NM_006389.5(HYOU1):c.920C>T (p.Ala307Val) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 15, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002019344.4
Allele description [Variation Report for NM_006389.5(HYOU1):c.920C>T (p.Ala307Val)]
NM_006389.5(HYOU1):c.920C>T (p.Ala307Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
PREDICTED: Homo sapiens ArfGAP with SH3 domain, ankyrin repeat and PH domain 1 (...
PREDICTED: Homo sapiens ArfGAP with SH3 domain, ankyrin repeat and PH domain 1 (ASAP1), transcript variant X1, mRNAgi|2462619491|ref|XM_054360515.1|Nucleotide
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Last Updated: Sep 29, 2024