ClinVar Miner

List of variants in gene ALDH7A1 reported as uncertain significance by Invitae

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Total variants: 41
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HGVS dbSNP
NM_001182.4(ALDH7A1):c.1010T>G (p.Phe337Cys) rs747834606
NM_001182.4(ALDH7A1):c.1046G>C (p.Arg349Thr) rs553114356
NM_001182.4(ALDH7A1):c.1084C>T (p.Pro362Ser) rs532800318
NM_001182.4(ALDH7A1):c.1163C>G (p.Ala388Gly)
NM_001182.4(ALDH7A1):c.119C>G (p.Ala40Gly)
NM_001182.4(ALDH7A1):c.1301A>G (p.Tyr434Cys) rs747597620
NM_001182.4(ALDH7A1):c.1356A>C (p.Lys452Asn)
NM_001182.4(ALDH7A1):c.1451A>G (p.Asn484Ser)
NM_001182.4(ALDH7A1):c.1520A>C (p.Glu507Ala) rs80049945
NM_001182.4(ALDH7A1):c.154G>C (p.Glu52Gln) rs765562932
NM_001182.4(ALDH7A1):c.1559C>T (p.Ser520Phe) rs1554097854
NM_001182.4(ALDH7A1):c.16C>T (p.Arg6Cys)
NM_001182.4(ALDH7A1):c.203C>A (p.Thr68Asn) rs58528748
NM_001182.4(ALDH7A1):c.20C>T (p.Ala7Val)
NM_001182.4(ALDH7A1):c.246+6A>T rs759910341
NM_001182.4(ALDH7A1):c.247G>A (p.Ala83Thr)
NM_001182.4(ALDH7A1):c.263A>T (p.Tyr88Phe) rs376294954
NM_001182.4(ALDH7A1):c.283G>A (p.Ala95Thr)
NM_001182.4(ALDH7A1):c.31_33delCACinsGAG (p.His11Glu) rs796052269
NM_001182.4(ALDH7A1):c.354C>T (p.Gly118=) rs149228266
NM_001182.4(ALDH7A1):c.355G>A (p.Asp119Asn) rs1212969829
NM_001182.4(ALDH7A1):c.359C>G (p.Ala120Gly) rs549279821
NM_001182.4(ALDH7A1):c.364C>T (p.Arg122Trp) rs370624118
NM_001182.4(ALDH7A1):c.542A>G (p.Gln181Arg) rs796052257
NM_001182.4(ALDH7A1):c.553G>A (p.Val185Ile) rs61757685
NM_001182.4(ALDH7A1):c.553G>T (p.Val185Leu) rs61757685
NM_001182.4(ALDH7A1):c.56C>T (p.Ser19Phe) rs566243475
NM_001182.4(ALDH7A1):c.575C>T (p.Thr192Met) rs376917645
NM_001182.4(ALDH7A1):c.577G>A (p.Ala193Thr) rs773503933
NM_001182.4(ALDH7A1):c.664A>G (p.Thr222Ala) rs777829351
NM_001182.4(ALDH7A1):c.682G>A (p.Val228Met) rs201832111
NM_001182.4(ALDH7A1):c.686C>T (p.Ala229Val) rs1473102872
NM_001182.4(ALDH7A1):c.79G>C (p.Ala27Pro) rs1060502950
NM_001182.4(ALDH7A1):c.8G>A (p.Arg3His) rs759866910
NM_001182.4(ALDH7A1):c.8G>T (p.Arg3Leu) rs759866910
NM_001182.4(ALDH7A1):c.914C>G (p.Ala305Gly) rs141775154
NM_001182.4(ALDH7A1):c.936C>G (p.Ser312Arg)
NM_001182.4(ALDH7A1):c.952G>A (p.Ala318Thr)
NM_001182.4(ALDH7A1):c.952G>C (p.Ala318Pro) rs936151635
NM_001182.4(ALDH7A1):c.987G>T (p.Arg329Ser)
NM_001182.4(ALDH7A1):c.995C>G (p.Thr332Ser)

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