ClinVar Miner

List of variants in gene XIAP reported as likely benign for X-linked lymphoproliferative syndrome

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 69
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001167.4(XIAP):c.978G>A (p.Gly326=) rs376282989 0.00035
NM_001167.4(XIAP):c.688G>A (p.Val230Ile) rs144884904 0.00032
NM_001167.4(XIAP):c.1242A>G (p.Leu414=) rs147262472 0.00015
NM_001167.4(XIAP):c.73G>C (p.Glu25Gln) rs781204574 0.00013
NM_001167.4(XIAP):c.844G>A (p.Glu282Lys) rs777303823 0.00012
NM_001167.4(XIAP):c.962C>G (p.Ala321Gly) rs182340753 0.00007
NM_001167.4(XIAP):c.1100A>G (p.Asp367Gly) rs200273554 0.00006
NM_001167.4(XIAP):c.1149G>A (p.Gly383=) rs374184914 0.00005
NM_001167.4(XIAP):c.933G>A (p.Lys311=) rs749597959 0.00005
NM_001167.4(XIAP):c.180C>T (p.Thr60=) rs370447539 0.00004
NM_001167.4(XIAP):c.1257A>G (p.Lys419=) rs757641017 0.00003
NM_001167.4(XIAP):c.870T>C (p.Tyr290=) rs770461720 0.00003
NM_001167.4(XIAP):c.1191T>G (p.Ile397Met) rs760574724 0.00002
NM_001167.4(XIAP):c.435G>T (p.Gln145His) rs759909620 0.00002
NM_001167.4(XIAP):c.446T>C (p.Ile149Thr) rs774308309 0.00002
NM_001167.4(XIAP):c.465G>A (p.Pro155=) rs751634597 0.00002
NM_001167.4(XIAP):c.1100-14A>C rs753279953 0.00001
NM_001167.4(XIAP):c.1300+12T>G rs2053507953 0.00001
NM_001167.4(XIAP):c.1314A>G (p.Glu438=) rs199833128 0.00001
NM_001167.4(XIAP):c.1380C>T (p.Ile460=) rs753857961 0.00001
NM_001167.4(XIAP):c.1452C>T (p.Cys484=) rs61757635 0.00001
NM_001167.4(XIAP):c.183G>T (p.Val61=) rs144938731 0.00001
NM_001167.4(XIAP):c.327T>C (p.Gly109=) rs774062590 0.00001
NM_001167.4(XIAP):c.369C>T (p.Ser123=) rs1211342947 0.00001
NM_001167.4(XIAP):c.549G>A (p.Glu183=) rs1308704581 0.00001
NM_001167.4(XIAP):c.606T>C (p.Cys202=) rs777129433 0.00001
NM_001167.4(XIAP):c.666A>G (p.Arg222=) rs1319323088 0.00001
NM_001167.4(XIAP):c.72A>G (p.Val24=) rs1209504379 0.00001
NM_001167.4(XIAP):c.878-4G>A rs371671137 0.00001
NM_001167.4(XIAP):c.978-6G>A rs912189497 0.00001
NM_001167.4(XIAP):c.1053T>C (p.Cys351=) rs2053405322
NM_001167.4(XIAP):c.1056+13T>A rs2522596525
NM_001167.4(XIAP):c.1056+21_1056+22del rs2148096290
NM_001167.4(XIAP):c.1056+28_1056+60dup rs768263227
NM_001167.4(XIAP):c.1057-13A>G
NM_001167.4(XIAP):c.1057-20A>G rs2522599043
NM_001167.4(XIAP):c.1071G>A (p.Glu357=) rs369835712
NM_001167.4(XIAP):c.1100-14A>T rs753279953
NM_001167.4(XIAP):c.1101T>C (p.Asp367=) rs2148107324
NM_001167.4(XIAP):c.1141C>A (p.Arg381=)
NM_001167.4(XIAP):c.1206C>T (p.Ser402=)
NM_001167.4(XIAP):c.1251T>C (p.Ala417=)
NM_001167.4(XIAP):c.1300+10G>T rs2522614792
NM_001167.4(XIAP):c.1300+17T>C rs2148107543
NM_001167.4(XIAP):c.1301-17A>T rs769635462
NM_001167.4(XIAP):c.1301-20A>C rs1424655367
NM_001167.4(XIAP):c.1301-6_1301-5del rs2522625119
NM_001167.4(XIAP):c.1323A>G (p.Leu441=) rs2148112163
NM_001167.4(XIAP):c.1407C>T (p.Val469=)
NM_001167.4(XIAP):c.1437C>T (p.Asp479=) rs781127670
NM_001167.4(XIAP):c.168T>C (p.Gly56=) rs1602544077
NM_001167.4(XIAP):c.18T>C (p.Phe6=) rs2053344531
NM_001167.4(XIAP):c.249C>T (p.His83=) rs752664980
NM_001167.4(XIAP):c.261C>T (p.Ser87=) rs2522584772
NM_001167.4(XIAP):c.283G>A (p.Gly95Ser) rs745844064
NM_001167.4(XIAP):c.300T>C (p.Asn100=) rs2148089584
NM_001167.4(XIAP):c.345C>T (p.Tyr115=)
NM_001167.4(XIAP):c.408T>C (p.His136=) rs2522585260
NM_001167.4(XIAP):c.438T>G (p.Val146=) rs1569477857
NM_001167.4(XIAP):c.486T>C (p.Ser162=) rs2053349352
NM_001167.4(XIAP):c.491A>G (p.Glu164Gly) rs749031811
NM_001167.4(XIAP):c.588C>T (p.Asp196=) rs1569477880
NM_001167.4(XIAP):c.738T>C (p.Ser246=) rs2522586208
NM_001167.4(XIAP):c.778C>T (p.Pro260Ser) rs2148090201
NM_001167.4(XIAP):c.804G>A (p.Arg268=) rs2522586405
NM_001167.4(XIAP):c.819G>A (p.Gly273=) rs2148090248
NM_001167.4(XIAP):c.873T>C (p.Ala291=)
NM_001167.4(XIAP):c.877+8_877+9del rs1355498168
NM_001167.4(XIAP):c.984A>G (p.Lys328=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.