Submitter | Handle | CPQ_GEN_INCA | Submitter SNP ID | rs5751738 | RefSNP(rs#) | clustering in process | Submitted Batch ID | Human_Comprehensive_Cancer_Panel_blood | Submitted Date | Jan 27, 2021 | Publication Cited | [1] Analysis of retinoblastoma with a panel of 160 genes- 90 novel, somatic, pathogenic mutations | First entry to dbSNP | Jan 27 2021 12:00:00:000AM |
| Resource Links | Submitted Gene Name | N.D | Submitted Gene ID | N.D. | Submitted SNP Synonyms | N.D | Submitted linkout | N.D |
| Assay | Species | Homo sapiens | Molecular Type | Genomic | Method | SUB8494678 | Ascertainment Samplesize | 46 | Population | PanelRB |
| Allele | Observed Allele | G/C | Ancestral Allele | N.D. | Allele Origin | N/A | SNP Class | SNV | CpG Code | N.D. |
| Validation | Validation Status | Not Validated | HWE Goodness of Fit | not applicable | Homozygote Detected | | PCR Confirmed | | In Expressed Sequence | |
| Variation | Frequency Submission | N.D. | Genotype Summary | N.D. | Genotype Submission | N.D. | Haplotype | N.D. |
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>gnl|dbSNP|ss5236854562|allelePos=26|len=51|taxid=9606|alleles='G/C'|mol=Genomic CTGTGTGTTA CGTGGGAACA GTCCC
S
TTTCCTGCCA GCTGCCTGTC AGGCA
There is no frequency submission for ss5236854562.
No sufficient data to compute Hardy-weinberg probability for ss5236854562.
There is no individual genotype data for ss5236854562.
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