NM_000136.3(FANCC):c.1450C>A (p.Gln484Lys) AND Fanconi anemia
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 26, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001945361.6
Allele description [Variation Report for NM_000136.3(FANCC):c.1450C>A (p.Gln484Lys)]
NM_000136.3(FANCC):c.1450C>A (p.Gln484Lys)
Condition(s)
-
HSC1RH111 normalized infant brain cDNA Homo sapiens cDNA clone c-1rh11, mRNA seq...
HSC1RH111 normalized infant brain cDNA Homo sapiens cDNA clone c-1rh11, mRNA sequencegi|573200|gnl|dbEST|73246|emb|Z4407Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024