NM_004260.4(RECQL4):c.98C>T (p.Ala33Val) AND Baller-Gerold syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003508721.2
Allele description [Variation Report for NM_004260.4(RECQL4):c.98C>T (p.Ala33Val)]
NM_004260.4(RECQL4):c.98C>T (p.Ala33Val)
Condition(s)
-
Homo sapiens regulator of G protein signaling 20 (RGS20), transcript variant 5, ...
Homo sapiens regulator of G protein signaling 20 (RGS20), transcript variant 5, mRNAgi|1676317523|ref|NM_001286675.2|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024