SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3663986 | snp | C/G | 0.5 | 0 | intron-variant | Trpc4ap | Mm_Celera | 2:155672180 | TGAGAGATAATCCCT[C/G]ACTAACCTGGAACTA | 56407 |
rs3664038 | snp | A/G | 0.5 | 0 | intron-variant | Trpc4ap | Mm_Celera | 2:155672207 | ACTAACTACATAGTA[A/G]AGGATAGACAACCTT | 56407 |
rs4135944 | snp | C/T | 0.5 | 0 | intron-variant | Trpc4ap | Mm_Celera | 2:155676392 | TGACTCACAACCATC[C/T]GTAATGAGATCTGAT | 56407 |
rs4135981 | snp | A/G | 0.5 | 0 | intron-variant | Trpc4ap | Mm_Celera | 2:155676422 | TACCCTCTTCTGGAG[A/G]CAGCTACAGTGTACT | 56407 |
rs4140365 | snp | A/G | 0.5 | 0 | intron-variant | Trpc4ap | Mm_Celera | 2:155676330 | GCGGTTAACAGCACC[A/G]ACTGTTCTTCCTAAG | 56407 |
rs13466891 | snp | C/G | 0.375 | 0.216506 | downstream-variant-500B, utr-variant-3-prime | Myh7b, Trpc4ap | Mm_Celera | 2:155634554 | AATGCTGCCTTCCCC[C/G]GGGTCTGCCCATCTC | 56407 |
rs13466892 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | Myh7b, Trpc4ap | GRCm38.p3 | 2:155634457 | ATCCAGGAGGCTCCC[C/T]AGAAGTGGGGGGAGC | 56407 |
rs13466893 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | Myh7b, Trpc4ap | Mm_Celera | 2:155634463 | GTGTTCATCCAGGAG[A/G]CTCCCTAGAAGTGGG | 56407 |
rs13466894 | snp | C/T | 0.473373 | 0.11227 | synonymous-codon | Trpc4ap | GRCm38.p3 | 2:155645015 | GATCCCAGGACTCAA[C/T]AATTTGTTCGACAAA | 56407 |
rs27308568 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Trpc4ap | Mm_Celera | 2:155678708 | GTCCAAGAAAACCCC[C/T]TTCATGACTAGAGAG | 56407 |
rs27308569 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trpc4ap | Mm_Celera | 2:155678395 | AAATGGAAGGTTAAG[A/G]AAACAAATACAATGC | 56407 |
rs27308570 | snp | C/T | 0.5 | 0 | intron-variant | Trpc4ap | Mm_Celera | 2:155676852 | TGTCAAACCATAGGA[C/T]AATTTCCTCAACAAA | 56407 |
rs27308571 | snp | C/T | 0.5 | 0 | intron-variant | Trpc4ap | Mm_Celera | 2:155676791 | TGTAAGTTCATCACA[C/T]GTCAACACCAATCAA | 56407 |
rs27308572 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Trpc4ap | Mm_Celera | 2:155676621 | TACAGCAATAGCTCT[A/G]TGCTGTTGATCTGAT | 56407 |
rs27308573 | snp | C/G/T | 0.132653 | 0.220748 | intron-variant | Trpc4ap | Mm_Celera | 2:155674675 | CACTGTGTTTTAGAT[C/G/T]ATGGCATGAGGGGGT | 56407 |
rs27308574 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trpc4ap | Mm_Celera | 2:155674649 | ATGAACAAGTCTCAT[A/G]ATTCTATCTACACTG | 56407 |
rs27308575 | snp | C/T | 0.5 | 0 | intron-variant | Trpc4ap | Mm_Celera | 2:155674604 | TTTAATAATGTTGGG[C/T]TTGTCTGAATACACA | 56407 |
rs27308576 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trpc4ap | Mm_Celera | 2:155673318 | AAGACTCCAAATTCA[A/G]CTGTGTTTTCTCTAC | 56407 |
rs27308577 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Trpc4ap | Mm_Celera | 2:155673284 | ACTTGTCAGTCTACG[A/C]TTTCCCCAGTGCACA | 56407 |
rs27308578 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trpc4ap | Mm_Celera | 2:155673234 | TAAAGCTGTAGCCTA[C/T]GCCCTGCTCCTGACA | 56407 |
rs27308579 | snp | C/G | 0.486111 | 0.0821678 | intron-variant | Trpc4ap | Mm_Celera | 2:155673209 | CCAAACAGCCAAGGA[C/G]CCCAGCAAATAAAGC | 56407 |
rs27308580 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Trpc4ap | Mm_Celera | 2:155672912 | ACAGCTCATACAAAA[A/G]CTGGCTATTTCTAAA | 56407 |
rs27308581 | snp | C/T | 0.5 | 0 | intron-variant | Trpc4ap | Mm_Celera | 2:155672571 | GAGACAGCACTCAAG[C/T]TGGAAAACAAGCGTC | 56407 |
rs27308582 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trpc4ap | Mm_Celera | 2:155672480 | TACACAGGTTACAAC[C/T]GTGGCTCCAGTTGCT | 56407 |
rs27308583 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Trpc4ap | Mm_Celera | 2:155672024 | GTTTGCAGAATGAAT[A/C]AAGTGTACCACACAC | 56407 |
rs27308584 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Trpc4ap | Mm_Celera | 2:155671459 | CCAGCAGCAGCTTGC[A/C]AGGGTACCAGGAAGG | 56407 |
rs27308585 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trpc4ap | Mm_Celera | 2:155670503 | CACTCTGTACGCTTT[A/G]GTACTTCAAATAAAT | 56407 |
rs27308586 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trpc4ap | Mm_Celera | 2:155670420 | ACGCATCTAAACCAA[A/G]AACAGCTCTGGTACA | 56407 |
rs27308587 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trpc4ap | Mm_Celera | 2:155669236 | TTTTAAAAGCTTGTT[C/T]CAGGGGCTGGTGAGA | 56407 |
rs27308588 | snp | A/G | 0.375 | 0.216506 | intron-variant | Trpc4ap | Mm_Celera | 2:155669179 | TGGACAGCATATCCG[A/G]GATACCTTGAGCCAA | 56407 |
rs27308589 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Trpc4ap | Mm_Celera | 2:155668071 | TTATAAAGATGGCTA[C/T]GGTTGATGGGCTGCT | 56407 |
rs27308590 | snp | A/C | 0.18 | 0.24 | intron-variant | Trpc4ap | Mm_Celera | 2:155667054 | CACGCAGTCATCAAG[A/C]ATTTGCTCACTACTC | 56407 |
rs27308591 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trpc4ap | Mm_Celera | 2:155666745 | GAGGTGCACAACCCC[A/G]CGAATGAGCCATGCA | 56407 |
rs27308592 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Trpc4ap | Mm_Celera | 2:155666186 | GTAAGTGGGCCGCAA[C/T]GGGAGGAGTACTCAC | 56407 |
rs27308593 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Trpc4ap | Mm_Celera | 2:155665981 | TTGTCACCTTTCAAC[A/T]GGTAATGGTGAGTCT | 56407 |
rs27308594 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trpc4ap | Mm_Celera | 2:155665955 | CTGTGACATGGGTAC[A/G]CCACCAACACTTGTC | 56407 |
rs27308595 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Trpc4ap | Mm_Celera | 2:155665708 | CCAGCACAGGTGCTC[C/T]AACAGCTCGCTCGCT | 56407 |
rs27308596 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Trpc4ap | Mm_Celera | 2:155665632 | TTTTTCCTATTTCAA[A/T]AAAGTGGCTCTAAGG | 56407 |
rs27308597 | snp | A/T | 0.18 | 0.24 | intron-variant | Trpc4ap | Mm_Celera | 2:155665424 | AAACCTTTCGCCCTA[A/T]TATCTACCTGTGCTT | 56407 |
rs27308598 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Trpc4ap | Mm_Celera | 2:155664406 | ATCTTGGAGAACCAA[C/T]AGGCTTTAAGTCTCC | 56407 |
rs27308599 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trpc4ap | Mm_Celera | 2:155664276 | CAAATGACTTCTCAC[C/T]GGGACCTCCATGGCT | 56407 |
rs27308600 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trpc4ap | Mm_Celera | 2:155664102 | GTCCAGACAAAAGCC[C/T]GCTGACTAATGTGAG | 56407 |
rs27308601 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Trpc4ap | Mm_Celera | 2:155663509 | CATGGATGGAACCCA[C/G]CGGCATAAGGAGCAC | 56407 |
rs27308602 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Trpc4ap | Mm_Celera | 2:155663292 | GGATCTAAAGCTCAA[G/T]CAGAGAGCTGGCTTG | 56407 |
rs27308603 | snp | C/T | 0.18 | 0.24 | intron-variant | Trpc4ap | Mm_Celera | 2:155662969 | TGATGAGCTACAGAG[C/T]AAGTGTCATGGTAGT | 56407 |
rs27308604 | snp | C/G | 0.18 | 0.24 | intron-variant | Trpc4ap | Mm_Celera | 2:155662955 | TGCCCTTAAACCTGT[C/G]ATGAGCTACAGAGTA | 56407 |
rs27308605 | snp | C/T | 0.42 | 0.183303 | intron-variant | Trpc4ap | Mm_Celera | 2:155662803 | GAGCGAGAACGTAAA[C/T]GAGGCCCTAACGAGC | 56407 |
rs27308606 | snp | G/T | 0.42 | 0.183303 | intron-variant | Trpc4ap | Mm_Celera | 2:155662678 | CTAAGTGAAAGCTGG[G/T]TAACAGTGTGTGGGT | 56407 |
rs27308607 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Trpc4ap | Mm_Celera | 2:155662396 | ACTTGGGTAGCACAG[A/G]CAGGAATAAGAAGGC | 56407 |
rs27308608 | snp | A/G | 0.42 | 0.183303 | intron-variant | Trpc4ap | Mm_Celera | 2:155662362 | AGGCACCTACAGAGC[A/G]TGGTGGAACCTATCA | 56407 |
rs27308609 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Trpc4ap | Mm_Celera | 2:155662348 | CACATGTAACATCAA[A/G]GCACCTACAGAGCGT | 56407 |
rs27308610 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Trpc4ap | GRCm38.p3 | 2:155661181 | TCCCCTAAGCCACTG[A/C/T]CCTGCCCTGAGTGTT | 56407 |
rs27308611 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Trpc4ap | Mm_Celera | 2:155660523 | CACTAAACAGGCAAA[C/T]GATCCCTAGACACAG | 56407 |
rs27308612 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Trpc4ap | Mm_Celera | 2:155659764 | TCCTGGGATTCCTAA[A/G]TAACTCATGGGAGAA | 56407 |
rs27308613 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Trpc4ap | Mm_Celera | 2:155659679 | CTAGGGTCTTAGGAG[A/T]GCTACTGAAAGGTGT | 56407 |
rs27308614 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Trpc4ap | Mm_Celera | 2:155659138 | CAGAGGTGCTCCTGT[C/G]CACATGCACTCAGGA | 56407 |
rs27308615 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Trpc4ap | Mm_Celera | 2:155658850 | GTGTGATGTGATATA[A/G]ACCTTCCTTGTGACT | 56407 |
rs27308616 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Trpc4ap | Mm_Celera | 2:155658162 | ATTTACCCTGAAGGT[A/G]TGCCTGTTCTCACTG | 56407 |
rs27308617 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trpc4ap | Mm_Celera | 2:155657685 | CAAAAAAGAGAGAGG[C/T]GCTGTAGTAAGAGCC | 56407 |
rs27308618 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trpc4ap | Mm_Celera | 2:155657203 | GAGCTAATGAACTTC[A/G]TCCTGAAACATAAGA | 56407 |
rs27308619 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Trpc4ap | Mm_Celera | 2:155656816 | GCCTAAGATGCACAC[A/G]GCAAGAAGTCTGGCA | 56407 |
rs27308620 | snp | C/T | 0.5 | 0 | intron-variant | Trpc4ap | Mm_Celera | 2:155656088 | GAGAGTGGCATTAAG[C/T]ACACACGAGGCTCTG | 56407 |
rs27308621 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Trpc4ap | Mm_Celera | 2:155655941 | TGGTGTGCTATGGGT[A/G]GAGAGAGCCCAGAGG | 56407 |
rs27308622 | snp | C/T | 0.32 | 0.24 | intron-variant | Trpc4ap | Mm_Celera | 2:155655479 | TGGAAAGAGAGAGCT[C/T]AGTGATTAAGAACGC | 56407 |
rs27308623 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Trpc4ap | Mm_Celera | 2:155655295 | TTTTTGTTCAAAACT[A/G]TCAAGAGCAGGAGCA | 56407 |
rs27308624 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trpc4ap | Mm_Celera | 2:155655247 | TTAAGGATAAACATA[C/T]AGACTGTTAAACAAT | 56407 |
rs27308625 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Trpc4ap | Mm_Celera | 2:155655099 | GAATAATGTTCTTTT[G/T]GTAATGGTAAAAATA | 56407 |
rs27308626 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trpc4ap | Mm_Celera | 2:155653381 | CAGTGTAGGACTGCA[C/T]TAAGGAAAATTCTAC | 56407 |
rs27308627 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trpc4ap | Mm_Celera | 2:155652934 | CTGGAAAGGTAACAG[A/G]CTACATATACTCCCA | 56407 |
rs27308628 | snp | G/T | 0.42 | 0.183303 | intron-variant | Trpc4ap | Mm_Celera | 2:155652112 | AAGCATGGAAAAGGT[G/T]CAGAGGGATGGGAAG | 56407 |
rs27308629 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Trpc4ap | Mm_Celera | 2:155651920 | GCCAGGGTCGCTGCA[C/T]CCCTATGGGCATCCT | 56407 |
rs27308630 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trpc4ap | Mm_Celera | 2:155651687 | CATACATATGTCACA[C/T]CCAGCAGACTAGAAT | 56407 |
rs27308631 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Trpc4ap | Mm_Celera | 2:155651085 | GGTTAGACAGCAGAT[A/C]CCGGGCCAGACTCGG | 56407 |
rs27308632 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trpc4ap | Mm_Celera | 2:155650980 | GTTCTCTTTATTCCC[C/T]ACTGAACAAGAGCCC | 56407 |
rs27308633 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Trpc4ap | Mm_Celera | 2:155650152 | GGAGCGGGAAAGAGA[A/G]AATCCAAGTCTTTGT | 56407 |
rs27308634 | snp | C/T | 0.42 | 0.183303 | intron-variant | Trpc4ap | Mm_Celera | 2:155650050 | CCTGCACACTGTCAC[C/T]ACCTAGAGATGCTGC | 56407 |
rs27308635 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trpc4ap | Mm_Celera | 2:155649083 | AGTCTAGAATCTAAC[C/T]CTAGGATCAGCTACA | 56407 |
rs27308636 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Trpc4ap | Mm_Celera | 2:155649026 | CCTCTCGTTATGAAC[A/C]GACTATCCCTGTTAT | 56407 |
rs27308637 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Trpc4ap | Mm_Celera | 2:155648889 | TGGAGGAAATGCTCA[C/G]ATGTGTGTCAGGACG | 56407 |
rs27308638 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Trpc4ap | Mm_Celera | 2:155648327 | TTGTTTCTGGCTGCT[A/G]TGACATGAACAGCTC | 56407 |
rs27308639 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Trpc4ap | Mm_Celera | 2:155646058 | TGATCCCTCTAAACA[G/T]CGATCCAAAACAAAA | 56407 |
rs27308640 | snp | C/G | 0.244898 | 0.249948 | synonymous-codon | Trpc4ap | Mm_Celera | 2:155645057 | AGCAATCATCCTGTG[C/G]ACCTGTGTAAGGATG | 56407 |
rs27308641 | snp | C/G | 0.42 | 0.183303 | intron-variant | Trpc4ap | Mm_Celera | 2:155644858 | TGAGGCCCTCAGGGT[C/G]AGCAGTGGTTCTTAA | 56407 |
rs27308642 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Trpc4ap | Mm_Celera | 2:155644309 | CTGTGGAAAGACTCA[C/T]TCTAAGTTACTAACT | 56407 |
rs27308643 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trpc4ap | Mm_Celera | 2:155644250 | TGCAAACGCAGAAGA[C/T]ACAGGATATTTCCAC | 56407 |
rs27308644 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Trpc4ap | Mm_Celera | 2:155644161 | GTGTGAAAACCCAGA[C/T]ACAAGCTGCTGGCAC | 56407 |
rs27308645 | snp | A/C/T | 0.486111 | 0.0821678 | intron-variant | Trpc4ap | GRCm38.p3 | 2:155644055 | GGCTCCTCTAAAGCG[A/C/T]GAGCCAAAGTGTGTC | 56407 |
rs27308646 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Trpc4ap | Mm_Celera | 2:155643856 | CCAAAGGGAAACCTA[C/T]TGATCTCAGAAAGGC | 56407 |
rs27308647 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Trpc4ap | Mm_Celera | 2:155643529 | GTGACATCCCTGTCT[A/T]GCTACACTGCTTCTT | 56407 |
rs27308648 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Trpc4ap | Mm_Celera | 2:155643473 | ACATATTAAAGCTAC[A/G]TTTGTCACAACACTT | 56407 |
rs27308649 | snp | C/T | 0.142012 | 0.225474 | synonymous-codon | Trpc4ap | Mm_Celera | 2:155643430 | GAGAAGTCTCAAAAA[C/T]TGGATCTTCAAGGTG | 56407 |
rs27308650 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Trpc4ap | Mm_Celera | 2:155643290 | GGAGCACAGCCTCAC[A/C]GATATTGGGGGCTCC | 56407 |
rs27308651 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Trpc4ap | Mm_Celera | 2:155643244 | ATTCGGTGCTCAGAT[A/G]GAAGGAAGGGTTGTC | 56407 |
rs27308652 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Trpc4ap | Mm_Celera | 2:155643238 | GGAAAGATTCGGTGC[C/T]CAGATAGAAGGAAGG | 56407 |
rs27308653 | snp | C/T | 0.5 | 0 | intron-variant | Trpc4ap | Mm_Celera | 2:155643150 | CTAAGAGGCTAGTCA[C/T]TGCACAAGGGTGTTG | 56407 |
rs27308654 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Trpc4ap | Mm_Celera | 2:155643133 | AGTCAGGGACTCTGC[A/G]GCTAAGAGGCTAGTC | 56407 |
rs27308655 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Trpc4ap | Mm_Celera | 2:155642577 | CTCTCCCAAATGTAC[C/T]CTACATGACAGCAGG | 56407 |
rs27308656 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Trpc4ap | Mm_Celera | 2:155642392 | CTGCCTCTTCATCCC[A/G]GTCAGGCCTCTGCTC | 56407 |
rs27308657 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Trpc4ap | Mm_Celera | 2:155642202 | CCCTGTTGTGTGAAC[A/C]CCTAGGGAGTGATCA | 56407 |
rs27308658 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Trpc4ap | Mm_Celera | 2:155642165 | CCATGTCATTATTGA[A/C]AATGCTTACCCAATT | 56407 |