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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CCSER1_chr4_90122394_91610295 | 91046088 | G | GATTCTTC others(5894): Show |
intron_variant | MODIFIER | HG01243.hp2 HG02717.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0020 | a0001c0001t0003g0012 a0001c0001t0020g0033 |
2 | 38 | 0.0526 | 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 | 38 | 0.0263 | 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 | 38 | 0.0263 | 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 | 38 | 0.0526 | 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 | 38 | 0.0526 | 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 | 170 | 0.0059 | 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 | a0009 | a0009c0036 | a0009c0036t0001 | a0009c0036t0001g0139 | 1 | 282 | 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 | 38 | 0.0790 | 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 | a0001c0001t0001g0155 | 1 | 370 | 0.0027 | 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 | a0001c0002t0002g0237 | 1 | 344 | 0.0029 | 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 | a0001c0001t0001g0037 | 1 | 370 | 0.0027 | 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 | a0001c0001t0001g0271 | 1 | 334 | 0.0030 | 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 | a0001c0001t0001g0284 a0001c0002t0001g0285 a0001c0002t0001g0286 |
3 | 334 | 0.0090 | 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 | a0001c0001t0001g0242 | 1 | 334 | 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 | 44 | 0.0227 | 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 | a0001c0002t0002g0235 | 1 | 344 | 0.0029 | 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 | a0001c0002t0001g0281 | 1 | 334 | 0.0030 | 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 | a0001c0001t0001g0249 a0001c0002t0001g0250 a0001c0002t0001g0251 |
3 | 334 | 0.0090 | 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 | a0001c0002t0001g0147 | 1 | 334 | 0.0030 | 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 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(10): Show |
15 | 334 | 0.0449 | 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 | a0001c0002t0001g0145 | 1 | 334 | 0.0030 | 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 | a0001c0001t0001g0204 | 1 | 279 | 0.0036 | 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 | a0001c0002t0001g0282 | 1 | 334 | 0.0030 | 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 | a0001c0001t0001g0016 | 2 | 334 | 0.0060 | 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 | a0001c0001t0001g0091 a0001c0001t0001g0093 |
2 | 334 | 0.0060 | 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 | a0001c0001t0001g0185 | 1 | 334 | 0.0030 | 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 | a0001c0003t0002g0081 | 1 | 334 | 0.0030 | 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 | a0001c0001t0001g0136 | 1 | 334 | 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 | 206056136 | G | GAGAGCCC others(5904): Show |
intron_variant | MODIFIER | HG00544.hp1 NA18955.hp2 NA18992.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 |
3 | 334 | 0.0090 | 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 | a0001c0001t0001g0273 | 1 | 334 | 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 | 206056813 | A | AAAAAAAA others(5904): Show |
intron_variant | MODIFIER | NA19075.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0239 | 1 | 334 | 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 | a0001c0001t0001g0266 | 1 | 334 | 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 | a0001c0001t0001g0163 | 1 | 334 | 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 | 206057479 | G | GGTGGAGT others(5904): Show |
intron_variant | MODIFIER | NA18977.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0164 | 1 | 334 | 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 | a0001c0001t0001g0161 | 1 | 334 | 0.0030 | 5912 | c.-97 others(5929): 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 | HG00621.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0241 | 1 | 334 | 0.0030 | 5912 | c.-97 others(5929): 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(5905): Show |
intron_variant | MODIFIER | NA19085.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0144 | 1 | 334 | 0.0030 | 5912 | c.-97 others(5929): 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(5905): Show |
intron_variant | MODIFIER | HG00323.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0162 | 1 | 334 | 0.0030 | 5912 | c.-97 others(5929): 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(5905): Show |
intron_variant | MODIFIER | NA19082.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0146 | 1 | 334 | 0.0030 | 5912 | c.-97 others(5929): 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(5905): Show |
intron_variant | MODIFIER | HG00323.hp2 HG00741.hp2 HG01074.hp2 others(9): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0001t0012a0001c0002t0001others(1): Show | a0001c0001t0001g0137 a0001c0001t0001g0152 a0001c0001t0001g0153 others(9): Show |
12 | 334 | 0.0359 | 5912 | c.-97 others(5929): 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(5905): Show |
intron_variant | MODIFIER | HG02129.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0138 | 1 | 334 | 0.0030 | 5912 | c.-97 others(5929): 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(5905): Show |
intron_variant | MODIFIER | HG02145.hp2 HG02257.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | 334 | 0.0060 | 5912 | c.-97 others(5929): 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(5905): Show |
intron_variant | MODIFIER | NA19072.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0195 | 1 | 334 | 0.0030 | 5912 | c.-97 others(5929): 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(5905): Show |
intron_variant | MODIFIER | NA19065.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0196 | 1 | 334 | 0.0030 | 5912 | c.-97 others(5929): 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(5905): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(56): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0001t0009a0001c0002t0001others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(46): Show |
59 | 334 | 0.1767 | 5912 | c.-97 others(5929): 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(5905): Show |
intron_variant | MODIFIER | HG01516.hp2 HG03654.hp2 HG03927.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0064 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | 334 | 0.0120 | 5912 | c.-97 others(5929): 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(5905): Show |
intron_variant | MODIFIER | HG00609.hp2 HG02056.hp2 HG03669.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0001 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0283 others(1): Show |
4 | 334 | 0.0120 | 5912 | c.-97 others(5929): 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(5905): Show |
intron_variant | MODIFIER | NA18989.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0245 | 1 | 334 | 0.0030 | 5912 | c.-97 others(5929): 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(5905): Show |
intron_variant | MODIFIER | HG01261.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0296 | 1 | 334 | 0.0030 | 5912 | c.-97 others(5929): 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(5905): Show |
intron_variant | MODIFIER | HG02056.hp1 NA18971.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | 334 | 0.0060 | 5912 | c.-97 others(5929): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | TogoVar |