ClinVar Miner

List of variants in gene CARD14 reported as benign for psoriasis

Included ClinVar conditions (7):
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Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_001366385.1(CARD14):c.675+26G>A rs4889991 0.77525
NM_001366385.1(CARD14):c.633G>A (p.Glu211=) rs4889990 0.37893
NM_001366385.1(CARD14):c.1641G>C (p.Arg547Ser) rs2066964 0.35511
NM_001366385.1(CARD14):c.676-6G>A rs28674001 0.31201
NM_001366385.1(CARD14):c.1323C>T (p.Asp441=) rs11658460 0.10192
NM_001366385.1(CARD14):c.1753G>A (p.Val585Ile) rs34367357 0.06519
NM_001366385.1(CARD14):c.1170C>T (p.Phe390=) rs74951924 0.03377
NM_001366385.1(CARD14):c.1264G>A (p.Glu422Lys) rs61751629 0.02212
NM_001366385.1(CARD14):c.1789C>T (p.Arg597Trp) rs73429414 0.01118
NM_001366385.1(CARD14):c.1517C>T (p.Pro506Leu) rs61751630 0.00959
NM_001366385.1(CARD14):c.1499+13G>A rs114086314 0.00912
NM_001366385.1(CARD14):c.843+16C>T rs143622685 0.00868
NM_001366385.1(CARD14):c.1476C>T (p.Phe492=) rs144710573 0.00483
NM_001366385.1(CARD14):c.709A>C (p.Asn237His) rs114218658 0.00457
NM_001366385.1(CARD14):c.185G>A (p.Arg62Gln) rs115582620 0.00439
NM_001366385.1(CARD14):c.1662C>T (p.Gly554=) rs149971215 0.00397
NM_001366385.1(CARD14):c.378G>A (p.Glu126=) rs138552007 0.00247
NM_001366385.1(CARD14):c.1065C>T (p.Cys355=) rs140246774 0.00228
NM_001366385.1(CARD14):c.1806G>A (p.Ser602=) rs113127952 0.00193
NM_001366385.1(CARD14):c.329T>C (p.Val110Ala) rs138139140 0.00180
NM_001366385.1(CARD14):c.526G>C (p.Asp176His) rs144475004 0.00168
NM_001366385.1(CARD14):c.796C>T (p.Arg266Cys) rs138616955 0.00128
NM_001366385.1(CARD14):c.1090-15C>T rs377287985 0.00119
NM_001366385.1(CARD14):c.1356+18G>A rs190983667 0.00107
NM_001366385.1(CARD14):c.211+20C>T rs539713605 0.00069
NM_001366385.1(CARD14):c.960G>A (p.Glu320=) rs144207494 0.00065
NM_001366385.1(CARD14):c.1518G>A (p.Pro506=) rs111586978 0.00056
NM_001366385.1(CARD14):c.1386G>A (p.Thr462=) rs146882682 0.00034
NM_001366385.1(CARD14):c.964-18G>A rs201163546 0.00029
NM_001366385.1(CARD14):c.27C>T (p.Ser9=) rs9895931 0.00026
NM_001366385.1(CARD14):c.212-19G>A rs200725256 0.00024
NM_001366385.1(CARD14):c.1090-10T>C rs778853453 0.00021
NM_001366385.1(CARD14):c.1091C>T (p.Ala364Val) rs141698692 0.00014
NM_001366385.1(CARD14):c.1797C>A (p.Thr599=) rs530338890 0.00010
NM_001366385.1(CARD14):c.936C>T (p.Ala312=) rs774862255 0.00007
NM_001366385.1(CARD14):c.1395C>T (p.Arg465=) rs759000751 0.00006
NM_001366385.1(CARD14):c.843+10G>A rs367767898 0.00004
NM_001366385.1(CARD14):c.1428C>T (p.Pro476=) rs368432283 0.00003
NM_001366385.1(CARD14):c.1430C>T (p.Ala477Val) rs546212263 0.00002
NM_001366385.1(CARD14):c.1851+16C>T rs146951890 0.00001
NM_001366385.1(CARD14):c.922C>T (p.Leu308=) rs537507973 0.00001
NM_001366385.1(CARD14):c.1356+18_1356+19del rs756509461
NM_001366385.1(CARD14):c.1371G>A (p.Ser457=) rs62074378
NM_001366385.1(CARD14):c.1659-17C>T rs374698233
NM_001366385.1(CARD14):c.1738C>T (p.Leu580=) rs562930550
NM_001366385.1(CARD14):c.599G>A (p.Ser200Asn) rs114688446
NM_001366385.1(CARD14):c.599G>T (p.Ser200Ile) rs114688446
NM_001366385.1(CARD14):c.669G>A (p.Gln223=)
NM_001366385.1(CARD14):c.931C>A (p.Arg311=) rs145167842

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