ClinVar Miner

List of variants in gene ATAD3A reported as likely benign for not provided

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Gene type:
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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_001170535.3(ATAD3A):c.168G>A (p.Glu56=) rs564012773 0.00793
NM_001170535.3(ATAD3A):c.1749C>T (p.Pro583=) rs138170400 0.00444
NM_001170535.3(ATAD3A):c.1089+8C>T rs200282209 0.00411
NM_001170535.3(ATAD3A):c.19A>G (p.Ile7Val) rs201314162 0.00329
NM_001170535.3(ATAD3A):c.1703A>T (p.Lys568Met) rs41285840 0.00291
NM_001170535.3(ATAD3A):c.1119C>T (p.Tyr373=) rs141422827 0.00270
NM_001170535.3(ATAD3A):c.571G>A (p.Ala191Thr) rs2986576 0.00214
NM_001170535.3(ATAD3A):c.646G>T (p.Ala216Ser) rs2767471 0.00200
NM_001170535.3(ATAD3A):c.1266C>T (p.Thr422=) rs149995099 0.00105
NM_001170535.3(ATAD3A):c.1615-7C>T rs543696394 0.00104
NM_001170535.3(ATAD3A):c.1615-8C>T rs533279074 0.00104
NM_001170535.3(ATAD3A):c.360C>T (p.Ser120=) rs571690031 0.00037
NM_001170535.3(ATAD3A):c.1227T>C (p.Phe409=) rs575132198 0.00027
NM_001170535.3(ATAD3A):c.1693C>T (p.His565Tyr) rs200344678 0.00027
NM_001170535.3(ATAD3A):c.486C>T (p.Ser162=) rs138279686 0.00025
NM_001170535.3(ATAD3A):c.1725A>G (p.Glu575=) rs147777956 0.00021
NM_001170535.3(ATAD3A):c.1239G>A (p.Ala413=) rs138094382 0.00019
NM_001170535.3(ATAD3A):c.1732G>A (p.Gly578Arg) rs200240134 0.00013
NM_001170535.3(ATAD3A):c.993C>T (p.Ile331=) rs138624825 0.00005
NM_001170535.3(ATAD3A):c.384C>T (p.Ala128=) rs763685989 0.00003
NM_001170535.3(ATAD3A):c.1602C>T (p.Ala534=) rs780963309 0.00001
NM_001170535.3(ATAD3A):c.672G>A (p.Glu224=) rs776672631 0.00001
NM_001170535.3(ATAD3A):c.1005A>C (p.Thr335=)
NM_001170535.3(ATAD3A):c.1014C>T (p.Thr338=)
NM_001170535.3(ATAD3A):c.1041C>T (p.Asn347=)
NM_001170535.3(ATAD3A):c.1053C>T (p.Tyr351=)
NM_001170535.3(ATAD3A):c.1170C>T (p.Thr390=)
NM_001170535.3(ATAD3A):c.1197C>G (p.Ala399=)
NM_001170535.3(ATAD3A):c.1347G>A (p.Leu449=)
NM_001170535.3(ATAD3A):c.1488G>A (p.Pro496=)
NM_001170535.3(ATAD3A):c.1623G>A (p.Ala541=)
NM_001170535.3(ATAD3A):c.1647G>C (p.Leu549=)
NM_001170535.3(ATAD3A):c.1650C>T (p.Thr550=)
NM_001170535.3(ATAD3A):c.1671C>T (p.Arg557=)
NM_001170535.3(ATAD3A):c.1698G>A (p.Gln566=)
NM_001170535.3(ATAD3A):c.1721C>T (p.Ala574Val)
NM_001170535.3(ATAD3A):c.1737T>C (p.Arg579=)
NM_001170535.3(ATAD3A):c.283-81G>A
NM_001170535.3(ATAD3A):c.330G>A (p.Ala110=)
NM_001170535.3(ATAD3A):c.39T>A (p.Gly13=)
NM_001170535.3(ATAD3A):c.414G>A (p.Arg138=)
NM_001170535.3(ATAD3A):c.492G>A (p.Gln164=)
NM_001170535.3(ATAD3A):c.639G>C (p.Leu213=)
NM_001170535.3(ATAD3A):c.730T>C (p.Trp244Arg)
NM_001170535.3(ATAD3A):c.750+10C>A rs569633380
NM_001170535.3(ATAD3A):c.792C>T (p.Ala264=) rs142477467
NM_001170535.3(ATAD3A):c.876G>C (p.Thr292=)
NM_001170535.3(ATAD3A):c.907-5G>A
NM_001170535.3(ATAD3A):c.939C>T (p.Asp313=)
NM_001170535.3(ATAD3A):c.966C>T (p.Pro322=)

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