ClinVar Miner

List of variants in gene TRAPPC11 reported as uncertain significance for Inborn genetic diseases

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Gene type:
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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_021942.6(TRAPPC11):c.2851+5G>A rs373713956 0.00034
NM_021942.6(TRAPPC11):c.1901A>G (p.Asn634Ser) rs148567547 0.00026
NM_021942.6(TRAPPC11):c.3086C>T (p.Ser1029Leu) rs201494083 0.00014
NM_021942.6(TRAPPC11):c.1654G>A (p.Asp552Asn) rs374195797 0.00013
NM_021942.6(TRAPPC11):c.151A>G (p.Ile51Val) rs141053214 0.00009
NM_021942.6(TRAPPC11):c.1766A>G (p.Gln589Arg) rs146053783 0.00009
NM_021942.6(TRAPPC11):c.1058C>G (p.Ala353Gly) rs200078740 0.00006
NM_021942.6(TRAPPC11):c.1244G>A (p.Gly415Glu) rs150383310 0.00006
NM_021942.6(TRAPPC11):c.1337A>G (p.Tyr446Cys) rs149572534 0.00003
NM_021942.6(TRAPPC11):c.2749C>T (p.Leu917Phe) rs554771345 0.00003
NM_021942.6(TRAPPC11):c.3029A>T (p.Glu1010Val) rs773678506 0.00003
NM_021942.6(TRAPPC11):c.899A>T (p.Asp300Val) rs768253464 0.00003
NM_021942.6(TRAPPC11):c.3002T>A (p.Val1001Asp) rs200989029 0.00002
NM_021942.6(TRAPPC11):c.1135C>T (p.Pro379Ser) rs201932605 0.00001
NM_021942.6(TRAPPC11):c.143G>A (p.Arg48Gln) rs1473309875 0.00001
NM_021942.6(TRAPPC11):c.2678A>G (p.Lys893Arg) rs759008736 0.00001
NM_021942.6(TRAPPC11):c.779A>G (p.His260Arg) rs764083534 0.00001
NM_021942.6(TRAPPC11):c.1079G>A (p.Arg360Gln)
NM_021942.6(TRAPPC11):c.1214A>G (p.Asp405Gly)
NM_021942.6(TRAPPC11):c.1217T>G (p.Leu406Arg)
NM_021942.6(TRAPPC11):c.1361A>C (p.His454Pro)
NM_021942.6(TRAPPC11):c.1374G>T (p.Gln458His)
NM_021942.6(TRAPPC11):c.1493C>G (p.Thr498Arg)
NM_021942.6(TRAPPC11):c.1747G>A (p.Asp583Asn)
NM_021942.6(TRAPPC11):c.1958C>T (p.Thr653Ile)
NM_021942.6(TRAPPC11):c.1987A>G (p.Lys663Glu)
NM_021942.6(TRAPPC11):c.2077A>C (p.Asn693His) rs374682349
NM_021942.6(TRAPPC11):c.2147C>A (p.Ala716Asp) rs143990563
NM_021942.6(TRAPPC11):c.2530C>T (p.Arg844Cys) rs149626892
NM_021942.6(TRAPPC11):c.2563G>A (p.Val855Ile)
NM_021942.6(TRAPPC11):c.2632G>A (p.Glu878Lys)
NM_021942.6(TRAPPC11):c.2666A>C (p.Asp889Ala)
NM_021942.6(TRAPPC11):c.2744C>T (p.Thr915Met)
NM_021942.6(TRAPPC11):c.2851+5G>T
NM_021942.6(TRAPPC11):c.3164C>T (p.Ala1055Val)
NM_021942.6(TRAPPC11):c.3309C>A (p.Phe1103Leu)
NM_021942.6(TRAPPC11):c.445+4T>A
NM_021942.6(TRAPPC11):c.557T>C (p.Ile186Thr)
NM_021942.6(TRAPPC11):c.830A>G (p.Lys277Arg)
NM_021942.6(TRAPPC11):c.917T>C (p.Ile306Thr)
NM_021942.6(TRAPPC11):c.979G>C (p.Gly327Arg)

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