NM_004863.4(SPTLC2):c.*1612G>A AND Neuropathy, hereditary sensory and autonomic, type 1C
- Germline classification:
- Uncertain significance (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:
- RCV001116476.4
Allele description [Variation Report for NM_004863.4(SPTLC2):c.*1612G>A]
NM_004863.4(SPTLC2):c.*1612G>A
Condition(s)
-
PREDICTED: Mus musculus TRM5 tRNA methyltransferase 5 (Trmt5), transcript varian...
PREDICTED: Mus musculus TRM5 tRNA methyltransferase 5 (Trmt5), transcript variant X3, misc_RNAgi|1907089559|ref|XR_872724.4|Nucleotide
-
AGENCOURT_7572794 NIH_MGC_92 Homo sapiens cDNA clone IMAGE:6044485 5', mRNA sequ...
AGENCOURT_7572794 NIH_MGC_92 Homo sapiens cDNA clone IMAGE:6044485 5', mRNA sequencegi|20409918|gnl|dbEST|12226659|gb|B 18.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Apr 9, 2023