Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.156880036C>GCA342940308NTRK1c.1904C>G (p.Pro635Arg)
c.*676C>G (n.*676C>G)
c.2084C>G (p.Pro695Arg)
c.52C>G
c.2075C>G (p.Pro692Arg)
c.2066C>G (p.Pro689Arg)
c.1976C>G (p.Pro659Arg)
n.2537C>G
n.36C>G
dbSNP
1g.156880036C>ACA342940307NTRK1c.1904C>A (p.Pro635Gln)
c.*676C>A (n.*676C>A)
c.2084C>A (p.Pro695Gln)
c.52C>A
c.2075C>A (p.Pro692Gln)
c.2066C>A (p.Pro689Gln)
c.1976C>A (p.Pro659Gln)
n.2537C>A
n.36C>A
dbSNP
1g.156880036C>TCA256288NTRK1c.1904C>T (p.Pro635Leu)
c.*676C>T (n.*676C>T)
c.2084C>T (p.Pro695Leu)
c.52C>T
c.2075C>T (p.Pro692Leu)
c.2066C>T (p.Pro689Leu)
c.1976C>T (p.Pro659Leu)
n.2537C>T
n.36C>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
1g.156880036C=CA1141581096NTRK1c.1904C= (p.Pro635=)
c.*676C= (n.*676C=)
c.2084C= (p.Pro695=)
c.52C=
c.2075C= (p.Pro692=)
c.2066C= (p.Pro689=)
c.1976C= (p.Pro659=)
n.2537C=
n.36C=
dbSNP

Number of alleles fetched