ClinVar Miner

List of variants in gene GPD1L reported as likely benign by Ambry Genetics

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Gene type:
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Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_015141.4(GPD1L):c.370A>G (p.Ile124Val) rs72552293 0.00291
NM_015141.4(GPD1L):c.981G>A (p.Val327=) rs144877595 0.00195
NM_015141.4(GPD1L):c.659G>A (p.Arg220His) rs72546648 0.00130
NM_015141.4(GPD1L):c.520G>A (p.Glu174Lys) rs112122950 0.00034
NM_015141.4(GPD1L):c.813G>T (p.Arg271=) rs35464343 0.00031
NM_015141.4(GPD1L):c.459C>T (p.Asn153=) rs375532052 0.00019
NM_015141.4(GPD1L):c.467A>G (p.Asn156Ser) rs139494055 0.00019
NM_015141.4(GPD1L):c.1038C>T (p.Ser346=) rs147092668 0.00016
NM_015141.4(GPD1L):c.445C>T (p.Leu149=) rs146738300 0.00015
NM_015141.4(GPD1L):c.837C>T (p.Phe279=) rs376724853 0.00013
NM_015141.4(GPD1L):c.192A>G (p.Lys64=) rs72546651 0.00011
NM_015141.4(GPD1L):c.876G>A (p.Glu292=) rs72546642 0.00010
NM_015141.4(GPD1L):c.555T>A (p.Thr185=) rs151196281 0.00009
NM_015141.4(GPD1L):c.897C>T (p.Leu299=) rs192905901 0.00009
NM_015141.4(GPD1L):c.906G>A (p.Pro302=) rs200045526 0.00009
NM_015141.4(GPD1L):c.870G>T (p.Glu290Asp) rs751812984 0.00008
NM_015141.4(GPD1L):c.951A>G (p.Leu317=) rs746611202 0.00008
NM_015141.4(GPD1L):c.651C>T (p.Asp217=) rs149641866 0.00006
NM_015141.4(GPD1L):c.996C>T (p.Tyr332=) rs149423659 0.00006
NM_015141.4(GPD1L):c.246C>T (p.Ser82=) rs377378878 0.00004
NM_015141.4(GPD1L):c.817C>T (p.Arg273Cys) rs72552294 0.00004
NM_015141.4(GPD1L):c.132A>G (p.Glu44=) rs200273033 0.00002
NM_015141.4(GPD1L):c.54A>G (p.Ser18=) rs147773109 0.00002
NM_015141.4(GPD1L):c.774C>T (p.Cys258=) rs753955088 0.00002
NM_015141.4(GPD1L):c.232A>G (p.Met78Val) rs762018216 0.00001
NM_015141.4(GPD1L):c.291C>T (p.His97=) rs1007252272 0.00001
NM_015141.4(GPD1L):c.384C>T (p.Pro128=) rs779990114 0.00001
NM_015141.4(GPD1L):c.810G>A (p.Gly270=) rs945877751 0.00001
NM_015141.4(GPD1L):c.822G>A (p.Arg274=) rs759180118 0.00001
NM_015141.4(GPD1L):c.1008A>T (p.Pro336=)
NM_015141.4(GPD1L):c.1035G>T (p.Gln345His) rs780760018
NM_015141.4(GPD1L):c.1053A>G (p.Thr351=)
NM_015141.4(GPD1L):c.105C>T (p.Ala35=)
NM_015141.4(GPD1L):c.189A>G (p.Val63=)
NM_015141.4(GPD1L):c.195T>C (p.Tyr65=) rs1700540170
NM_015141.4(GPD1L):c.345G>A (p.Ala115=) rs149167213
NM_015141.4(GPD1L):c.345G>T (p.Ala115=) rs149167213
NM_015141.4(GPD1L):c.411C>A (p.Ile137=)
NM_015141.4(GPD1L):c.48-4G>A
NM_015141.4(GPD1L):c.480A>C (p.Ala160=)
NM_015141.4(GPD1L):c.504C>T (p.Ile168=)
NM_015141.4(GPD1L):c.528C>A (p.Gly176=)
NM_015141.4(GPD1L):c.570T>C (p.Ile190=)
NM_015141.4(GPD1L):c.573C>T (p.Thr191=)
NM_015141.4(GPD1L):c.603C>G (p.Leu201=)
NM_015141.4(GPD1L):c.612G>A (p.Ala204=)
NM_015141.4(GPD1L):c.639T>G (p.Ala213=)
NM_015141.4(GPD1L):c.648C>T (p.Cys216=)
NM_015141.4(GPD1L):c.763C>G (p.Leu255Val)
NM_015141.4(GPD1L):c.783C>T (p.Ala261=)
NM_015141.4(GPD1L):c.813G>A (p.Arg271=) rs35464343
NM_015141.4(GPD1L):c.861A>G (p.Glu287=)
NM_015141.4(GPD1L):c.936C>G (p.Leu312=)
NM_015141.4(GPD1L):c.967T>C (p.Leu323=)
NM_015141.4(GPD1L):c.978A>C (p.Ala326=) rs1553663699

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