SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs15127 | snp | A/C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | CRKL | GRCh38.p7 | 22:20953333 | ACCTGTCCTTCTGCT[A/C/T]CTTTAGAAAACAGAA | 1399 |
rs737892 | snp | C/T | 0.44252 | 0.159487 | intron-variant | CRKL | GRCh38.p7 | 22:20918446 | TTTTTTTTTTTTCCC[C/T]CTCACGAGGCTGTTT | 1399 |
rs737893 | snp | C/T | 0.320814 | 0.239761 | intron-variant | CRKL | GRCh38.p7 | 22:20934613 | GCCTTCTTGCTCTTT[C/T]TTGTTCCCAAAGCCT | 1399 |
rs737894 | snp | A/G | 0.32153 | 0.239548 | utr-variant-3-prime, nc-transcript-variant | CRKL | GRCh38.p7 | 22:20950120 | TGGAGAGAAGTTGAC[A/G]TGGAAAGGGTCTTCC | 1399 |
rs737895 | snp | C/G | 0.338523 | 0.233803 | downstream-variant-500B | CRKL | GRCh38.p7 | 22:20953947 | CCAAAAGAGAAATCT[C/G]CCTCCCAGAGTGTCT | 1399 |
rs929201 | snp | C/T | 0.00716266 | 0.059414 | utr-variant-5-prime, nc-transcript-variant | CRKL | GRCh38.p7 | 22:20917542 | TCGAGTTCGGTGCCT[C/T]GTGTGACGGCGGGGG | 1399 |
rs929202 | snp | A/G | 0.441841 | 0.160303 | intron-variant | CRKL | GRCh38.p7 | 22:20920050 | CCAATTTAAGGAGTT[A/G]AGAATCTTAGAACCC | 1399 |
rs1043235 | snp | A/G | 0.476227 | 0.106402 | utr-variant-3-prime, intron-variant | CRKL | GRCh38.p7 | 22:20952112 | TGAGTGGAGTTTCCA[A/G]CAGAGGGAGGAATGT | 1399 |
rs1043242 | snp | A/G | 0.440609 | 0.161766 | utr-variant-3-prime, intron-variant | CRKL | GRCh38.p7 | 22:20952455 | TTCTGCACTCCAGAT[A/G]TGTGCCAAAACTAGT | 1399 |
rs1043260 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | CRKL | GRCh38.p7 | 22:20953303 | TAACTGCTGTCGGTG[C/T]GGACGCTGTGCTGGT | 1399 |
rs1043264 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | CRKL | GRCh38.p7 | 22:20953304 | AACTGCTGTCGGTGT[A/G]GACGCTGTGCTGGTT | 1399 |
rs1548410 | snp | C/T | 0.309401 | 0.24284 | utr-variant-3-prime, nc-transcript-variant | CRKL | GRCh38.p7 | 22:20950175 | TGGGACTGATTCTGT[C/T]GTGTTCACCAGAGAA | 1399 |
rs1978098 | snp | C/T | 0.132066 | 0.220435 | intron-variant | CRKL | GRCh38.p7 | 22:20934583 | GTCCTATTCCTTGTT[C/T]GCCCCAAATTCTCAG | 1399 |
rs2023715 | snp | C/T | 0.131038 | 0.219882 | intron-variant | CRKL | GRCh38.p7 | 22:20946556 | GTGCTTCCTCTTAAT[C/T]TGTTGATAAGGTCAG | 1399 |
rs2023716 | snp | A/C | 0.202035 | 0.245356 | intron-variant | CRKL | GRCh38.p7 | 22:20946607 | TTGCCCCGTGAACTG[A/C]GTTGGTATCTACCCA | 1399 |
rs2106538 | snp | C/T | 0.338523 | 0.233803 | intron-variant | CRKL | GRCh38.p7 | 22:20944027 | gctattcaggttcct[C/T]gcaattctatatgaa | 1399 |
rs2266951 | snp | A/G | 0.226188 | 0.248863 | intron-variant | CRKL | GRCh38.p7 | 22:20919153 | CAAAATATCAGAACT[A/G]TATATTGATACTGTG | 1399 |
rs2266952 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | CRKL | GRCh38.p7 | 22:20945767 | GGGCAGGCAGTGGAC[C/T]CATGCAGCTCCGTGA | 1399 |
rs2266953 | snp | C/T | 0.442655 | 0.159323 | intron-variant | CRKL | GRCh38.p7 | 22:20948637 | CCAAAGTTCATGGCA[C/T]GGACCATTGGACTGT | 1399 |
rs2266954 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | CRKL | GRCh38.p7 | 22:20948721 | CGCCGGCTGGTCTCA[A/G]ACTCCTGGGCTCAAG | 1399 |
rs2266955 | snp | A/G | 0.441977 | 0.16014 | intron-variant | CRKL | GRCh38.p7 | 22:20949423 | TGCATTCCAGCCTGG[A/G]CGACAGACCCCGTCT | 1399 |
rs2266956 | snp | C/T | 0.347032 | 0.230401 | intron-variant | CRKL | GRCh38.p7 | 22:20949530 | TCACTTGAGCCCAGG[C/T]GTTAGAGGTTACATT | 1399 |
rs2285547 | snp | C/T | 0.33875 | 0.233717 | utr-variant-3-prime, intron-variant | CRKL | GRCh38.p7 | 22:20952770 | ACTAGAGGGCATTGA[C/T]TGGTTAAAAACTTGT | 1399 |
rs3171744 | snp | C/T | | | utr-variant-3-prime, intron-variant | CRKL | GRCh38.p7 | 22:20951941 | CTGCGGCAGTTGCCG[C/T]TTCTGGTTAGGTGTG | 1399 |
rs3180409 | snp | C/T | 0 | 0 | missense, nc-transcript-variant | CRKL | GRCh38.p7 | 22:20918205 | GAGTTTTACAAGATC[C/T]ACTACCTGGACACCA | 1399 |
rs3180410 | snp | A/T | 0 | 0 | missense, nc-transcript-variant | CRKL | GRCh38.p7 | 22:20933816 | TCTGTCTCAGCACCC[A/T]ACCTGCCTACAGCAG | 1399 |
rs3182906 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CRKL | GRCh38.p7 | 22:20953490 | TTAAAGATCATAAAC[C/T]TCAGGCAATAATATT | 1399 |
rs3819652 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | CRKL | GRCh38.p7 | 22:20932609 | TGAGATTATAAAAAT[A/C]AATTTAAACCAGGTA | 1399 |
rs3827296 | snp | C/G | 0.339203 | 0.233544 | intron-variant | CRKL | GRCh38.p7 | 22:20926175 | ATTAATGTAGATGAT[C/G]GGCAGGAACCTAGGA | 1399 |
rs4508706 | snp | A/G | 0 | 0 | upstream-variant-2KB | CRKL | GRCh38.p7 | 22:20916161 | gggaggatcccttga[A/G]atggggaaatcaagg | 1399 |
rs4624490 | snp | A/G | 0.442113 | 0.159977 | intron-variant | CRKL | GRCh38.p7 | 22:20922317 | tgagccaccctctcc[A/G]gccTGGGAGTGTGTT | 1399 |
rs4820671 | snp | A/C | 0.338296 | 0.233889 | intron-variant | CRKL | GRCh38.p7 | 22:20920862 | CCTTTCTCTGACCCT[A/C]CCCCTCACGTTCAGC | 1399 |
rs4820673 | snp | C/T | 0.320814 | 0.239761 | intron-variant | CRKL | GRCh38.p7 | 22:20943672 | ttattctttccctgt[C/T]gaatagacttggcac | 1399 |
rs4820674 | snp | A/G | 0.320814 | 0.239761 | intron-variant | CRKL | GRCh38.p7 | 22:20943765 | ctggagactgaggtg[A/G]gaagattgcttgagc | 1399 |
rs4822687 | snp | C/T | 0.442249 | 0.159814 | intron-variant | CRKL | GRCh38.p7 | 22:20920741 | ACCTTTGTACCTTTG[C/T]ACCTTTGCTCCAGCT | 1399 |
rs4822700 | snp | C/T | 0.321053 | 0.23969 | intron-variant | CRKL | GRCh38.p7 | 22:20946020 | CAGCATACATTCATG[C/T]ATTTGCATACAACTT | 1399 |
rs4822707 | snp | G/T | 0.226779 | 0.248919 | intron-variant | CRKL | GRCh38.p7 | 22:20949402 | AATGAGCTGTAATCG[G/T]GCCACTGCATTCCAG | 1399 |
rs5752261 | snp | C/T | 0.131381 | 0.220067 | intron-variant | CRKL | GRCh38.p7 | 22:20920765 | TCCAGCTGTTGGCTC[C/T]TCACTGACTGCCTTA | 1399 |
rs5752263 | snp | C/G | 0.321053 | 0.23969 | intron-variant | CRKL | GRCh38.p7 | 22:20922313 | gatgtgagccaccct[C/G]tccggccTGGGAGTG | 1399 |
rs5752268 | snp | C/T | 0.320814 | 0.239761 | intron-variant | CRKL | GRCh38.p7 | 22:20929313 | GGGACTACAGGCGCC[C/T]GCCACCACGCTCAGC | 1399 |
rs5752272 | snp | A/C | 0.391805 | 0.252207 | intron-variant | CRKL | GRCh38.p7 | 22:20932274 | CCACTATGCCCGGCT[A/C]ATTTTTTGTCTGTTT | 1399 |
rs5752273 | snp | A/G | 0.321292 | 0.23962 | intron-variant | CRKL | GRCh38.p7 | 22:20933355 | agcctgggcaacaga[A/G]caagactccatctcc | 1399 |
rs5752274 | snp | A/G | 0.339429 | 0.233457 | intron-variant | CRKL | GRCh38.p7 | 22:20933623 | cagtgagctaagatc[A/G]cgctattgcactcca | 1399 |
rs5752284 | snp | C/T | 0.320814 | 0.239761 | intron-variant | CRKL | GRCh38.p7 | 22:20938456 | CTGAATAGCTGTAGA[C/T]AGGTGAGCATGCTGG | 1399 |
rs5752304 | snp | C/T | 0.164546 | 0.234942 | intron-variant | CRKL | GRCh38.p7 | 22:20947939 | TCCACCCACTTCAGC[C/T]TCCCAAAGTGCTGGG | 1399 |
rs5752307 | snp | C/T | 0.225597 | 0.248806 | intron-variant | CRKL | GRCh38.p7 | 22:20948754 | GTCCTCCCACCTCAG[C/T]CTGCCAAGGACCTGG | 1399 |
rs5761353 | snp | G/T | 0 | 0 | upstream-variant-2KB | CRKL | GRCh38.p7 | 22:20917174 | TCCCTCTCGGCTCCA[G/T]CTGTTTTCCTGCCAG | 1399 |
rs5761361 | snp | G/T | 0.442113 | 0.159977 | intron-variant | CRKL | GRCh38.p7 | 22:20918737 | GCTGGGACTACTGGC[G/T]CACGCCACCACACCC | 1399 |
rs5761368 | snp | A/G | 0.338976 | 0.23363 | intron-variant | CRKL | GRCh38.p7 | 22:20923183 | TGTACTGTACTCAGC[A/G]GACTTTGAGCATTAC | 1399 |
rs5761382 | snp | A/G/T | 0.491394 | 0.231548 | intron-variant | CRKL | GRCh38.p7 | 22:20929330 | CCACCACGCTCAGCT[A/G/T]ATTTTTTTGTATTTT | 1399 |
rs5761386 | snp | G/T | 0.338523 | 0.233803 | intron-variant | CRKL | GRCh38.p7 | 22:20931558 | CTGACAGATGCAGGG[G/T]TCGTCCCTAAGGCTG | 1399 |
rs5761424 | snp | A/G | 0.322721 | 0.23919 | intron-variant | CRKL | GRCh38.p7 | 22:20938913 | GAATTGAAGTCAGTG[A/G]AACAGATCGTGTGGA | 1399 |
rs5761429 | snp | A/G | 0.155656 | 0.231515 | intron-variant | CRKL | GRCh38.p7 | 22:20939365 | cctgcctcagcctcc[A/G]gagtagctgggacta | 1399 |
rs5761433 | snp | A/G | 0.155987 | 0.23165 | intron-variant | CRKL | GRCh38.p7 | 22:20940126 | GTTATGTCATCTAGC[A/G]TATTCATTACCCTCC | 1399 |
rs5761449 | snp | A/T | 0.499891 | 0.00738737 | intron-variant | CRKL | GRCh38.p7 | 22:20941509 | TATACATATGTGTGT[A/T]TGTGTATGTGTATAT | 1399 |
rs5761450 | snp | G/T | 0.125182 | 0.216612 | intron-variant | CRKL | GRCh38.p7 | 22:20941528 | gtatgtgtatatata[G/T]atatattttatgtgt | 1399 |
rs5761455 | snp | C/G | 0.338523 | 0.233803 | intron-variant | CRKL | GRCh38.p7 | 22:20941809 | ACCTTGGCTAGGCTG[C/G]TCTTGAACTCCTGAC | 1399 |
rs5761460 | snp | C/T | 0.125182 | 0.216612 | intron-variant | CRKL | GRCh38.p7 | 22:20942963 | agcagctgtaccata[C/T]tccattccaaccagc | 1399 |
rs5761464 | snp | C/G | 0.103438 | 0.202533 | intron-variant | CRKL | GRCh38.p7 | 22:20943730 | gggtgtggtggtgca[C/G]acctgtaatcccagg | 1399 |
rs5761467 | snp | A/G | 0.321053 | 0.23969 | intron-variant | CRKL | GRCh38.p7 | 22:20944785 | cagagcctcactccc[A/G]ctccattgcccaggc | 1399 |
rs5761470 | snp | C/T | 0.212728 | 0.247206 | intron-variant | CRKL | GRCh38.p7 | 22:20946717 | GGTGTAGAGCACCCC[C/T]CCCTCCAAAAAAAAA | 1399 |
rs5761471 | snp | A/C/G | | | intron-variant | CRKL | GRCh38.p7 | 22:20947261 | ttttttttttcaata[A/C/G]aagctaggtctcact | 1399 |
rs5844448 | in-del | -/A | 0.488057 | 0.0763479 | upstream-variant-2KB | CRKL | GRCh38.p7 | 22:20915406 | AGTCCGTATCAGAAT[-/A]AAAAAAAAAAAAAAG | 1399 |
rs5844449 | in-del | -/T | 0.400325 | 0.199756 | intron-variant | CRKL | GRCh38.p7 | 22:20918431 | GGATAAGAGGATGCG[-/T]TTTTTTTTTTTCCCT | 1399 |
rs5844450 | in-del | -/A | 0.322721 | 0.23919 | intron-variant | CRKL | GRCh38.p7 | 22:20924557 | GAATTTGATTCAGAG[-/A]AAAATACAAGAACAT | 1399 |
rs5997038 | snp | A/G | 0.338523 | 0.233803 | intron-variant | CRKL | GRCh38.p7 | 22:20925517 | GAGACTTCGTCTCGG[A/G]AAACAAAAAACAAAC | 1399 |
rs5997064 | snp | A/G | 0.33875 | 0.233717 | intron-variant | CRKL | GRCh38.p7 | 22:20945289 | tgagccaccgcaccc[A/G]gcttggaattacttt | 1399 |
rs6004914 | snp | A/G | 0.202651 | 0.245475 | intron-variant | CRKL | GRCh38.p7 | 22:20920299 | CGAGGTCAGGAGTTC[A/G]AGACCATCTTGGCCA | 1399 |
rs6004917 | snp | A/G | 0.226484 | 0.248892 | intron-variant | CRKL | GRCh38.p7 | 22:20921571 | ATGAAGCTAAGACCT[A/G]AGGGTAAAGAAGAAC | 1399 |
rs6004944 | snp | A/C | 0.226188 | 0.248863 | intron-variant | CRKL | GRCh38.p7 | 22:20928468 | tctcaaaaaaattta[A/C]aaaacaagccaaaaa | 1399 |
rs6005013 | snp | A/G | 0.324145 | 0.238752 | intron-variant | CRKL | GRCh38.p7 | 22:20947704 | TTTTTTTTTGAGACA[A/G]GGTCTTGCTCTGTCA | 1399 |
rs6005034 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | CRKL | GRCh38.p7 | 22:20953109 | TATTTTTGAAAAGGG[A/G]TGATGTGGTTTTTTG | 1399 |
rs7287892 | snp | A/C | 0.338523 | 0.233803 | intron-variant | CRKL | GRCh38.p7 | 22:20937041 | GTTTTTAGTAGAGAC[A/C]GGGTTTCACTATGTT | 1399 |
rs7288034 | snp | C/G | 0.488606 | 0.0746142 | upstream-variant-2KB | CRKL | GRCh38.p7 | 22:20916535 | ctggtgacagagcga[C/G]actccgtcgaaagaa | 1399 |
rs7290490 | snp | C/T | 0.320814 | 0.239761 | intron-variant | CRKL | GRCh38.p7 | 22:20936975 | AAGCGATTCTTCTGC[C/T]TCAGCCTCTCAAGTA | 1399 |
rs7292964 | snp | C/T | 0.320335 | 0.239902 | intron-variant | CRKL | GRCh38.p7 | 22:20942259 | tatcaaaacttcatt[C/T]cttGTCCCAGCATGG | 1399 |
rs8139149 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | CRKL | GRCh38.p7 | 22:20942468 | tttgttaatccattt[A/G]tctcttgatggatac | 1399 |
rs8140283 | snp | A/G | 0.338296 | 0.233889 | intron-variant | CRKL | GRCh38.p7 | 22:20936072 | gactgaggtggaaca[A/G]ttgcttgaaccaggt | 1399 |
rs8142366 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | CRKL | GRCh38.p7 | 22:20948518 | TGCAAGAACCTTTCA[A/G]AGTTGGAaggaaact | 1399 |
rs9608541 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | CRKL | GRCh38.p7 | 22:20926659 | AGCTTAGATGGGATC[A/C/T]CCCAGAATGAGGAGG | 1399 |
rs9608579 | snp | A/C | 0.5 | 0 | intron-variant | CRKL | GRCh38.p7 | 22:20946733 | CCCTCCAAAAAAAAA[A/C]AACAGATTGATCTGC | 1399 |
rs9613273 | snp | C/T | 0.347473 | 0.230215 | intron-variant | CRKL | GRCh38.p7 | 22:20918464 | CACGAGGCTGTTTCT[C/T]AATGTGAAGAGGATG | 1399 |
rs9613274 | snp | A/G | 0.320814 | 0.239761 | intron-variant | CRKL | GRCh38.p7 | 22:20918880 | CAGGCGTGAGCCACC[A/G]CACCCGGCCAAAAAC | 1399 |
rs9613291 | snp | A/G | 0.442385 | 0.15965 | intron-variant | CRKL | GRCh38.p7 | 22:20922701 | TTTTTTTGAGACCAA[A/G]TCTCCCTCTGTCCCC | 1399 |
rs9613292 | snp | A/G | 0.472896 | 0.113214 | intron-variant | CRKL | GRCh38.p7 | 22:20923358 | cttggctcactgcaa[A/G]ctccgcctcctgggt | 1399 |
rs9613367 | snp | A/G | 0 | 0 | intron-variant | CRKL | GRCh38.p7 | 22:20941517 | TGTGTGTTTGTGTAT[A/G]TGTATATATATATAT | 1399 |
rs9613368 | snp | A/G | | | intron-variant | CRKL | GRCh38.p7 | 22:20941519 | TGTGTTTGTGTATGT[A/G]TATATATATATATAT | 1399 |
rs9613369 | snp | A/T | 0.5 | 0 | intron-variant | CRKL | GRCh38.p7 | 22:20941588 | tgtgtgtatATATAt[A/T]ttttttttttttttt | 1399 |
rs9613388 | snp | G/T | 0.029116 | 0.117091 | utr-variant-3-prime, nc-transcript-variant | CRKL | GRCh38.p7 | 22:20951185 | ACTCCACTCACTGAA[G/T]CCCAGACCTCCGTGC | 1399 |
rs9620650 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | CRKL | GRCh38.p7 | 22:20930806 | ctgcctcagcctccc[A/G]agtggctgggactac | 1399 |
rs9620655 | snp | G/T | 0.338523 | 0.233803 | intron-variant | CRKL | GRCh38.p7 | 22:20937935 | AGTGCAGTGGCATGA[G/T]CTCCGCTCGCTGCAA | 1399 |
rs9625098 | snp | C/T | | | intron-variant | CRKL | GRCh38.p7 | 22:20918352 | CATATTCCCCGCATT[C/T]TGAACCAAATTATTT | 1399 |
rs9625149 | snp | C/G | 0.0678174 | 0.1712 | intron-variant | CRKL | GRCh38.p7 | 22:20946718 | GTGTAGAGCACCCCT[C/G]CCTCCAAAAAAAAAA | 1399 |
rs9625171 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | CRKL | GRCh38.p7 | 22:20950744 | TAAACAGGTTAAGTA[A/G]CAGGTTGGGTTTTTA | 1399 |
rs9917575 | snp | A/G | 0.131038 | 0.219882 | intron-variant | CRKL | GRCh38.p7 | 22:20932700 | TTGTAATTTGAAAAG[A/G]CATTCAGAATAGTAA | 1399 |
rs10660912 | in-del | -/AA/AAG/AAGAAAAG | 0 | 0 | upstream-variant-2KB | CRKL | GRCh38.p7 | 22:20916629 | AAGAAAAGAAAAGAA[-/AA/AAG/AAGAAAAG]AAGAAAAGAAAGAAA | 1399 |
rs11269946 | in-del | -/ACAGGAGGGACCTGTATA | 0.322007 | 0.239405 | intron-variant | CRKL | GRCh38.p7 | 22:20921515 | TAGTAAGATCAATAT[-/ACAGGAGGGACCTGTATA]ACAGGAGGGACCTAC | 1399 |
rs11317560 | in-del | -/A | | | upstream-variant-2KB | CRKL | GRCh38.p7 | 22:20916635 | AAGAAAAGAAAAAAG[-/A]AAAGAAAGAAAGAAA | 1399 |
rs11327549 | in-del | -/T | 0.327211 | 0.237778 | intron-variant | CRKL | GRCh38.p7 | 22:20939408 | ACCACGCCCGGCTAA[-/T]TTTTTTTTTTGTATT | 1399 |
rs11451684 | in-del | -/A | | | intron-variant | CRKL | GRCh38.p7 | 22:20925187 | CGAGACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA | 1399 |