ClinVar Miner

List of variants in gene KIF1A reported as likely benign by Ambry Genetics

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Gene type:
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Total variants: 37
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HGVS dbSNP
NM_004321.7(KIF1A):c.1011C>T (p.Asn337=) rs1485121388
NM_004321.7(KIF1A):c.1110C>T (p.Arg370=) rs369641508
NM_004321.7(KIF1A):c.1410C>T (p.Ala470=) rs375180690
NM_004321.7(KIF1A):c.1569C>T (p.Gly523=)
NM_004321.7(KIF1A):c.204G>T (p.Ala68=) rs141052770
NM_004321.7(KIF1A):c.2595C>G (p.Pro865=) rs140783695
NM_004321.7(KIF1A):c.2631C>T (p.Gly877=) rs751977290
NM_004321.7(KIF1A):c.2655G>C (p.Val885=) rs186881889
NM_004321.7(KIF1A):c.2782G>A (p.Val928Met) rs183359489
NM_004321.7(KIF1A):c.2829C>A (p.Ile943=) rs373045276
NM_004321.7(KIF1A):c.2956C>T (p.Pro986Ser) rs143037290
NM_004321.7(KIF1A):c.297G>A (p.Thr99=)
NM_004321.7(KIF1A):c.2985C>T (p.Arg995=)
NM_004321.7(KIF1A):c.3027G>A (p.Ala1009=) rs200149062
NM_004321.7(KIF1A):c.3030C>T (p.Ser1010=)
NM_004321.7(KIF1A):c.3042C>G (p.Ala1014=) rs370286749
NM_004321.7(KIF1A):c.3273C>T (p.Asp1091=)
NM_004321.7(KIF1A):c.3369G>A (p.Arg1123=) rs371024769
NM_004321.7(KIF1A):c.3549T>C (p.His1183=) rs184931664
NM_004321.7(KIF1A):c.3585C>T (p.Arg1195=) rs144520412
NM_004321.7(KIF1A):c.3627C>T (p.Asp1209=)
NM_004321.7(KIF1A):c.3633C>A (p.Ser1211=)
NM_004321.7(KIF1A):c.4071C>T (p.Gly1357=) rs375309925
NM_004321.7(KIF1A):c.411C>T (p.Asn137=) rs1447851714
NM_004321.7(KIF1A):c.4278C>T (p.Ser1426=) rs373703367
NM_004321.7(KIF1A):c.4301C>T (p.Ala1434Val) rs141441058
NM_004321.7(KIF1A):c.4446C>T (p.Ser1482=) rs371737085
NM_004321.7(KIF1A):c.4548C>T (p.Tyr1516=) rs202049905
NM_004321.7(KIF1A):c.4614G>A (p.Leu1538=) rs187810230
NM_004321.7(KIF1A):c.4740G>A (p.Gly1580=) rs143815273
NM_004321.7(KIF1A):c.4767G>A (p.Thr1589=) rs201733233
NM_004321.7(KIF1A):c.4929G>A (p.Ala1643=)
NM_004321.7(KIF1A):c.654C>T (p.His218=)
NM_004321.7(KIF1A):c.657C>T (p.Ala219=) rs531993959
NM_004321.7(KIF1A):c.693C>T (p.Asp231=) rs772411022
NM_004321.7(KIF1A):c.849C>T (p.Ser283=) rs187442951
NM_004321.7(KIF1A):c.927C>T (p.Ser309=)

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