Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.49457791dup | CA3847075 | MMUT | c.656dup (p.Asn219LysfsTer2) | dbSNP ExAC gnomAD v2 |
6 | g.49457791del | CA2499218333 | MMUT | c.656del (p.Asn219MetfsTer4) | ClinVar dbSNP |
6 | g.49457789T>A | CA249731 | MMUT | c.655A>T (p.Asn219Tyr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49457789T>C | CA364404270 | MMUT | c.655A>G (p.Asn219Asp) | |
6 | g.49457789T>G | CA364404271 | MMUT | c.655A>C (p.Asn219His) | |
6 | g.49457789T= | CA1627392109 | MMUT | c.655A= (p.Asn219=) | |
6 | g.49457790T>A | CA364404272 | MMUT | c.654A>T (p.Gln218His) | |
6 | g.49457790T>C | CA450608788 | MMUT | c.654A>G (p.Gln218=) | |
6 | g.49457790T>G | CA364404273 | MMUT | c.654A>C (p.Gln218His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49457790T= | CA1627395125 | MMUT | c.654A= (p.Gln218=) | |
6 | g.49457791T>A | CA364404275 | MMUT | c.653A>T (p.Gln218Leu) | |
6 | g.49457791T>C | CA358798 | MMUT | c.653A>G (p.Gln218Arg) | ClinVar dbSNP |
6 | g.49457791T>G | CA364404274 | MMUT | c.653A>C (p.Gln218Pro) | |
6 | g.49457791T= | CA1627395138 | MMUT | c.653A= (p.Gln218=) | |
6 | g.49457792G>A | CA3847076 | MMUT | c.652C>T (p.Gln218Ter) | dbSNP ExAC gnomAD v2 |
6 | g.49457792G>C | CA364404276 | MMUT | c.652C>G (p.Gln218Glu) | ClinVar dbSNP |
6 | g.49457792G= | CA1627395151 | MMUT | c.652C= (p.Gln218=) | |
6 | g.49457792G>T | CA364404277 | MMUT | c.652C>A (p.Gln218Lys) | |
6 | g.49457793G>A | CA450608789 | MMUT | c.651C>T (p.Ile217=) | dbSNP |
6 | g.49457793G>C | CA364404278 | MMUT | c.651C>G (p.Ile217Met) | |
6 | g.49457793G= | CA1627395162 | MMUT | c.651C= (p.Ile217=) | |
6 | g.49457793G>T | CA450608790 | MMUT | c.651C>A (p.Ile217=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
6 | g.49457794A= | CA1627395169 | MMUT | c.650T= (p.Ile217=) | |
6 | g.49457794A>C | CA364404279 | MMUT | c.650T>G (p.Ile217Ser) | |
6 | g.49457794A>G | CA364404280 | MMUT | c.650T>C (p.Ile217Thr) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.49457794A>T | CA364404281 | MMUT | c.650T>A (p.Ile217Asn) | |
6 | g.49457795T>A | CA364404282 | MMUT | c.649A>T (p.Ile217Phe) | |
6 | g.49457795T>C | CA364404283 | MMUT | c.649A>G (p.Ile217Val) | |
6 | g.49457795T>G | CA364404284 | MMUT | c.649A>C (p.Ile217Leu) | |
6 | g.49457796G>A | CA3847077 | MMUT | c.648C>T (p.Thr216=) | ClinVar dbSNP ExAC gnomAD v2 |
6 | g.49457796G>C | CA450608791 | MMUT | c.648C>G (p.Thr216=) | |
6 | g.49457796G= | CA1627395171 | MMUT | c.648C= (p.Thr216=) | |
6 | g.49457796G>T | CA450608792 | MMUT | c.648C>A (p.Thr216=) | |
6 | g.49457797G>A | CA364404285 | MMUT | c.647C>T (p.Thr216Ile) | |
6 | g.49457797G>C | CA364404286 | MMUT | c.647C>G (p.Thr216Ser) | |
6 | g.49457797G= | CA1627395174 | MMUT | c.647C= (p.Thr216=) | |
6 | g.49457797G>T | CA364404287 | MMUT | c.647C>A (p.Thr216Asn) | ClinVar dbSNP |
6 | g.49457798T>A | CA364404288 | MMUT | c.646A>T (p.Thr216Ser) | |
6 | g.49457798T>C | CA364404289 | MMUT | c.646A>G (p.Thr216Ala) | |
6 | g.49457798T>G | CA364404290 | MMUT | c.646A>C (p.Thr216Pro) | |
6 | g.49457799A>C | CA450608795 | MMUT | c.645T>G (p.Gly215=) | |
6 | g.49457799A>G | CA450608794 | MMUT | c.645T>C (p.Gly215=) | ClinVar |
6 | g.49457799A>T | CA450608793 | MMUT | c.645T>A (p.Gly215=) | |
6 | g.49457800C>A | CA364404292 | MMUT | c.644G>T (p.Gly215Val) | |
6 | g.49457800C= | CA1627395179 | MMUT | c.644G= (p.Gly215=) | |
6 | g.49457800C>G | CA364404291 | MMUT | c.644G>C (p.Gly215Ala) | |
6 | g.49457800C>T | CA3847078 | MMUT | c.644G>A (p.Gly215Asp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49457801C>A | CA16618294 | MMUT | c.643G>T (p.Gly215Cys) | ClinVar dbSNP gnomAD v4 |
6 | g.49457801C= | CA1627395185 | MMUT | c.643G= (p.Gly215=) | |
6 | g.49457801C>G | CA364404293 | MMUT | c.643G>C (p.Gly215Arg) |