ClinVar Miner

List of variants in gene SLC35A2 reported as benign for congenital disorder of glycosylation type II

Included ClinVar conditions (28):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_005660.3(SLC35A2):c.43C>A (p.Pro15Thr) rs55719932 0.01547
NM_005660.3(SLC35A2):c.990C>T (p.Leu330=) rs146079657 0.00069
NM_005660.3(SLC35A2):c.72G>T (p.Glu24Asp) rs374961453 0.00057
NM_005660.3(SLC35A2):c.1078G>A (p.Val360Ile) rs138190020 0.00045
NM_005660.3(SLC35A2):c.561C>T (p.Ala187=) rs370394797 0.00036
NM_005660.3(SLC35A2):c.1056T>C (p.Ser352=) rs56111636 0.00024
NM_005660.3(SLC35A2):c.12T>G (p.Val4=) rs782793880 0.00023
NM_005660.3(SLC35A2):c.169G>A (p.Ala57Thr) rs151120284 0.00011
NM_005660.3(SLC35A2):c.112A>C (p.Ile38Leu) rs782268788 0.00008
NM_005660.3(SLC35A2):c.1039G>A (p.Ala347Thr) rs781948153 0.00006
NM_005660.3(SLC35A2):c.92-11G>A rs368406784 0.00006
NM_005660.3(SLC35A2):c.1063G>A (p.Ala355Thr) rs376547003 0.00005
NM_005660.3(SLC35A2):c.639C>T (p.Ser213=) rs782301792 0.00005
NM_005660.3(SLC35A2):c.74C>T (p.Pro25Leu) rs781993117 0.00005
NM_005660.3(SLC35A2):c.771C>T (p.Ala257=) rs782663029 0.00005
NM_005660.3(SLC35A2):c.828C>T (p.Leu276=) rs782113085 0.00005
NM_005660.3(SLC35A2):c.90G>C (p.Ala30=) rs1057522337 0.00005
NM_005660.3(SLC35A2):c.1062C>T (p.Ser354=) rs142781476 0.00004
NM_005660.3(SLC35A2):c.1145C>T (p.Thr382Met) rs781801728 0.00004
NM_005660.3(SLC35A2):c.8C>T (p.Ala3Val) rs946472167 0.00004
NM_005660.3(SLC35A2):c.1015A>G (p.Ser339Gly) rs782789576 0.00003
NM_005660.3(SLC35A2):c.941G>A (p.Arg314His) rs920606773 0.00003
NM_005660.3(SLC35A2):c.1112C>T (p.Pro371Leu) rs782673464 0.00002
NM_005660.3(SLC35A2):c.1129C>T (p.Arg377Cys) rs782483874 0.00002
NM_005660.3(SLC35A2):c.279C>T (p.Asn93=) rs782206039 0.00002
NM_005660.3(SLC35A2):c.345C>T (p.Leu115=) rs782476110 0.00002
NM_005660.3(SLC35A2):c.562G>A (p.Gly188Ser) rs1023107993 0.00002
NM_005660.3(SLC35A2):c.1025G>A (p.Arg342Gln) rs781897678 0.00001
NM_005660.3(SLC35A2):c.1110A>G (p.Pro370=) rs782273947 0.00001
NM_005660.3(SLC35A2):c.263C>T (p.Ala88Val) rs375442287 0.00001
NM_005660.3(SLC35A2):c.818G>C (p.Gly273Ala) rs1557042798 0.00001
NM_005660.3(SLC35A2):c.819C>T (p.Gly273=) rs1271812540 0.00001
NM_005660.3(SLC35A2):c.826C>T (p.Leu276Phe) rs782737391 0.00001
NM_005660.3(SLC35A2):c.1042A>G (p.Ile348Val)
NM_005660.3(SLC35A2):c.1050TGCCTC[1] (p.349AS[3]) rs781977360
NM_005660.3(SLC35A2):c.1058CCTCCG[1] (p.349AS[3]) rs782439562
NM_005660.3(SLC35A2):c.1068C>T (p.Ser356=)
NM_005660.3(SLC35A2):c.1069G>A (p.Gly357Arg) rs782347244
NM_005660.3(SLC35A2):c.1130G>A (p.Arg377His) rs369048466
NM_005660.3(SLC35A2):c.1130G>C (p.Arg377Pro) rs369048466
NM_005660.3(SLC35A2):c.1163+16G>T
NM_005660.3(SLC35A2):c.292G>A (p.Val98Ile)
NM_005660.3(SLC35A2):c.439C>T (p.Leu147=)
NM_005660.3(SLC35A2):c.578G>A (p.Arg193Gln) rs1602338782
NM_005660.3(SLC35A2):c.610G>A (p.Ala204Thr) rs2147487234
NM_005660.3(SLC35A2):c.66A>G (p.Ala22=)
NM_005660.3(SLC35A2):c.91+9G>C

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