NM_001001991.3(PAMR1):c.607C>T (p.Arg203Trp) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 19, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004500194.1
Allele description [Variation Report for NM_001001991.3(PAMR1):c.607C>T (p.Arg203Trp)]
NM_001001991.3(PAMR1):c.607C>T (p.Arg203Trp)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens BAC clone RP13-492C18 from 7, complete sequence
Homo sapiens BAC clone RP13-492C18 from 7, complete sequencegi|18042312|gb|AC092423.5||gnl|wugs 3-492C18Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 7, 2024