SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs31954373 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Rasd2 | GRCm38.p3 | 8:75221061 | TGCAGCCATGGCCTA[C/G]CACATTTGAGTCGTG | 75141 |
rs31954384 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B | Rasd2 | Mm_Celera | 8:75224320 | AGACTGGCCGAGGAG[C/T]CAGATACTGTGACAT | 75141 |
rs31954387 | snp | A/G | 0.48 | 0.0979796 | downstream-variant-500B | Rasd2 | GRCm38.p3 | 8:75224380 | TTGCTACAGTGACCA[A/G]CCTGGTAATATGAGT | 75141 |
rs31954390 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Rasd2 | GRCm38.p3 | 8:75224513 | ATAGGGATGGTAGGC[A/G]GTGCCATCTAGAAGG | 75141 |
rs31954393 | snp | C/G | 0.497778 | 0.0332592 | downstream-variant-500B | Rasd2 | GRCm38.p3 | 8:75224607 | AACAGTCAATCTTTC[C/G]AAGTTGAGAAGGGAT | 75141 |
rs31955745 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rasd2 | Mm_Celera | 8:75221074 | TACCACATTTGAGTC[A/G]TGTGACCTTGGGCAG | 75141 |
rs31955748 | snp | C/T | 0.32 | 0.24 | intron-variant | Rasd2 | Mm_Celera | 8:75221366 | AGATGCAAACCAAAG[C/T]TCCCTCTCACCAACA | 75141 |
rs31955751 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rasd2 | Mm_Celera | 8:75221518 | GACCATATCTGAGTC[C/T]ACCTGGGTGTGCCTC | 75141 |
rs31956264 | snp | C/T | 0.48 | 0.0979796 | synonymous-codon | Rasd2 | GRCm38.p3 | 8:75221987 | GAACACTAATGTGAA[C/T]GAGATGTTCTATGTG | 75141 |
rs31956267 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Rasd2 | Mm_Celera | 8:75222062 | GCACCATAAGATCTC[C/T]GTGCAGTACGGCGAT | 75141 |
rs31956269 | snp | A/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75222375 | TCTTGTTTCCTGGAC[A/T]CCTCCTGTGAGCCGT | 75141 |
rs31956271 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75222389 | CACCTCCTGTGAGCC[A/G]TGAGTGTGGTTCCTT | 75141 |
rs31956273 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75222416 | CCTTTGTGGGAGGAC[A/G]GAGACATGTCTAGGG | 75141 |
rs31957365 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75222465 | CGAGACAAGCTTTCC[A/G]TGGGAGGGATGCAAA | 75141 |
rs31957367 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75222593 | TGCTCCCTCTGTTCA[C/G]ACCAGCTTGGTCTCA | 75141 |
rs31957369 | snp | G/T | 0.495868 | 0.0452663 | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75222816 | agagagagagagaCC[G/T]GTGTCCCCCAGATCA | 75141 |
rs31957371 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75222948 | GTAAGAGGCCAATGC[C/T]TTGTCTTTGACCGGG | 75141 |
rs31958354 | snp | A/G | 0.495 | 0.0497494 | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75223025 | TCCCAGGCAGGCTGT[A/G]TTCTGCCCAGTGTCC | 75141 |
rs31958357 | snp | A/C | 0.32 | 0.24 | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75223083 | ACAGTCACAGCAGTA[A/C]TCTCCTGCCCTCTGG | 75141 |
rs31958360 | snp | A/G | 0.487535 | 0.077957 | utr-variant-3-prime | Rasd2 | GRCm38.p3 | 8:75223111 | TGGAGAGGATGACTG[A/G]GCTTTGAGAGAGTGA | 75141 |
rs31958363 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75223355 | GTGGAGCAGTTGAGA[A/G]CCAGAGCCGAGTCCA | 75141 |
rs31959145 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75223517 | ATTAGTACTGCAGCT[A/G]GCCCATTTGAGATGA | 75141 |
rs31959147 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime | Rasd2 | GRCm38.p3 | 8:75223539 | TTGAGATGACTCTGG[A/G]TAAAGACACCTGCTG | 75141 |
rs31959150 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75223549 | TCTGGGTAAAGACAC[C/T]TGCTGCCAAGCTTTC | 75141 |
rs31959153 | snp | A/G | 0.49827 | 0.0293608 | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75223582 | CCTGAGTTTGGTCCC[A/G]GGGTTCCATGTGGTG | 75141 |
rs31959926 | snp | A/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75223839 | GGATCATGTTACATA[A/T]GCCTTCCTCAGAGCA | 75141 |
rs31959929 | snp | A/C | 0.475309 | 0.108333 | utr-variant-3-prime | Rasd2 | GRCm38.p3 | 8:75223935 | CAGACTCCATACACA[A/C]ACCTGCTGCTCAGCA | 75141 |
rs31959932 | snp | C/T | 0.493827 | 0.0552116 | utr-variant-3-prime | Rasd2 | GRCm38.p3 | 8:75223954 | TGCTGCTCAGCACAA[C/T]TGCTTCAGCACCTGC | 75141 |
rs31960665 | snp | C/T | 0.475309 | 0.108333 | utr-variant-3-prime | Rasd2 | GRCm38.p3 | 8:75224048 | ATGGCCTGGTCCATC[C/T]GGTCAAGCTCTACTG | 75141 |
rs31960668 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75224070 | GCTCTACTGCCTGGA[C/T]CTCTGTGTACACTAT | 75141 |
rs31960671 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Rasd2 | GRCm38.p3 | 8:75224166 | TCTGTCTGGGTCAAG[A/G]CCTCCTTGCATACAA | 75141 |
rs31961464 | snp | C/T | 0.48 | 0.0979796 | downstream-variant-500B | Rasd2 | GRCm38.p3 | 8:75224218 | TTTGGAGGATGAAAC[C/T]CAAATAAGGAGATTG | 75141 |
rs32633215 | snp | C/T | 0.5 | 0 | intron-variant | Rasd2 | GRCm38.p3 | 8:75216662 | TGATGCCTGCAGAAG[C/T]ATCTGCAATGTCTCT | 75141 |
rs32634538 | snp | A/C | 0.5 | 0 | intron-variant | Rasd2 | GRCm38.p3 | 8:75214472 | TTTAACCTATCCTAG[A/C]GTCCCTTGAGCTTTG | 75141 |
rs32817031 | snp | A/G | 0.5 | 0 | intron-variant | Rasd2 | GRCm38.p3 | 8:75216757 | TCACAGGTCAGTTCA[A/G]TGGGGGACATCAGGG | 75141 |
rs32865175 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rasd2 | GRCm38.p3 | 8:75215461 | AGAGTCCCCATCTGT[C/T]CCTGCAGAGCGTCTC | 75141 |
rs33119505 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Rasd2 | GRCm38.p3 | 8:75212318 | TGCGCAGGACCAGGA[A/T]TTGAAGGGAACACAG | 75141 |
rs33526412 | snp | A/G | 0.5 | 0 | intron-variant | Rasd2 | GRCm38.p3 | 8:75219204 | CGAGCAGGGACCAGC[A/G]TTTGATCCCCAGCAC | 75141 |
rs33609744 | snp | C/T | 0.5 | 0 | intron-variant | Rasd2 | GRCm38.p3 | 8:75214479 | TATCCTAGCGTCCCT[C/T]GAGCTTTGGAGCATT | 75141 |
rs47896788 | snp | A/C | | | intron-variant | Rasd2 | GRCm38.p3 | 8:75215948 | TCATTCCCCTGCCCC[A/C]AACCCCACTCTGGCA | 75141 |
rs48886683 | snp | C/T | | | intron-variant | Rasd2 | GRCm38.p3 | 8:75216100 | GGAGCCACAGATGCT[C/T]TGTCACCTGGCTTCC | 75141 |
rs51488798 | snp | A/T | | | intron-variant | Rasd2 | GRCm38.p3 | 8:75214780 | TGACTACTCAGAGAG[A/T]CTGCCCAAAGAAAAG | 75141 |
rs51738976 | snp | A/G | | | downstream-variant-500B | Rasd2 | GRCm38.p3 | 8:75224228 | GAAACCCAAATAAGG[A/G]GATTGTGCCTGGCCT | 75141 |
rs52135253 | snp | A/G | | | utr-variant-3-prime | Rasd2 | GRCm38.p3 | 8:75222733 | GGGGgagagagaaag[A/G]gagagagagagagag | 75141 |
rs52194591 | snp | A/G | | | utr-variant-3-prime | Rasd2 | GRCm38.p3 | 8:75222721 | CCTTGAGTGGAGGGG[A/G]GAGAGAGAAAGGGAG | 75141 |
rs52446581 | snp | A/G | | | utr-variant-3-prime | Rasd2 | GRCm38.p3 | 8:75222730 | GAGGGGGgagagaga[A/G]agggagagagagaga | 75141 |
rs211749404 | in-del | -/A | | | intron-variant | Rasd2 | Mm_Celera | 8:75219215 | CAGCGTTTGATCCCC[-/A]GCACACAGACCAAGA | 75141 |
rs212086553 | snp | A/C | | | intron-variant | Rasd2 | Mm_Celera | 8:75215905 | ACATTGCAGATGCTT[A/C]TGCAGGCTTCAGGCT | 75141 |
rs212225196 | snp | A/G | | | intron-variant | Rasd2 | Mm_Celera | 8:75215091 | TGTGGCAGGTAGTGT[A/G]GTGAACCTGGCTCTG | 75141 |
rs212608363 | snp | A/T | | | intron-variant | Rasd2 | Mm_Celera | 8:75217395 | ATAATGATAAAAAAA[A/T]AATGGCTGAGGTATC | 75141 |
rs213058873 | snp | A/G | | | intron-variant | Rasd2 | Mm_Celera | 8:75218014 | GCTGTATGTGAGGAG[A/G]AGCCTACCATGATGC | 75141 |
rs213209079 | snp | A/G | | | intron-variant | Rasd2 | Mm_Celera | 8:75220132 | TTTTCAATTATAAAA[A/G]TGATACAAAGGCAAA | 75141 |
rs213264601 | snp | C/G | | | intron-variant | Rasd2 | Mm_Celera | 8:75220960 | CTAGTGTGGGCTGCA[C/G]TTTCTTACTTATCCT | 75141 |
rs213799955 | in-del | -/TCTTCTGTTT | | | intron-variant | Rasd2 | Mm_Celera | 8:75216276 | CCCTCCCTCCGTGAG[-/TCTTCTGTTT]TCTTCTGTTTTCTCT | 75141 |
rs213888098 | snp | A/G | | | intron-variant | Rasd2 | Mm_Celera | 8:75214884 | TGAGCTGAGTGCACA[A/G]ACCAGATCACTCAGA | 75141 |
rs214217820 | in-del | -/CAG | | | intron-variant | Rasd2 | Mm_Celera | 8:75221177 | GAGGTGCCCAGGAAA[-/CAG]CATGTGTGCCTACTC | 75141 |
rs214308680 | snp | C/G | | | intron-variant | Rasd2 | Mm_Celera | 8:75215980 | TTAGGATTTGTCTTT[C/G]CCCACTGTGGAGTTA | 75141 |
rs214369483 | snp | A/C/G | | | intron-variant | Rasd2 | Mm_Celera | 8:75216750 | CACAGACTCACAGGT[A/C/G]AGTTCAGTGGGGGAC | 75141 |
rs214892406 | snp | A/G | | | intron-variant | Rasd2 | Mm_Celera | 8:75218142 | GCACCAGAAGCTGTG[A/G]AATAAGGAGCGCTGC | 75141 |
rs214959909 | snp | C/T | | | intron-variant | Rasd2 | Mm_Celera | 8:75219815 | TACTACCAAGAACCC[C/T]ACAAACTGCCCCCTT | 75141 |
rs215418152 | snp | A/G | | | intron-variant | Rasd2 | Mm_Celera | 8:75221155 | AATCTTCCCCATGGG[A/G]GTATTATGAGGTGCC | 75141 |
rs215479529 | snp | C/T | | | upstream-variant-2KB | Rasd2 | Mm_Celera | 8:75212415 | TCCACCCCTTCCAAG[C/T]CTCGCCCGCACATCT | 75141 |
rs215481927 | snp | A/G | | | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75222413 | GTTCCTTTGTGGGAG[A/G]ACGGAGACATGTCTA | 75141 |
rs215543136 | snp | A/G | | | upstream-variant-2KB | Rasd2 | Mm_Celera | 8:75212928 | GAGGTTGGGAGGTCA[A/G]GAGCGGGTTCCCACA | 75141 |
rs216006511 | in-del | -/ACAC | | | intron-variant | Rasd2 | Mm_Celera | 8:75219671 | TGCACACATACACAA[-/ACAC]ACACACACACACACA | 75141 |
rs216011556 | snp | A/G | | | intron-variant | Rasd2 | Mm_Celera | 8:75215021 | CCCCAGAGCCTAGGG[A/G]AGGAGTCAGGACTAC | 75141 |
rs216067870 | snp | C/T | | | intron-variant | Rasd2 | Mm_Celera | 8:75215791 | GTCTGGTCCTAAAAC[C/T]CTGATGTCCCCACTG | 75141 |
rs216736880 | snp | A/G | | | downstream-variant-500B | Rasd2 | Mm_Celera | 8:75224509 | ATCCATAGGGATGGT[A/G]GGCGGTGCCATCTAG | 75141 |
rs217126783 | snp | C/G | | | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75223653 | TGGTACCCCTAGCGC[C/G]CCCCCCCCCCCCCAT | 75141 |
rs217193962 | snp | C/T | | | upstream-variant-2KB | Rasd2 | Mm_Celera | 8:75212235 | GCACAGAGCTCTCAC[C/T]CAGGCTTTCCTGCCT | 75141 |
rs217649053 | in-del | -/G | | | upstream-variant-2KB | Rasd2 | GRCm38.p3 | 8:75212705 | TCAGGGACGGGAAGA[-/G]CTAGGTCCCACCAAG | 75141 |
rs217777632 | snp | A/G | | | intron-variant | Rasd2 | Mm_Celera | 8:75216783 | CAGGGTTTTAGGACC[A/G]GAACTCCACCACATG | 75141 |
rs217999214 | snp | G/T | | | intron-variant | Rasd2 | Mm_Celera | 8:75217297 | GGCATGAGCAGAGTC[G/T]GTGCATACCTAGAGA | 75141 |
rs218600423 | snp | C/T | | | intron-variant | Rasd2 | Mm_Celera | 8:75218424 | GAAGTCCTTCAGGGA[C/T]CCTAGCCAATGGCTT | 75141 |
rs218658929 | snp | C/T | | | intron-variant | Rasd2 | Mm_Celera | 8:75219910 | TCTGCTTAAGGAACT[C/T]AAGGTGGGCCTGGGT | 75141 |
rs218897126 | snp | A/C | | | intron-variant | Rasd2 | Mm_Celera | 8:75218892 | AGGCTATGTCTAGGA[A/C]ACTGAGGCAGAGTGG | 75141 |
rs218913830 | snp | A/G | | | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75223639 | CCACACATCCATCAT[A/G]GTACCCCTAGCGCGC | 75141 |
rs219377186 | in-del | -/TTCTGTTTTT | | | intron-variant | Rasd2 | Mm_Celera | 8:75216288 | GAGTCTTCTGTTTTC[-/TTCTGTTTTT]TCTCTTCCTTCATTC | 75141 |
rs219407647 | snp | A/T | | | upstream-variant-2KB | Rasd2 | Mm_Celera | 8:75213001 | TCCCAGGCCCGTGCC[A/T]TACGGTCTTCCGGTC | 75141 |
rs219492800 | snp | A/T | | | intron-variant | Rasd2 | Mm_Celera | 8:75220643 | CTTCCTAGTTCATGC[A/T]GTACATGTGTGTCAT | 75141 |
rs219658079 | snp | C/T | | | upstream-variant-2KB | Rasd2 | Mm_Celera | 8:75213928 | GCCCAGCTCCGGGCG[C/T]CGCGCGCAGGAGGAT | 75141 |
rs219822011 | snp | A/G | | | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75224013 | TCCTGAGTATACCAG[A/G]TACTTGTCCAGGCAA | 75141 |
rs219876653 | snp | A/G | | | intron-variant | Rasd2 | Mm_Celera | 8:75214714 | GCCTCAGAGGGACAA[A/G]AAAGAGTCCCTGCAA | 75141 |
rs219925451 | snp | C/T | | | upstream-variant-2KB | Rasd2 | Mm_Celera | 8:75213695 | CCGGAGTCGTGCCCC[C/T]TCCCCTTCAGCGCGG | 75141 |
rs219929302 | snp | C/T | | | intron-variant | Rasd2 | Mm_Celera | 8:75215417 | AGGTGAGATTGGACT[C/T]GGGCAGCCACTCAAC | 75141 |
rs220199010 | in-del | -/TC | | | intron-variant | Rasd2 | Mm_Celera | 8:75215617 | ATTCAGTTCCCCACT[-/TC]TCTCTAGACCACCAA | 75141 |
rs220579798 | snp | A/T | | | intron-variant | Rasd2 | Mm_Celera | 8:75216407 | TTGGGAGGCCTGGCT[A/T]GAAGCTGGGACAAGG | 75141 |
rs220636085 | snp | C/T | | | intron-variant | Rasd2 | Mm_Celera | 8:75216908 | AGCATGGGACAGGCC[C/T]TTCTTCCTGGGACCT | 75141 |
rs220694657 | snp | C/T | | | intron-variant | Rasd2 | Mm_Celera | 8:75217411 | AATGGCTGAGGTATC[C/T]AGATGAGGCTGTGGT | 75141 |
rs220728736 | snp | A/G | | | intron-variant | Rasd2 | Mm_Celera | 8:75216832 | GGCTGACATAGCCAC[A/G]GTGACCTGGATAGAA | 75141 |
rs220747989 | snp | C/T | | | intron-variant | Rasd2 | Mm_Celera | 8:75219519 | acggacacagataca[C/T]gcacacatacacaca | 75141 |
rs220858049 | snp | C/T | | | intron-variant | Rasd2 | Mm_Celera | 8:75219133 | ATCCCTGGATAGAAA[C/T]AGAAGGGAGCATACG | 75141 |
rs220918724 | snp | A/G | | | intron-variant | Rasd2 | Mm_Celera | 8:75220322 | TGGTTCTGGGCACAA[A/G]AGATGCACAGGGCTG | 75141 |
rs221033687 | snp | C/T | | | intron-variant | Rasd2 | Mm_Celera | 8:75216379 | CTGACTCTCTCCTTT[C/T]ATTCATTGTGTCTTG | 75141 |
rs221183802 | in-del | -/CGCCCCC | | | utr-variant-3-prime | Rasd2 | Mm_Celera | 8:75223652 | ATGGTACCCCTAGCG[-/CGCCCCC]CCCCCCCCATGAATT | 75141 |
rs221782213 | snp | C/T | | | intron-variant | Rasd2 | Mm_Celera | 8:75215492 | ATAAGAATAAGGCAG[C/T]CCCAGCATGACATGC | 75141 |
rs221820612 | snp | A/C | | | upstream-variant-2KB | Rasd2 | Mm_Celera | 8:75213462 | GAGCGCAGCTAGCGG[A/C]GTCGGGCGAGGAGCA | 75141 |
rs221823507 | snp | C/T | | | intron-variant | Rasd2 | Mm_Celera | 8:75216271 | CGCACCCCCTCCCTC[C/T]GTGAGTCTTCTGTTT | 75141 |
rs221824692 | snp | C/T | | | intron-variant | Rasd2 | Mm_Celera | 8:75217739 | AGCTCATAGCTCACA[C/T]TCACCTGGGACTGAG | 75141 |
rs221908155 | snp | A/G | | | intron-variant | Rasd2 | Mm_Celera | 8:75214232 | GCTTTATACACGTAG[A/G]GCATTAAGCTCACTA | 75141 |