NM_212482.4(FN1):c.6336T>C (p.Pro2112=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 30, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002500044.1
Allele description [Variation Report for NM_212482.4(FN1):c.6336T>C (p.Pro2112=)]
NM_212482.4(FN1):c.6336T>C (p.Pro2112=)
Condition(s)
-
Homo sapiens regulator of G protein signaling 2 (RGS2), mRNA
Homo sapiens regulator of G protein signaling 2 (RGS2), mRNAgi|1519316072|ref|NM_002923.4|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024