NM_001122630.2(CDKN1C):c.574_575insACCCGG (p.Pro191_Ala192insAspPro) AND Beckwith-Wiedemann syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 24, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001410418.13
Allele description [Variation Report for NM_001122630.2(CDKN1C):c.574_575insACCCGG (p.Pro191_Ala192insAspPro)]
NM_001122630.2(CDKN1C):c.574_575insACCCGG (p.Pro191_Ala192insAspPro)
Condition(s)
-
Homo sapiens SH2 domain containing 4A (SH2D4A), mRNA
Homo sapiens SH2 domain containing 4A (SH2D4A), mRNAgi|21361890|ref|NM_022071.2|Nucleotide
-
LOC4345046 [Oryza sativa Japonica Group]
LOC4345046 [Oryza sativa Japonica Group]Gene ID:4345046Gene
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See more...Assertion and evidence details
Last Updated: Oct 20, 2024