view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARFRP1_chr20_63693647_63712976 | 63693708 | A | ACCACCTC others(5887): Show |
downstream_gene_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0043 | 1 | 224 | 0.0045 | 5894 | c.*67 others(5905): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4938 | chr20 | TogoVar | |||||||
CHL1_chr3_191763_414417 | 262424 | C | CAGATCTA others(5888): Show |
intron_variant | MODIFIER | HG02559.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0079 | 1 | 127 | 0.0079 | 5895 | c.-95 others(5914): Show |
CHL1 | ENSG00000134121.10 | transcript | ENST00000256509.7 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
LRRC27_chr10_132327193_132386508 | 132364461 | C | CCACCCAC others(5889): Show |
intron_variant | MODIFIER | HG01515.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0151 | 1 | 256 | 0.0039 | 5896 | c.129 others(5913): Show |
LRRC27 | ENSG00000148814.18 | transcript | ENST00000368614.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(5890): Show |
upstream_gene_variant | MODIFIER | HG02809.hp2 | a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0179 | 1 | 8 | 0.1250 | 5897 | c.-45 others(5906): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5891): Show |
intron_variant | MODIFIER | HG01884.hp1 | a0003 | a0003c0005 | a0003c0005t0010 | a0003c0005t0010g0004 | 1 | 5 | 0.2000 | 5898 | c.217 others(5919): Show |
CCSER1 | ENSG00000184305.16 | transcript | ENST00000509176.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5892): Show |
intron_variant | MODIFIER | HG02723.hp1 HG02809.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0008a0002c0002t0003 | a0001c0001t0008g0038 a0002c0002t0003g0013 |
2 | 6 | 0.3333 | 5899 | c.217 others(5920): Show |
CCSER1 | ENSG00000184305.16 | transcript | ENST00000509176.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5892): Show |
intron_variant | MODIFIER | HG01099.hp1 | a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0028 | 1 | 5 | 0.2000 | 5899 | c.217 others(5920): Show |
CCSER1 | ENSG00000184305.16 | transcript | ENST00000509176.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5892): Show |
intron_variant | MODIFIER | HG02258.hp1 HG03239.hp1 HG03516.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0006a0001c0003t0002 | a0001c0001t0001g0024 a0001c0001t0006g0023 a0001c0003t0002g0026 |
3 | 7 | 0.4286 | 5899 | c.217 others(5920): Show |
CCSER1 | ENSG00000184305.16 | transcript | ENST00000509176.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5892): Show |
intron_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0017 | 1 | 5 | 0.2000 | 5899 | c.217 others(5920): Show |
CCSER1 | ENSG00000184305.16 | transcript | ENST00000509176.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5893): Show |
intron_variant | MODIFIER | HG02109.hp1 HG03139.hp1 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0003a0001c0008t0019 | a0001c0001t0003g0034 a0001c0008t0019g0029 |
2 | 6 | 0.3333 | 5900 | c.217 others(5921): Show |
CCSER1 | ENSG00000184305.16 | transcript | ENST00000509176.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5893): Show |
intron_variant | MODIFIER | HG03209.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0036 | 1 | 5 | 0.2000 | 5900 | c.217 others(5921): Show |
CCSER1 | ENSG00000184305.16 | transcript | ENST00000509176.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5893): Show |
intron_variant | MODIFIER | NA19240.hp1 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0035 | 1 | 5 | 0.2000 | 5900 | c.217 others(5921): Show |
CCSER1 | ENSG00000184305.16 | transcript | ENST00000509176.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5893): Show |
intron_variant | MODIFIER | HG01243.hp1 NA19240.hp2 |
a0001a0005 | a0001c0001a0005c0007 | a0001c0001t0007a0005c0007t0012 | a0001c0001t0007g0007 a0005c0007t0012g0010 |
2 | 6 | 0.3333 | 5900 | c.217 others(5921): Show |
CCSER1 | ENSG00000184305.16 | transcript | ENST00000509176.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5893): Show |
intron_variant | MODIFIER | HG02717.hp2 HG02897.hp2 HG03130.hp1 others(3): Show |
a0001a0002a0004 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0004a0001c0003t0002a0002c0002t0001others(3): Show | a0001c0001t0004g0005 a0001c0003t0002g0014 a0002c0002t0001g0006 others(3): Show |
6 | 10 | 0.6000 | 5900 | c.217 others(5921): Show |
CCSER1 | ENSG00000184305.16 | transcript | ENST00000509176.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5893): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0003 | a0003c0005 | a0003c0005t0005 | a0003c0005t0005g0011 | 1 | 5 | 0.2000 | 5900 | c.217 others(5921): Show |
CCSER1 | ENSG00000184305.16 | transcript | ENST00000509176.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5894): Show |
intron_variant | MODIFIER | HG01243.hp2 HG02717.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0020 | a0001c0001t0003g0012 a0001c0001t0020g0033 |
2 | 6 | 0.3333 | 5901 | c.217 others(5922): Show |
CCSER1 | ENSG00000184305.16 | transcript | ENST00000509176.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5894): Show |
intron_variant | MODIFIER | HG01099.hp2 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0019 | 1 | 5 | 0.2000 | 5901 | c.217 others(5922): Show |
CCSER1 | ENSG00000184305.16 | transcript | ENST00000509176.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5894): Show |
intron_variant | MODIFIER | HG03017.hp2 | a0002 | a0002c0002 | a0002c0002t0017 | a0002c0002t0017g0008 | 1 | 5 | 0.2000 | 5901 | c.217 others(5922): Show |
CCSER1 | ENSG00000184305.16 | transcript | ENST00000509176.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5894): Show |
intron_variant | MODIFIER | HG02897.hp1 HG03209.hp1 |
a0002a0006 | a0002c0002a0006c0006 | a0002c0002t0018a0006c0006t0016 | a0002c0002t0018g0009 a0006c0006t0016g0020 |
2 | 6 | 0.3333 | 5901 | c.217 others(5922): Show |
CCSER1 | ENSG00000184305.16 | transcript | ENST00000509176.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5894): Show |
intron_variant | MODIFIER | HG02809.hp1 NA18906.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0008 | a0001c0001t0001g0002 a0002c0002t0008g0030 |
2 | 6 | 0.3333 | 5901 | c.217 others(5922): Show |
CCSER1 | ENSG00000184305.16 | transcript | ENST00000509176.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
EHMT1_chr9_137614005_137841127 | 137716460 | T | TGGGGGAG others(5898): Show |
intron_variant | MODIFIER | HG01496.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0009 | 1 | 129 | 0.0078 | 5905 | c.86- others(5916): Show |
EHMT1 | ENSG00000181090.21 | transcript | ENST00000460843.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PIEZO1_chr16_88710338_88790220 | 88731953 | G | GGGGAGAG others(5898): Show |
intron_variant | MODIFIER | HG04199.hp1 | a0010 | a0010c0036 | a0010c0036t0001 | a0010c0036t0001g0139 | 1 | 280 | 0.0036 | 5905 | c.299 others(5920): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | |||||||
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5899): Show |
intron_variant | MODIFIER | HG01192.hp1 HG02258.hp2 HG02723.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004a0001c0001t0011 | a0001c0001t0002g0027 a0001c0001t0004g0022 a0001c0001t0011g0003 |
3 | 7 | 0.4286 | 5906 | c.217 others(5927): Show |
CCSER1 | ENSG00000184305.16 | transcript | ENST00000509176.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
CLPTM1L_chr5_1312752_1350099 | 1333664 | T | TGAGGATA others(5900): Show |
intron_variant | MODIFIER | NA18944.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0026 | 1 | 55 | 0.0182 | 5907 | c.891 others(5922): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
ACTN2_chr1_236681499_236769631 | 236715026 | C | CCACTGAA others(5902): Show |
intron_variant | MODIFIER | HG02132.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0235 | 1 | 173 | 0.0058 | 5909 | c.127 others(5926): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
CLPTM1L_chr5_1312752_1350099 | 1333664 | T | TGAGGATA others(5902): Show |
intron_variant | MODIFIER | NA18998.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0057 | 1 | 55 | 0.0182 | 5909 | c.891 others(5924): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
RHEX_chr1_206048173_206107449 | 206054127 | A | AAAAAAAA others(5902): Show |
intron_variant | MODIFIER | HG01256.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 319 | 0.0031 | 5909 | c.-97 others(5924): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RHEX_chr1_206048173_206107449 | 206054127 | A | AAAAAAAA others(5902): Show |
intron_variant | MODIFIER | HG00544.hp2 HG00609.hp1 NA19075.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0029 a0001c0002t0001g0172 a0001c0002t0001g0178 |
3 | 321 | 0.0093 | 5909 | c.-97 others(5924): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RHEX_chr1_206048173_206107449 | 206057461 | C | CCACAAAA others(5902): Show |
intron_variant | MODIFIER | NA18997.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0231 | 1 | 332 | 0.0030 | 5909 | c.-97 others(5926): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TRPM2_chr21_44348621_44447644 | 44407131 | A | ATTCCTCC others(5902): Show |
intron_variant | MODIFIER | HG04199.hp1 | a0009 | a0009c0011 | a0009c0011t0001 | a0009c0011t0001g0010 | 1 | 4 | 0.2500 | 5909 | c.296 others(5926): Show |
TRPM2 | ENSG00000142185.18 | transcript | ENST00000397928.6 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236714890 | T | TACCACTG others(5903): Show |
intron_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0233 | 1 | 241 | 0.0041 | 5910 | c.127 others(5927): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RHEX_chr1_206048173_206107449 | 206052634 | G | GAAACCAG others(5903): Show |
upstream_gene_variant | MODIFIER | HG02602.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0170 | 1 | 325 | 0.0031 | 5910 | c.-72 others(5919): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 538 | chr1 | TogoVar | |||||||
RHEX_chr1_206048173_206107449 | 206054127 | A | AAAAAAAA others(5903): Show |
intron_variant | MODIFIER | NA18747.hp1 NA18945.hp2 NA18982.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0151 a0001c0002t0001g0134 a0001c0002t0001g0174 |
3 | 321 | 0.0093 | 5910 | c.-97 others(5925): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RHEX_chr1_206048173_206107449 | 206054302 | A | AAAAAAAT others(5903): Show |
intron_variant | MODIFIER | NA19065.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0003 | 1 | 317 | 0.0032 | 5910 | c.-97 others(5927): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RHEX_chr1_206048173_206107449 | 206054302 | A | AAAAAAAT others(5903): Show |
intron_variant | MODIFIER | HG00280.hp2 HG00741.hp1 HG01515.hp2 others(12): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0136 a0001c0001t0001g0156 a0001c0001t0001g0159 others(10): Show |
15 | 331 | 0.0453 | 5910 | c.-97 others(5927): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RHEX_chr1_206048173_206107449 | 206055734 | G | GGCCCCAG others(5903): Show |
intron_variant | MODIFIER | NA19055.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0074 | 1 | 306 | 0.0033 | 5910 | c.-97 others(5927): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PHRF1_chr11_571470_617222 | 585658 | T | TTGAGGTA others(5904): Show |
intron_variant | MODIFIER | NA18952.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0203 | 1 | 13 | 0.0769 | 5911 | c.215 others(5928): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
RHEX_chr1_206048173_206107449 | 206052634 | G | GAAACCAG others(5904): Show |
upstream_gene_variant | MODIFIER | NA19084.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0176 | 1 | 325 | 0.0031 | 5911 | c.-72 others(5920): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 538 | chr1 | TogoVar | |||||||
RHEX_chr1_206048173_206107449 | 206052634 | G | GAAACCAG others(5904): Show |
upstream_gene_variant | MODIFIER | NA18962.hp2 NA19066.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020 | 2 | 326 | 0.0061 | 5911 | c.-72 others(5920): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 538 | chr1 | TogoVar | |||||||
RHEX_chr1_206048173_206107449 | 206052634 | G | GAAACCAG others(5904): Show |
upstream_gene_variant | MODIFIER | HG02698.hp1 HG03927.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0127 |
2 | 326 | 0.0061 | 5911 | c.-72 others(5920): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 538 | chr1 | TogoVar | |||||||
RHEX_chr1_206048173_206107449 | 206052634 | G | GAAACCAG others(5904): Show |
upstream_gene_variant | MODIFIER | NA18969.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0154 | 1 | 325 | 0.0031 | 5911 | c.-72 others(5920): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 538 | chr1 | TogoVar | |||||||
RHEX_chr1_206048173_206107449 | 206052634 | G | GAAACCAG others(5904): Show |
upstream_gene_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0049 | 1 | 325 | 0.0031 | 5911 | c.-72 others(5920): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 538 | chr1 | TogoVar | |||||||
RHEX_chr1_206048173_206107449 | 206054611 | C | CACAGGTT others(5904): Show |
intron_variant | MODIFIER | NA18990.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0064 | 1 | 217 | 0.0046 | 5911 | c.-97 others(5928): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RHEX_chr1_206048173_206107449 | 206056136 | G | GAGAGCCC others(5904): Show |
intron_variant | MODIFIER | HG00544.hp1 NA18955.hp2 NA18992.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | 197 | 0.0152 | 5911 | c.-97 others(5928): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RHEX_chr1_206048173_206107449 | 206056136 | G | GAGAGCCC others(5904): Show |
intron_variant | MODIFIER | HG00438.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0248 | 1 | 195 | 0.0051 | 5911 | c.-97 others(5928): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RHEX_chr1_206048173_206107449 | 206056813 | A | AAAAAAAA others(5904): Show |
intron_variant | MODIFIER | NA19075.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0122 | 1 | 332 | 0.0030 | 5911 | c.-97 others(5928): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RHEX_chr1_206048173_206107449 | 206057282 | G | GAGAATTG others(5904): Show |
intron_variant | MODIFIER | NA18982.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0241 | 1 | 328 | 0.0030 | 5911 | c.-97 others(5928): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RHEX_chr1_206048173_206107449 | 206057324 | C | CCCAAAAG others(5904): Show |
intron_variant | MODIFIER | HG02300.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0096 | 1 | 245 | 0.0041 | 5911 | c.-97 others(5928): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RHEX_chr1_206048173_206107449 | 206057479 | G | GGTGGAGT others(5904): Show |
intron_variant | MODIFIER | NA18977.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0097 | 1 | 332 | 0.0030 | 5911 | c.-97 others(5928): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RHEX_chr1_206048173_206107449 | 206054611 | C | CACAGGTT others(5905): Show |
intron_variant | MODIFIER | HG02074.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0123 | 1 | 217 | 0.0046 | 5912 | c.-97 others(5929): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | TogoVar |