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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
RHEX_chr1_206048173_206107449 | 206054611 | C | CACAGGTT others(5905): Show |
intron_variant | MODIFIER | HG00621.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0126 | 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 | ||||||
RHEX_chr1_206048173_206107449 | 206055734 | G | GGCCCCAG others(5905): Show |
intron_variant | MODIFIER | NA19085.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0073 | 1 | 306 | 0.0033 | 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 | a0001c0001t0001g0095 | 1 | 306 | 0.0033 | 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 | a0001c0001t0001g0075 | 1 | 195 | 0.0051 | 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 | a0001c0001t0001a0001c0001t0008a0001c0002t0001others(1): Show | a0001c0001t0001g0047 a0001c0001t0001g0084 a0001c0001t0001g0085 others(9): Show |
12 | 206 | 0.0583 | 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 | a0001c0001t0001g0048 | 1 | 195 | 0.0051 | 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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | 196 | 0.0102 | 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 | a0001c0001t0001g0185 | 1 | 195 | 0.0051 | 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 | a0001c0001t0001g0186 | 1 | 195 | 0.0051 | 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 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(41): Show |
59 | 253 | 0.2332 | 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 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(1): Show |
4 | 198 | 0.0202 | 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 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0235 others(1): Show |
4 | 198 | 0.0202 | 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 | a0001c0001t0001g0236 | 1 | 195 | 0.0051 | 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 | a0001c0001t0001g0242 | 1 | 195 | 0.0051 | 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 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | 196 | 0.0102 | 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 | NA19074.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0245 | 1 | 195 | 0.0051 | 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 | NA19010.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0246 | 1 | 195 | 0.0051 | 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 | HG02027.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0247 | 1 | 195 | 0.0051 | 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 | HG03831.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0251 | 1 | 195 | 0.0051 | 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 | 206056877 | G | GTTATTTC others(5905): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00735.hp2 HG01106.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 a0001c0001t0001g0082 a0001c0001t0001g0083 |
5 | 331 | 0.0151 | 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 | 206056877 | G | GTTATTTC others(5905): Show |
intron_variant | MODIFIER | HG02293.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0189 | 1 | 327 | 0.0031 | 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 | 206057282 | G | GAGAATTG others(5905): Show |
intron_variant | MODIFIER | NA18961.hp1 NA19068.hp1 NA19091.hp2 |
a0001a0005 | a0001c0001a0005c0009 | a0001c0001t0001a0005c0009t0001 | a0001c0001t0001g0190 a0001c0001t0001g0192 a0005c0009t0001g0191 |
3 | 330 | 0.0091 | 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(5906): Show |
intron_variant | MODIFIER | NA19004.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0187 | 1 | 195 | 0.0051 | 5913 | c.-97 others(5930): 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(5906): Show |
intron_variant | MODIFIER | HG00597.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0188 | 1 | 195 | 0.0051 | 5913 | c.-97 others(5930): Show |
RHEX | ENSG00000263961.8 | transcript | ENST00000331555.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RBFOX2_chr22_35733736_36033824 | 35735298 | T | TCCACCTG others(5910): Show |
downstream_gene_variant | MODIFIER | HG01081.hp1 HG03490.hp1 HG03492.hp2 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0113 a0001c0001t0003g0114 a0001c0001t0003g0116 |
3 | 25 | 0.1200 | 5917 | c.*89 others(5928): Show |
RBFOX2 | ENSG00000100320.24 | transcript | ENST00000695854.1 | protein_coding | 3437 | chr22 | TogoVar | |||||||
RBFOX2_chr22_35733736_36033824 | 35735298 | T | TCCACCTG others(5911): Show |
downstream_gene_variant | MODIFIER | HG01192.hp2 HG01496.hp2 HG01515.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0017 | a0001c0001t0001g0078 a0001c0001t0001g0107 a0001c0001t0017g0071 |
3 | 25 | 0.1200 | 5918 | c.*89 others(5929): Show |
RBFOX2 | ENSG00000100320.24 | transcript | ENST00000695854.1 | protein_coding | 3437 | chr22 | TogoVar | |||||||
MUC12_chr7_100964565_101023936 | 101004216 | T | TAGCCCCA others(5912): Show |
disruptive_inframe_insertion | MODERATE | HG01261.hp2 | a0060 | a0060c0226 | a0060c0226t0001 | a0060c0226t0001g0058 | 1 | 15 | 0.0667 | 5919 | c.136 others(5930): Show |
p.Pro others(5934): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||
MUC12_chr7_100964565_101023936 | 101004216 | T | TAGCCCCA others(5912): Show |
disruptive_inframe_insertion | MODERATE | HG04115.hp2 | a0115 | a0115c0094 | a0115c0094t0001 | a0115c0094t0001g0120 | 1 | 15 | 0.0667 | 5919 | c.136 others(5930): Show |
p.Pro others(5934): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||
MUC12_chr7_100964565_101023936 | 101004216 | T | TAGCCCCA others(5912): Show |
disruptive_inframe_insertion | MODERATE | NA18967.hp2 | a0122 | a0122c0105 | a0122c0105t0001 | a0122c0105t0001g0211 | 1 | 15 | 0.0667 | 5919 | c.136 others(5930): Show |
p.Pro others(5934): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||
MUC12_chr7_100964565_101023936 | 101004216 | T | TAGCCCCA others(5912): Show |
disruptive_inframe_insertion | MODERATE | HG02155.hp2 | a0004 | a0004c0003 | a0004c0003t0001 | a0004c0003t0001g0113 | 1 | 15 | 0.0667 | 5919 | c.136 others(5930): Show |
p.Pro others(5934): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||
RBFOX2_chr22_35733736_36033824 | 35735298 | T | TCCACCTG others(5912): Show |
downstream_gene_variant | MODIFIER | HG02559.hp1 HG02683.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0020 | a0001c0001t0001g0055 a0001c0001t0020g0115 |
2 | 24 | 0.0833 | 5919 | c.*89 others(5930): Show |
RBFOX2 | ENSG00000100320.24 | transcript | ENST00000695854.1 | protein_coding | 3437 | chr22 | TogoVar | |||||||
YBEY_chr21_46281342_46302751 | 46293666 | G | GCAAGTTA others(5912): Show |
intron_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0207 | 1 | 277 | 0.0036 | 5919 | c.339 others(5936): Show |
YBEY | ENSG00000182362.14 | transcript | ENST00000397701.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
ARFRP1_chr20_63693647_63712976 | 63693708 | A | ACCACCTC others(5913): Show |
downstream_gene_variant | MODIFIER | HG02523.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0025 | 1 | 224 | 0.0045 | 5920 | c.*67 others(5931): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4938 | chr20 | TogoVar | |||||||
RBFOX2_chr22_35733736_36033824 | 35735298 | T | TCCACCTG others(5914): Show |
downstream_gene_variant | MODIFIER | HG02280.hp2 HG02818.hp2 HG02886.hp1 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0012 | a0001c0001t0006g0082 a0001c0001t0006g0090 a0001c0001t0012g0020 |
3 | 25 | 0.1200 | 5921 | c.*89 others(5932): Show |
RBFOX2 | ENSG00000100320.24 | transcript | ENST00000695854.1 | protein_coding | 3437 | chr22 | TogoVar | |||||||
SERINC2_chr1_31408213_31439678 | 31432164 | A | ATAGGGTG others(5915): Show |
intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0086 | 1 | 325 | 0.0031 | 5922 | c.101 others(5939): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PTP4A3_chr8_141387021_141437454 | 141415697 | G | GTAGGGGG others(5919): Show |
intron_variant | MODIFIER | HG00408.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0087 | 1 | 322 | 0.0031 | 5926 | c.-85 others(5945): Show |
PTP4A3 | ENSG00000184489.13 | transcript | ENST00000521578.6 | protein_coding | 1/5 | chr8 | TogoVar | |||||||
RBFOX2_chr22_35733736_36033824 | 35735298 | T | TCCACCTG others(5919): Show |
downstream_gene_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0108 | 1 | 23 | 0.0435 | 5926 | c.*89 others(5937): Show |
RBFOX2 | ENSG00000100320.24 | transcript | ENST00000695854.1 | protein_coding | 3437 | chr22 | TogoVar | |||||||
SERINC2_chr1_31408213_31439678 | 31432174 | T | TAGGGTGG others(5924): Show |
intron_variant | MODIFIER | NA18984.hp2 | a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0164 | 1 | 228 | 0.0044 | 5931 | c.101 others(5948): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
USP12_chr13_27061156_27176811 | 27063931 | A | AGGGAGGA others(5927): Show |
downstream_gene_variant | MODIFIER | HG03017.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0072 | 1 | 62 | 0.0161 | 5934 | c.*53 others(5945): Show |
USP12 | ENSG00000152484.14 | transcript | ENST00000282344.11 | protein_coding | 2224 | chr13 | TogoVar | |||||||
CLPTM1L_chr5_1312752_1350099 | 1333664 | T | TGAGGATA others(5930): Show |
intron_variant | MODIFIER | HG02273.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 | 1 | 55 | 0.0182 | 5937 | c.891 others(5952): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
CLPTM1L_chr5_1312752_1350099 | 1333664 | T | TGAGGATA others(5931): Show |
intron_variant | MODIFIER | HG01361.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0010 | 1 | 55 | 0.0182 | 5938 | c.891 others(5953): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
PIEZO1_chr16_88710338_88790220 | 88731922 | A | AGGAGGGC others(5931): Show |
intron_variant | MODIFIER | NA19010.hp1 | a0080 | a0080c0114 | a0080c0114t0001 | a0080c0114t0001g0171 | 1 | 34 | 0.0294 | 5938 | c.299 others(5953): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | |||||||
SPAAR_chr9_35904490_35916686 | 35914257 | G | GGTGTGTG others(5933): Show |
downstream_gene_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0001 | 1 | 417 | 0.0024 | 5940 | c.*35 others(5951): Show |
SPAAR | ENSG00000235387.5 | transcript | ENST00000443779.3 | protein_coding | 2572 | chr9 | TogoVar | |||||||
TMEM242_chr6_157284025_157328519 | 157311780 | G | GTGCCCCA others(5934): Show |
intron_variant | MODIFIER | HG01433.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0157 | 1 | 317 | 0.0032 | 5941 | c.327 others(5958): Show |
TMEM242 | ENSG00000215712.11 | transcript | ENST00000400788.9 | protein_coding | 3/3 | chr6 | TogoVar | |||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(5937): Show |
upstream_gene_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0083 | 1 | 8 | 0.1250 | 5944 | c.-45 others(5953): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
ARFRP1_chr20_63693647_63712976 | 63693729 | A | ACCACCAC others(5942): Show |
downstream_gene_variant | MODIFIER | HG04204.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 | 1 | 167 | 0.0060 | 5949 | c.*67 others(5960): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4917 | chr20 | TogoVar | |||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(5942): Show |
upstream_gene_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0105 | 1 | 8 | 0.1250 | 5949 | c.-45 others(5958): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
FAM227A_chr22_38573118_38661392 | 38644446 | A | ACTATGCT others(5943): Show |
intron_variant | MODIFIER | NA18939.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0264 | 1 | 225 | 0.0044 | 5950 | c.225 others(5967): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | TogoVar | |||||||
FAM227A_chr22_38573118_38661392 | 38644446 | A | ACTATGCT others(5943): Show |
intron_variant | MODIFIER | NA18961.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0266 | 1 | 225 | 0.0044 | 5950 | c.225 others(5967): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | TogoVar | |||||||
CLPTM1L_chr5_1312752_1350099 | 1333251 | C | CGGATGAG others(5949): Show |
intron_variant | MODIFIER | HG03688.hp2 | a0002 | a0002c0003 | a0002c0003t0004 | a0002c0003t0004g0198 | 1 | 302 | 0.0033 | 5956 | c.891 others(5973): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar |