ClinVar Miner

List of variants reported as uncertain significance for Fanconi anemia complementation group G by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 37
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HGVS dbSNP
NM_004629.1(FANCG):c.*101A>G rs751616369
NM_004629.1(FANCG):c.*250C>T rs535188841
NM_004629.1(FANCG):c.-1C>T rs587777946
NM_004629.1(FANCG):c.-311T>A rs886063900
NM_004629.1(FANCG):c.-348A>G rs376750755
NM_004629.1(FANCG):c.-488G>A rs752617227
NM_004629.1(FANCG):c.-491G>A rs886063901
NM_004629.1(FANCG):c.1252G>A (p.Glu418Lys) rs886063896
NM_004629.1(FANCG):c.1538G>A (p.Arg513Gln) rs17885240
NM_004629.1(FANCG):c.1545C>T (p.Ala515=) rs201422773
NM_004629.1(FANCG):c.161dup (p.His55fs) rs886063898
NM_004629.1(FANCG):c.1652A>C (p.Tyr551Ser) rs1447816480
NM_004629.1(FANCG):c.1689G>C (p.Arg563=) rs138855718
NM_004629.1(FANCG):c.1808C>T (p.Ser603Phe) rs17878854
NM_004629.1(FANCG):c.20C>T (p.Ser7Phe) rs35984312
NM_004629.1(FANCG):c.366G>C (p.Trp122Cys) rs546023787
NM_004629.1(FANCG):c.458C>G (p.Ala153Gly)
NM_004629.1(FANCG):c.478G>A (p.Ala160Thr) rs140534765
NM_004629.1(FANCG):c.880G>A (p.Gly294Arg) rs886063897
NM_004629.1(FANCG):c.957G>A (p.Pro319=) rs145092954
NM_004629.2(FANCG):c.*141A>G
NM_004629.2(FANCG):c.*77C>T
NM_004629.2(FANCG):c.-276G>A
NM_004629.2(FANCG):c.-56G>A
NM_004629.2(FANCG):c.1002A>T (p.Leu334=)
NM_004629.2(FANCG):c.1027C>G (p.Gln343Glu)
NM_004629.2(FANCG):c.1152A>C (p.Pro384=)
NM_004629.2(FANCG):c.1155C>T (p.Pro385=)
NM_004629.2(FANCG):c.1157C>A (p.Pro386His)
NM_004629.2(FANCG):c.1345C>T (p.Pro449Ser)
NM_004629.2(FANCG):c.1434-6C>T
NM_004629.2(FANCG):c.1448T>C (p.Leu483Pro)
NM_004629.2(FANCG):c.292C>A (p.Arg98=)
NM_004629.2(FANCG):c.724C>T (p.Arg242Trp)
NM_004629.2(FANCG):c.794C>T (p.Ala265Val)
NM_004629.2(FANCG):c.944G>A (p.Ser315Asn)
NM_004629.2(FANCG):c.999C>T (p.Asp333=)

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