ClinVar Miner

List of variants in gene IQSEC2 reported as likely benign for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 36
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HGVS dbSNP
NM_001111125.3(IQSEC2):c.1000-9C>T rs1556864744
NM_001111125.3(IQSEC2):c.108G>A (p.Leu36=) rs1602383725
NM_001111125.3(IQSEC2):c.1188G>A (p.Glu396=) rs782503727
NM_001111125.3(IQSEC2):c.120G>A (p.Gln40=) rs1057522131
NM_001111125.3(IQSEC2):c.132C>T (p.Ile44=) rs1556880287
NM_001111125.3(IQSEC2):c.1554C>G (p.Leu518=) rs782768601
NM_001111125.3(IQSEC2):c.1712G>A (p.Gly571Asp) rs1569302404
NM_001111125.3(IQSEC2):c.2018G>A (p.Ser673Asn)
NM_001111125.3(IQSEC2):c.2271C>T (p.Tyr757=) rs1556862965
NM_001111125.3(IQSEC2):c.2328C>T (p.Ile776=) rs781978108
NM_001111125.3(IQSEC2):c.2750-9C>T rs1556861395
NM_001111125.3(IQSEC2):c.2775C>T (p.Pro925=) rs371055459
NM_001111125.3(IQSEC2):c.2890-6G>A rs184248834
NM_001111125.3(IQSEC2):c.294C>T (p.His98=) rs1556880235
NM_001111125.3(IQSEC2):c.3420C>A (p.Leu1140=) rs1602259971
NM_001111125.3(IQSEC2):c.3501+7G>T rs1221336765
NM_001111125.3(IQSEC2):c.3523C>T (p.Arg1175Cys)
NM_001111125.3(IQSEC2):c.3546T>G (p.Pro1182=) rs1602258133
NM_001111125.3(IQSEC2):c.3555A>C (p.Pro1185=) rs1315062158
NM_001111125.3(IQSEC2):c.3561G>C (p.Pro1187=) rs1286507586
NM_001111125.3(IQSEC2):c.3669G>A (p.Pro1223=) rs782744933
NM_001111125.3(IQSEC2):c.3735C>T (p.His1245=) rs797045630
NM_001111125.3(IQSEC2):c.3870T>C (p.Leu1290=) rs1057521625
NM_001111125.3(IQSEC2):c.3924G>A (p.Pro1308=) rs1460397663
NM_001111125.3(IQSEC2):c.396C>T (p.Asp132=) rs1556880172
NM_001111125.3(IQSEC2):c.4119T>C (p.Pro1373=) rs1602256870
NM_001111125.3(IQSEC2):c.4293C>T (p.Ile1431=) rs782536136
NM_001111125.3(IQSEC2):c.4317C>T (p.Pro1439=) rs1216934275
NM_001111125.3(IQSEC2):c.4353C>G (p.Pro1451=) rs1556858970
NM_001111125.3(IQSEC2):c.435C>T (p.Thr145=) rs782726368
NM_001111125.3(IQSEC2):c.507G>A (p.Glu169=) rs1556880086
NM_001111125.3(IQSEC2):c.618C>T (p.Ser206=) rs370573314
NM_001111125.3(IQSEC2):c.699C>G (p.Leu233=) rs1411580863
NM_001111125.3(IQSEC2):c.837C>T (p.Ser279=) rs374638286
NM_001111125.3(IQSEC2):c.960G>C (p.Ser320=) rs782062867
NM_001111125.3(IQSEC2):c.987G>T (p.Leu329=) rs1419492759

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