NM_001370549.1(SLC16A11):c.709C>T (p.Pro237Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 2, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004088982.1
Allele description [Variation Report for NM_001370549.1(SLC16A11):c.709C>T (p.Pro237Ser)]
NM_001370549.1(SLC16A11):c.709C>T (p.Pro237Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens catenin delta 1 (CTNND1), transcript variant 21, mRNA
Homo sapiens catenin delta 1 (CTNND1), transcript variant 21, mRNAgi|332688219|ref|NM_001206890.1|Nucleotide
-
bcl-2-like protein 13 isoform X1 [Homo sapiens]
bcl-2-like protein 13 isoform X1 [Homo sapiens]gi|2462584471|ref|XP_054181411.1|Protein
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Niumbaha superba isolate MNHN2016x2807 recombination activating protein 2 (RAG2)...
Niumbaha superba isolate MNHN2016x2807 recombination activating protein 2 (RAG2) gene, partial cdsgi|1344455010|gb|MF038395.1|Nucleotide
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Niumbaha superba isolate K13x322 recombination activating protein 2 (RAG2) gene,...
Niumbaha superba isolate K13x322 recombination activating protein 2 (RAG2) gene, partial cdsgi|1344455008|gb|MF038394.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024