ClinVar Miner

List of variants in gene SIN3A reported as pathogenic for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 33
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NC_000015.9:g.(?_75664320)_(75722716_?)del
NM_001145358.2(SIN3A):c.1006C>T (p.Gln336Ter)
NM_001145358.2(SIN3A):c.1009-9A>G
NM_001145358.2(SIN3A):c.1122dup (p.Glu375fs) rs2073604192
NM_001145358.2(SIN3A):c.1138del (p.Leu380fs)
NM_001145358.2(SIN3A):c.1160dup (p.Leu388fs) rs2073603561
NM_001145358.2(SIN3A):c.1411C>T (p.Arg471Ter)
NM_001145358.2(SIN3A):c.1509dup (p.Val504fs)
NM_001145358.2(SIN3A):c.1519_1523del (p.Phe507fs)
NM_001145358.2(SIN3A):c.1551G>A (p.Trp517Ter)
NM_001145358.2(SIN3A):c.1609C>T (p.Arg537Ter) rs757034687
NM_001145358.2(SIN3A):c.1657C>T (p.Arg553Ter) rs1555444885
NM_001145358.2(SIN3A):c.1675C>T (p.Arg559Ter) rs1555444879
NM_001145358.2(SIN3A):c.1773G>A (p.Trp591Ter)
NM_001145358.2(SIN3A):c.1912A>T (p.Lys638Ter) rs1567341422
NM_001145358.2(SIN3A):c.2019T>G (p.Tyr673Ter) rs1595897112
NM_001145358.2(SIN3A):c.2094-1G>T rs2073273656
NM_001145358.2(SIN3A):c.2152C>T (p.Arg718Ter) rs1444395453
NM_001145358.2(SIN3A):c.2353_2356del (p.Gln785fs) rs2141426359
NM_001145358.2(SIN3A):c.23_24del (p.Gln8fs) rs2141571783
NM_001145358.2(SIN3A):c.2448dup (p.His817fs)
NM_001145358.2(SIN3A):c.2626_2629del (p.Leu876fs)
NM_001145358.2(SIN3A):c.2675G>A (p.Trp892Ter) rs1555443627
NM_001145358.2(SIN3A):c.2689C>T (p.Arg897Ter) rs1064796919
NM_001145358.2(SIN3A):c.2809_2810del (p.Lys937fs) rs1555443600
NM_001145358.2(SIN3A):c.2844_2847del (p.Lys948fs) rs1555443581
NM_001145358.2(SIN3A):c.3025C>T (p.Gln1009Ter)
NM_001145358.2(SIN3A):c.3303C>G (p.Tyr1101Ter) rs778623853
NM_001145358.2(SIN3A):c.3400del (p.Arg1134fs) rs1555441161
NM_001145358.2(SIN3A):c.366+1G>T rs2141540743
NM_001145358.2(SIN3A):c.663dup (p.Pro222fs)
NM_001145358.2(SIN3A):c.763del (p.Gln255fs) rs1595907762
NM_001145358.2:c.474-574_1408-735dup

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.