ClinVar Miner

List of variants in gene FANCE reported as likely benign for Fanconi anemia complementation group E

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP
NM_021922.2(FANCE):c.1053T>G (p.Leu351=) rs755165473
NM_021922.2(FANCE):c.1278G>A (p.Met426Ile) rs758380315
NM_021922.2(FANCE):c.1316+10C>T rs200479051
NM_021922.2(FANCE):c.1333C>T (p.Pro445Ser) rs141551053
NM_021922.2(FANCE):c.1509C>T (p.Asn503=) rs147166240
NM_021922.2(FANCE):c.1572G>A (p.Arg524=) rs115195341
NM_021922.2(FANCE):c.210G>A (p.Glu70=) rs1008512809
NM_021922.2(FANCE):c.284A>G (p.Gln95Arg) rs149097636
NM_021922.2(FANCE):c.52C>T (p.Pro18Ser) rs552241929
NM_021922.2(FANCE):c.552A>C (p.Pro184=) rs138182352
NM_021922.2(FANCE):c.561A>G (p.Glu187=) rs1554121329
NM_021922.2(FANCE):c.696G>A (p.Glu232=) rs147356927
NM_021922.2(FANCE):c.798G>A (p.Ser266=) rs746542545
NM_021922.2(FANCE):c.999C>T (p.Leu333=) rs776082827
NM_021922.3(FANCE):c.1114-4G>A rs368422520
NM_021922.3(FANCE):c.792C>T (p.Asp264=) rs758132363

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