ClinVar Miner

List of variants in gene PPA2 reported as benign for not provided

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Gene type:
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Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_176869.3(PPA2):c.268-256T>A rs2046880 0.89627
NM_176869.3(PPA2):c.940-91C>G rs2726526 0.64415
NM_176869.3(PPA2):c.442-200T>C rs2713863 0.60281
NM_176869.3(PPA2):c.656-328A>C rs2726454 0.59908
NM_176869.3(PPA2):c.655+228T>C rs2726514 0.58917
NM_176869.3(PPA2):c.869+290G>A rs2636706 0.36141
NM_176869.3(PPA2):c.656-125C>T rs1490594 0.36077
NM_176869.3(PPA2):c.846G>C (p.Lys282Asn) rs13787 0.36065
NM_176869.3(PPA2):c.656-211A>G rs2713870 0.36062
NM_176869.3(PPA2):c.976+170C>T rs11301777 0.29129
NM_176869.3(PPA2):c.656-268C>T rs17035551 0.18430
NM_176869.3(PPA2):c.656-146A>G rs17035550 0.18406
NM_176869.3(PPA2):c.27C>T (p.Arg9=) rs4699179 0.15486
NM_176869.3(PPA2):c.940-79C>T rs72665979 0.12620
NM_176869.3(PPA2):c.940-278C>T rs72665980 0.12618
NM_176869.3(PPA2):c.*262A>G rs112734002 0.12608
NM_176869.3(PPA2):c.940-319A>G rs34248474 0.10007
NM_176869.3(PPA2):c.976+312A>G rs35206705 0.09995
NM_176869.3(PPA2):c.157+259G>A rs113639727 0.04423
NM_176869.3(PPA2):c.939+156A>G rs78201873 0.04102
NM_176869.3(PPA2):c.321+249A>G rs193136512 0.03936
NM_176869.3(PPA2):c.441+179A>C rs72950601 0.03910
NM_176869.3(PPA2):c.268-79T>C rs72952259 0.03736
NM_176869.3(PPA2):c.268-19G>T rs112044972 0.03601
NM_176869.3(PPA2):c.268-314T>C rs17035600 0.03597
NM_176869.3(PPA2):c.322-37A>G rs11097889 0.03593
NM_176869.3(PPA2):c.267+177A>T rs191124324 0.03585
NM_176869.3(PPA2):c.267+177_267+178insG rs141782383 0.03581
NM_176869.3(PPA2):c.158-125G>A rs77806360 0.03219
NM_176869.3(PPA2):c.64A>G (p.Thr22Ala) rs35571699 0.02096
NM_176869.3(PPA2):c.441+5C>G rs111967703 0.02057
NM_176869.3(PPA2):c.222+184A>G rs76601279 0.02049
NM_176869.3(PPA2):c.939+286A>G rs114945266 0.01707
NM_176869.3(PPA2):c.940-193dup rs11399157 0.01682
NM_176869.3(PPA2):c.477G>A (p.Thr159=) rs139651138 0.01242
NM_176869.3(PPA2):c.939+17C>T rs7679119 0.00788
NM_176869.3(PPA2):c.727G>T (p.Val243Leu) rs148492084 0.00747
NM_176869.3(PPA2):c.513C>T (p.Cys171=) rs138826533 0.00285
NM_176869.3(PPA2):c.180T>C (p.Ile60=) rs140134079 0.00142
NM_176869.3(PPA2):c.251G>A (p.Arg84Gln) rs146135315 0.00106
NM_176869.3(PPA2):c.442-17T>A rs575289677 0.00096
NM_176869.3(PPA2):c.222+4T>A rs200307466 0.00081
NM_176869.3(PPA2):c.627G>A (p.Ala209=) rs189755896 0.00025
NM_176869.3(PPA2):c.442-15A>T rs551515553 0.00023
NM_176869.3(PPA2):c.901C>T (p.Arg301Cys) rs112301391 0.00022
NM_176869.3(PPA2):c.528+19A>G rs181437213 0.00014
NM_176869.3(PPA2):c.441+14T>G rs192764857 0.00011
NM_176869.3(PPA2):c.*52_*53insACTCTTTTTCCCCAAG rs16345
NM_176869.3(PPA2):c.158-100C>G rs73836216
NM_176869.3(PPA2):c.268-15del rs2110305892
NM_176869.3(PPA2):c.322-138C>A rs11097890
NM_176869.3(PPA2):c.441+259del rs35970605
NM_176869.3(PPA2):c.442-16A>T rs2713862
NM_176869.3(PPA2):c.442-17dup
NM_176869.3(PPA2):c.442-7del rs753176486
NM_176869.3(PPA2):c.442-7dup
NM_176869.3(PPA2):c.529-170_529-165del rs140043365
NM_176869.3(PPA2):c.656-78C>G rs1490593
NM_176869.3(PPA2):c.784-19TTTG[2] rs34331553
NM_176869.3(PPA2):c.869+35_869+36insTTATT rs70964660
NM_176869.3(PPA2):c.939+291C>T rs66988826
NM_176869.3(PPA2):c.976+14del
NM_176869.3(PPA2):c.976+232G>A rs36112402
NM_176869.3(PPA2):c.976+246del rs34420247
NM_176869.3(PPA2):c.976+315del rs147156921

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