NM_203282.4(ZNF254):c.227G>T (p.Arg76Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004115969.1
Allele description [Variation Report for NM_203282.4(ZNF254):c.227G>T (p.Arg76Leu)]
NM_203282.4(ZNF254):c.227G>T (p.Arg76Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens GS homeobox 2 (GSX2), mRNA
Homo sapiens GS homeobox 2 (GSX2), mRNAgi|1519315608|ref|NM_133267.3|Nucleotide
-
Homo sapiens BAC clone RP11-367N1 from 4, complete sequence
Homo sapiens BAC clone RP11-367N1 from 4, complete sequencegi|23308141|gb|AC110298.5||gnl|wugs 1-367N1Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024