Annotation Detail
Information
- Associated Genes
- TPM1
- Associated Variants
-
TPM1 p.Glu234Lys (p.E234K)
(
ENST00000267996.11,
ENST00000317516.12,
ENST00000358278.7,
ENST00000561266.6,
ENST00000560959.5,
ENST00000714017.1,
ENST00000559556.5,
ENST00000560970.6,
ENST00000558910.3,
ENST00000334895.10,
ENST00000714014.1,
ENST00000559397.6,
ENST00000357980.9,
ENST00000714013.1,
ENST00000651577.1,
ENST00000560615.6,
ENST00000651704.1,
ENST00000288398.10,
ENST00000403994.9,
ENST00000404484.9,
ENST00000559281.6 )
TPM1 p.Glu234Lys (p.E234K) ( ENST00000267996.11, ENST00000288398.10, ENST00000317516.12, ENST00000334895.10, ENST00000357980.9, ENST00000358278.7, ENST00000403994.9, ENST00000404484.9, ENST00000558910.3, ENST00000559281.6, ENST00000559397.6, ENST00000559556.5, ENST00000560615.6, ENST00000560959.5, ENST00000560970.6, ENST00000561266.6, ENST00000651577.1, ENST00000651704.1, ENST00000714013.1, ENST00000714014.1, ENST00000714017.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001018005.2(TPM1):c.574G>A (p.Glu192Lys) AND not provided
- ClinVar Allele ID
- 40542
- ClinVar RefSeq Alternation Syntax
- NM_001018020.2:c.639+450G>A
- ClinVar RefSeq Alternation Syntax
- NM_001018006.2:c.639+450G>A
- ClinVar RefSeq Alternation Syntax
- NM_000366.6:c.639+450G>A
- ClinVar RefSeq Alternation Syntax
- NM_001365781.2:c.531+450G>A
- ClinVar RefSeq Alternation Syntax
- NM_001365780.1:c.466G>A
- ClinVar RefSeq Alternation Syntax
- NM_001365776.1:c.574G>A
- ClinVar RefSeq Alternation Syntax
- NM_001365778.1:c.700G>A
- ClinVar RefSeq Alternation Syntax
- NM_001365782.1:c.466G>A
- ClinVar RefSeq Alternation Syntax
- NM_001018004.2:c.574G>A
- ClinVar RefSeq Alternation Syntax
- NM_001018008.2:c.466G>A
- ClinVar RefSeq Alternation Syntax
- NM_001018007.2:c.574G>A
- ClinVar RefSeq Alternation Syntax
- NM_001301244.2:c.574G>A
- ClinVar RefSeq Alternation Syntax
- NM_001330346.2:c.466G>A
- ClinVar RefSeq Alternation Syntax
- NM_001330351.2:c.531+450G>A
- ClinVar RefSeq Alternation Syntax
- NM_001330344.2:c.531+450G>A
- ClinVar RefSeq Alternation Syntax
- NM_001301289.2:c.466G>A
- ClinVar RefSeq Alternation Syntax
- NM_001365779.1:c.574G>A
- ClinVar RefSeq Alternation Syntax
- NM_001018005.2:c.574G>A
- ClinVar RefSeq Alternation Syntax
- NM_001365777.1:c.574G>A
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2023-10-19
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000024578
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs