Annotation Detail
Information
- Associated Genes
- MTRR
- Associated Variants
-
MTRR c.1557+95G>A
(
ENST00000264668.6,
ENST00000440940.7 )
MTRR c.1557+95G>A ( ENST00000264668.6, ENST00000440940.7 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_002454.3(MTRR):c.1557+95G>A AND not provided
- ClinVar Allele ID
- 1222236
- ClinVar RefSeq Alternation Syntax
- NM_001364441.2:c.1557+95G>A
- ClinVar RefSeq Alternation Syntax
- NM_001364442.2:c.1557+95G>A
- ClinVar RefSeq Alternation Syntax
- NM_024010.4:c.1557+95G>A
- ClinVar RefSeq Alternation Syntax
- NM_002454.3:c.1557+95G>A
- ClinVar RefSeq Alternation Syntax
- NM_001364440.2:c.1557+95G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-06-29
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001617034
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs