List of variants in gene FANCA reported as uncertain significance by Counsyl

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 44

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.623C>T (p.Ser208Leu)	rs144420697	0.00325
NM_000135.4(FANCA):c.1549C>T (p.Arg517Trp)	rs587778309	0.00011
NM_000135.4(FANCA):c.3069G>T (p.Glu1023Asp)	rs373986283	0.00008
NM_000135.4(FANCA):c.3349-3C>T	rs373861415	0.00006
NM_000135.4(FANCA):c.1510C>T (p.Arg504Cys)	rs200291237	0.00004
NM_000135.4(FANCA):c.2567T>C (p.Leu856Ser)	rs370085403	0.00004
NM_000135.4(FANCA):c.2944A>G (p.Thr982Ala)	rs587778317	0.00003
NM_000135.4(FANCA):c.3761A>T (p.Glu1254Val)	rs750773229	0.00003
NM_000135.4(FANCA):c.457C>G (p.Gln153Glu)	rs774448881	0.00003
NM_000135.4(FANCA):c.553C>A (p.Leu185Ile)	rs587778323	0.00003
NM_000135.4(FANCA):c.1038G>C (p.Trp346Cys)	rs750257902	0.00002
NM_000135.4(FANCA):c.2008C>T (p.Arg670Cys)	rs587778312	0.00002
NM_000135.4(FANCA):c.3316G>A (p.Glu1106Lys)	rs777825824	0.00002
NM_000135.4(FANCA):c.3482C>T (p.Thr1161Met)	rs142833057	0.00002
NM_000135.4(FANCA):c.2582C>T (p.Ser861Phe)	rs980582362	0.00001
NM_000135.4(FANCA):c.2903C>T (p.Ser968Leu)	rs779162871	0.00001
NM_000135.4(FANCA):c.2941T>C (p.Cys981Arg)	rs191943709	0.00001
NM_000135.4(FANCA):c.343G>A (p.Gly115Arg)	rs769824282	0.00001
NM_000135.4(FANCA):c.793-3C>G	rs749688050	0.00001
NM_000135.4(FANCA):c.839C>T (p.Ala280Val)	rs767092317	0.00001
NM_000135.4(FANCA):c.1273G>C (p.Asp425His)	rs1555561398
NM_000135.4(FANCA):c.1304G>T (p.Arg435Leu)	rs1060501879
NM_000135.4(FANCA):c.1360-16_1363dup	rs1555556321
NM_000135.4(FANCA):c.1475A>G (p.His492Arg)	rs925457555
NM_000135.4(FANCA):c.1566+2C>T	rs1316950815
NM_000135.4(FANCA):c.1625A>T (p.Glu542Val)	rs587778310
NM_000135.4(FANCA):c.1682C>T (p.Thr561Met)	rs148154682
NM_000135.4(FANCA):c.168_173del (p.Leu57_Asn58del)	rs1060501881
NM_000135.4(FANCA):c.1776+7A>G	rs1555552070
NM_000135.4(FANCA):c.2492TCT[1] (p.Phe832del)	rs1310756192
NM_000135.4(FANCA):c.2519C>G (p.Ala840Gly)	rs587778313
NM_000135.4(FANCA):c.2593A>G (p.Ile865Val)	rs878853662
NM_000135.4(FANCA):c.2859C>A (p.Asp953Glu)	rs149112292
NM_000135.4(FANCA):c.2959G>C (p.Ala987Pro)	rs752735858
NM_000135.4(FANCA):c.2982C>G (p.Ser994Arg)	rs1555540072
NM_000135.4(FANCA):c.3164G>T (p.Arg1055Leu)	rs1429943036
NM_000135.4(FANCA):c.3359_3361del (p.Cys1120del)	rs1314042335
NM_000135.4(FANCA):c.3422C>A (p.Ala1141Asp)	rs587778318
NM_000135.4(FANCA):c.3602AAG[1] (p.Glu1202del)	rs1380850249
NM_000135.4(FANCA):c.3703CAA[1] (p.Gln1236del)	rs1555535513
NM_000135.4(FANCA):c.3725_3727del (p.Ile1242del)	rs1441710252
NM_000135.4(FANCA):c.752C>T (p.Ser251Leu)	rs878853666
NM_000135.4(FANCA):c.964C>T (p.His322Tyr)	rs772768595
NM_000135.4(FANCA):c.971T>G (p.Leu324Arg)	rs1447363475

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