NM_000218.3(KCNQ1):c.*806C>T AND Short QT syndrome type 2
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000274123.7
Allele description [Variation Report for NM_000218.3(KCNQ1):c.*806C>T]
NM_000218.3(KCNQ1):c.*806C>T
Condition(s)
-
Rattus norvegicus C-x(9)-C motif containing 1 (Cmc1), transcript variant 1, mRNA...
Rattus norvegicus C-x(9)-C motif containing 1 (Cmc1), transcript variant 1, mRNA; nuclear gene for mitochondrial productgi|312839829|ref|NM_001199225.1|Nucleotide
-
ankyrin-like protein [Vaccinia virus]
ankyrin-like protein [Vaccinia virus]gi|66275813|ref|YP_232898.1|Protein
-
aldh2.1 aldehyde dehydrogenase 2 family member, tandem duplicate 1 [Danio rerio]
aldh2.1 aldehyde dehydrogenase 2 family member, tandem duplicate 1 [Danio rerio]Gene ID:393462Gene
-
393462[uid] AND (alive[prop]) (1)
Gene
-
Homo sapiens solute carrier family 6 member 4 (SLC6A4) gene, exon 11 and partial...
Homo sapiens solute carrier family 6 member 4 (SLC6A4) gene, exon 11 and partial cdsgi|190889231|gb|EU796619.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Dec 24, 2023