NM_006509.4(RELB):c.314C>T (p.Pro105Leu) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001890823.5
Allele description [Variation Report for NM_006509.4(RELB):c.314C>T (p.Pro105Leu)]
NM_006509.4(RELB):c.314C>T (p.Pro105Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens solute carrier family 35 member B1 (SLC35B1), transcript variant 1,...
Homo sapiens solute carrier family 35 member B1 (SLC35B1), transcript variant 1, mRNAgi|1653961869|ref|NM_005827.4|Nucleotide
-
Homo sapiens COL18A1 antisense RNA 1 (COL18A1-AS1), transcript variant 2, long n...
Homo sapiens COL18A1 antisense RNA 1 (COL18A1-AS1), transcript variant 2, long non-coding RNAgi|226958363|ref|NR_027498.1|Nucleotide
-
Childhood Astrocytomas Treatment (PDQ®) - PDQ Cancer Information Summaries
Childhood Astrocytomas Treatment (PDQ®) - PDQ Cancer Information Summaries
-
Homo sapiens paired immunoglobin like type 2 receptor alpha (PILRA), transcript ...
Homo sapiens paired immunoglobin like type 2 receptor alpha (PILRA), transcript variant 1, mRNAgi|1520687840|ref|NM_013439.3|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024