NM_003179.3(SYP):c.456G>A (p.Met152Ile) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003480407.1
Allele description [Variation Report for NM_003179.3(SYP):c.456G>A (p.Met152Ile)]
NM_003179.3(SYP):c.456G>A (p.Met152Ile)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens chromosome 18, clone RP11-650P15, complete sequence
Homo sapiens chromosome 18, clone RP11-650P15, complete sequencegi|19033940|gnl|WIBR|L5633|gb|AC021 |Nucleotide
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See more...Assertion and evidence details
Last Updated: Jan 6, 2024