ClinVar Miner

List of variants in gene LOC114827827, NPPA studied for Atrial fibrillation, familial, 6

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Total variants: 24
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HGVS dbSNP
NM_006172.4(NPPA):c.112A>G (p.Met38Val)
NM_006172.4(NPPA):c.135C>T (p.Asp45=) rs148712945
NM_006172.4(NPPA):c.171C>T (p.Val57=) rs61757262
NM_006172.4(NPPA):c.172G>A (p.Val58Met) rs768114654
NM_006172.4(NPPA):c.176C>T (p.Pro59Leu) rs759999149
NM_006172.4(NPPA):c.190A>C (p.Ser64Arg) rs61757261
NM_006172.4(NPPA):c.197C>T (p.Pro66Leu) rs150794709
NM_006172.4(NPPA):c.198G>A (p.Pro66=) rs767807184
NM_006172.4(NPPA):c.208G>T (p.Ala70Ser)
NM_006172.4(NPPA):c.219_227del (p.Ser75_Leu77del) rs1557442938
NM_006172.4(NPPA):c.23C>T (p.Thr8Ile) rs142653342
NM_006172.4(NPPA):c.252C>T (p.Thr84=) rs755212754
NM_006172.4(NPPA):c.253G>A (p.Gly85Arg) rs749353276
NM_006172.4(NPPA):c.272A>G (p.Gln91Arg) rs201879717
NM_006172.4(NPPA):c.273_274GA[2] (p.Asp93fs) rs774165756
NM_006172.4(NPPA):c.292G>A (p.Gly98Arg) rs142022010
NM_006172.4(NPPA):c.350C>T (p.Ala117Val)
NM_006172.4(NPPA):c.352C>A (p.Leu118Met)
NM_006172.4(NPPA):c.367C>A (p.Arg123=)
NM_006172.4(NPPA):c.370A>G (p.Ser124Gly) rs1215729892
NM_006172.4(NPPA):c.425G>A (p.Ser142Asn) rs781197146
NM_006172.4(NPPA):c.78T>A (p.Asn26Lys) rs770401799
NM_006172.4(NPPA):c.83T>C (p.Met28Thr) rs142116829
NM_006172.4(NPPA):c.85T>C (p.Tyr29His)

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