ClinVar Miner

List of variants in gene ALG13 reported as uncertain significance by Ambry Genetics

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Gene type:
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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_001099922.3(ALG13):c.104A>G (p.Asn35Ser) rs149808406 0.00035
NM_001099922.3(ALG13):c.13T>C (p.Phe5Leu) rs199754211 0.00014
NM_001099922.3(ALG13):c.1313C>A (p.Thr438Lys) rs367783946 0.00013
NM_001099922.3(ALG13):c.1277A>G (p.Asn426Ser) rs1208820400 0.00009
NM_001099922.3(ALG13):c.756T>G (p.Phe252Leu) rs915629293 0.00007
NM_001099922.3(ALG13):c.880C>G (p.Pro294Ala) rs753556936 0.00005
NM_001099922.3(ALG13):c.350A>T (p.His117Leu) rs754497897 0.00004
NM_001099922.3(ALG13):c.1822G>C (p.Asp608His) rs374870130 0.00002
NM_001099922.3(ALG13):c.1619C>T (p.Ala540Val) rs1234385710 0.00001
NM_001099922.3(ALG13):c.245-4G>T rs761270344 0.00001
NM_001099922.3(ALG13):c.2573A>G (p.Asn858Ser) rs756238772 0.00001
NM_001099922.3(ALG13):c.2758C>A (p.Pro920Thr) rs748792396 0.00001
NM_001099922.3(ALG13):c.3278C>T (p.Ser1093Phe) rs1465704791 0.00001
NM_001099922.3(ALG13):c.3406G>T (p.Gly1136Cys) rs376207448 0.00001
NM_001099922.3(ALG13):c.652A>G (p.Asn218Asp) rs886042566 0.00001
NM_001099922.3(ALG13):c.916C>G (p.Leu306Val) rs1248942119 0.00001
NM_001099922.3(ALG13):c.-1C>T
NM_001099922.3(ALG13):c.1310G>C (p.Gly437Ala)
NM_001099922.3(ALG13):c.1709G>A (p.Gly570Glu)
NM_001099922.3(ALG13):c.1831C>G (p.Leu611Val) rs199505558
NM_001099922.3(ALG13):c.1838C>G (p.Pro613Arg)
NM_001099922.3(ALG13):c.2106T>G (p.Ser702Arg) rs797044876
NM_001099922.3(ALG13):c.2351A>C (p.Asn784Thr)
NM_001099922.3(ALG13):c.3330A>T (p.Gln1110His)
NM_001099922.3(ALG13):c.3370G>A (p.Ala1124Thr)
NM_001099922.3(ALG13):c.344A>G (p.Gln115Arg)
NM_001099922.3(ALG13):c.869G>A (p.Arg290Gln) rs1939809151
NM_001099922.3(ALG13):c.952C>T (p.Arg318Cys) rs775191661

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