2904A>G
16g.79599049T>GCA396535088MAFc.854A>C (p.Glu285Ala)
n.2904A>C
16g.79599050C>ACA396535089MAFc.853G>T (p.Glu285Ter)
n.2903G>T
16g.79599050C=CA2235931003MAFc.853G= (p.Glu285=)
n.2903G=
16g.79599050C>GCA396535090MAFc.853G>C (p.Glu285Gln)
n.2903G>C
dbSNP
16g.79599050C>TCA396535091MAFc.853G>A (p.Glu285Lys)
n.2903G>A
16g.79599051C>ACA396535092MAFc.852G>T (p.Glu284Asp)
n.2902G>T
16g.79599051C>GCA396535093MAFc.852G>C (p.Glu284Asp)
n.2902G>C
16g.79599051C>TCA496509118MAFc.852G>A (p.Glu284=)
n.2902G>A
16g.79599052T>ACA396535094MAFc.851A>T (p.Glu284Val)
n.2901A>T
16g.79599052T>CCA396535095MAFc.851A>G (p.Glu284Gly)
n.2901A>G
dbSNP
16g.79599052T>GCA396535096MAFc.851A>C (p.Glu284Ala)
n.2901A>C
gnomAD v4
16g.79599052T=CA2235931006MAFc.851A= (p.Glu284=)
n.2901A=
16g.79599053C>ACA396535098MAFc.850G>T (p.Glu284Ter)
n.2900G>T
gnomAD v4
16g.79599053C=CA2235931010MAFc.850G= (p.Glu284=)
n.2900G=
16g.79599053C>GCA8184020MAFc.850G>C (p.Glu284Gln)
n.2900G>C
dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched