GRCh37/hg19 10p12.1(chr10:25133682-25277446)x1 AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 22, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000846016.2
Allele description [Variation Report for GRCh37/hg19 10p12.1(chr10:25133682-25277446)x1]
GRCh37/hg19 10p12.1(chr10:25133682-25277446)x1
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
Chain H, CS2pt1p2_A10L Fab heavy chain
Chain H, CS2pt1p2_A10L Fab heavy chaingi|2559884535|pdb|8TEA|HProtein
-
Homo sapiens RPL13A, U32, U33, U34, U35, RPS11, U35 genes for ibosomal protein L...
Homo sapiens RPL13A, U32, U33, U34, U35, RPS11, U35 genes for ibosomal protein L13a and S11, U32, U33, U34, U35, and U35 snoRNA, complete cds and sequencegi|6552364|dbj|AB028893.1|Nucleotide
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Last Updated: Dec 11, 2022