SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8149556 | snp | A/G | | | synonymous-codon | Psen2 | Rn_Celera | 13:98514244 | CACCAGGTTGTCTGT[A/G]GAGAAGTAAAAGATG | 81751 |
rs8149885 | snp | C/T | | | utr-variant-3-prime | Psen2 | Rn_Celera | 13:98514070 | TTATTCTTTTTTTTT[C/T]TTTTGTAAGGAAAGA | 81751 |
rs8174647 | snp | A/T | | | missense | Psen2 | Rn_Celera | 13:98529021 | CTCACATTCATGGCC[A/T]CTGATAGCGAGGAAG | 81751 |
rs8174937 | snp | C/T | | | synonymous-codon | Psen2 | Rn_Celera | 13:98515515 | GACGCTGGCCTGCTT[C/T]ATCGCCATCCTCATT | 81751 |
rs105851495 | snp | A/C | 0 | 0 | intron-variant | Psen2 | Rn_Celera | 13:98534595 | CATTTTGTCAAAGGA[A/C]CAGTCACGTCCATGG | 81751 |
rs105959136 | snp | C/G | 0 | 0 | intron-variant | Psen2 | Rn_Celera | 13:98517345 | AAATGCAGAAGAAAA[C/G]TAAAAGCCTATCTGT | 81751 |
rs197937143 | snp | A/C | 0 | 0 | intron-variant | Psen2 | Rn_Celera | 13:98523612 | TCCGGAAAAAAAAGA[A/C]CCAAAAAAAAAAAAA | 81751 |