NM_005144.5(HR):c.1947G>A (p.Thr649=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003845380.2
Allele description [Variation Report for NM_005144.5(HR):c.1947G>A (p.Thr649=)]
NM_005144.5(HR):c.1947G>A (p.Thr649=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens cDNA FLJ12203 fis, clone MAMMA1000914
Homo sapiens cDNA FLJ12203 fis, clone MAMMA1000914gi|10433624|dbj|AK022265.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024