ClinVar Miner

List of variants in gene RB1 reported by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 54
Download table as spreadsheet
HGVS dbSNP
NM_000321.2(RB1):c.*1022C>T rs886050283
NM_000321.2(RB1):c.*1268G>A rs571383547
NM_000321.2(RB1):c.*1459T>C rs886050284
NM_000321.2(RB1):c.*1527_*1528delTT rs540108904
NM_000321.2(RB1):c.*1540A>G rs768155412
NM_000321.2(RB1):c.*1544T>C rs886050285
NM_000321.2(RB1):c.*162T>G rs886050273
NM_000321.2(RB1):c.*1635T>A rs886050286
NM_000321.2(RB1):c.*1687T>C rs4151635
NM_000321.2(RB1):c.*172G>A rs143536240
NM_000321.2(RB1):c.*184A>T rs4151630
NM_000321.2(RB1):c.*398G>T rs886050274
NM_000321.2(RB1):c.*413T>G rs886050275
NM_000321.2(RB1):c.*435A>G rs886050276
NM_000321.2(RB1):c.*448_*451delATCT rs746086958
NM_000321.2(RB1):c.*463T>A rs4151631
NM_000321.2(RB1):c.*512A>C rs886050278
NM_000321.2(RB1):c.*604A>T rs886050279
NM_000321.2(RB1):c.*673G>T rs886050280
NM_000321.2(RB1):c.*703G>T rs139023385
NM_000321.2(RB1):c.*788C>A rs886050281
NM_000321.2(RB1):c.*964C>G rs4151633
NM_000321.2(RB1):c.*998G>A rs886050282
NM_000321.2(RB1):c.-153G>T rs886050266
NM_000321.2(RB1):c.-156C>A rs886050265
NM_000321.2(RB1):c.-69G>C rs753117180
NM_000321.2(RB1):c.-81G>A rs886050267
NM_000321.2(RB1):c.1140C>T (p.Asn380=) rs117865557
NM_000321.2(RB1):c.1306C>A (p.Gln436Lys) rs4151534
NM_000321.2(RB1):c.1333-9dupT rs766968771
NM_000321.2(RB1):c.1390-11A>G rs200658795
NM_000321.2(RB1):c.1390-14A>T rs9535023
NM_000321.2(RB1):c.1574C>G (p.Ala525Gly) rs4151539
NM_000321.2(RB1):c.1696-4A>G rs143685082
NM_000321.2(RB1):c.1707A>G (p.Leu569=) rs3092895
NM_000321.2(RB1):c.1770T>C (p.Cys590=) rs145310579
NM_000321.2(RB1):c.1961-12T>C rs201697122
NM_000321.2(RB1):c.2003G>A (p.Arg668His) rs551747882
NM_000321.2(RB1):c.2091C>G (p.Asp697Glu) rs3092903
NM_000321.2(RB1):c.2106+8A>G rs750581965
NM_000321.2(RB1):c.2463A>G (p.Thr821=) rs370088029
NM_000321.2(RB1):c.2521-11G>A rs4151624
NM_000321.2(RB1):c.2652A>C (p.Glu884Asp) rs765537411
NM_000321.2(RB1):c.2664-10T>A rs3092904
NM_000321.2(RB1):c.299G>C (p.Gly100Ala) rs886050268
NM_000321.2(RB1):c.380+10C>G rs187110786
NM_000321.2(RB1):c.380+12T>C rs3092881
NM_000321.2(RB1):c.393C>G (p.Phe131Leu) rs749495284
NM_000321.2(RB1):c.42C>T (p.Ala14=) rs148980395
NM_000321.2(RB1):c.608-4delT rs762805947
NM_000321.2(RB1):c.616T>C (p.Leu206=) rs886050270
NM_000321.2(RB1):c.862-15C>A rs115108608
NM_000321.2(RB1):c.929G>A (p.Gly310Glu) rs200844292
NM_000321.2(RB1):c.953C>G (p.Ser318Cys) rs886050271

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.