Annotation Detail
Information
- Associated Genes
- IMPDH1
- Associated Variants
-
IMPDH1 p.Val353Ile (p.V353I)
(
ENST00000338791.11,
ENST00000348127.11,
ENST00000354269.9,
ENST00000419067.6,
ENST00000470772.5,
ENST00000480861.5,
ENST00000496200.5 )
IMPDH1 p.Val353Ile (p.V353I) ( ENST00000338791.11, ENST00000348127.11, ENST00000354269.9, ENST00000419067.6, ENST00000470772.5, ENST00000480861.5, ENST00000496200.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000883.4(IMPDH1):c.1057G>A (p.Val353Ile) AND not provided
- ClinVar Allele ID
- 29874
- ClinVar RefSeq Alternation Syntax
- NM_000883.4:c.1057G>A
- ClinVar RefSeq Alternation Syntax
- NM_001304521.2:c.850G>A
- ClinVar RefSeq Alternation Syntax
- NM_001142574.2:c.787G>A
- ClinVar RefSeq Alternation Syntax
- NM_183243.3:c.949G>A
- ClinVar RefSeq Alternation Syntax
- NM_001142573.2:c.802G>A
- ClinVar RefSeq Alternation Syntax
- NM_001142575.2:c.727G>A
- ClinVar RefSeq Alternation Syntax
- NM_001102605.2:c.1027G>A
- ClinVar RefSeq Alternation Syntax
- NM_001142576.2:c.958G>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2022-09-10
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002513068
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs