| NM_001532
|
| Transcript: | NM_001532 [Chr.11(-): 66129992-66139291 GRCh37] |
| Id: | SLC29A2_exon12 |
| Position: | Chr.11(-): 66130854-66131081 GRCh37 |
| Chr.11(-): 65887430-65887657 NCBI36 | |
| Sequence: | GTGGAGCTGGGTCCAGATTTAGACCCAGCATTTTCTAAGAGCTCCTGTTCCCGGGTGTTCTAGGCAGGTGCTGCCACACG
AGAGGGAGGTGGCCGGCGCCCTCATGACCTTCTTCCTGGCCCTGGGACTTTCCTGTGGAGCCTCCCTCTCCTTCCTCTTC AAGGCGCTGCTCTGAAGTGGCCCCTCCAGGCTCTTTGGCAGCCTCTTCTCGACGTCTCCTTCCGGAGC Color Legend: SNP UTR CODING |
| Sample Sets: | Set-I |
| Assays: | SLC29A2_12_PCR |
PMT impact: P - Public D - Discovered E - Exclusive (dbSNP build 137)
Array availability: I - found on Illumina Human1M-Duo BeadChip (2011-04-21) A - found on Affymetrix Genome-Wide SNP Array 6.0 (2011-06-21)
| Feature | PMT SNP ID | dbSNP/ PubMed | SNP Array Availability | Genomic Position | Transcript Position | Coding Position | Nucleotide Change | Strand, '+' or '-' | Amino Acid Position | Amino Acid Change | Statistics | Sample Set | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| no variants | |||||||||||||
Transmembrane prediction:
Non-synonymous amino acid changes shown in red, indels (insertions and deletions) in blue, and synonymous changes in green. Exon(s) indicated by black outlines.