NM_000179.3(MSH6):c.818G>T (p.Gly273Val) AND Hereditary cancer
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 23, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003491994.1
Allele description [Variation Report for NM_000179.3(MSH6):c.818G>T (p.Gly273Val)]
NM_000179.3(MSH6):c.818G>T (p.Gly273Val)
Condition(s)
- Name:
- Hereditary cancer
- Identifiers:
- MedGen: C1333600
-
Prom2 prominin 2 [Mus musculus]
Prom2 prominin 2 [Mus musculus]Gene ID:192212Gene
-
192212[uid] AND (alive[prop]) (1)
Gene
-
Mus musculus exophilin 5, mRNA (cDNA clone MGC:141574 IMAGE:40087301), complete ...
Mus musculus exophilin 5, mRNA (cDNA clone MGC:141574 IMAGE:40087301), complete cdsgi|111309318|gb|BC120905.1|Nucleotide
-
Homo sapiens nucleolar protein family 6 (RNA-associated), mRNA (cDNA clone MGC:2...
Homo sapiens nucleolar protein family 6 (RNA-associated), mRNA (cDNA clone MGC:20838 IMAGE:4423152), complete cdsgi|40226130|gb|BC030139.2|Nucleotide
-
Homo sapiens nucleolar protein family 6 (RNA-associated), mRNA (cDNA clone IMAGE...
Homo sapiens nucleolar protein family 6 (RNA-associated), mRNA (cDNA clone IMAGE:4100186), partial cdsgi|39645212|gb|BC008852.2|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Oct 20, 2024