NM_021259.3(PGAP6):c.1936A>G (p.Met646Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004253493.1
Allele description [Variation Report for NM_021259.3(PGAP6):c.1936A>G (p.Met646Val)]
NM_021259.3(PGAP6):c.1936A>G (p.Met646Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
SRP007642 (12)
SRA
-
Homo sapiens cDNA: FLJ23123 fis, clone LNG08039
Homo sapiens cDNA: FLJ23123 fis, clone LNG08039gi|10439707|dbj|AK026776.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024