ClinVar Miner

List of variants in gene combination LOC114827827, NPPA reported as likely benign for atrial fibrillation

Included ClinVar conditions (49):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_006172.4(NPPA):c.292G>A (p.Gly98Arg) rs142022010 0.00242
NM_006172.4(NPPA):c.83T>C (p.Met28Thr) rs142116829 0.00217
NM_006172.4(NPPA):c.190A>C (p.Ser64Arg) rs61757261 0.00165
NM_006172.4(NPPA):c.171C>T (p.Val57=) rs61757262 0.00106
NM_006172.4(NPPA):c.135C>T (p.Asp45=) rs148712945 0.00063
NM_006172.4(NPPA):c.352C>A (p.Leu118Met) rs147081122 0.00060
NM_006172.4(NPPA):c.198G>A (p.Pro66=) rs767807184 0.00010
NM_006172.4(NPPA):c.375G>A (p.Leu125=) rs765926210 0.00010
NM_006172.4(NPPA):c.390C>T (p.Cys130=) rs774295577 0.00006
NM_006172.4(NPPA):c.124-7T>C rs574725428 0.00005
NM_006172.4(NPPA):c.272A>G (p.Gln91Arg) rs201879717 0.00005
NM_006172.4(NPPA):c.252C>T (p.Thr84=) rs755212754 0.00004
NM_006172.4(NPPA):c.393C>T (p.Phe131=) rs768567024 0.00002
NM_006172.4(NPPA):c.111G>C (p.Leu37=) rs751792176 0.00001
NM_006172.4(NPPA):c.24C>T (p.Thr8=) rs548535773 0.00001
NM_006172.4(NPPA):c.255G>A (p.Gly85=) rs1557442880 0.00001
NM_006172.4(NPPA):c.291C>T (p.Leu97=) rs941079012 0.00001
NM_006172.4(NPPA):c.102C>T (p.Asn34=)
NM_006172.4(NPPA):c.123+17G>A
NM_006172.4(NPPA):c.123+17G>C rs761089549
NM_006172.4(NPPA):c.123+7C>T
NM_006172.4(NPPA):c.124-12C>T
NM_006172.4(NPPA):c.124-20T>C rs373867029
NM_006172.4(NPPA):c.124-28_124-19del
NM_006172.4(NPPA):c.124-5T>C
NM_006172.4(NPPA):c.165T>C (p.Asp55=) rs941150669
NM_006172.4(NPPA):c.196C>A (p.Pro66Thr)
NM_006172.4(NPPA):c.210G>A (p.Ala70=)
NM_006172.4(NPPA):c.264C>T (p.Ser88=) rs1645075676
NM_006172.4(NPPA):c.297G>C (p.Arg99=)
NM_006172.4(NPPA):c.327C>T (p.Ala109=)
NM_006172.4(NPPA):c.336A>G (p.Lys112=)
NM_006172.4(NPPA):c.351G>A (p.Ala117=) rs1473148185
NM_006172.4(NPPA):c.363C>T (p.Ala121=)
NM_006172.4(NPPA):c.387C>T (p.Ser129=)
NM_006172.4(NPPA):c.423G>A (p.Gln141=)
NM_006172.4(NPPA):c.426C>T (p.Ser142=) rs747448548
NM_006172.4(NPPA):c.435C>T (p.Gly145=)
NM_006172.4(NPPA):c.441C>T (p.Asn147=)
NM_006172.4(NPPA):c.450+16G>A
NM_006172.4(NPPA):c.450+20G>A
NM_006172.4(NPPA):c.450+8G>A
NM_006172.4(NPPA):c.45G>A (p.Leu15=)
NM_006172.4(NPPA):c.45G>T (p.Leu15=)
NM_006172.4(NPPA):c.93C>A (p.Ala31=) rs374257969
NM_006172.4(NPPA):c.93C>T (p.Ala31=) rs374257969
NM_006172.4(NPPA):c.9C>A (p.Ser3=) rs1557443346

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