NM_000059.4(BRCA2):c.7806-14T>C AND Fanconi anemia complementation group D1
- 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:
- RCV000386451.13
Allele description [Variation Report for NM_000059.4(BRCA2):c.7806-14T>C]
NM_000059.4(BRCA2):c.7806-14T>C
Condition(s)
-
UFM1P3 UFM1 pseudogene 3 [Homo sapiens]
UFM1P3 UFM1 pseudogene 3 [Homo sapiens]Gene ID:100506633Gene
-
LOC105375733 [Homo sapiens]
LOC105375733 [Homo sapiens]Gene ID:105375733Gene
-
NMTRQ-TTG11-1 nuclear-encoded mitochondrial tRNA-Gln (TTG) 11-1 [Homo sapiens]
NMTRQ-TTG11-1 nuclear-encoded mitochondrial tRNA-Gln (TTG) 11-1 [Homo sapiens]Gene ID:100189501Gene
-
RNA5SP271 RNA, 5S ribosomal pseudogene 271 [Homo sapiens]
RNA5SP271 RNA, 5S ribosomal pseudogene 271 [Homo sapiens]Gene ID:100873524Gene
-
RPL7L1P18 RPL7L1 pseudogene 18 [Homo sapiens]
RPL7L1P18 RPL7L1 pseudogene 18 [Homo sapiens]Gene ID:100131013Gene
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Last Updated: Sep 16, 2024