| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193334784 | snp | A/G | 0.0198 | 0.0975088 | intron-variant, synonymous-codon | gly-9, ? | WS195 | III:11288291 | TGTCATATTGCTATT[A/G]TTCACGTGATGAATG | 176558 |
| rs193334785 | snp | A/G | 0.147875 | 0.22819 | synonymous-codon, intron-variant | ?, gly-9 | WS195 | III:11289668 | TTTTGAATGATCTAT[A/G]CATTGAGGGAATTCC | 176558 |
| rs193600977 | snp | A/G | | | intron-variant | gly-9, ? | WS195 | III:11287476 | AATATCGATTTTCCC[A/G]GAAAAAGAGAAAAAT | 176558 |
| rs193600978 | snp | G/T | | | intron-variant | ?, gly-9 | WS195 | III:11287514 | TTTCTTTAAAAAAAA[G/T]AGACCAACTTGACAT | 176558 |
| rs193600979 | snp | C/T | | | intron-variant | gly-9, ? | WS195 | III:11288051 | CCTCGGCCACCAACA[C/T]TACTAATTTTTTTCA | 176558 |
| rs193600980 | snp | C/T | | | intron-variant | ?, gly-9 | WS195 | III:11289125 | AAGGCAGGAAAAAAA[C/T]AAGCAGGTAGTCGCG | 176558 |
| rs193600981 | snp | A/G | | | intron-variant | gly-9, ? | WS195 | III:11289150 | GTCGCGGAGGCAGGC[A/G]TGTAGGCAAGTAGGC | 176558 |
| rs353126752 | in-del | -/T | | | intron-variant | ?, gly-9 | WS195 | III:11290271 | TTTCAGATTTCAGCA[-/T]TTTTTTTCTTTTCTG | 176558 |