NM_019043.4(APBB1IP):c.1865C>T (p.Ala622Val) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- May 8, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000947236.4
Allele description [Variation Report for NM_019043.4(APBB1IP):c.1865C>T (p.Ala622Val)]
NM_019043.4(APBB1IP):c.1865C>T (p.Ala622Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens clone DNA108771 C20orf16 (UNQ3039) mRNA, complete cds
Homo sapiens clone DNA108771 C20orf16 (UNQ3039) mRNA, complete cdsgi|37181313|gb|AY358104.1|Nucleotide
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Last Updated: Sep 29, 2024