NM_198994.3(TGM6):c.1501G>A (p.Val501Met) AND Spinocerebellar ataxia type 35
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000323219.5
Allele description [Variation Report for NM_198994.3(TGM6):c.1501G>A (p.Val501Met)]
NM_198994.3(TGM6):c.1501G>A (p.Val501Met)
Condition(s)
-
Homo sapiens inosine triphosphatase (ITPA), transcript variant 7, mRNA
Homo sapiens inosine triphosphatase (ITPA), transcript variant 7, mRNAgi|1676318174|ref|NM_001324236.2|Nucleotide
-
Mus musculus integrin alpha L (Itgal), transcript variant 2, mRNA
Mus musculus integrin alpha L (Itgal), transcript variant 2, mRNAgi|359751456|ref|NM_008400.3|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Apr 9, 2023