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Characterized by: Sanger Center, Cambridge Laboratory Internal ID: scsnp-AL137795.9_35135 dbSNP Acc# 1383206 Submit Date: 12 Jul 2000 Release Date: Confirmed: n/a 
| Ornamentation | Ambiguity Codes | |||||
|---|---|---|---|---|---|---|
| This Polymorphism | M | a/c | V | a/c/g | ||
| Other Polymorphism (link) | N | a/c/g/t | H | a/c/t | ||
| Repeat masked region | R | a/g | D | a/g/t | ||
| Mapping Primer | W | a/t | S | c/g | ||
| Confirmation Primer | B | c/g/t | Y | c/t | ||
| K | g/t | |||||
Tracefile Position Reversed p1_0t378f07.q1cSCF 96 no AL137795 (genomic alignment) 35135 no 
Allele Times seen a 1 g 1 
| Band | GenBank Entry | Contig | Chrom | 
|---|---|---|---|
| 1p36.31-1p36.33 | AL137795.10 | NT_000002 | Chr1 | 
| Relative Position | 33893 | 234039 | 8567.0 kb | 
| Accession# | Pval | Cliq_begin | Cliq_end | Acc_begin | Acc_end | Description | 
|---|---|---|---|---|---|---|
| AL137795.10 | 9.50e-78 | -81 | 187 | 33878 | 34027 | Human DNA sequence from clone RP5-1096P7 on chromosome 1p36.31-36.33, complete sequence. | 
 
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