NM_001171109.2(FAM133A):c.662A>G (p.Lys221Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 27, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004239356.1
Allele description [Variation Report for NM_001171109.2(FAM133A):c.662A>G (p.Lys221Arg)]
NM_001171109.2(FAM133A):c.662A>G (p.Lys221Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens ADP ribosylation factor like GTPase 6 (ARL6), transcript variant 12...
Homo sapiens ADP ribosylation factor like GTPase 6 (ARL6), transcript variant 12, non-coding RNAgi|1889749951|ref|NR_136602.3|Nucleotide
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See more...Assertion and evidence details
Last Updated: Jun 2, 2024