NM_203416.4(CD163):c.2240G>C (p.Ser747Thr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 13, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004199671.1
Allele description [Variation Report for NM_203416.4(CD163):c.2240G>C (p.Ser747Thr)]
NM_203416.4(CD163):c.2240G>C (p.Ser747Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens arylformamidase (AFMID), transcript variant 12, non-coding RNA
Homo sapiens arylformamidase (AFMID), transcript variant 12, non-coding RNAgi|1890391776|ref|NR_027083.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024