SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6231372 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | Map3k9 | Mm_Celera | 12:81782711 | ttgagagcattgact[G/T]ctccagaggacccag | 338372 |
rs6231891 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Map3k9 | Mm_Celera | 12:81782787 | gaaatgacatacttg[A/G]ctggtctctatgggc | 338372 |
rs6231929 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | Map3k9 | Mm_Celera | 12:81782804 | tggtctctatgggca[C/G]taggaatgcacatgg | 338372 |
rs6261003 | snp | C/T | 0.5 | 0 | intron-variant | Map3k9, LOC105244954 | Mm_Celera | 12:81763364 | ctcgggaggcagagg[C/T]aggcagatttctgag | 338372 |
rs6261454 | snp | C/T | 0.5 | 0 | intron-variant | Map3k9, LOC105244954 | Mm_Celera | 12:81763447 | agagaaaccctgtct[C/T]gaaaaaccaaaaaaa | 338372 |
rs6355412 | snp | C/T | 0.5 | 0 | intron-variant | Map3k9 | Mm_Celera | 12:81727555 | TGGAGCTGTTTCAGG[C/T]CTAGGCTCTTCCANT | 338372 |
rs6355430 | snp | A/G | 0.5 | 0 | intron-variant | Map3k9 | Mm_Celera | 12:81727569 | GNCTAGGCTCTTCCA[A/G]TGTAAGGGACAAAGG | 338372 |
rs6355794 | snp | C/T | 0.5 | 0 | intron-variant | Map3k9 | Mm_Celera | 12:81727585 | TGTAAGGGACAAAGG[C/T]CCCCGGACAGCCCCA | 338372 |
rs6356300 | snp | A/G | 0.5 | 0 | intron-variant | Map3k9 | Mm_Celera | 12:81727698 | ATGAATGGGGAGGGG[A/G]AATTCACTTTACTGA | 338372 |
rs6366578 | snp | C/G | 0.5 | 0 | intron-variant | Map3k9 | Mm_Celera | 12:81775654 | AAATAGAGATGGAAA[C/G]TATTTTCTGGCTGCC | 338372 |
rs6389303 | snp | A/G | 0.5 | 0 | intron-variant | Map3k9 | Mm_Celera | 12:81737587 | agagggagtgggagg[A/G]gcttgggggggaggg | 338372 |
rs6390387 | snp | C/T | 0.375 | 0.216506 | intron-variant | Map3k9 | Mm_Celera | 12:81737781 | CCAAGAATTACACTA[C/T]TAgattgaggatgtg | 338372 |
rs6390985 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Map3k9 | Mm_Celera | 12:81737904 | AGGCTGGGAAATAAA[A/G]AGAAACTGTACTTCT | 338372 |
rs13481560 | snp | C/T | 0.38875 | 0.207962 | intron-variant | Map3k9, LOC105244954 | GRCm38.p3 | 12:81765850 | AATCCTGGGAAGGAC[C/T]TCAGACACTATCTCG | 338372 |
rs29122829 | snp | A/G | 0.32 | 0.24 | intron-variant | Map3k9 | Mm_Celera | 12:81769367 | CATCTCCATAGTGAA[A/G]GCTGCTGGATGCTGC | 338372 |
rs29126168 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Map3k9 | GRCm38.p3 | 12:81717216 | GCTTCTCCCCTCCTG[C/T]CCTGGTAGGAAAGGC | 338372 |
rs29140389 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Map3k9 | GRCm38.p3 | 12:81716186 | CCCTTATCTTATTCC[A/G]ACAGGAATAAACTAA | 338372 |
rs29143448 | snp | G/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Map3k9, LOC105244954 | GRCm38.p3 | 12:81759228 | ACTGACACCAGCTGC[G/T]GTTGTGTCATCCGGT | 338372 |
rs29146245 | snp | A/C | 0.459184 | 0.136902 | utr-variant-3-prime | Map3k9 | GRCm38.p3 | 12:81717293 | CCATCTTGCTGCTAC[A/C]TTCACACCTGACAAC | 338372 |
rs29157217 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime | Map3k9 | GRCm38.p3 | 12:81718816 | CAGCATGGAGCCAGG[A/G]TTGGGTCTAGACACC | 338372 |
rs29159509 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Map3k9 | Mm_Celera | 12:81715835 | AGAGGACACAACTCC[C/T]TGGGAAAGCGGTGAT | 338372 |
rs29172258 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Map3k9 | GRCm38.p3 | 12:81715107 | GTACCTTGAAAGACA[C/T]GAAGAGAAAAGGCCA | 338372 |
rs29174612 | snp | C/T | 0.48 | 0.0979796 | utr-variant-3-prime | Map3k9 | GRCm38.p3 | 12:81718635 | CACAGCCACAGCCTT[C/T]AGGGCCCATTGTTCT | 338372 |
rs29195862 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Map3k9 | GRCm38.p3 | 12:81718571 | AAAGTCGGGGGCTCT[A/G]CACCCGTGGTGGAGC | 338372 |
rs29200869 | snp | A/G | 0.5 | 0 | intron-variant | Map3k9 | Mm_Celera | 12:81771484 | AAGGAAGGAAGGAAG[A/G]AAGGAAGAAAGAAAG | 338372 |
rs29490108 | snp | A/T | 0.5 | 0 | utr-variant-3-prime | Map3k9 | Mm_Celera | 12:81716005 | ACACCCCCAAGTCTG[A/T]CCACACATTCTTGGG | 338372 |
rs33843993 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Map3k9 | GRCm38.p3 | 12:81715673 | CGGCAGAGACCCAGG[A/G]CCTTCTCGGTGCTGG | 338372 |
rs33845958 | snp | C/T | 0.391111 | 0.206368 | utr-variant-3-prime | Map3k9 | GRCm38.p3 | 12:81717029 | CATCCATGGCATGGT[C/T]GGTGCTCAGCCCTAA | 338372 |
rs45655752 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Map3k9 | Mm_Celera | 12:81770950 | ATACCTAATTGTTCA[C/T]ATTCTCAGAAAAGAA | 338372 |
rs45662472 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Map3k9 | Mm_Celera | 12:81739984 | GAGGAGCTGTGTAAA[C/T]GTGCAGACTGTCTCC | 338372 |
rs45694450 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Map3k9 | Mm_Celera | 12:81754786 | GCAGGGCCAGCCTGA[C/T]TCTTCGGCCCTGGCA | 338372 |
rs45701479 | snp | C/T | 0.277778 | 0.248452 | intron-variant, downstream-variant-500B | Map3k9 | Mm_Celera | 12:81728173 | CCTTAGAATTTATAC[C/T]AATGTCAGAGGTAGC | 338372 |
rs45722704 | snp | C/G | 0.32 | 0.24 | intron-variant | Map3k9 | Mm_Celera | 12:81770606 | TTACACTTCCACCAT[C/G]CTGGCCCAGATTTCT | 338372 |
rs45760073 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Map3k9 | Mm_Celera | 12:81742102 | AAAGATACCTGCCAA[C/T]GTTCTAGAATTCAGA | 338372 |
rs45766066 | snp | C/T | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Map3k9 | Mm_Celera | 12:81728946 | CTAGAAGGGCATTAA[C/T]ATGTGGTTAGTTGGG | 338372 |
rs45797960 | snp | C/G | 0.132653 | 0.220748 | synonymous-codon | Map3k9 | Mm_Celera | 12:81732071 | GCGTTTCTTCACCCG[C/G]GGCTTTTCCTGGCAC | 338372 |
rs45831711 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Map3k9 | Mm_Celera | 12:81734374 | CCTAGAAAATAGAGC[C/T]CTGAATTTAGGGAAC | 338372 |
rs45843817 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Map3k9 | Mm_Celera | 12:81738600 | TTCCCAGTGTAGAAG[C/T]GTTGTACTAATAGTC | 338372 |
rs45849394 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Map3k9 | Mm_Celera | 12:81733738 | CCAGATTTGGCTCTG[C/T]CCAGACATCGCAGGG | 338372 |
rs45851646 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Map3k9, LOC105244954 | Mm_Celera | 12:81761749 | GAAAGCAACGAGCTT[C/T]GTGTTCACAACCAAG | 338372 |
rs45862547 | snp | G/T | 0.32 | 0.24 | intron-variant | Map3k9 | Mm_Celera | 12:81770667 | CCCTGCCTGGCTCTC[G/T]CAGAATGGTAAGGAT | 338372 |
rs45892555 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Map3k9 | Mm_Celera | 12:81747315 | GATGTACCGGTGCAA[A/T]ATGGACTGTGGGCTA | 338372 |
rs45906486 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Map3k9 | Mm_Celera | 12:81731833 | CCAATGGACGTTCCC[C/T]GAAAGGCCTGGCAGC | 338372 |
rs45925231 | snp | A/G | 0.32 | 0.24 | intron-variant | Map3k9 | Mm_Celera | 12:81750651 | GGTATGGCGACTTAC[A/G]GCATAATGCAGTCGG | 338372 |
rs45948855 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Map3k9 | Mm_Celera | 12:81756024 | TGTGTTTACACAGTC[A/G]GCCTCCAGAGGACTA | 338372 |
rs45967954 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Map3k9 | Mm_Celera | 12:81736508 | GGCTACAGAATGAGC[C/T]ACGACAGACGTATTA | 338372 |
rs45968645 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Map3k9, LOC105244954 | Mm_Celera | 12:81759965 | GCCCTAAGTTCAAAG[C/T]CCAGACATGGATGCT | 338372 |
rs46031313 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k9 | Mm_Celera | 12:81750370 | TTCCCATCAACGGGT[A/G]TCCCTAGGCCTCCAA | 338372 |
rs46056232 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Map3k9 | Mm_Celera | 12:81739744 | ACACATCCTATCACC[A/G]CAGAAGCAAAGAACA | 338372 |
rs46066353 | snp | A/G | 0.32 | 0.24 | intron-variant | Map3k9, LOC105244954 | Mm_Celera | 12:81763955 | AGGAAAAGGGGGTTC[A/G]CAGTGTAAGACGGGG | 338372 |
rs46087190 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Map3k9 | Mm_Celera | 12:81753480 | CCCTGACTAAGACAC[C/T]ACCGAAGTTATTACT | 338372 |
rs46131331 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k9, LOC105244954 | Mm_Celera | 12:81764680 | AAAAGGAGCACAGGT[A/G]GAGGCGAGTTTCTCC | 338372 |
rs46132558 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Map3k9 | Mm_Celera | 12:81742481 | TGCATCTAGGGTCCT[A/G]TGTACACTGGGCAGG | 338372 |
rs46165846 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Map3k9, LOC105244954 | Mm_Celera | 12:81761387 | CACACTATCTGAAGG[A/G]AACATCTCTGGGGAA | 338372 |
rs46172434 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k9 | Mm_Celera | 12:81768543 | GAAGACAGCTGTTGA[A/G]TTCCCATGCTGTAAG | 338372 |
rs46183886 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Map3k9 | Mm_Celera | 12:81727514 | AGCTGTGCTCTGCCC[G/T]TCCAATCAGCAAACC | 338372 |
rs46200354 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Map3k9 | Mm_Celera | 12:81751069 | TAAGTTTTGGTATAA[A/G]CCTTTTTGCATGAAA | 338372 |
rs46203778 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Map3k9, LOC105244954 | Mm_Celera | 12:81760039 | ATTCTAGTCTCTGTT[C/T]CCAGTCTTTTCCTTC | 338372 |
rs46307636 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Map3k9 | Mm_Celera | 12:81750250 | AATACACCAGCACCT[A/T]TGCACACGTGAAAAA | 338372 |
rs46323784 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime | Map3k9 | GRCm38.p3 | 12:81717087 | AAAGATGGCAGGAGC[A/G]AGGGCAACACAGAAC | 338372 |
rs46346496 | snp | A/G | 0.32 | 0.24 | intron-variant | Map3k9 | Mm_Celera | 12:81770306 | CAGCACCGACAGGGA[A/G]ATACCATGTTATACC | 338372 |
rs46351032 | snp | A/C/G | 0.244898 | 0.249948 | intron-variant | Map3k9 | GRCm38.p3 | 12:81740505 | CACTCCAATAATTCA[A/C/G]AGAGTAACCATAGTT | 338372 |
rs46371212 | snp | C/T | 0.32 | 0.24 | intron-variant | Map3k9 | Mm_Celera | 12:81731130 | AGTTCTGAGTTTCAG[C/T]CTCCTCCTCATCTGT | 338372 |
rs46382210 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Map3k9 | Mm_Celera | 12:81756308 | CTTGGGGGCAAGGAG[A/G]CCCAAAGGCTCGAAA | 338372 |
rs46395618 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Map3k9 | GRCm38.p3 | 12:81729712 | TGTGAGCTCTTTCTG[C/T]CCAAGTGTTCCTGGT | 338372 |
rs46401034 | snp | A/G | 0.260355 | 0.249785 | utr-variant-3-prime | Map3k9 | GRCm38.p3 | 12:81717980 | TGAGCCATATGGAAT[A/G]GGCAACTTTAGCCTT | 338372 |
rs46404723 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Map3k9 | Mm_Celera | 12:81753962 | CATAAGATGGAACAA[A/C]GCAGAGGATCCTAGG | 338372 |
rs46411704 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | Map3k9 | Mm_Celera | 12:81714952 | CCACCACAAGGAACC[A/G]GGAGTAACCAGTATG | 338372 |
rs46412950 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k9 | Mm_Celera | 12:81730365 | AGTGAACAACGGGAC[A/G]AGGAACAGGAAGGCT | 338372 |
rs46462284 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Map3k9 | Mm_Celera | 12:81770477 | ATTAGCAAGGCAAGG[C/T]CTCCTTCCCAGGAGG | 338372 |
rs46477255 | snp | C/T | 0.32 | 0.24 | intron-variant | Map3k9 | Mm_Celera | 12:81770926 | CTTTCATACTCACCA[C/T]TGAAATCTATACCTA | 338372 |
rs46519776 | snp | A/G | 0.32 | 0.24 | intron-variant | Map3k9 | Mm_Celera | 12:81767869 | ATACCCCCTATGCAT[A/G]GACAAAGTGCACAGA | 338372 |
rs46576007 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Map3k9 | Mm_Celera | 12:81754385 | CCATGGGGACTTTAC[C/T]TTCATCTCCCTGGCC | 338372 |
rs46593208 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Map3k9, LOC105244954 | Mm_Celera | 12:81764570 | CAGGAGGCAGTGAGA[A/G]CTAGCACTTCCTGCG | 338372 |
rs46604169 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k9, LOC105244954 | Mm_Celera | 12:81762434 | CTATGGACATTTTTG[A/G]CTGTTTCATTGCGTT | 338372 |
rs46627680 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Map3k9, LOC105244954 | Mm_Celera | 12:81761434 | AGGAGTTCCACTGCC[A/G]CCCTCTCAATGTGTT | 338372 |
rs46688349 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k9, LOC105244954 | Mm_Celera | 12:81766326 | CAGAGAGAATACACT[A/G]GAGCACCAAGTTACG | 338372 |
rs46695863 | snp | C/T | 0.391111 | 0.206368 | intron-variant, utr-variant-3-prime | Map3k9 | GRCm38.p3 | 12:81729664 | AGTGAGAGAGACAGT[C/T]ACATCATCTGCCTCT | 338372 |
rs46722831 | snp | C/G | 0.297521 | 0.245442 | intron-variant | Map3k9 | Mm_Celera | 12:81747957 | TCTTTCCTACTCTTT[C/G]TTCTTCCTTGCTGAG | 338372 |
rs46729939 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Map3k9 | Mm_Celera | 12:81744301 | GCTGGACCCCAGGAA[A/G]CTACTGCAGAGTGAC | 338372 |
rs46776143 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Map3k9, LOC105244954 | Mm_Celera | 12:81764385 | TTGTCCTGGAGTGAA[A/T]GTAATAATCAGATGA | 338372 |
rs46778453 | snp | C/T | | | intron-variant | Map3k9 | Mm_Celera | 12:81777944 | CTATTCTGAATAAAG[C/T]TTGAAGCAAAAGTTT | 338372 |
rs46808763 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Map3k9 | Mm_Celera | 12:81747326 | GCAATATGGACTGTG[G/T]GCTACAGAAGGGGTA | 338372 |
rs46832351 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Map3k9 | Mm_Celera | 12:81746996 | CATTGCTAGTTCTTC[C/T]TCAGCAGCTAAACCC | 338372 |
rs46848793 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k9 | Mm_Celera | 12:81747008 | TTCTTCAGCAGCTAA[A/G]CCCAACTGCACACAA | 338372 |
rs46850500 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k9 | Mm_Celera | 12:81747367 | TCAGCCTGCATGCCT[A/G]CACCAGTTACTTAAG | 338372 |
rs46854004 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Map3k9 | Mm_Celera | 12:81748001 | TCTTCTGACCCAGTG[C/T]AGGTTGTTTACTCCC | 338372 |
rs46863302 | snp | G/T | 0.32 | 0.24 | upstream-variant-2KB | Map3k9 | Mm_Celera | 12:81784459 | CTCTCAAAGCATGCT[G/T]TTTAGCGTCAGCGAC | 338372 |
rs46875531 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Map3k9 | GRCm38.p3 | 12:81753677 | CAGACATTTCTCCAG[C/T]CATCCAGGCGCTATT | 338372 |
rs46901140 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Map3k9, LOC105244954 | Mm_Celera | 12:81765459 | TGCAAGAGGCAAATG[C/T]AAGTCACAGCAAAGC | 338372 |
rs46908287 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Map3k9, LOC105244954 | Mm_Celera | 12:81756540 | AAGAGGCAGTCCCTG[A/G]ATGTGGGCAGGTCAG | 338372 |
rs46909270 | snp | C/T | 0.32 | 0.24 | intron-variant | Map3k9 | Mm_Celera | 12:81756140 | ACACCCCATGTTCAT[C/T]AAAACTTGCCAGGTA | 338372 |
rs46911250 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Map3k9 | Mm_Celera | 12:81770436 | GACATGCAGTCTCCT[A/G]CCCTCTCATGCAAAC | 338372 |
rs46926462 | snp | C/T | 0.124444 | 0.216185 | missense | Map3k9 | Mm_Celera | 12:81729795 | CCTCTTTTGGAACAA[C/T]TGAGCTCCGGCCCCA | 338372 |
rs46929965 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Map3k9, LOC105244954 | Mm_Celera | 12:81756638 | CATAAGTAACCAGAA[C/T]GTCCAACTTGTGTGG | 338372 |
rs46947981 | snp | A/G | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Map3k9, LOC105244954 | Mm_Celera | 12:81767770 | GAGGCACCTCAGTGT[A/G]GATGTGCTCTTTTGC | 338372 |
rs46977674 | snp | A/C | 0.32 | 0.24 | intron-variant | Map3k9 | Mm_Celera | 12:81731228 | GTTGTTAGTGCATAG[A/C]AATGTCCTGGTACAG | 338372 |
rs46994844 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Map3k9 | Mm_Celera | 12:81750425 | GTGAGCTCTAAGTAA[C/G]GGTTGAAGGGTTAGA | 338372 |
rs47017738 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Map3k9 | Mm_Celera | 12:81746787 | GTCTCTAAGAAGTAG[A/G]AAGATGACACTCCCT | 338372 |
rs47068293 | snp | A/C/T | 0.408163 | 0.193609 | intron-variant | Map3k9 | GRCm38.p3 | 12:81751104 | CTGTATACTGAAAAT[A/C/T]CAAATGAATCAGGCA | 338372 |