NM_016139.4(CHCHD2):c.50+241T>C AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Apr 2, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001535339.2
Allele description [Variation Report for NM_016139.4(CHCHD2):c.50+241T>C]
NM_016139.4(CHCHD2):c.50+241T>C
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
transcription factor IIIB 90 kDa subunit isoform X5 [Homo sapiens]
transcription factor IIIB 90 kDa subunit isoform X5 [Homo sapiens]gi|2462539941|ref|XP_054231887.1|Protein
-
transcription factor IIIB 90 kDa subunit isoform X9 [Homo sapiens]
transcription factor IIIB 90 kDa subunit isoform X9 [Homo sapiens]gi|2462539949|ref|XP_054231891.1|Protein
-
PREDICTED: Homo sapiens BRF1 RNA polymerase III transcription initiation factor ...
PREDICTED: Homo sapiens BRF1 RNA polymerase III transcription initiation factor subunit (BRF1), transcript variant X13, mRNAgi|2217297241|ref|XM_024449553.2|Nucleotide
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Last Updated: Dec 24, 2023