NM_005861.4(STUB1):c.771C>T (p.Ile257=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003312319.11
Allele description
NM_005861.4(STUB1):c.771C>T (p.Ile257=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens mRNA; cDNA DKFZp686E01209 (from clone DKFZp686E01209)
Homo sapiens mRNA; cDNA DKFZp686E01209 (from clone DKFZp686E01209)gi|34367757|emb|BX648595.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024