ClinVar Miner

List of variants in gene TRAIP reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 77
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HGVS dbSNP gnomAD frequency
NM_005879.3(TRAIP):c.303G>A (p.Gln101=) rs145932323 0.00538
NM_005879.3(TRAIP):c.1067T>C (p.Ile356Thr) rs145654028 0.00083
NM_005879.3(TRAIP):c.323G>A (p.Arg108Gln) rs186312616 0.00039
NM_005879.3(TRAIP):c.1407G>A (p.Ser469=) rs146951959 0.00036
NM_005879.3(TRAIP):c.1344G>A (p.Gln448=) rs144112402 0.00016
NM_005879.3(TRAIP):c.1287+10T>C rs370712427 0.00013
NM_005879.3(TRAIP):c.1038-7C>T rs535151842 0.00007
NM_005879.3(TRAIP):c.603T>C (p.Cys201=) rs531391341 0.00006
NM_005879.3(TRAIP):c.1248C>T (p.Gly416=) rs771177157 0.00001
NM_005879.3(TRAIP):c.1004G>T (p.Gly335Val) rs144992965
NM_005879.3(TRAIP):c.1011C>T (p.Tyr337=)
NM_005879.3(TRAIP):c.1032G>A (p.Lys344=)
NM_005879.3(TRAIP):c.1037+11G>A
NM_005879.3(TRAIP):c.1037+9T>C
NM_005879.3(TRAIP):c.1044A>G (p.Pro348=)
NM_005879.3(TRAIP):c.1056C>T (p.Val352=)
NM_005879.3(TRAIP):c.1086+17A>G
NM_005879.3(TRAIP):c.1086+8C>G
NM_005879.3(TRAIP):c.1131A>C (p.Pro377=)
NM_005879.3(TRAIP):c.1158T>C (p.Pro386=)
NM_005879.3(TRAIP):c.1206C>G (p.Pro402=)
NM_005879.3(TRAIP):c.1236+10G>A
NM_005879.3(TRAIP):c.1236+14C>T
NM_005879.3(TRAIP):c.1237-20A>G
NM_005879.3(TRAIP):c.1242G>A (p.Arg414=)
NM_005879.3(TRAIP):c.1260C>T (p.Leu420=)
NM_005879.3(TRAIP):c.1288-14G>A
NM_005879.3(TRAIP):c.1288-4C>T
NM_005879.3(TRAIP):c.1317T>C (p.Pro439=)
NM_005879.3(TRAIP):c.1335G>A (p.Lys445=)
NM_005879.3(TRAIP):c.156+10T>C
NM_005879.3(TRAIP):c.156+8T>A
NM_005879.3(TRAIP):c.157-11C>T
NM_005879.3(TRAIP):c.157-15del
NM_005879.3(TRAIP):c.157-4C>A
NM_005879.3(TRAIP):c.240+17T>C
NM_005879.3(TRAIP):c.241-14G>C
NM_005879.3(TRAIP):c.241-20T>A
NM_005879.3(TRAIP):c.280+17C>T
NM_005879.3(TRAIP):c.280+18G>A
NM_005879.3(TRAIP):c.281-11C>T
NM_005879.3(TRAIP):c.281-20G>A
NM_005879.3(TRAIP):c.301C>G (p.Gln101Glu)
NM_005879.3(TRAIP):c.330G>A (p.Thr110=)
NM_005879.3(TRAIP):c.345T>C (p.Asn115=)
NM_005879.3(TRAIP):c.409-6C>T
NM_005879.3(TRAIP):c.470G>A (p.Arg157His)
NM_005879.3(TRAIP):c.503+12G>A
NM_005879.3(TRAIP):c.504-13G>A
NM_005879.3(TRAIP):c.513T>G (p.Leu171=)
NM_005879.3(TRAIP):c.51C>A (p.Ser17=)
NM_005879.3(TRAIP):c.54C>G (p.Arg18=)
NM_005879.3(TRAIP):c.54C>T (p.Arg18=)
NM_005879.3(TRAIP):c.579G>A (p.Ala193=)
NM_005879.3(TRAIP):c.617+15C>A
NM_005879.3(TRAIP):c.618-10C>T
NM_005879.3(TRAIP):c.624C>T (p.Tyr208=)
NM_005879.3(TRAIP):c.663G>T (p.Val221=)
NM_005879.3(TRAIP):c.706-14A>G
NM_005879.3(TRAIP):c.706-8_706-5del
NM_005879.3(TRAIP):c.729G>A (p.Leu243=)
NM_005879.3(TRAIP):c.72C>T (p.His24=)
NM_005879.3(TRAIP):c.744A>G (p.Leu248=)
NM_005879.3(TRAIP):c.796-15C>T
NM_005879.3(TRAIP):c.796-9C>T
NM_005879.3(TRAIP):c.816G>A (p.Thr272=)
NM_005879.3(TRAIP):c.81C>T (p.His27=)
NM_005879.3(TRAIP):c.864C>T (p.Val288=)
NM_005879.3(TRAIP):c.885-12C>G
NM_005879.3(TRAIP):c.885-17G>C
NM_005879.3(TRAIP):c.898G>A (p.Glu300Lys)
NM_005879.3(TRAIP):c.924A>G (p.Pro308=)
NM_005879.3(TRAIP):c.927C>T (p.Ser309=)
NM_005879.3(TRAIP):c.945T>C (p.Asp315=)
NM_005879.3(TRAIP):c.98+9C>T
NM_005879.3(TRAIP):c.99-14G>C
NM_005879.3(TRAIP):c.996C>T (p.Ser332=)

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