NM_000059.4(BRCA2):c.267G>T (p.Pro89=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 10, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001637051.3
Allele description [Variation Report for NM_000059.4(BRCA2):c.267G>T (p.Pro89=)]
NM_000059.4(BRCA2):c.267G>T (p.Pro89=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Amanita supravolvata voucher RET 103-7 18S ribosomal RNA gene, partial sequence;...
Amanita supravolvata voucher RET 103-7 18S ribosomal RNA gene, partial sequence; internal transcribed spacer 1, 5.8S ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequencegi|1652651804|gb|KP258995.2|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024