ClinVar Miner

List of variants in gene GATAD1 reported as uncertain significance for cardiovascular disorder

Included ClinVar conditions (1435):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_021167.5(GATAD1):c.604G>A (p.Ala202Thr) rs564747350 0.00048
NM_021167.5(GATAD1):c.512G>A (p.Arg171Lys) rs540654499 0.00011
NM_021167.5(GATAD1):c.375+3A>G rs1227573993 0.00007
NM_021167.5(GATAD1):c.766A>G (p.Thr256Ala) rs778560008 0.00007
NM_021167.5(GATAD1):c.770C>T (p.Pro257Leu) rs145306938 0.00006
NM_021167.5(GATAD1):c.578C>G (p.Ser193Cys) rs780188711 0.00005
NM_021167.5(GATAD1):c.721C>T (p.Pro241Ser) rs779832718 0.00005
NM_021167.5(GATAD1):c.646A>T (p.Met216Leu) rs778197140 0.00004
NM_021167.5(GATAD1):c.524A>G (p.Gln175Arg) rs145592666 0.00003
NM_021167.5(GATAD1):c.539A>T (p.Glu180Val) rs764831879 0.00003
NM_021167.5(GATAD1):c.406A>G (p.Ile136Val) rs200665705 0.00002
NM_021167.5(GATAD1):c.613A>G (p.Ile205Val) rs794729022 0.00002
NM_021167.5(GATAD1):c.299A>G (p.Tyr100Cys) rs200072145 0.00001
NM_021167.5(GATAD1):c.308C>T (p.Ala103Val) rs374329900 0.00001
NM_021167.5(GATAD1):c.311C>T (p.Pro104Leu) rs768140033 0.00001
NM_021167.5(GATAD1):c.431A>G (p.Tyr144Cys) rs200584566 0.00001
NM_021167.5(GATAD1):c.466T>G (p.Ser156Ala) rs754965302 0.00001
NM_021167.5(GATAD1):c.515G>C (p.Gly172Ala) rs1237515001 0.00001
NM_021167.5(GATAD1):c.611A>G (p.Tyr204Cys) rs922487847 0.00001
NC_000007.13:g.(?_92077044)_(92085876_?)del
NM_021167.5(GATAD1):c.288A>T (p.Arg96Ser)
NM_021167.5(GATAD1):c.307G>T (p.Ala103Ser) rs1789290199
NM_021167.5(GATAD1):c.311_312delinsAA (p.Pro104Gln) rs1789291007
NM_021167.5(GATAD1):c.353G>A (p.Arg118Lys) rs1789292576
NM_021167.5(GATAD1):c.389C>A (p.Pro130His) rs1789390751
NM_021167.5(GATAD1):c.411C>G (p.Ile137Met) rs1157446233
NM_021167.5(GATAD1):c.424A>G (p.Ile142Val)
NM_021167.5(GATAD1):c.503C>G (p.Ala168Gly)
NM_021167.5(GATAD1):c.538G>C (p.Glu180Gln)
NM_021167.5(GATAD1):c.547G>A (p.Ala183Thr)
NM_021167.5(GATAD1):c.575T>C (p.Leu192Pro) rs370960226
NM_021167.5(GATAD1):c.583C>A (p.Pro195Thr)
NM_021167.5(GATAD1):c.604G>C (p.Ala202Pro)
NM_021167.5(GATAD1):c.604G>T (p.Ala202Ser) rs564747350
NM_021167.5(GATAD1):c.627G>T (p.Glu209Asp) rs2115885370
NM_021167.5(GATAD1):c.632A>T (p.Asp211Val) rs2115885418
NM_021167.5(GATAD1):c.647T>C (p.Met216Thr)
NM_021167.5(GATAD1):c.691A>G (p.Lys231Glu) rs2115885587
NM_021167.5(GATAD1):c.698G>A (p.Arg233Gln)
NM_021167.5(GATAD1):c.740G>T (p.Gly247Val)
NM_021167.5(GATAD1):c.770dup (p.Ala258fs)
NM_021167.5(GATAD1):c.777A>G (p.Ile259Met)
NM_021167.5(GATAD1):c.787G>C (p.Glu263Gln)
NM_021167.5(GATAD1):c.791C>T (p.Ser264Leu)

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