NM_000365.6(TPI1):c.192G>A (p.Ala64=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001511228.8
Allele description [Variation Report for NM_000365.6(TPI1):c.192G>A (p.Ala64=)]
NM_000365.6(TPI1):c.192G>A (p.Ala64=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens cDNA clone IMAGE:4121824, partial cds
Homo sapiens cDNA clone IMAGE:4121824, partial cdsgi|33871715|gb|BC007739.2|Nucleotide
-
Sequence 677 from Patent EP1270724
Sequence 677 from Patent EP1270724gi|28798866|emb|AX646485.1||pat|EP| 24|677Nucleotide
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Last Updated: Sep 29, 2024