| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193319501 | snp | G/T | 0.0198 | 0.0975088 | missense | C44E4.1, ? | WS195 | I:4612920 | TTCGGATCACTGACA[G/T]CATTCGTTCCACCAT | 172068 |
| rs193319502 | snp | C/T | 0.0203024 | 0.0986865 | intron-variant | C44E4.1 | WS195 | I:4621720 | GAACTGCAGGACCAA[C/T]CAGCGATTTGCTCCG | 172068 |
| rs193573661 | snp | A/C | | | utr-variant-3-prime | ? | WS195 | I:4610166 | TTGATTAAATATTTT[A/C]TTTATTAAAAACTCT | 172068 |
| rs193573662 | snp | C/T | | | intron-variant | ?, C44E4.1 | WS195 | I:4611882 | GCGGTAATTCTAAAA[C/T]TCGGTGCTTTCAAAT | 172068 |
| rs193573663 | snp | A/T | | | intron-variant | C44E4.1 | WS195 | I:4616594 | CAAAAAAATGAAAAA[A/T]TTTTTTTTGAGGTCT | 172068 |
| rs193573664 | snp | A/T | | | intron-variant | C44E4.1 | WS195 | I:4616647 | ATTGGCCGATATTGT[A/T]CGTCGGAAAATAAAT | 172068 |
| rs193573665 | snp | A/T | | | intron-variant | C44E4.1 | WS195 | I:4618124 | CAAAATTTTCTTAAA[A/T]TTCCAATTTAATTAA | 172068 |
| rs193573666 | snp | C/T | | | missense | C44E4.1 | WS195 | I:4620224 | TCAATCGGAATAGTT[C/T]CAGCGATTTTCGCGA | 172068 |
| rs193573667 | snp | A/G | | | intron-variant | C44E4.1 | WS195 | I:4622777 | TGCATTGTGGCAACT[A/G]AAAATTCGAAATTAT | 172068 |
| rs353105373 | snp | A/G | | | intron-variant | C44E4.1 | WS195 | I:4616781 | ATTTTCAACTTTTTG[A/G]TCCAAAATAATTTTC | 172068 |
| rs353107631 | snp | C/T | | | intron-variant | C44E4.1 | WS195 | I:4621814 | TGGCTTAATCTATCT[C/T]GATTTTTCAATATTT | 172068 |
| rs353131990 | in-del | -/A | | | intron-variant | C44E4.1 | WS195 | I:4616154 | CGCCTGAAAATTTCG[-/A]AAAAAAAAAATTTCA | 172068 |
| rs353141771 | in-del | -/T | | | intron-variant | C44E4.1 | WS195 | I:4621264 | GAAATTTTTCAATTG[-/T]TTTTTTTTTTCAATT | 172068 |
| rs353145121 | in-del | -/T | | | intron-variant | C44E4.1 | WS195 | I:4621409 | TGCTAAACGTTGCGA[-/T]TTTTTTTTGATTTTC | 172068 |
| rs353150911 | snp | C/T | | | intron-variant | C44E4.1 | WS195 | I:4619472 | TTTTAAAAAGTTTTT[C/T]AGACAAAAAAATTCT | 172068 |
| rs353163584 | snp | A/T | | | intron-variant | ?, C44E4.1 | WS195 | I:4613037 | AACTAGAAAAAGTTT[A/T]AAATTTTGGGTTTTA | 172068 |