Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.38414872A>TCA370730499FGFR1c.1884T>A (p.Asn628Lys)
c.1872T>A (p.Asn624Lys)
n.2777T>A
n.706T>A
n.574T>A
c.2064T>A (p.Asn688Lys)
n.2572T>A
c.1605T>A (p.Asn535Lys)
c.*1530T>A (n.*1530T>A)
c.*1851T>A (n.*1851T>A)
n.3378T>A
c.1611T>A (p.Asn537Lys)
c.1854T>A (p.Asn618Lys)
c.*934T>A (n.*934T>A)
c.1617T>A (p.Asn539Lys)
c.1878T>A (p.Asn626Lys)
c.1977T>A (p.Asn659Lys)
n.4163T>A
n.1406T>A
c.84T>A (p.Asn28Lys)
n.430T>A
c.*779T>A (n.*779T>A)
c.1860T>A (p.Asn620Lys)
c.1983T>A (p.Asn661Lys)
c.1716T>A (p.Asn572Lys)
c.1710T>A (p.Asn570Lys)
c.1593T>A (p.Asn531Lys)
c.1971T>A (p.Asn657Lys)
c.1704T>A (p.Asn568Lys)
c.912T>A (p.Asn304Lys)
n.2157T>A
 dbSNP
8g.38414872A>CCA357150FGFR1c.1884T>G (p.Asn628Lys)
c.1872T>G (p.Asn624Lys)
n.2777T>G
n.706T>G
n.574T>G
c.2064T>G (p.Asn688Lys)
n.2572T>G
c.1605T>G (p.Asn535Lys)
c.*1530T>G (n.*1530T>G)
c.*1851T>G (n.*1851T>G)
n.3378T>G
c.1611T>G (p.Asn537Lys)
c.1854T>G (p.Asn618Lys)
c.*934T>G (n.*934T>G)
c.1617T>G (p.Asn539Lys)
c.1878T>G (p.Asn626Lys)
c.1977T>G (p.Asn659Lys)
n.4163T>G
n.1406T>G
c.84T>G (p.Asn28Lys)
n.430T>G
c.*779T>G (n.*779T>G)
c.1860T>G (p.Asn620Lys)
c.1983T>G (p.Asn661Lys)
c.1716T>G (p.Asn572Lys)
c.1710T>G (p.Asn570Lys)
c.1593T>G (p.Asn531Lys)
c.1971T>G (p.Asn657Lys)
c.1704T>G (p.Asn568Lys)
c.912T>G (p.Asn304Lys)
n.2157T>G
 ClinVar dbSNP
8g.38414872A>GCA460395884FGFR1c.1884T>C (p.Asn628=)
c.1872T>C (p.Asn624=)
n.2777T>C
n.706T>C
n.574T>C
c.2064T>C (p.Asn688=)
n.2572T>C
c.1605T>C (p.Asn535=)
c.*1530T>C (n.*1530T>C)
c.*1851T>C (n.*1851T>C)
n.3378T>C
c.1611T>C (p.Asn537=)
c.1854T>C (p.Asn618=)
c.*934T>C (n.*934T>C)
c.1617T>C (p.Asn539=)
c.1878T>C (p.Asn626=)
c.1977T>C (p.Asn659=)
n.4163T>C
n.1406T>C
c.84T>C (p.Asn28=)
n.430T>C
c.*779T>C (n.*779T>C)
c.1860T>C (p.Asn620=)
c.1983T>C (p.Asn661=)
c.1716T>C (p.Asn572=)
c.1710T>C (p.Asn570=)
c.1593T>C (p.Asn531=)
c.1971T>C (p.Asn657=)
c.1704T>C (p.Asn568=)
c.912T>C (p.Asn304=)
n.2157T>C
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched