SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3686436 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Cttn | GRCm38.p3 | 7:144447603 | AATCACACCAAGCCC[A/G]CCCTCTGCTCTGTCG | 13043 |
rs6212186 | snp | C/T | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144468670 | CAGTCAGAGAGGACC[C/T]AGTCACAGGATGGAG | 13043 |
rs6213681 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cttn | GRCm38.p3 | 7:144468930 | GACGGTGTGGAGTTA[C/T]GCCAGGTGCCTTCCC | 13043 |
rs6213704 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cttn | GRCm38.p3 | 7:144468956 | TTCCCGACTAACAGG[C/T]CAAAGTCTGAAGGGC | 13043 |
rs6214127 | snp | A/G | 0.5 | 0 | intron-variant | Cttn | Mm_Celera | 7:144469016 | GTTAAAGGCATAACT[A/G]NCATAAGCCCTCAAT | 13043 |
rs6214128 | snp | C/T | 0.5 | 0 | intron-variant | Cttn | Mm_Celera | 7:144469017 | TTAAAGGCATAACTN[C/T]CATAAGCCCTCAATT | 13043 |
rs6244811 | snp | C/T | 0.5 | 0 | intron-variant | Cttn | Mm_Celera | 7:144437817 | AGACTGGGTAACAGG[C/T]CCNGGTTCAAAACTA | 13043 |
rs6244814 | snp | A/T | 0.5 | 0 | intron-variant | Cttn | Mm_Celera | 7:144437820 | CTGGGTAACAGGNCC[A/T]GGTTCAAAACTAAGC | 13043 |
rs6246602 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Cttn | Mm_Celera | 7:144438149 | GATGGAGGGACCAGA[A/T]ACCTCCTAGAAACAA | 13043 |
rs6247101 | snp | C/T | 0.5 | 0 | intron-variant | Cttn | Mm_Celera | 7:144438215 | attgggagtcagagg[C/T]aggcggatctctgag | 13043 |
rs6264587 | snp | A/G | 0.5 | 0 | intron-variant | Cttn | Mm_Celera | 7:144439251 | TAGGTACTTCCCTTG[A/G]CTCCTGGTCCCAGCT | 13043 |
rs6279099 | snp | C/T | 0.5 | 0 | intron-variant | Cttn | Mm_Celera | 7:144439647 | AGAGTATGGGAGACT[C/T]GAGGCAGGAAGGAAG | 13043 |
rs6279130 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Cttn | Mm_Celera | 7:144439667 | CAGGAAGGAAGCAAG[C/G]ACTCCACAGAGCTTC | 13043 |
rs6353510 | snp | A/T | 0.5 | 0 | intron-variant | Cttn | GRCm38.p3 | 7:144444084 | cataaaataaataaa[A/T]ctttaaaaagaagaa | 13043 |
rs6354122 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cttn | GRCm38.p3 | 7:144444229 | GTCCCAACTTCCTTC[A/G]GTGATGAACAGTGAT | 13043 |
rs13459241 | snp | C/T | | | utr-variant-3-prime | Cttn | GRCm38.p3 | 7:144436800 | CATCTGCTGATGCTT[C/T]GGGGCATGTCCTGCC | 13043 |
rs31056571 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cttn | GRCm38.p3 | 7:144438401 | TTCCTGGGCTAGTGA[C/T]GCTGAGTTCCATAAG | 13043 |
rs31253254 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cttn | GRCm38.p3 | 7:144445339 | CCTCAGTCTCCCAAA[C/T]GCTGAGATGATGTCA | 13043 |
rs31323121 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Cttn | GRCm38.p3 | 7:144461568 | TGATTTCTGTAAATG[C/T]CACCTAGAGTCCCAT | 13043 |
rs31488022 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cttn | GRCm38.p3 | 7:144437139 | GACTCAGATGGGATT[A/G]TCACCTGACCAGGGG | 13043 |
rs31543615 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Cttn | GRCm38.p3 | 7:144451354 | CTGAAGGGACGGCTG[A/G]ATACAGCTACAGGGT | 13043 |
rs31543619 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Cttn | GRCm38.p3 | 7:144471213 | AAGAACTGATCAAAT[A/G]CAGCTTGGGGAGAAA | 13043 |
rs31700350 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Cttn | Mm_Celera | 7:144448349 | GGGCAGGAAGGAACA[C/T]TGGCATCTGTGCAGT | 13043 |
rs31715583 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Cttn | GRCm38.p3 | 7:144472840 | CACCAAGCCTGACAA[C/T]CTGAGTTCAATGCTA | 13043 |
rs31877359 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Cttn | Mm_Celera | 7:144469526 | ACCAAGAGGAAACAA[A/G]GGAACATACCAGGCC | 13043 |
rs31970069 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Cttn | GRCm38.p3 | 7:144460607 | GAGCAGGCTCCACTC[A/C]CTCATCTTGGGGCAA | 13043 |
rs32037695 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Cttn | Mm_Celera | 7:144472306 | GCAAATGTGCACCAC[C/T]CCACCCACCATCCTC | 13043 |
rs32086595 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Cttn | GRCm38.p3 | 7:144445141 | GCCACCCTGCTCAGC[A/G]ACCTGACACAGACTA | 13043 |
rs32086730 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Cttn | GRCm38.p3 | 7:144458041 | ACATGAACAAAGGAC[A/C]GAGCCTGAAGTATAC | 13043 |
rs32091379 | snp | A/C | 0.375 | 0.216506 | intron-variant | Cttn | GRCm38.p3 | 7:144465118 | GAAGGGCAGGTTTGC[A/C]ATTTGGGGGGCACAG | 13043 |
rs32123901 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cttn | GRCm38.p3 | 7:144468922 | ATGCTCAGGACGGTG[C/T]GGAGTTACGCCAGGT | 13043 |
rs32140259 | snp | A/G | 0.32 | 0.24 | intron-variant | Cttn | GRCm38.p3 | 7:144443050 | GACAGAGGGTGAGGG[A/G]AAATGGAAAAGGAAC | 13043 |
rs32224911 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cttn | Mm_Celera | 7:144466945 | TGCTGGGGTTGAGAC[C/T]GGGGTCTTACTCCAC | 13043 |
rs32232675 | snp | A/C | 0.375 | 0.216506 | utr-variant-3-prime | Cttn | Mm_Celera | 7:144436897 | GGAAGCAGAAACCAA[A/C]TCAAACACACGCAGA | 13043 |
rs32352254 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cttn | GRCm38.p3 | 7:144463075 | TTACTCAAAGCCATC[C/T]CACACCCTCAGCAGC | 13043 |
rs32368791 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cttn | GRCm38.p3 | 7:144469509 | CCCCATCCCTCACAC[A/G]GACCAAGAGGAAACA | 13043 |
rs32443104 | snp | C/T | 0.5 | 0 | intron-variant | Cttn | Mm_Celera | 7:144444778 | TCTCCTATCTAGTGA[C/T]TGAGGTGAAAGGGGA | 13043 |
rs32451378 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cttn | GRCm38.p3 | 7:144443949 | GTTAAGAGCACTGAC[C/T]GCTCTTCCAGAGGTC | 13043 |
rs32484100 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Cttn | GRCm38.p3 | 7:144470614 | CTCCCGTCCAGGCCC[G/T]GCACCCTGACAACTC | 13043 |
rs32500743 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cttn | GRCm38.p3 | 7:144447193 | GAATGGCCATGCCTG[A/G]CTGGCAGGAGGTGGG | 13043 |
rs36241493 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cttn | Mm_Celera | 7:144444965 | CCGGAAGTGTTCAGA[A/G]ACCACAGCCCAGGGG | 13043 |
rs36254785 | snp | A/T | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144463711 | CTCTCATGCCTAACT[A/T]GTATGCCCTGAGACC | 13043 |
rs36276149 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cttn | Mm_Celera | 7:144461549 | AGATCAGCAGATAGA[A/G]GGTTGATTTCTGTAA | 13043 |
rs36279474 | snp | C/T | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144442840 | ATCTGGATGTTTAGA[C/T]ATTTGTGGCTGCTAC | 13043 |
rs36284517 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Cttn | Mm_Celera | 7:144466360 | ACAGGAACCAGAGGA[C/G]TCCGCAGATTCAAAG | 13043 |
rs36284909 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Cttn | Mm_Celera | 7:144437576 | TAGAACCATGTTCCC[A/T]GCCTGCACAGTGGGT | 13043 |
rs36287951 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cttn | Mm_Celera | 7:144467063 | TCTGTGTAATCTGGG[A/G]TCTAAATAAGGCCCC | 13043 |
rs36303090 | snp | A/T | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144447098 | ATGAACACTGCTCTC[A/T]GAACAGCCTCGTGGC | 13043 |
rs36303140 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cttn | Mm_Celera | 7:144466060 | TACCTATGAAGAGAA[A/G]ACTGGAGGCTCAGCA | 13043 |
rs36327931 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Cttn | GRCm38.p3 | 7:144466601 | GCTGCGGCAGAGACA[A/G]GACAGCCTGCCTCTA | 13043 |
rs36360222 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Cttn | GRCm38.p3 | 7:144438773 | TCCAGTACCTGCTTG[A/G]TAGTGGCCAGGAGCC | 13043 |
rs36385261 | snp | C/T | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144442384 | ATGTCTGGCAGTATT[C/T]CCTCCAAGGTGGGCC | 13043 |
rs36388335 | snp | C/G | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144459882 | TAGTGAGTTCTAGGG[C/G]AAGCTCAGAAGGGCA | 13043 |
rs36389531 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Cttn | Mm_Celera | 7:144448138 | CACCTGACTACATAT[A/C]ATCATTCTTAAACTC | 13043 |
rs36391046 | snp | G/T | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144451325 | TTAAAGCTACTCCAG[G/T]CTTCAAGGTTTGCCT | 13043 |
rs36425155 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Cttn | Mm_Celera | 7:144452319 | GCCAATGCATGCGGC[A/C]CTCGAGGCATGGAGG | 13043 |
rs36439650 | snp | G/T | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144462512 | GTGGGACCAGACAGG[G/T]AAACTCAGCAGGACT | 13043 |
rs36468236 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Cttn | Mm_Celera | 7:144445761 | GGGGCACCAACACTG[C/T]ACCCCACATAGCCAC | 13043 |
rs36475969 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Cttn | Mm_Celera | 7:144467121 | CTGAAATGAACATGA[A/C]TGCTTCTGACTGCAA | 13043 |
rs36482155 | snp | A/C | 0.375 | 0.216506 | intron-variant | Cttn | Mm_Celera | 7:144439328 | AGCCAGTGTTCCAAC[A/C]CTTGGCCCAGAAGGA | 13043 |
rs36503632 | snp | A/G | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144451288 | CGCAGAAGCAGGATC[A/G]GAACTGGATGGTAAA | 13043 |
rs36503978 | snp | C/T | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144460917 | GCTTCCAGACTCTGT[C/T]GTGCTCACAAAGCCG | 13043 |
rs36529716 | snp | A/G | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144448251 | TGGGAGATGCCCAGG[A/G]TGAAGCCAACCACAG | 13043 |
rs36533388 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cttn | Mm_Celera | 7:144453486 | CAAGCTCTTGATTTT[C/T]AAATACTGGTAAACA | 13043 |
rs36536379 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Cttn | Mm_Celera | 7:144437484 | GAATGGAAGTGCTGA[C/T]GTGACAGAGAGGGGC | 13043 |
rs36544176 | snp | C/T | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144442419 | TGGTAAGGAAAAAAA[C/T]CATTGCTGAGCCAAG | 13043 |
rs36544646 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Cttn | Mm_Celera | 7:144469467 | TCACTGGGCACAACA[G/T]GGAATTCCTTCTCCC | 13043 |
rs36545356 | snp | C/T | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144467437 | TATGGATGTGTCTGT[C/T]TGTGTCCATGTATGG | 13043 |
rs36547465 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cttn | Mm_Celera | 7:144458323 | GTTCAAGGCTATAGA[C/T]CTACCAATAGGCAAT | 13043 |
rs36588373 | snp | G/T | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144447323 | TCCTCAATGCCAGCC[G/T]CTGACTAACACACTT | 13043 |
rs36589263 | snp | C/T | 0.32 | 0.24 | utr-variant-5-prime | Cttn | GRCm38.p3 | 7:144465979 | TGCTGGGAAAAGCAG[C/T]TCAGAGTCTGTCCGA | 13043 |
rs36593037 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Cttn | Mm_Celera | 7:144451207 | TCTGATCTGGGCCTG[A/T]TGATCTAACATTGAC | 13043 |
rs36627076 | snp | C/T | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144456946 | TACAGACTCAATCAT[C/T]ACTGACCCGGTCTGT | 13043 |
rs36636279 | snp | A/C | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144457576 | CCATGGAGTCAGAGG[A/C]TACCTGTGAACTGCT | 13043 |
rs36651458 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Cttn | Mm_Celera | 7:144461000 | TGGGGCCTCTGACAA[A/T]GTAAAACAGCTACTA | 13043 |
rs36659912 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Cttn | Mm_Celera | 7:144447373 | AACAGGGCTCTCAGC[C/T]ACCACACACCTGGTC | 13043 |
rs36674044 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cttn | Mm_Celera | 7:144439628 | GGGAGCCCTGAGTCC[A/G]GGCAGAGTATGGGAG | 13043 |
rs36681349 | snp | C/G | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144457268 | CCAGGCTGAGAGAAT[C/G]AGAACAGCCTCAGGT | 13043 |
rs36692049 | snp | A/G | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144451161 | GAATCACGGGAACAC[A/G]CGCACTGGTCCAGTA | 13043 |
rs36697267 | snp | A/G | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144458900 | TCCTGGCAACACAGA[A/G]CCCCAACTGAGTGCC | 13043 |
rs36699165 | snp | A/G | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144440768 | CCCCCTGGTCTTCAG[A/G]GCTGTGGCATCAAGT | 13043 |
rs36702717 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Cttn | Mm_Celera | 7:144451229 | AACATTGACCAAAGC[A/G]TAAAGGAACAAACAA | 13043 |
rs36733782 | snp | C/T | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144447263 | AGTGCACAAGGTCAG[C/T]GGTCGCCATCTTTAC | 13043 |
rs36788286 | snp | A/G | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144437445 | CCATGCATCCTATAA[A/G]ACAGTGCTCAAGTAA | 13043 |
rs36788721 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cttn | Mm_Celera | 7:144439373 | GACATGCCTCTGTTG[A/G]TTGGGCCACTTGCTA | 13043 |
rs36790876 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cttn | Mm_Celera | 7:144454599 | TGAAAAGATTAGAAG[A/G]AACACAGGAACAAAA | 13043 |
rs36809213 | snp | C/T | 0.336735 | 0.234472 | utr-variant-3-prime | Cttn | GRCm38.p3 | 7:144436527 | TGGTCCCCTTTCCTC[C/T]TCTTCCAAACACTGG | 13043 |
rs36833070 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Cttn | GRCm38.p3 | 7:144436026 | TTGCTCAAGGAAGCC[A/G]TGGAGGCACCCAGGT | 13043 |
rs36836639 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cttn | Mm_Celera | 7:144461414 | GTCAGCGAGATTGCT[A/G]TCCTGTTTGTTCACT | 13043 |
rs36865197 | snp | C/T | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144456922 | TGACCTTCGGTTTCA[C/T]AGTCAAACTACAGAC | 13043 |
rs36899447 | snp | G/T | 0.231111 | 0.249285 | upstream-variant-2KB | Cttn | Mm_Celera | 7:144472875 | AATAAGTAGCCCACT[G/T]TGTGTCTTGGTTTCT | 13043 |
rs36961494 | snp | G/T | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144455144 | ATGACAATCAGGTGC[G/T]GTGCTATAACCAAGC | 13043 |
rs36970047 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Cttn | Mm_Celera | 7:144466050 | GATCAATGATTACCT[A/G]TGAAGAGAAGACTGG | 13043 |
rs36970398 | snp | A/G | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144447359 | CTTATGTCTTCTGCA[A/G]CAGGGCTCTCAGCCA | 13043 |
rs37053998 | snp | C/T | 0.42 | 0.183303 | utr-variant-3-prime | Cttn | GRCm38.p3 | 7:144436213 | CCTCATTGCAGGCTG[C/T]TCAGGGGTCATGAGC | 13043 |
rs37062294 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cttn | Mm_Celera | 7:144457655 | GGGAGCCGGCAGTCC[C/T]GGCCATCACGCACCT | 13043 |
rs37071807 | snp | G/T | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144446023 | TCCACAGTCACTGGG[G/T]CTCGGCTCCCCTTCC | 13043 |
rs37137037 | snp | C/T | 0.32 | 0.24 | intron-variant | Cttn | Mm_Celera | 7:144463153 | ACATGGCTAGGTCTC[C/T]TGTCCATTATCTGTG | 13043 |
rs37140124 | snp | C/T | 0.396694 | 0.202437 | utr-variant-3-prime | Cttn | GRCm38.p3 | 7:144436814 | CGAAGCATCAGCAGA[C/T]GTATTAAATATAAAG | 13043 |
rs37151732 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Cttn | Mm_Celera | 7:144455399 | CCCACAAACTGTGCA[C/G]ACAGAGTTCAGCTCA | 13043 |