NM_001370326.1(ANKFN1):c.1131A>T (p.Arg377Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004164655.1
Allele description [Variation Report for NM_001370326.1(ANKFN1):c.1131A>T (p.Arg377Ser)]
NM_001370326.1(ANKFN1):c.1131A>T (p.Arg377Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
PREDICTED: Homo sapiens cyclin C (CCNC), transcript variant X6, mRNA
PREDICTED: Homo sapiens cyclin C (CCNC), transcript variant X6, mRNAgi|2462611192|ref|XM_054356696.1|Nucleotide
-
PREDICTED: Homo sapiens cyclin C (CCNC), transcript variant X5, mRNA
PREDICTED: Homo sapiens cyclin C (CCNC), transcript variant X5, mRNAgi|2462611190|ref|XM_054356695.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024