NM_031296.3(RAB33B):c.*590T>C AND Smith-McCort dysplasia 2
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000400758.5
Allele description [Variation Report for NM_031296.3(RAB33B):c.*590T>C]
NM_031296.3(RAB33B):c.*590T>C
Condition(s)
-
Shewanella sp. 10N.286.52.B9, whole genome shotgun sequencing project
Shewanella sp. 10N.286.52.B9, whole genome shotgun sequencing projectgi|1326455132|gb|MCTY00000000.1|MCT 0000Nucleotide
-
Homo sapiens dynein 2 intermediate chain 2 (DYNC2I2), RefSeqGene on chromosome 9
Homo sapiens dynein 2 intermediate chain 2 (DYNC2I2), RefSeqGene on chromosome 9gi|595763551|ref|NG_034056.1|Nucleotide
-
Homo sapiens SVH-C (SVH) mRNA, complete cds; alternatively spliced
Homo sapiens SVH-C (SVH) mRNA, complete cds; alternatively splicedgi|25246386|gb|AY150852.1|Nucleotide
-
USP6NL USP6 N-terminal like [Pan troglodytes]
USP6NL USP6 N-terminal like [Pan troglodytes]Gene ID:466011Gene
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023