SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6172573 | snp | C/T | 0.375 | 0.216506 | intron-variant, utr-variant-5-prime | Herc1, Gm30447 | Mm_Celera | 9:66352312 | CAGTTCCTTTCAACA[C/T]GGATGCATTGATTTG | 235439 |
rs6173270 | snp | G/T | 0.5 | 0 | intron-variant, utr-variant-5-prime | Herc1, Gm30447 | Mm_Celera | 9:66352456 | TAACGCATTGAAATG[G/T]NTAACACGTTAGAGG | 235439 |
rs6173271 | snp | A/T | 0.5 | 0 | intron-variant, utr-variant-5-prime | Herc1, Gm30447 | Mm_Celera | 9:66352457 | AACGCATTGAAATGN[A/T]TAACACGTTAGAGGA | 235439 |
rs6178572 | snp | A/G | 0.290657 | 0.246672 | missense, nc-transcript-variant | Herc1 | Mm_Celera | 9:66433339 | GAAGAAAAGGGTAAC[A/G]TCTTGCTGACAGGAA | 235439 |
rs6178732 | snp | C/T | 0.5 | 0 | intron-variant | Herc1 | Mm_Celera | 9:66397772 | ctctccctcccctcc[C/T]actcccccctcngcc | 235439 |
rs6178749 | snp | C/T | 0.5 | 0 | intron-variant | Herc1 | Mm_Celera | 9:66397784 | tccnactcccccctc[C/T]gcctccccctctccc | 235439 |
rs6254391 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Herc1 | Mm_Celera | 9:66488802 | TAAATAGCATGACAT[A/G]ATTTATAACTTTGTT | 235439 |
rs6254488 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Herc1 | Mm_Celera | 9:66488855 | ATATAGTCTGTGACA[A/T]GTTAATAGTTGCTTT | 235439 |
rs6256109 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Herc1 | Mm_Celera | 9:66489097 | TTCCCAAGGACATTA[A/G]CCAGACTTCCTGACA | 235439 |
rs6361121 | snp | C/T | 0.5 | 0 | intron-variant | Herc1 | Mm_Celera | 9:66506987 | agatgaagctgagag[C/T]tctacatcttcatct | 235439 |
rs6361588 | snp | C/T | 0.5 | 0 | intron-variant | Herc1 | Mm_Celera | 9:66507023 | tatctgctagcagaa[C/T]actggctaccacatg | 235439 |
rs6362722 | snp | A/G | 0.5 | 0 | intron-variant | Herc1 | Mm_Celera | 9:66507267 | AAGAAGCCATTTTCA[A/G]CTGTGTACTTTAAAA | 235439 |
rs6363284 | snp | C/T | 0.5 | 0 | intron-variant | Herc1 | Mm_Celera | 9:66507363 | tttgtgagttcaagg[C/T]ctgcctggtctgcat | 235439 |
rs6363789 | snp | A/T | 0.5 | 0 | intron-variant | Herc1 | Mm_Celera | 9:66507457 | TTTTAATTAAAATTT[A/T]NAAAACCCTCTTTCC | 235439 |
rs6364338 | snp | G/T | 0.5 | 0 | intron-variant | Herc1 | Mm_Celera | 9:66507533 | gaccagaggaaggtg[G/T]atctctgtgagtttg | 235439 |
rs6364379 | snp | A/G | 0.5 | 0 | intron-variant | Herc1 | Mm_Celera | 9:66507553 | ctgtgagtttgaggg[A/G]acagccaaagctata | 235439 |
rs6375594 | snp | G/T | 0.32 | 0.24 | intron-variant | Herc1 | Mm_Celera | 9:66382038 | AAGATCACAAAGGGT[G/T]CATTTTTCTGTCATG | 235439 |
rs6376143 | snp | C/T | 0.5 | 0 | intron-variant | Herc1 | Mm_Celera | 9:66382137 | tgtatattcttggac[C/T]agagagtggcancat | 235439 |
rs6376154 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Herc1 | GRCm38.p3 | 9:66348738 | gggagagagagagag[A/G]ngagagagagggagg | 235439 |
rs6376166 | snp | A/C | 0.5 | 0 | intron-variant | Herc1 | Mm_Celera | 9:66382149 | gacnagagagtggca[A/C]catctggaggtgtgg | 235439 |
rs6376650 | snp | A/C | 0.5 | 0 | intron-variant | Herc1 | Mm_Celera | 9:66382225 | tgtgggtgtgggctt[A/C]anaccctcaccctag | 235439 |
rs6376651 | snp | A/G | 0.5 | 0 | intron-variant | Herc1 | Mm_Celera | 9:66382227 | tgggtgtgggcttna[A/G]accctcaccctagtt | 235439 |
rs6376691 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Herc1 | Mm_Celera | 9:66348848 | gggctgcaaagctca[C/T]atttgggggcagggt | 235439 |
rs6376746 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Herc1 | Mm_Celera | 9:66348882 | acaggtcggaactga[A/G]ggatgcagggagaat | 235439 |
rs6377708 | snp | C/T | 0.5 | 0 | intron-variant | Herc1 | Mm_Celera | 9:66382412 | tttttataagacttg[C/T]cttggtcatagtgtc | 235439 |
rs13463823 | snp | C/T | | | synonymous-codon | Herc1 | Mm_Celera | 9:66501980 | TGATGGTAAAATGGT[C/T]CCCATAATCCCTGGA | 235439 |
rs13473778 | snp | C/G | | | missense, nc-transcript-variant | Herc1 | Mm_Celera | 9:66450922 | GGGGGACATTGAGCA[C/G]AAACCTGAGAGTGAA | 235439 |
rs13473779 | snp | C/G | | | missense, nc-transcript-variant | Herc1 | Mm_Celera | 9:66451022 | TCAGAAAATGAAATA[C/G]CTTCATTTTCTTTAG | 235439 |
rs13473780 | snp | C/G | | | synonymous-codon, nc-transcript-variant | Herc1 | Mm_Celera | 9:66450829 | GGACCTAACATATCT[C/G]ACAGGCATTCATGAA | 235439 |
rs29684858 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc1 | Mm_Celera | 9:66403252 | GCAGGAATTCTGTGA[A/G]AGTTTATTAGTTTTA | 235439 |
rs29786024 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Herc1 | Mm_Celera | 9:66465052 | ATTTTGAAGTTTTTT[C/T]TATCCTAATTGTGGA | 235439 |
rs29891724 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Herc1 | Mm_Celera | 9:66494883 | TCTCTCTCTCCCTCT[C/G]TCTCTCTCTTGGGGT | 235439 |
rs29933583 | snp | G/T | 0.375 | 0.216506 | intron-variant | Herc1 | Mm_Celera | 9:66358379 | TTCTTGCGCGCGCGC[G/T]CTCTCTCTCTCTCTC | 235439 |
rs29980948 | snp | C/G | 0.375 | 0.216506 | intron-variant | Herc1 | Mm_Celera | 9:66444737 | CTGGTTCAATTTCCA[C/G]CACCAATATGGCAGC | 235439 |
rs29984475 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Herc1 | Mm_Celera | 9:66505211 | TTTTCCATGTGTGCT[C/T]GTGTGCCAGGGTCCA | 235439 |
rs30036037 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc1 | Mm_Celera | 9:66356907 | AAACCTCTCAGCTAC[A/T]GGGAACAGTGTTACT | 235439 |
rs30132328 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Herc1 | Mm_Celera | 9:66439049 | AGACTTTATGTGACA[C/T]TAGGCTAAAATACAG | 235439 |
rs30342417 | snp | A/T | 0.375 | 0.216506 | intron-variant | Herc1 | Mm_Celera | 9:66396811 | ATACGTATTAATTAC[A/T]CTTTTCAAAATTTTA | 235439 |
rs30434530 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc1 | Mm_Celera | 9:66389147 | CATGTCTTTAAAAAA[A/T]TTTTTTTTCATTAGG | 235439 |
rs30517365 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Herc1 | Mm_Celera | 9:66429384 | TCTGTCCTTCAATCT[C/G]GGCAGCAAATACCTC | 235439 |
rs33633453 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc1 | Mm_Celera | 9:66477367 | CAAACACAATATAAC[C/T]TAAAGATACACTAGT | 235439 |
rs33648233 | snp | C/G | 0.475309 | 0.108333 | intron-variant | Herc1 | Mm_Celera | 9:66445919 | CAAGCAAACAGTTTA[C/G]GATTGTATATTCTAT | 235439 |
rs33765407 | snp | A/G | 0.18 | 0.24 | missense, nc-transcript-variant | Herc1 | Mm_Celera | 9:66451217 | GGCTGTAGTAAATAT[A/G]CTGAGCTCTTGCTGA | 235439 |
rs36262868 | snp | A/T | 0.32 | 0.24 | synonymous-codon, nc-transcript-variant | Herc1 | Mm_Celera | 9:66474786 | ACCATTTGCAGTAGG[A/T]TATTTTGATGGAAAA | 235439 |
rs36264931 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66474431 | GAAGAACATGGTACA[A/G]TGCCTTAATACCAAC | 235439 |
rs36266773 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Herc1 | Mm_Celera | 9:66489392 | AACTCAGTTTTCTGT[A/G]GCTTTGACTAAAGAT | 235439 |
rs36270588 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66478216 | AGACTAAAGGCTCAT[A/G]TAATAACCAGTTTTA | 235439 |
rs36307694 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Herc1 | Mm_Celera | 9:66496078 | CAACCAGGTAAGGTG[C/T]TGGACTGGGAAGTGG | 235439 |
rs36343211 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Herc1 | Mm_Celera | 9:66503833 | CCTTGTTCCTCTCTC[A/G]GTGAATTGTCCCTTT | 235439 |
rs36362845 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Herc1 | Mm_Celera | 9:66486254 | AGTGGTACAGGTCAG[A/G]CACAGCATTCATAAG | 235439 |
rs36381640 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Herc1 | Mm_Celera | 9:66484638 | CTGTAATCAGAAGCA[G/T]AGTAGTCAAAGGTTA | 235439 |
rs36445347 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66487600 | TGCATAAAGACATTG[A/T]AAGTGTTTCTCAATA | 235439 |
rs36446216 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66487555 | GTTCCTGTGTGTCAG[C/T]GTTGAGTTGTATAAC | 235439 |
rs36458611 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66502653 | GGCTGCACGTGAGGA[C/G]TATCTTCTTTTTTGT | 235439 |
rs36459293 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Herc1 | Mm_Celera | 9:66502095 | CAGGTAAGATGAACT[A/G]TCATGGTGCAGGAAG | 235439 |
rs36471609 | snp | C/T | 0.473373 | 0.11227 | intron-variant, downstream-variant-500B | Herc1 | Mm_Celera | 9:66474996 | AATATTCTATCACTA[C/T]ACAAAGTCTTTGTGG | 235439 |
rs36504117 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Herc1 | Mm_Celera | 9:66489929 | CAGATGCCGAGGAGT[C/T]AGTCTGTAGTTTTAT | 235439 |
rs36513261 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66484501 | CTCTTTCTCCACCAG[A/T]CTTTAGTAGCTTCCT | 235439 |
rs36514840 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66496699 | CCTGTGGATCACCAT[C/T]TATGAGAGGAAGGAA | 235439 |
rs36515427 | snp | A/G | 0.32 | 0.24 | intron-variant | Herc1 | Mm_Celera | 9:66470651 | ACAGTAGTTGCTTTT[A/G]TGTCGACATGTTGCA | 235439 |
rs36526311 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Herc1 | Mm_Celera | 9:66486465 | TTTAATATTAGAATG[A/G]ACTTAACTTTCCCAA | 235439 |
rs36543701 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Herc1 | Mm_Celera | 9:66481377 | GATTAAAGACTGCTG[A/T]AAAGGGGATTTACCT | 235439 |
rs36544200 | snp | C/T | 0.32 | 0.24 | intron-variant | Herc1 | Mm_Celera | 9:66485071 | TAGAAAGGTTAGAAA[C/T]TGTGACCTGATTGTA | 235439 |
rs36584083 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66506316 | CTCGGAATGATCCTT[G/T]CCTTGACTGTGTCCT | 235439 |
rs36620091 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66504309 | TTTGAGTCATGGAGA[C/T]ACCACAGCACACTTT | 235439 |
rs36677241 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66490072 | AGAGACAAGATAATC[C/T]TTCCAACACATGCCT | 235439 |
rs36730226 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Herc1 | Mm_Celera | 9:66472661 | TCAAGTGGGATTTCA[A/G]TAGTTATTACAAGTC | 235439 |
rs36742511 | snp | A/T | 0.32 | 0.24 | intron-variant | Herc1 | Mm_Celera | 9:66495829 | CTTGTGTTCACTGTT[A/T]GAGAGTTTTCAAAAT | 235439 |
rs36782374 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Herc1 | Mm_Celera | 9:66484132 | GAACTTCATTTTATA[C/T]GTAGCCTCCAAATAA | 235439 |
rs36788344 | snp | A/G | 0.32 | 0.24 | intron-variant | Herc1 | Mm_Celera | 9:66487777 | ACGAATTATTTAGGA[A/G]TCTTGGGAATTGTAC | 235439 |
rs36796893 | snp | A/C | 0.32 | 0.24 | intron-variant | Herc1 | Mm_Celera | 9:66501468 | TGTAACTCCTGACTT[A/C]CTGTGTTCTCCAATC | 235439 |
rs36805488 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66476246 | ATGTATAAGGCCATA[A/G]AGTTACCTAAGGGAA | 235439 |
rs36810367 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Herc1 | Mm_Celera | 9:66470862 | ACATAGAACAGCAGC[C/T]GTGAAACTTTGCACT | 235439 |
rs36820703 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66496101 | GGAAGTGGTACCCAC[A/G]ATGGACTTGCCAGAG | 235439 |
rs36826513 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Herc1 | Mm_Celera | 9:66491185 | ACAGGTTGAATGTCA[C/T]TCTTTTTAAGAACAC | 235439 |
rs36834267 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66484373 | ATCTTCTAGGCATGG[C/T]ACTGTATTCCCAAAC | 235439 |
rs36860915 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Herc1 | Mm_Celera | 9:66500781 | CGTGTTTTCTCTCTC[A/G]CACACAAGCACACAT | 235439 |
rs36863102 | snp | C/T | 0.132653 | 0.220748 | missense, nc-transcript-variant | Herc1 | Mm_Celera | 9:66474752 | CTGTCACCTGCATTG[C/T]TTGGTTCAGTGAAGA | 235439 |
rs36912748 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66501512 | GTAAAGTCAGATGTT[G/T]TCTACCTCTTTCTGT | 235439 |
rs36920899 | snp | A/G/T | 0.132653 | 0.220748 | intron-variant | Herc1 | Mm_Celera | 9:66483782 | TTTGATTGTAGATGC[A/G/T]TGTGTTTCTGTAGAG | 235439 |
rs36948811 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Herc1 | Mm_Celera | 9:66506096 | AACTGCTCCTGTCGA[C/T]AGAACTTTGCCTCCT | 235439 |
rs36990876 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66505506 | CCTGTCTCTCCAGCA[C/T]ACCGTGTTCTTTTGC | 235439 |
rs37031358 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Herc1 | Mm_Celera | 9:66499303 | TTAAGAAGGCTTACA[A/G]TTGGGCCCTGTACAT | 235439 |
rs37060416 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Herc1 | Mm_Celera | 9:66484586 | ATCTCATGGTTCTGA[A/T]TTATTTCATTCAGAT | 235439 |
rs37086146 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Herc1 | Mm_Celera | 9:66476805 | CAAGACACACAAACT[C/T]GTGAATCTGGGAGTC | 235439 |
rs37100528 | snp | C/T | 0.336735 | 0.234472 | synonymous-codon, nc-transcript-variant | Herc1 | Mm_Celera | 9:66473484 | GAGTCTCCAGAGTTA[C/T]TGCTGGTGGGACGGA | 235439 |
rs37104888 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Herc1 | Mm_Celera | 9:66473859 | TTAAAAGTTAGAGCT[A/G]TGGAATAGGGGAATC | 235439 |
rs37155298 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Herc1 | Mm_Celera | 9:66503957 | CTTAGCATCATACTG[C/T]ATCCAGTCAGTTTTT | 235439 |
rs37204694 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Herc1 | Mm_Celera | 9:66471723 | GTGAGAGATACTGTT[A/G]ACTAAGAATATCCTA | 235439 |
rs37214974 | snp | A/C | 0.32 | 0.24 | intron-variant | Herc1 | Mm_Celera | 9:66490572 | CCATTCAGCTGTGGA[A/C]GAATCCATTGATGAA | 235439 |
rs37240430 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66480595 | CCATGCCTTTTCTTA[C/T]AAGTCTGAGAACTGG | 235439 |
rs37244708 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Herc1 | Mm_Celera | 9:66488631 | TTTCAGCATGTTACC[A/C]ATGAATTGTGCATCT | 235439 |
rs37246894 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66488637 | CATGTTACCAATGAA[C/T]TGTGCATCTTTCAAA | 235439 |
rs37277223 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Herc1 | Mm_Celera | 9:66474531 | GTGAGGTCATGTCTT[C/T]TACTCGTAACTAACA | 235439 |
rs37308631 | snp | A/C | 0.32 | 0.24 | intron-variant | Herc1 | Mm_Celera | 9:66487862 | GGAAACAACACATAA[A/C]ATTTTTCAGTTAAGA | 235439 |
rs37356548 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Herc1 | GRCm38.p3 | 9:66492705 | CAGAAACCAGTGTGT[C/G/T]TTAAGTAAGAGTTCT | 235439 |
rs37418839 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Herc1 | Mm_Celera | 9:66497977 | GTGGTGACACGTGAA[C/G]ATGTTCATGGAGGAG | 235439 |
rs37427297 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66484753 | TCATCTAAAATGTCC[A/G]TAAATGTGTTAGAGA | 235439 |
rs37470530 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66494135 | AAGTATTACAAAATC[A/T]TTATAGTCATTTTTT | 235439 |
rs37482451 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc1 | Mm_Celera | 9:66479239 | GAAAGAACCAGTCTT[C/T]CTGATCCTTTGGGTT | 235439 |