ClinVar Miner

List of variants studied for Schimke immuno-osseous dysplasia by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 58
Download table as spreadsheet
HGVS dbSNP
NC_000002.12:g.216412428T>C
NC_000002.12:g.216412444G>C
NC_000002.12:g.216412482C>G
NM_001127207.2(SMARCAL1):c.2542G>T (p.Glu848Ter) rs119473033
NM_014140.3(SMARCAL1):c.*13G>T rs760333596
NM_014140.3(SMARCAL1):c.*30T>G rs186052380
NM_014140.3(SMARCAL1):c.-114G>A rs561221026
NM_014140.3(SMARCAL1):c.-137A>G rs115172989
NM_014140.3(SMARCAL1):c.-141G>A rs542884297
NM_014140.3(SMARCAL1):c.-164G>A rs767342189
NM_014140.3(SMARCAL1):c.-170C>T rs886055614
NM_014140.3(SMARCAL1):c.-200G>A rs79352134
NM_014140.3(SMARCAL1):c.-218C>T rs3755141
NM_014140.3(SMARCAL1):c.-48C>A rs576450027
NM_014140.3(SMARCAL1):c.-82T>C rs886055615
NM_014140.3(SMARCAL1):c.1129G>C (p.Glu377Gln) rs2066518
NM_014140.3(SMARCAL1):c.1196C>T (p.Thr399Met) rs139872089
NM_014140.3(SMARCAL1):c.1212G>A (p.Ala404=) rs2066525
NM_014140.3(SMARCAL1):c.1243A>G (p.Ser415Gly) rs58848916
NM_014140.3(SMARCAL1):c.1251G>A (p.Thr417=) rs372331472
NM_014140.3(SMARCAL1):c.1271A>T (p.Asp424Val) rs2066520
NM_014140.3(SMARCAL1):c.127G>A (p.Ala43Thr) rs2066524
NM_014140.3(SMARCAL1):c.1407C>T (p.Ile469=) rs750621192
NM_014140.3(SMARCAL1):c.1413C>T (p.Ile471=) rs149599324
NM_014140.3(SMARCAL1):c.1414G>A (p.Ala472Thr) rs571392819
NM_014140.3(SMARCAL1):c.1485+8G>A rs886055617
NM_014140.3(SMARCAL1):c.1947C>T (p.Asp649=) rs2066526
NM_014140.3(SMARCAL1):c.1995C>T (p.Ala665=) rs151241914
NM_014140.3(SMARCAL1):c.2070T>C (p.Thr690=) rs2066527
NM_014140.3(SMARCAL1):c.2114C>T (p.Thr705Ile) rs200644381
NM_014140.3(SMARCAL1):c.2225C>T (p.Thr742Met) rs2271336
NM_014140.3(SMARCAL1):c.2226G>A (p.Thr742=) rs2271335
NM_014140.3(SMARCAL1):c.2528+15G>A rs200879397
NM_014140.3(SMARCAL1):c.2641A>C (p.Lys881Gln) rs190386780
NM_014140.3(SMARCAL1):c.2658_2659delinsTT (p.Gln887Ter) rs1559140275
NM_014140.3(SMARCAL1):c.341G>A (p.Arg114His) rs11555797
NM_014140.3(SMARCAL1):c.423T>C (p.Tyr141=) rs35907255
NM_014140.3(SMARCAL1):c.600G>A (p.Ser200=) rs530505647
NM_014140.3(SMARCAL1):c.72A>G (p.Arg24=) rs199805770
NM_014140.3(SMARCAL1):c.76G>A (p.Glu26Lys) rs886055616
NM_014140.3(SMARCAL1):c.812-15T>C rs375588610
NM_014140.3(SMARCAL1):c.863-9C>G rs188833040
NM_014140.3(SMARCAL1):c.901C>G (p.Pro301Ala) rs146084305
NM_014140.3(SMARCAL1):c.927C>T (p.Ser309=) rs139949668
NM_014140.3(SMARCAL1):c.945C>G (p.Ser315Arg) rs2066522
NM_014140.3(SMARCAL1):c.960C>T (p.Ala320=) rs2066513
NM_014140.4(SMARCAL1):c.1147+8G>A rs759562755
NM_014140.4(SMARCAL1):c.1160G>A (p.Arg387His)
NM_014140.4(SMARCAL1):c.1469G>A (p.Arg490His)
NM_014140.4(SMARCAL1):c.1785C>T (p.Ile595=) rs145825654
NM_014140.4(SMARCAL1):c.1944C>T (p.Ser648=) rs752241342
NM_014140.4(SMARCAL1):c.2295G>A (p.Glu765=)
NM_014140.4(SMARCAL1):c.2316A>G (p.Gln772=)
NM_014140.4(SMARCAL1):c.532G>T (p.Ala178Ser)
NM_014140.4(SMARCAL1):c.693A>C (p.Gln231His)
NM_014140.4(SMARCAL1):c.748G>C (p.Val250Leu)
NM_014140.4(SMARCAL1):c.863-4G>T
NM_014140.4(SMARCAL1):c.961G>A (p.Gly321Ser)

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.