Annotation Detail
Information
- Associated Genes
- TMPRSS6
- Associated Variants
-
TMPRSS6 p.Ser352= (p.S352=)
(
ENST00000346753.9,
ENST00000381792.6,
ENST00000406725.6,
ENST00000406856.7,
ENST00000442782.7,
ENST00000676104.1 )
TMPRSS6 p.Ser352= (p.S352=) ( ENST00000346753.9, ENST00000381792.6, ENST00000406725.6, ENST00000406856.7, ENST00000442782.7, ENST00000676104.1 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_001374504.1(TMPRSS6):c.1056G>A (p.Ser352=) AND not specified
- ClinVar Allele ID
- 257675
- ClinVar RefSeq Alternation Syntax
- NM_001289001.2:c.1056G>A
- ClinVar RefSeq Alternation Syntax
- NM_153609.4:c.1056G>A
- ClinVar RefSeq Alternation Syntax
- NM_001374504.1:c.1056G>A
- ClinVar RefSeq Alternation Syntax
- NM_001289000.2:c.1056G>A
- Clinical Significance Description
- Benign
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000247391
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs