Item | Value |
---|---|
geneid | 23039 |
ensemblid | ENSG00000130227.17 |
hgncid | 14108 |
symbol | XPO7 |
name | exportin 7 |
refseq_nuc | NM_015024.5 |
refseq_prot | NP_055839.3 |
ensembl_nuc | ENST00000252512.14 |
ensembl_prot | ENSP00000252512.9 |
mane_status | MANE Select |
chr | chr8 |
start | 21919662 |
end | 22006585 |
strand | + |
ver | v1.2 |
region | chr8:21919662-22006585 |
region5000 | chr8:21914662-22011585 |
regionname0 | XPO7_chr8_21919662_22006585 |
regionname5000 | XPO7_chr8_21914662_22011585 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1087 | 339 | 86 | 63 | 144 | 12 | 32 | 110 | XPO7_chr8_21914662_22011585 | XPO7 | MADHV others(1082): Show |
chr8 | 21914662 | 22011585 |
a0002 | 0/0 | 1087 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | MADHV others(1082): Show |
chr8 | 21914662 | 22011585 |
a0003 | 0/0 | 1087 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | MADHV others(1082): Show |
chr8 | 21914662 | 22011585 |
a0004 | 0/0 | 1087 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | MADHV others(1082): Show |
chr8 | 21914662 | 22011585 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3261 | 116 | 18 | 28 | 54 | 2 | 13 | XPO7_chr8_21914662_22011585 | XPO7 | ATGGC others(3256): Show |
chr8 | 21914662 | 22011585 | ||
a0001c0002 | 0/0 | 3261 | 109 | 50 | 11 | 36 | 0 | 12 | XPO7_chr8_21914662_22011585 | XPO7 | ATGGC others(3256): Show |
chr8 | 21914662 | 22011585 | ||
a0001c0003 | 0/1 | 3261 | 86 | 14 | 16 | 45 | 4 | 6 | XPO7_chr8_21914662_22011585 | XPO7 | ATGGC others(3256): Show |
chr8 | 21914662 | 22011585 | ||
a0001c0004 | 0/0 | 3261 | 15 | 1 | 8 | 0 | 6 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | ATGGC others(3256): Show |
chr8 | 21914662 | 22011585 | ||
a0001c0005 | 0/0 | 3261 | 4 | 1 | 0 | 2 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | ATGGC others(3256): Show |
chr8 | 21914662 | 22011585 | ||
a0001c0006 | 0/0 | 3261 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | ATGGC others(3256): Show |
chr8 | 21914662 | 22011585 | ||
a0001c0007 | 0/0 | 3261 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | ATGGC others(3256): Show |
chr8 | 21914662 | 22011585 | ||
a0001c0008 | 0/0 | 3261 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | ATGGC others(3256): Show |
chr8 | 21914662 | 22011585 | ||
a0001c0009 | 0/0 | 3261 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | ATGGC others(3256): Show |
chr8 | 21914662 | 22011585 | ||
a0001c0010 | 0/0 | 3261 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | ATGGC others(3256): Show |
chr8 | 21914662 | 22011585 | ||
a0002c0013 | 0/0 | 3261 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | ATGGC others(3256): Show |
chr8 | 21914662 | 22011585 | ||
a0003c0012 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | ATGGC others(3256): Show |
chr8 | 21914662 | 22011585 | ||
a0004c0011 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | ATGGC others(3256): Show |
chr8 | 21914662 | 22011585 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 1/0 | 4870 | 113 | 17 | 28 | 53 | 2 | 12 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0001t0010 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0001t0011 | 0/0 | 4870 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0001t0013 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0002t0001 | 0/0 | 4870 | 88 | 37 | 11 | 30 | 0 | 10 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0002t0002 | 0/0 | 4870 | 2 | 0 | 0 | 1 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0002t0004 | 0/0 | 4871 | 7 | 2 | 0 | 5 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4866): Show |
chr8 | 21914662 | 22011585 |
a0001c0002t0005 | 0/0 | 4870 | 5 | 5 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0002t0006 | 0/0 | 4870 | 3 | 3 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0002t0007 | 0/0 | 4870 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0002t0008 | 0/0 | 4870 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0002t0009 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0003t0001 | 0/1 | 4870 | 76 | 13 | 16 | 36 | 4 | 6 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0003t0002 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0003t0003 | 0/0 | 4879 | 8 | 0 | 0 | 8 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4874): Show |
chr8 | 21914662 | 22011585 |
a0001c0003t0012 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0004t0001 | 0/0 | 4870 | 15 | 1 | 8 | 0 | 6 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0005t0002 | 0/0 | 4870 | 4 | 1 | 0 | 2 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0006t0005 | 0/0 | 4870 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0007t0001 | 0/0 | 4870 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0008t0002 | 0/0 | 4870 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0009t0002 | 0/0 | 4870 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0001c0010t0002 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0002c0013t0001 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0003c0012t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
a0004c0011t0002 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | AGCGC others(4865): Show |
chr8 | 21914662 | 22011585 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0010g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0011g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0013g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0004g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0006g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0006g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0006g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0007g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0008g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0009g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0012g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0005t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0005t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0005t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0005t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0006t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0006t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0007t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0007t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0008t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0008t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0009t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0009t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0010t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0002c0013t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0003c0012t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0004c0011t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0004 | t0001 | g0300 | EUR | GBR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0021 | EUR | GBR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00323 | hp1 | a0001 | c0004 | t0001 | g0296 | EUR | FIN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0035 | EUR | FIN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0322 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0101 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00558 | hp1 | a0001 | c0003 | t0001 | g0110 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0321 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00642 | hp1 | a0001 | c0004 | t0001 | g0313 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00673 | hp2 | a0001 | c0007 | t0001 | g0309 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0253 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0107 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00738 | hp2 | a0001 | c0004 | t0001 | g0297 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0063 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01069 | hp1 | a0001 | c0004 | t0001 | g0016 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01069 | hp2 | a0001 | c0003 | t0001 | g0081 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01070 | hp1 | a0001 | c0004 | t0001 | g0015 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01071 | hp1 | a0001 | c0004 | t0001 | g0310 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01071 | hp2 | a0001 | c0003 | t0001 | g0104 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0084 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0048 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01167 | hp2 | a0001 | c0003 | t0001 | g0061 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0080 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01168 | hp2 | a0001 | c0003 | t0001 | g0058 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0039 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01175 | hp1 | a0001 | c0004 | t0001 | g0302 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01255 | hp2 | a0001 | c0003 | t0001 | g0090 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01256 | hp2 | a0001 | c0003 | t0001 | g0033 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0053 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01261 | hp2 | a0001 | c0003 | t0001 | g0057 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0243 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0315 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0236 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0034 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0272 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01516 | hp1 | a0001 | c0004 | t0001 | g0312 | EUR | IBS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01516 | hp2 | a0001 | c0003 | t0001 | g0086 | EUR | IBS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0160 | EUR | IBS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01517 | hp2 | a0001 | c0004 | t0001 | g0016 | EUR | IBS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0306 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01934 | hp1 | a0001 | c0003 | t0001 | g0056 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0237 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02004 | hp2 | a0001 | c0004 | t0001 | g0301 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02027 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0267 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02055 | hp2 | a0001 | c0006 | t0005 | g0268 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02056 | hp1 | a0001 | c0003 | t0001 | g0114 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02071 | hp1 | a0001 | c0003 | t0001 | g0106 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02083 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02129 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02132 | hp2 | a0001 | c0003 | t0001 | g0082 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02145 | hp1 | a0001 | c0003 | t0001 | g0052 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0244 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0307 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | CDX | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | CDX | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02165 | hp1 | a0001 | c0003 | t0001 | g0078 | EAS | CDX | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | CDX | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0044 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0266 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0292 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02280 | hp2 | a0001 | c0002 | t0007 | g0010 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02300 | hp1 | a0001 | c0004 | t0001 | g0303 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0324 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02451 | hp1 | a0001 | c0004 | t0001 | g0304 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02572 | hp1 | a0001 | c0002 | t0005 | g0265 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0158 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02622 | hp1 | a0003 | c0012 | t0001 | g0250 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0251 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0291 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0258 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0279 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02809 | hp2 | a0001 | c0002 | t0009 | g0269 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02818 | hp2 | a0001 | c0002 | t0006 | g0317 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0067 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02895 | hp2 | a0001 | c0001 | t0013 | g0167 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0255 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0261 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02922 | hp2 | a0001 | c0002 | t0004 | g0289 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0047 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02965 | hp2 | a0001 | c0002 | t0005 | g0260 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02976 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03017 | hp2 | a0001 | c0003 | t0001 | g0087 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0256 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0252 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03139 | hp2 | a0001 | c0005 | t0002 | g0227 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03195 | hp1 | a0001 | c0002 | t0005 | g0264 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0262 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03239 | hp2 | a0001 | c0003 | t0001 | g0066 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03453 | hp1 | a0001 | c0002 | t0006 | g0318 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03453 | hp2 | a0001 | c0002 | t0007 | g0010 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03486 | hp1 | a0001 | c0003 | t0012 | g0069 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03486 | hp2 | a0001 | c0002 | t0005 | g0257 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03490 | hp1 | a0001 | c0003 | t0001 | g0119 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0316 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0320 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0254 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0091 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0060 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0281 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0278 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0298 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03710 | hp2 | a0001 | c0003 | t0001 | g0037 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | BEB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0299 | SAS | BEB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | BEB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0280 | SAS | BEB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03942 | hp1 | a0001 | c0003 | t0001 | g0103 | SAS | BEB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0311 | SAS | BEB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04115 | hp1 | a0001 | c0002 | t0008 | g0270 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0171 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | BEB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0283 | SAS | BEB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04199 | hp2 | a0001 | c0005 | t0002 | g0224 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0288 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04204 | hp2 | a0001 | c0001 | t0011 | g0246 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0271 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0305 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | CHB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0323 | EAS | CHB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0097 | EAS | CHB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | CHB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | YRI | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | YRI | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18940 | hp1 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18942 | hp1 | a0001 | c0003 | t0003 | g0102 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18944 | hp1 | a0001 | c0003 | t0001 | g0075 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18947 | hp1 | a0001 | c0003 | t0001 | g0100 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18947 | hp2 | a0001 | c0002 | t0004 | g0050 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18950 | hp2 | a0001 | c0003 | t0003 | g0085 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18953 | hp1 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18953 | hp2 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18957 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18957 | hp2 | a0001 | c0003 | t0001 | g0094 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18961 | hp2 | a0001 | c0002 | t0004 | g0049 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0077 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18965 | hp1 | a0001 | c0003 | t0003 | g0092 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18967 | hp2 | a0001 | c0003 | t0001 | g0073 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18968 | hp2 | a0001 | c0003 | t0001 | g0105 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18969 | hp2 | a0001 | c0003 | t0003 | g0070 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18970 | hp1 | a0001 | c0003 | t0003 | g0062 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18971 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18974 | hp2 | a0001 | c0003 | t0003 | g0111 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18975 | hp1 | a0001 | c0003 | t0001 | g0079 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18975 | hp2 | a0001 | c0005 | t0002 | g0146 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18978 | hp2 | a0001 | c0003 | t0001 | g0099 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18981 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18984 | hp1 | a0001 | c0009 | t0002 | g0076 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18985 | hp1 | a0001 | c0008 | t0002 | g0038 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18986 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18986 | hp2 | a0001 | c0003 | t0002 | g0294 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18988 | hp1 | a0001 | c0010 | t0002 | g0134 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18988 | hp2 | a0001 | c0003 | t0001 | g0096 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18989 | hp2 | a0001 | c0007 | t0001 | g0314 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18990 | hp2 | a0001 | c0003 | t0003 | g0041 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0116 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18995 | hp2 | a0001 | c0003 | t0003 | g0072 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18997 | hp2 | a0001 | c0009 | t0002 | g0074 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19005 | hp2 | a0001 | c0003 | t0001 | g0108 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19007 | hp1 | a0001 | c0003 | t0001 | g0083 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19011 | hp2 | a0001 | c0008 | t0002 | g0059 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19030 | hp1 | a0001 | c0002 | t0005 | g0293 | AFR | LWK | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19030 | hp2 | a0001 | c0002 | t0004 | g0290 | AFR | LWK | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | LWK | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | LWK | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19066 | hp1 | a0001 | c0003 | t0001 | g0098 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19068 | hp2 | a0001 | c0003 | t0001 | g0117 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19074 | hp2 | a0001 | c0003 | t0001 | g0095 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19076 | hp1 | a0001 | c0001 | t0010 | g0142 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19078 | hp1 | a0001 | c0005 | t0002 | g0151 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19078 | hp2 | a0001 | c0003 | t0001 | g0093 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19085 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19086 | hp2 | a0001 | c0003 | t0001 | g0088 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19088 | hp2 | a0001 | c0003 | t0001 | g0112 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19089 | hp2 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19090 | hp1 | a0001 | c0003 | t0001 | g0113 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0040 | AFR | YRI | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0259 | AFR | YRI | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA20129 | hp1 | a0001 | c0002 | t0006 | g0319 | AFR | ASW | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0159 | AFR | ASW | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA20752 | hp1 | a0001 | c0004 | t0001 | g0295 | EUR | TSI | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0118 | EUR | TSI | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA20805 | hp1 | a0001 | c0004 | t0001 | g0015 | EUR | TSI | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA20805 | hp2 | a0001 | c0003 | t0001 | g0055 | EUR | TSI | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01123 | hp2 | a0002 | c0013 | t0001 | g0089 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0036 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0043 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02559 | hp2 | a0001 | c0006 | t0005 | g0263 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0068 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | USA | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG06807 | hp2 | a0004 | c0011 | t0002 | g0163 | AFR | USA | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | USA | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | USA | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0042 | AFR | LWK | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | LWK | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0120 | REF | REF | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0168 | REF | REF | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:21989038 | C | A | 1 | a0004 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.1823C>A | p.Pro608Gln | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/28 | 1932/4870 | 1823/3264 | 608/1087 | chr8 | 21989038 | |||
chr8:21998827 | A | G | 1 | a0003 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.2418A>G | p.Ile806Met | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 22/28 | 2527/4870 | 2418/3264 | 806/1087 | chr8 | 21998827 | |||
chr8:22002221 | G | C | 1 | a0002 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.2892G>C | p.Glu964Asp | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/28 | 3001/4870 | 2892/3264 | 964/1087 | chr8 | 22002221 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:21976454 | C | T | 4 | a0001c0003 a0001c0008 a0001c0009 others(1): Show |
90 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(87): Show |
synonymous_variant | LOW | c.696C>T | p.Ile232Ile | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/28 | 805/4870 | 696/3264 | 232/1087 | chr8 | 21976454 | |||
chr8:21980161 | T | C | 1 | a0001c0010 | 1 | NA18988.hp1 | synonymous_variant | LOW | c.915T>C | p.Ser305Ser | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/28 | 1024/4870 | 915/3264 | 305/1087 | chr8 | 21980161 | |||
chr8:21989075 | G | C | 8 | a0001c0002 a0001c0003 a0001c0004 others(5): Show |
219 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(216): Show |
synonymous_variant | LOW | c.1860G>C | p.Leu620Leu | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/28 | 1969/4870 | 1860/3264 | 620/1087 | chr8 | 21989075 | |||
chr8:21990344 | G | C | 1 | a0001c0004 | 15 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(12): Show |
splice_region_variant&synonymous_variant | LOW | c.1869G>C | p.Gly623Gly | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 17/28 | 1978/4870 | 1869/3264 | 623/1087 | chr8 | 21990344 | |||
chr8:21990368 | G | T | 1 | a0001c0006 | 2 | HG02055.hp2 HG02559.hp2 |
synonymous_variant | LOW | c.1893G>T | p.Val631Val | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 17/28 | 2002/4870 | 1893/3264 | 631/1087 | chr8 | 21990368 | |||
chr8:22005040 | A | G | 7 | a0001c0002 a0001c0003 a0001c0004 others(4): Show |
215 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(212): Show |
synonymous_variant | LOW | c.3216A>G | p.Ser1072Ser | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 3325/4870 | 3216/3264 | 1072/1087 | chr8 | 22005040 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:21919691 | G | T | 2 | a0001c0002t0005 a0001c0006t0005 |
7 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-80G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/28 | 80 | chr8 | 21919691 | ||||||
chr8:21919696 | G | GGCGGCGG others(2): Show |
1 | a0001c0003t0003 | 8 | NA18942.hp1 NA18950.hp2 NA18965.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-69_-61dupGGCAGCGG others(1): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/28 | 60 | INFO_REALIGN_3_PRIME | chr8 | 21919696 | |||||
chr8:21919703 | G | T | 1 | a0001c0001t0013 | 1 | HG02895.hp2 | 5_prime_UTR_variant | MODIFIER | c.-68G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/28 | 68 | chr8 | 21919703 | ||||||
chr8:21919705 | A | G | 1 | a0001c0001t0013 | 1 | HG02895.hp2 | 5_prime_UTR_variant | MODIFIER | c.-66A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/28 | 66 | chr8 | 21919705 | ||||||
chr8:21919715 | G | T | 1 | a0001c0003t0012 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-56G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/28 | 56 | chr8 | 21919715 | ||||||
chr8:22005380 | A | T | 1 | a0001c0002t0007 | 2 | HG02280.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*292A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 292 | chr8 | 22005380 | ||||||
chr8:22005635 | C | CA | 1 | a0001c0002t0004 | 7 | HG02922.hp2 NA18947.hp2 NA18957.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*556dupA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 557 | INFO_REALIGN_3_PRIME | chr8 | 22005635 | |||||
chr8:22005779 | G | A | 15 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0005 others(12): Show |
212 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*691G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 691 | chr8 | 22005779 | ||||||
chr8:22005929 | G | A | 1 | a0001c0002t0008 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*841G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 841 | chr8 | 22005929 | ||||||
chr8:22006035 | T | G | 1 | a0001c0002t0006 | 3 | HG02818.hp2 HG03453.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*947T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 947 | chr8 | 22006035 | ||||||
chr8:22006219 | T | A | 1 | a0001c0001t0010 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1131T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 1131 | chr8 | 22006219 | ||||||
chr8:22006419 | T | G | 1 | a0001c0001t0011 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1331T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 1331 | chr8 | 22006419 | ||||||
chr8:22006495 | C | T | 1 | a0001c0002t0009 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1407C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 1407 | chr8 | 22006495 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:21919805 | G | A | 6 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(3): Show |
6 | HG00140.hp2 HG00741.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+17G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21919805 | |||||||
chr8:21919820 | C | T | 1 | a0001c0001t0002g0324 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.18+32C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21919820 | |||||||
chr8:21919844 | G | C | 8 | a0001c0002t0001g0003 a0001c0002t0001g0023 a0001c0002t0001g0024 others(5): Show |
9 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+56G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21919844 | |||||||
chr8:21919874 | G | A | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.18+86G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21919874 | |||||||
chr8:21919965 | G | A | 92 | a0001c0002t0001g0046 a0001c0002t0001g0051 a0001c0002t0001g0064 others(89): Show |
98 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.18+177G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21919965 | |||||||
chr8:21919967 | C | T | 3 | a0001c0002t0001g0321 a0001c0002t0001g0322 a0001c0002t0001g0323 |
3 | HG00423.hp2 HG00621.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.18+179C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21919967 | |||||||
chr8:21919972 | G | C | 2 | a0001c0001t0002g0006 a0001c0001t0002g0121 |
3 | NA18959.hp1 NA18962.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.18+184G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21919972 | |||||||
chr8:21920084 | C | G | 178 | a0001c0001t0002g0316 a0001c0002t0001g0003 a0001c0002t0001g0013 others(175): Show |
189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.18+296C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21920084 | |||||||
chr8:21920109 | C | T | 1 | a0001c0002t0001g0029 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.18+321C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21920109 | |||||||
chr8:21920237 | C | T | 1 | a0001c0001t0002g0248 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.18+449C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21920237 | |||||||
chr8:21920280 | C | T | 28 | a0001c0001t0002g0316 a0001c0002t0001g0298 a0001c0002t0001g0299 others(25): Show |
30 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.18+492C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21920280 | |||||||
chr8:21920454 | G | A | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+666G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21920454 | |||||||
chr8:21920571 | T | C | 176 | a0001c0001t0002g0316 a0001c0002t0001g0003 a0001c0002t0001g0013 others(173): Show |
187 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.18+783T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21920571 | |||||||
chr8:21920669 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.18+881C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21920669 | |||||||
chr8:21920686 | C | G | 1 | a0001c0002t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+898C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21920686 | |||||||
chr8:21921100 | T | G | 1 | a0001c0001t0002g0122 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.18+1312T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21921100 | |||||||
chr8:21921189 | A | G | 1 | a0001c0002t0001g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.18+1401A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21921189 | |||||||
chr8:21921204 | G | C | 2 | a0001c0002t0001g0251 a0003c0012t0001g0250 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.18+1416G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21921204 | |||||||
chr8:21921266 | A | G | 1 | a0001c0001t0011g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.18+1478A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21921266 | |||||||
chr8:21921345 | A | T | 2 | a0001c0002t0004g0289 a0001c0002t0004g0290 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.18+1557A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21921345 | |||||||
chr8:21921562 | T | C | 1 | a0001c0002t0005g0293 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.18+1774T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21921562 | |||||||
chr8:21921880 | G | A | 1 | a0001c0002t0001g0007 | 2 | HG01257.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.18+2092G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21921880 | |||||||
chr8:21921969 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.18+2181G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21921969 | |||||||
chr8:21922107 | A | G | 1 | a0001c0002t0001g0288 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.18+2319A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21922107 | |||||||
chr8:21922162 | C | G | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+2374C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21922162 | |||||||
chr8:21922309 | CTT | C | 23 | a0001c0002t0001g0298 a0001c0002t0001g0299 a0001c0002t0001g0305 others(20): Show |
25 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.18+2523_18+2524del others(2): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21922309 | ||||||
chr8:21922426 | C | G | 73 | a0001c0001t0002g0242 a0001c0002t0001g0007 a0001c0002t0001g0228 others(70): Show |
75 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.18+2638C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21922426 | |||||||
chr8:21922442 | C | G | 23 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0251 others(20): Show |
23 | HG01433.hp1 HG02056.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.18+2654C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21922442 | |||||||
chr8:21922466 | C | T | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0009g0269 |
5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+2678C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21922466 | |||||||
chr8:21922585 | T | C | 20 | a0001c0002t0001g0124 a0001c0002t0001g0271 a0001c0002t0001g0272 others(17): Show |
20 | HG01433.hp1 HG02056.hp2 HG02738.hp2 others(17): Show |
intron_variant | MODIFIER | c.18+2797T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21922585 | |||||||
chr8:21922686 | C | T | 1 | a0001c0003t0012g0069 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.18+2898C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21922686 | |||||||
chr8:21922886 | A | G | 20 | a0001c0002t0001g0124 a0001c0002t0001g0271 a0001c0002t0001g0272 others(17): Show |
20 | HG01433.hp1 HG02056.hp2 HG02738.hp2 others(17): Show |
intron_variant | MODIFIER | c.18+3098A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21922886 | |||||||
chr8:21923016 | T | A | 2 | a0001c0002t0001g0252 a0001c0002t0001g0253 |
2 | HG00733.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.18+3228T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21923016 | |||||||
chr8:21923221 | C | G | 1 | a0001c0003t0001g0068 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.18+3433C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21923221 | |||||||
chr8:21923233 | A | G | 115 | a0001c0001t0002g0242 a0001c0002t0001g0007 a0001c0002t0001g0046 others(112): Show |
122 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.18+3445A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21923233 | |||||||
chr8:21923378 | A | G | 1 | a0001c0002t0001g0320 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.18+3590A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21923378 | |||||||
chr8:21923541 | T | C | 1 | a0001c0002t0009g0269 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18+3753T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21923541 | |||||||
chr8:21923872 | A | G | 15 | a0001c0002t0001g0273 a0001c0002t0001g0274 a0001c0002t0001g0275 others(12): Show |
15 | HG02056.hp2 HG02738.hp2 HG03688.hp1 others(12): Show |
intron_variant | MODIFIER | c.18+4084A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21923872 | |||||||
chr8:21924118 | C | T | 177 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(174): Show |
188 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.18+4330C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924118 | |||||||
chr8:21924355 | T | C | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.18+4567T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924355 | |||||||
chr8:21924447 | T | C | 1 | a0001c0002t0001g0228 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.18+4659T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924447 | |||||||
chr8:21924447 | T | TC | 171 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0018 others(168): Show |
178 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.18+4668dupC | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21924447 | ||||||
chr8:21924452 | C | G | 1 | a0001c0002t0001g0245 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.18+4664C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924452 | |||||||
chr8:21924598 | C | A | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.18+4810C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924598 | |||||||
chr8:21924651 | G | A | 2 | a0001c0001t0002g0011 a0001c0005t0002g0227 |
3 | HG00738.hp1 HG01099.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.18+4863G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924651 | |||||||
chr8:21924724 | T | G | 4 | a0001c0002t0001g0228 a0001c0002t0001g0229 a0001c0002t0001g0238 others(1): Show |
4 | HG02135.hp1 NA18940.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+4936T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924724 | |||||||
chr8:21924788 | C | T | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.18+5000C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924788 | |||||||
chr8:21924851 | T | G | 1 | a0001c0002t0001g0228 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.18+5063T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924851 | |||||||
chr8:21924897 | C | G | 5 | a0001c0002t0001g0274 a0001c0002t0001g0275 a0001c0002t0001g0276 others(2): Show |
5 | NA18612.hp1 NA18968.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+5109C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924897 | |||||||
chr8:21925052 | G | A | 1 | a0001c0003t0001g0032 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.18+5264G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925052 | |||||||
chr8:21925120 | A | G | 16 | a0001c0002t0001g0124 a0001c0002t0001g0273 a0001c0002t0001g0274 others(13): Show |
16 | HG02056.hp2 HG02738.hp2 HG03688.hp1 others(13): Show |
intron_variant | MODIFIER | c.18+5332A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925120 | |||||||
chr8:21925124 | A | G | 3 | a0001c0002t0001g0292 a0001c0006t0005g0263 a0001c0006t0005g0268 |
3 | HG02055.hp2 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.18+5336A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925124 | |||||||
chr8:21925169 | A | G | 4 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0251 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+5381A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925169 | |||||||
chr8:21925186 | C | T | 1 | a0001c0002t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+5398C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925186 | |||||||
chr8:21925386 | A | G | 1 | a0001c0001t0002g0170 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.18+5598A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925386 | |||||||
chr8:21925448 | T | G | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+5660T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925448 | |||||||
chr8:21925626 | T | C | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.18+5838T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925626 | |||||||
chr8:21925665 | T | C | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+5877T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925665 | |||||||
chr8:21925681 | G | C | 1 | a0001c0004t0001g0304 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.18+5893G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925681 | |||||||
chr8:21925771 | C | G | 1 | a0001c0001t0002g0169 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.18+5983C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925771 | |||||||
chr8:21925877 | T | C | 1 | a0001c0001t0002g0125 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.18+6089T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925877 | |||||||
chr8:21925958 | C | A | 1 | a0001c0002t0001g0256 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.18+6170C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925958 | |||||||
chr8:21926357 | G | A | 2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.18+6569G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21926357 | |||||||
chr8:21926555 | GT | G | 15 | a0001c0001t0002g0006 a0001c0001t0002g0121 a0001c0001t0002g0128 others(12): Show |
16 | HG00673.hp1 HG01099.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.18+6777delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21926555 | ||||||
chr8:21926627 | CGTT | C | 77 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0012 others(74): Show |
80 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.18+6842_18+6844del others(3): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21926627 | ||||||
chr8:21926693 | A | G | 1 | a0001c0001t0002g0133 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.18+6905A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21926693 | |||||||
chr8:21926774 | GA | G | 7 | a0001c0002t0001g0003 a0001c0002t0001g0023 a0001c0002t0001g0024 others(4): Show |
8 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+6994delA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21926774 | ||||||
chr8:21926897 | C | T | 1 | a0001c0002t0001g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.18+7109C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21926897 | |||||||
chr8:21927049 | T | G | 86 | a0001c0001t0002g0160 a0001c0002t0001g0003 a0001c0002t0001g0013 others(83): Show |
92 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.18+7261T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927049 | |||||||
chr8:21927139 | C | CT | 4 | a0001c0002t0001g0271 a0001c0002t0001g0272 a0001c0002t0001g0288 others(1): Show |
4 | HG01433.hp1 HG04115.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+7352dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21927139 | ||||||
chr8:21927141 | G | T | 1 | a0001c0002t0001g0315 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.18+7353G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927141 | |||||||
chr8:21927224 | TA | T | 116 | a0001c0001t0002g0226 a0001c0001t0002g0242 a0001c0002t0001g0007 others(113): Show |
123 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.18+7444delA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21927224 | ||||||
chr8:21927405 | A | G | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+7617A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927405 | |||||||
chr8:21927478 | A | G | 205 | a0001c0001t0002g0160 a0001c0001t0002g0226 a0001c0001t0002g0242 others(202): Show |
218 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.18+7690A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927478 | |||||||
chr8:21927505 | G | A | 4 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0251 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+7717G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927505 | |||||||
chr8:21927533 | C | A | 1 | a0001c0002t0001g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.18+7745C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927533 | |||||||
chr8:21927538 | C | CT | 6 | a0001c0001t0002g0122 a0001c0001t0002g0155 a0001c0001t0002g0215 others(3): Show |
6 | HG02040.hp2 HG02486.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+7771dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21927538 | ||||||
chr8:21927538 | CT | C | 86 | a0001c0001t0002g0128 a0001c0001t0002g0160 a0001c0002t0001g0003 others(83): Show |
92 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.18+7771delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21927538 | ||||||
chr8:21927558 | T | C | 113 | a0001c0001t0002g0226 a0001c0001t0002g0242 a0001c0002t0001g0007 others(110): Show |
120 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.18+7770T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927558 | |||||||
chr8:21927558 | T | TC | 3 | a0001c0002t0001g0245 a0001c0003t0001g0047 a0001c0003t0001g0067 |
3 | HG02886.hp2 HG02965.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.18+7770_18+7771ins others(1): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927558 | |||||||
chr8:21927618 | T | C | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+7830T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927618 | |||||||
chr8:21927725 | A | C | 1 | a0001c0002t0001g0024 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.18+7937A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927725 | |||||||
chr8:21927866 | C | A | 4 | a0001c0002t0001g0305 a0001c0002t0001g0306 a0001c0002t0001g0307 others(1): Show |
4 | HG01358.hp1 HG01928.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+8078C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927866 | |||||||
chr8:21927928 | G | C | 3 | a0001c0002t0005g0257 a0001c0002t0005g0264 a0001c0002t0005g0293 |
3 | HG03195.hp1 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.18+8140G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927928 | |||||||
chr8:21928070 | A | T | 1 | a0001c0001t0002g0012 | 2 | HG00438.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.18+8282A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21928070 | |||||||
chr8:21928102 | G | C | 1 | a0001c0002t0001g0308 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.18+8314G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21928102 | |||||||
chr8:21928236 | T | C | 7 | a0001c0002t0005g0257 a0001c0002t0005g0260 a0001c0002t0005g0264 others(4): Show |
7 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+8448T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21928236 | |||||||
chr8:21928443 | G | A | 1 | a0001c0003t0003g0070 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.18+8655G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21928443 | |||||||
chr8:21928545 | C | T | 1 | a0001c0002t0001g0277 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.18+8757C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21928545 | |||||||
chr8:21928787 | G | A | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.18+8999G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21928787 | |||||||
chr8:21928929 | A | T | 45 | a0001c0001t0002g0160 a0001c0002t0001g0003 a0001c0002t0001g0023 others(42): Show |
48 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.18+9141A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21928929 | |||||||
chr8:21929122 | C | T | 3 | a0001c0002t0002g0249 a0001c0002t0004g0289 a0001c0002t0004g0290 |
3 | HG02922.hp2 NA18981.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.18+9334C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21929122 | |||||||
chr8:21929130 | C | G | 2 | a0001c0002t0004g0289 a0001c0002t0004g0290 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.18+9342C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21929130 | |||||||
chr8:21929330 | G | A | 1 | a0001c0002t0005g0260 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.18+9542G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21929330 | |||||||
chr8:21929478 | C | T | 177 | a0001c0001t0002g0011 a0001c0001t0002g0160 a0001c0002t0001g0003 others(174): Show |
189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.18+9690C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21929478 | |||||||
chr8:21929643 | A | C | 1 | a0001c0003t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.18+9855A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21929643 | |||||||
chr8:21929668 | A | G | 8 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+9880A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21929668 | |||||||
chr8:21929802 | A | C | 1 | a0001c0002t0001g0251 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18+10014A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21929802 | |||||||
chr8:21930104 | C | T | 2 | a0001c0002t0004g0289 a0001c0002t0004g0290 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.18+10316C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930104 | |||||||
chr8:21930212 | G | T | 1 | a0001c0002t0001g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.18+10424G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930212 | |||||||
chr8:21930222 | G | A | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+10434G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930222 | |||||||
chr8:21930242 | T | C | 1 | a0001c0001t0002g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.18+10454T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930242 | |||||||
chr8:21930267 | A | G | 4 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+10479A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930267 | |||||||
chr8:21930270 | C | G | 1 | a0001c0005t0002g0224 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.18+10482C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930270 | |||||||
chr8:21930271 | C | T | 1 | a0001c0004t0001g0303 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.18+10483C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930271 | |||||||
chr8:21930388 | A | G | 6 | a0001c0002t0005g0257 a0001c0002t0005g0264 a0001c0002t0005g0265 others(3): Show |
6 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+10600A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930388 | |||||||
chr8:21930755 | G | A | 7 | a0001c0002t0005g0257 a0001c0002t0005g0260 a0001c0002t0005g0264 others(4): Show |
7 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+10967G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930755 | |||||||
chr8:21930858 | A | T | 1 | a0001c0004t0001g0302 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.18+11070A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930858 | |||||||
chr8:21931089 | C | A | 27 | a0001c0002t0001g0298 a0001c0002t0001g0299 a0001c0002t0001g0305 others(24): Show |
29 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.18+11301C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931089 | |||||||
chr8:21931168 | C | CT | 22 | a0001c0002t0001g0124 a0001c0002t0001g0271 a0001c0002t0001g0272 others(19): Show |
22 | HG01433.hp1 HG02004.hp2 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.18+11393dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21931168 | ||||||
chr8:21931168 | C | T | 1 | a0001c0002t0001g0253 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.18+11380C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931168 | |||||||
chr8:21931214 | G | A | 10 | a0001c0002t0001g0003 a0001c0002t0001g0023 a0001c0002t0001g0024 others(7): Show |
11 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.18+11426G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931214 | |||||||
chr8:21931308 | G | A | 2 | a0001c0001t0002g0178 a0001c0003t0001g0093 |
2 | HG01361.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.18+11520G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931308 | |||||||
chr8:21931354 | G | C | 1 | a0001c0003t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.18+11566G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931354 | |||||||
chr8:21931423 | T | G | 177 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(174): Show |
188 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.18+11635T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931423 | |||||||
chr8:21931425 | G | A | 92 | a0001c0002t0001g0046 a0001c0002t0001g0051 a0001c0002t0001g0064 others(89): Show |
98 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.18+11637G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931425 | |||||||
chr8:21931473 | C | T | 177 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(174): Show |
188 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.18+11685C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931473 | |||||||
chr8:21931846 | A | T | 1 | a0001c0002t0001g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.18+12058A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931846 | |||||||
chr8:21932120 | C | T | 5 | a0001c0002t0001g0256 a0001c0002t0001g0259 a0001c0002t0001g0261 others(2): Show |
5 | HG02055.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+12332C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21932120 | |||||||
chr8:21932593 | G | GC | 4 | a0001c0001t0002g0170 a0001c0001t0002g0179 a0001c0001t0002g0180 others(1): Show |
4 | HG01256.hp1 HG04184.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+12806dupC | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21932593 | ||||||
chr8:21932646 | T | TA | 50 | a0001c0003t0001g0005 a0001c0003t0001g0071 a0001c0003t0001g0073 others(47): Show |
51 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.18+12862dupA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21932646 | ||||||
chr8:21932729 | A | G | 1 | a0001c0002t0001g0254 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.18+12941A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21932729 | |||||||
chr8:21932784 | G | T | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+12996G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21932784 | |||||||
chr8:21932925 | A | G | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.18+13137A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21932925 | |||||||
chr8:21932968 | T | G | 26 | a0001c0002t0001g0051 a0001c0002t0004g0001 a0001c0002t0004g0049 others(23): Show |
31 | HG00323.hp2 HG01109.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.18+13180T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21932968 | |||||||
chr8:21933026 | C | T | 3 | a0001c0001t0002g0212 a0001c0001t0002g0213 a0001c0001t0002g0214 |
3 | NA19000.hp1 NA19005.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.18+13238C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21933026 | |||||||
chr8:21933027 | G | A | 3 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 |
3 | HG01934.hp2 HG02004.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.18+13239G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21933027 | |||||||
chr8:21933096 | A | AT | 17 | a0001c0001t0002g0011 a0001c0001t0002g0022 a0001c0001t0002g0127 others(14): Show |
20 | HG00735.hp1 HG00738.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.18+13330dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21933096 | ||||||
chr8:21933096 | AT | A | 51 | a0001c0001t0002g0128 a0001c0001t0002g0184 a0001c0002t0001g0252 others(48): Show |
53 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.18+13330delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21933096 | ||||||
chr8:21933096 | ATT | A | 105 | a0001c0002t0001g0046 a0001c0002t0001g0051 a0001c0002t0001g0064 others(102): Show |
111 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.18+13329_18+13330d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21933096 | ||||||
chr8:21933139 | C | T | 14 | a0001c0002t0001g0003 a0001c0002t0001g0023 a0001c0002t0001g0024 others(11): Show |
15 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.18+13351C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21933139 | |||||||
chr8:21933210 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.18+13422C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21933210 | |||||||
chr8:21933286 | G | C | 1 | a0001c0001t0002g0135 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.18+13498G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21933286 | |||||||
chr8:21933601 | C | G | 1 | a0001c0003t0001g0056 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.18+13813C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21933601 | |||||||
chr8:21933622 | A | G | 1 | a0001c0004t0001g0300 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.18+13834A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21933622 | |||||||
chr8:21933625 | T | G | 8 | a0001c0002t0001g0003 a0001c0002t0001g0023 a0001c0002t0001g0024 others(5): Show |
9 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+13837T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21933625 | |||||||
chr8:21934006 | T | A | 2 | a0001c0001t0002g0161 a0001c0001t0002g0217 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.18+14218T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934006 | |||||||
chr8:21934021 | C | T | 5 | a0001c0002t0005g0257 a0001c0002t0005g0260 a0001c0002t0005g0264 others(2): Show |
5 | HG02572.hp1 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+14233C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934021 | |||||||
chr8:21934046 | C | T | 178 | a0001c0001t0002g0160 a0001c0002t0001g0003 a0001c0002t0001g0013 others(175): Show |
189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.18+14258C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934046 | |||||||
chr8:21934136 | C | A | 3 | a0001c0003t0001g0071 a0001c0003t0001g0094 a0001c0003t0001g0095 |
3 | NA18953.hp2 NA18957.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.18+14348C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934136 | |||||||
chr8:21934163 | A | C | 1 | a0001c0002t0001g0259 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.18+14375A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934163 | |||||||
chr8:21934193 | A | C | 1 | a0001c0002t0005g0293 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.18+14405A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934193 | |||||||
chr8:21934261 | C | T | 54 | a0001c0003t0001g0005 a0001c0003t0001g0071 a0001c0003t0001g0073 others(51): Show |
55 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.18+14473C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934261 | |||||||
chr8:21934299 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.18+14511C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934299 | |||||||
chr8:21934415 | C | A | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.18+14627C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934415 | |||||||
chr8:21934476 | T | C | 1 | a0001c0003t0001g0032 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.18+14688T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934476 | |||||||
chr8:21934490 | G | A | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0009g0269 |
5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+14702G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934490 | |||||||
chr8:21934656 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.18+14868G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934656 | |||||||
chr8:21934839 | A | G | 7 | a0001c0002t0001g0256 a0001c0002t0001g0258 a0001c0002t0001g0259 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+15051A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934839 | |||||||
chr8:21934842 | C | T | 2 | a0001c0001t0002g0207 a0001c0002t0001g0153 |
2 | NA18985.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.18+15054C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934842 | |||||||
chr8:21934913 | T | C | 1 | a0001c0001t0002g0171 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.18+15125T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934913 | |||||||
chr8:21935057 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.18+15269T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21935057 | |||||||
chr8:21935070 | T | C | 1 | a0001c0002t0001g0156 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.18+15282T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21935070 | |||||||
chr8:21935120 | G | A | 3 | a0001c0002t0002g0249 a0001c0002t0004g0289 a0001c0002t0004g0290 |
3 | HG02922.hp2 NA18981.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.18+15332G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21935120 | |||||||
chr8:21935455 | ATTCTAGT others(154): Show |
A | 1 | a0001c0002t0001g0239 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.18+15670_18+15830d others(2): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21935455 | ||||||
chr8:21935468 | G | A | 1 | a0001c0002t0005g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.18+15680G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21935468 | |||||||
chr8:21935472 | G | C | 177 | a0001c0001t0002g0160 a0001c0002t0001g0003 a0001c0002t0001g0013 others(174): Show |
188 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.18+15684G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21935472 | |||||||
chr8:21935822 | T | TG | 181 | a0001c0001t0002g0011 a0001c0001t0002g0160 a0001c0002t0001g0003 others(178): Show |
193 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.18+16037dupG | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21935822 | ||||||
chr8:21935838 | C | G | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+16050C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21935838 | |||||||
chr8:21935885 | A | C | 1 | a0001c0002t0009g0269 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18+16097A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21935885 | |||||||
chr8:21936097 | A | G | 84 | a0001c0001t0002g0160 a0001c0002t0001g0003 a0001c0002t0001g0013 others(81): Show |
89 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.18+16309A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936097 | |||||||
chr8:21936115 | G | A | 1 | a0001c0002t0001g0274 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.18+16327G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936115 | |||||||
chr8:21936117 | C | G | 1 | a0001c0002t0009g0269 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18+16329C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936117 | |||||||
chr8:21936252 | T | TTG | 3 | a0001c0002t0001g0292 a0001c0006t0005g0263 a0001c0006t0005g0268 |
3 | HG02055.hp2 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.18+16467_18+16468d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21936252 | ||||||
chr8:21936400 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.18+16612A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936400 | |||||||
chr8:21936421 | G | T | 1 | a0001c0001t0002g0154 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.18+16633G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936421 | |||||||
chr8:21936530 | C | T | 178 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(175): Show |
189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.18+16742C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936530 | |||||||
chr8:21936604 | G | T | 1 | a0001c0003t0001g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.18+16816G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936604 | |||||||
chr8:21936619 | A | G | 1 | a0001c0002t0001g0272 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.18+16831A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936619 | |||||||
chr8:21936676 | T | C | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+16888T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936676 | |||||||
chr8:21936734 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.18+16946C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936734 | |||||||
chr8:21936768 | C | T | 1 | a0001c0005t0002g0151 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.18+16980C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936768 | |||||||
chr8:21936868 | T | C | 96 | a0001c0002t0001g0046 a0001c0002t0001g0051 a0001c0002t0001g0064 others(93): Show |
102 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.18+17080T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936868 | |||||||
chr8:21937097 | A | C | 1 | a0001c0002t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+17309A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21937097 | |||||||
chr8:21937249 | T | C | 1 | a0001c0001t0002g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.18+17461T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21937249 | |||||||
chr8:21937323 | G | T | 1 | a0001c0005t0002g0151 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.18+17535G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21937323 | |||||||
chr8:21937363 | C | T | 4 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0251 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+17575C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21937363 | |||||||
chr8:21937378 | A | G | 1 | a0001c0003t0001g0055 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.18+17590A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21937378 | |||||||
chr8:21937437 | G | A | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+17649G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21937437 | |||||||
chr8:21937750 | T | C | 2 | a0001c0002t0001g0252 a0001c0002t0001g0253 |
2 | HG00733.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.18+17962T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21937750 | |||||||
chr8:21938128 | G | T | 1 | a0001c0003t0001g0090 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.18+18340G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21938128 | |||||||
chr8:21938496 | A | G | 2 | a0001c0003t0001g0118 a0002c0013t0001g0089 |
2 | HG01123.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.18+18708A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21938496 | |||||||
chr8:21938575 | G | A | 6 | a0001c0002t0001g0003 a0001c0002t0001g0024 a0001c0002t0001g0025 others(3): Show |
7 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+18787G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21938575 | |||||||
chr8:21938779 | A | T | 1 | a0001c0001t0002g0206 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.18+18991A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21938779 | |||||||
chr8:21938927 | T | C | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+19139T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21938927 | |||||||
chr8:21939225 | C | CT | 174 | a0001c0001t0002g0160 a0001c0002t0001g0003 a0001c0002t0001g0013 others(171): Show |
184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.18+19450dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21939225 | ||||||
chr8:21939493 | T | C | 1 | a0001c0002t0001g0239 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.18+19705T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21939493 | |||||||
chr8:21939718 | A | G | 1 | a0001c0001t0002g0184 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.18+19930A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21939718 | |||||||
chr8:21940285 | G | A | 5 | a0001c0002t0001g0274 a0001c0002t0001g0275 a0001c0002t0001g0276 others(2): Show |
5 | NA18612.hp1 NA18968.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+20497G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21940285 | |||||||
chr8:21940300 | A | T | 1 | a0001c0003t0001g0071 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.18+20512A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21940300 | |||||||
chr8:21940474 | CT | C | 177 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(174): Show |
188 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.18+20699delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21940474 | ||||||
chr8:21940523 | G | C | 1 | a0001c0002t0005g0260 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.18+20735G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21940523 | |||||||
chr8:21940526 | G | A | 1 | a0001c0002t0001g0014 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.18+20738G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21940526 | |||||||
chr8:21940556 | A | G | 1 | a0001c0003t0001g0115 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.18+20768A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21940556 | |||||||
chr8:21940805 | C | T | 177 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(174): Show |
188 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.18+21017C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21940805 | |||||||
chr8:21940918 | C | T | 177 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(174): Show |
188 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.18+21130C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21940918 | |||||||
chr8:21941133 | C | CT | 58 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(55): Show |
61 | HG00733.hp2 HG01433.hp1 HG01891.hp1 others(58): Show |
intron_variant | MODIFIER | c.18+21358dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21941133 | ||||||
chr8:21941133 | C | CTT | 92 | a0001c0002t0001g0046 a0001c0002t0001g0051 a0001c0002t0001g0064 others(89): Show |
98 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.18+21357_18+21358d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21941133 | ||||||
chr8:21941270 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.18+21482C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21941270 | |||||||
chr8:21941364 | C | A | 1 | a0001c0003t0001g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.18+21576C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21941364 | |||||||
chr8:21941444 | A | C | 2 | a0001c0001t0002g0203 a0001c0001t0002g0204 |
2 | NA18949.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.18+21656A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21941444 | |||||||
chr8:21941734 | G | A | 84 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(81): Show |
89 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.18+21946G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21941734 | |||||||
chr8:21941787 | C | T | 2 | a0001c0001t0002g0132 a0001c0001t0002g0176 |
2 | HG00673.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.18+21999C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21941787 | |||||||
chr8:21941838 | G | A | 1 | a0001c0002t0001g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.18+22050G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21941838 | |||||||
chr8:21941874 | G | C | 2 | a0001c0003t0001g0048 a0001c0003t0001g0057 |
2 | HG01109.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.18+22086G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21941874 | |||||||
chr8:21941903 | A | G | 1 | a0001c0002t0001g0124 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.18+22115A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21941903 | |||||||
chr8:21942115 | A | G | 92 | a0001c0002t0001g0046 a0001c0002t0001g0051 a0001c0002t0001g0064 others(89): Show |
98 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.18+22327A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942115 | |||||||
chr8:21942182 | A | G | 19 | a0001c0002t0001g0124 a0001c0002t0001g0271 a0001c0002t0001g0272 others(16): Show |
19 | HG01433.hp1 HG02738.hp2 HG03688.hp1 others(16): Show |
intron_variant | MODIFIER | c.18+22394A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942182 | |||||||
chr8:21942226 | C | A | 92 | a0001c0002t0001g0046 a0001c0002t0001g0051 a0001c0002t0001g0064 others(89): Show |
98 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.18+22438C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942226 | |||||||
chr8:21942241 | T | G | 7 | a0001c0002t0005g0257 a0001c0002t0005g0260 a0001c0002t0005g0264 others(4): Show |
7 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+22453T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942241 | |||||||
chr8:21942348 | A | G | 7 | a0001c0002t0005g0257 a0001c0002t0005g0260 a0001c0002t0005g0264 others(4): Show |
7 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+22560A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942348 | |||||||
chr8:21942396 | T | A | 2 | a0001c0002t0004g0289 a0001c0002t0004g0290 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.18+22608T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942396 | |||||||
chr8:21942398 | A | C | 1 | a0001c0001t0002g0131 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.18+22610A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942398 | |||||||
chr8:21942430 | A | C | 24 | a0001c0001t0002g0160 a0001c0002t0001g0298 a0001c0002t0001g0299 others(21): Show |
26 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.18+22642A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942430 | |||||||
chr8:21942594 | G | A | 3 | a0001c0002t0001g0031 a0001c0002t0001g0251 a0003c0012t0001g0250 |
3 | HG02622.hp1 HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.18+22806G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942594 | |||||||
chr8:21942796 | G | A | 1 | a0001c0002t0001g0157 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.18+23008G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942796 | |||||||
chr8:21942800 | A | G | 1 | a0001c0010t0002g0134 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.18+23012A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942800 | |||||||
chr8:21942823 | T | C | 1 | a0001c0005t0002g0224 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.18+23035T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942823 | |||||||
chr8:21943012 | T | C | 1 | a0001c0002t0001g0157 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.18+23224T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943012 | |||||||
chr8:21943114 | A | G | 1 | a0001c0002t0001g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.18+23326A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943114 | |||||||
chr8:21943229 | A | G | 1 | a0001c0003t0001g0119 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.18+23441A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943229 | |||||||
chr8:21943282 | C | T | 2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.18+23494C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943282 | |||||||
chr8:21943289 | T | C | 3 | a0001c0001t0002g0162 a0001c0001t0002g0247 a0001c0005t0002g0224 |
3 | HG02135.hp2 HG02155.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.18+23501T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943289 | |||||||
chr8:21943463 | A | G | 1 | a0001c0002t0005g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-23394A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943463 | |||||||
chr8:21943522 | G | C | 1 | a0001c0002t0001g0320 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.19-23335G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943522 | |||||||
chr8:21943580 | C | T | 88 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(85): Show |
92 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.19-23277C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943580 | |||||||
chr8:21943581 | G | A | 8 | a0001c0002t0001g0230 a0001c0002t0001g0231 a0001c0002t0001g0232 others(5): Show |
8 | NA18949.hp2 NA18970.hp2 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-23276G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943581 | |||||||
chr8:21943630 | G | A | 184 | a0001c0001t0002g0011 a0001c0002t0001g0003 a0001c0002t0001g0013 others(181): Show |
197 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.19-23227G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943630 | |||||||
chr8:21943684 | T | C | 1 | a0001c0002t0001g0305 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.19-23173T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943684 | |||||||
chr8:21943970 | C | T | 1 | a0001c0005t0002g0224 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.19-22887C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943970 | |||||||
chr8:21943997 | C | G | 8 | a0001c0002t0001g0292 a0001c0002t0005g0257 a0001c0002t0005g0260 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-22860C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943997 | |||||||
chr8:21944041 | T | C | 20 | a0001c0001t0002g0006 a0001c0001t0002g0121 a0001c0001t0002g0128 others(17): Show |
21 | HG00673.hp1 HG01099.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.19-22816T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944041 | |||||||
chr8:21944121 | G | A | 1 | a0001c0001t0011g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.19-22736G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944121 | |||||||
chr8:21944223 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.19-22634C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944223 | |||||||
chr8:21944368 | G | A | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0009g0269 |
5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-22489G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944368 | |||||||
chr8:21944456 | A | C | 1 | a0001c0002t0001g0266 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.19-22401A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944456 | |||||||
chr8:21944485 | T | G | 9 | a0001c0003t0001g0073 a0001c0003t0001g0075 a0001c0003t0001g0077 others(6): Show |
9 | NA18747.hp1 NA18944.hp1 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-22372T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944485 | |||||||
chr8:21944607 | C | T | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.19-22250C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944607 | |||||||
chr8:21944686 | A | G | 182 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(179): Show |
194 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.19-22171A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944686 | |||||||
chr8:21944718 | C | A | 3 | a0001c0003t0001g0078 a0001c0003t0001g0079 a0001c0003t0001g0100 |
3 | HG02165.hp1 NA18947.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.19-22139C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944718 | |||||||
chr8:21944729 | G | A | 1 | a0001c0003t0001g0096 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.19-22128G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944729 | |||||||
chr8:21944761 | C | T | 53 | a0001c0003t0001g0005 a0001c0003t0001g0071 a0001c0003t0001g0073 others(50): Show |
54 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.19-22096C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944761 | |||||||
chr8:21944765 | T | G | 88 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(85): Show |
92 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.19-22092T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944765 | |||||||
chr8:21944779 | G | A | 88 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(85): Show |
92 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.19-22078G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944779 | |||||||
chr8:21944854 | T | A | 1 | a0001c0002t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.19-22003T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944854 | |||||||
chr8:21944921 | G | A | 94 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(91): Show |
102 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.19-21936G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944921 | |||||||
chr8:21945063 | C | T | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.19-21794C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945063 | |||||||
chr8:21945088 | C | T | 2 | a0001c0002t0004g0289 a0001c0002t0004g0290 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.19-21769C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945088 | |||||||
chr8:21945147 | C | T | 1 | a0001c0003t0001g0037 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.19-21710C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945147 | |||||||
chr8:21945150 | G | T | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.19-21707G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945150 | |||||||
chr8:21945175 | C | T | 2 | a0001c0003t0001g0060 a0001c0003t0001g0061 |
2 | HG01167.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.19-21682C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945175 | |||||||
chr8:21945211 | A | C | 1 | a0001c0001t0002g0226 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.19-21646A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945211 | |||||||
chr8:21945326 | A | G | 94 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(91): Show |
102 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.19-21531A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945326 | |||||||
chr8:21945349 | TAGAC | T | 54 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(51): Show |
60 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.19-21504_19-21501d others(6): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21945349 | ||||||
chr8:21945399 | A | T | 89 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(86): Show |
93 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.19-21458A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945399 | |||||||
chr8:21945497 | A | G | 183 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(180): Show |
195 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.19-21360A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945497 | |||||||
chr8:21945545 | A | T | 1 | a0001c0001t0002g0011 | 2 | HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.19-21312A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945545 | |||||||
chr8:21945580 | A | G | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0009g0269 |
5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-21277A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945580 | |||||||
chr8:21945814 | A | G | 3 | a0001c0002t0001g0228 a0001c0002t0001g0229 a0001c0002t0001g0238 |
3 | NA18940.hp2 NA18950.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.19-21043A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945814 | |||||||
chr8:21945891 | G | A | 1 | a0001c0002t0005g0293 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-20966G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945891 | |||||||
chr8:21945923 | G | A | 3 | a0001c0002t0006g0317 a0001c0002t0006g0318 a0001c0002t0006g0319 |
3 | HG02818.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.19-20934G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945923 | |||||||
chr8:21946214 | C | T | 24 | a0001c0002t0001g0051 a0001c0002t0001g0124 a0001c0002t0001g0271 others(21): Show |
26 | HG01433.hp1 HG02056.hp2 HG02738.hp2 others(23): Show |
intron_variant | MODIFIER | c.19-20643C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946214 | |||||||
chr8:21946224 | C | A | 92 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(89): Show |
100 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.19-20633C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946224 | |||||||
chr8:21946305 | A | C | 89 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(86): Show |
93 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.19-20552A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946305 | |||||||
chr8:21946368 | T | A | 2 | a0001c0003t0001g0004 a0001c0003t0001g0052 |
3 | HG01891.hp2 HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.19-20489T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946368 | |||||||
chr8:21946475 | C | T | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.19-20382C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946475 | |||||||
chr8:21946575 | A | G | 1 | a0001c0001t0002g0223 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.19-20282A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946575 | |||||||
chr8:21946580 | A | AC | 92 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(89): Show |
100 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.19-20277_19-20276i others(3): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946580 | |||||||
chr8:21946585 | A | AAAC | 51 | a0001c0002t0004g0289 a0001c0002t0004g0290 a0001c0003t0001g0005 others(48): Show |
52 | HG00558.hp1 HG00735.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.19-20272_19-20271i others(5): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946585 | |||||||
chr8:21946585 | A | AAACAAAA others(10): Show |
1 | a0001c0003t0001g0097 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.19-20272_19-20271i others(19): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946585 | |||||||
chr8:21946585 | A | AAC | 34 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(31): Show |
37 | HG00323.hp2 HG00741.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.19-20272_19-20271i others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946585 | |||||||
chr8:21946586 | C | A | 91 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(88): Show |
95 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.19-20271C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946586 | |||||||
chr8:21946586 | C | CA | 110 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0242 others(107): Show |
119 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.19-20259dupA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21946586 | ||||||
chr8:21946591 | A | AC | 4 | a0001c0002t0005g0257 a0001c0002t0005g0264 a0001c0002t0005g0293 others(1): Show |
4 | HG02622.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-20266_19-20265i others(3): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946591 | |||||||
chr8:21946640 | A | AT | 75 | a0001c0001t0002g0125 a0001c0001t0002g0149 a0001c0001t0002g0150 others(72): Show |
81 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.19-20196dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21946640 | ||||||
chr8:21946640 | A | ATT | 9 | a0001c0002t0001g0253 a0001c0002t0001g0259 a0001c0002t0001g0267 others(6): Show |
9 | HG00642.hp1 HG00733.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-20197_19-20196d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21946640 | ||||||
chr8:21946644 | T | G | 3 | a0001c0002t0001g0292 a0001c0006t0005g0263 a0001c0006t0005g0268 |
3 | HG02055.hp2 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.19-20213T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946644 | |||||||
chr8:21946807 | T | TTA | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0009g0269 |
5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-20050_19-20049i others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946807 | |||||||
chr8:21947172 | A | G | 1 | a0001c0002t0001g0299 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.19-19685A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21947172 | |||||||
chr8:21947474 | G | A | 2 | a0001c0007t0001g0309 a0001c0007t0001g0314 |
2 | HG00673.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.19-19383G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21947474 | |||||||
chr8:21947478 | A | G | 89 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(86): Show |
93 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.19-19379A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21947478 | |||||||
chr8:21947521 | A | G | 1 | a0001c0001t0002g0200 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.19-19336A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21947521 | |||||||
chr8:21947560 | A | G | 1 | a0001c0002t0001g0051 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.19-19297A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21947560 | |||||||
chr8:21947754 | T | C | 94 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(91): Show |
102 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.19-19103T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21947754 | |||||||
chr8:21947924 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.19-18933C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21947924 | |||||||
chr8:21947996 | G | C | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-18861G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21947996 | |||||||
chr8:21948109 | C | G | 24 | a0001c0001t0002g0160 a0001c0002t0001g0298 a0001c0002t0001g0299 others(21): Show |
26 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.19-18748C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948109 | |||||||
chr8:21948212 | G | T | 1 | a0001c0002t0001g0320 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.19-18645G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948212 | |||||||
chr8:21948420 | C | A | 1 | a0001c0001t0002g0203 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.19-18437C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948420 | |||||||
chr8:21948467 | G | A | 1 | a0001c0002t0001g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.19-18390G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948467 | |||||||
chr8:21948546 | C | T | 1 | a0001c0001t0002g0203 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.19-18311C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948546 | |||||||
chr8:21948584 | A | G | 1 | a0001c0001t0002g0127 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.19-18273A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948584 | |||||||
chr8:21948652 | A | G | 4 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0251 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-18205A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948652 | |||||||
chr8:21948671 | G | A | 1 | a0001c0002t0001g0299 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.19-18186G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948671 | |||||||
chr8:21948737 | G | A | 2 | a0001c0002t0004g0289 a0001c0002t0004g0290 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.19-18120G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948737 | |||||||
chr8:21949012 | C | T | 1 | a0001c0002t0001g0298 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.19-17845C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21949012 | |||||||
chr8:21949030 | A | G | 1 | a0001c0001t0002g0021 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.19-17827A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21949030 | |||||||
chr8:21949041 | G | T | 1 | a0001c0001t0002g0162 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.19-17816G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21949041 | |||||||
chr8:21949157 | C | A | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-17700C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21949157 | |||||||
chr8:21949265 | T | C | 1 | a0001c0003t0002g0294 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.19-17592T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21949265 | |||||||
chr8:21949278 | G | A | 2 | a0001c0001t0002g0011 a0001c0005t0002g0227 |
3 | HG00738.hp1 HG01099.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.19-17579G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21949278 | |||||||
chr8:21949292 | G | A | 27 | a0001c0002t0001g0298 a0001c0002t0001g0299 a0001c0002t0001g0305 others(24): Show |
29 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.19-17565G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21949292 | |||||||
chr8:21949541 | G | A | 1 | a0001c0001t0002g0248 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.19-17316G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21949541 | |||||||
chr8:21949714 | CTGTT | C | 89 | a0001c0001t0002g0181 a0001c0002t0001g0046 a0001c0002t0001g0064 others(86): Show |
93 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.19-17138_19-17135d others(6): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21949714 | ||||||
chr8:21950069 | C | A | 1 | a0001c0002t0009g0269 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.19-16788C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21950069 | |||||||
chr8:21950106 | T | C | 1 | a0001c0001t0002g0006 | 2 | NA18959.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.19-16751T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21950106 | |||||||
chr8:21950210 | G | A | 1 | a0001c0003t0001g0056 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.19-16647G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21950210 | |||||||
chr8:21950242 | G | A | 1 | a0001c0001t0002g0128 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.19-16615G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21950242 | |||||||
chr8:21950246 | A | G | 76 | a0001c0002t0001g0007 a0001c0002t0001g0153 a0001c0002t0001g0228 others(73): Show |
78 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.19-16611A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21950246 | |||||||
chr8:21950888 | G | C | 1 | a0001c0002t0001g0256 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.19-15969G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21950888 | |||||||
chr8:21950927 | G | T | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-15930G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21950927 | |||||||
chr8:21950959 | A | C | 1 | a0003c0012t0001g0250 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.19-15898A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21950959 | |||||||
chr8:21951090 | T | TTTAA | 3 | a0001c0002t0001g0023 a0001c0002t0001g0029 a0001c0003t0001g0087 |
3 | HG02976.hp2 HG03017.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.19-15742_19-15739d others(6): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21951090 | ||||||
chr8:21951205 | C | T | 8 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-15652C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951205 | |||||||
chr8:21951229 | A | G | 1 | a0002c0013t0001g0089 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-15628A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951229 | |||||||
chr8:21951263 | G | T | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.19-15594G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951263 | |||||||
chr8:21951334 | A | G | 7 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(4): Show |
8 | HG02280.hp2 HG02572.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-15523A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951334 | |||||||
chr8:21951462 | A | G | 3 | a0001c0001t0002g0148 a0001c0001t0002g0198 a0001c0001t0002g0199 |
3 | HG00621.hp1 NA18965.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.19-15395A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951462 | |||||||
chr8:21951504 | A | G | 34 | a0001c0002t0001g0003 a0001c0002t0001g0023 a0001c0002t0001g0024 others(31): Show |
37 | HG01433.hp1 HG01891.hp1 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.19-15353A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951504 | |||||||
chr8:21951587 | C | G | 3 | a0001c0003t0001g0048 a0001c0003t0001g0056 a0001c0003t0001g0057 |
3 | HG01109.hp1 HG01261.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.19-15270C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951587 | |||||||
chr8:21951662 | T | C | 3 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0021 |
3 | HG00140.hp2 HG01433.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.19-15195T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951662 | |||||||
chr8:21951829 | A | AT | 111 | a0001c0002t0001g0007 a0001c0002t0001g0046 a0001c0002t0001g0064 others(108): Show |
116 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.19-15027dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21951829 | ||||||
chr8:21951908 | G | T | 1 | a0001c0001t0002g0178 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.19-14949G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951908 | |||||||
chr8:21952074 | T | G | 7 | a0001c0002t0005g0257 a0001c0002t0005g0260 a0001c0002t0005g0264 others(4): Show |
7 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-14783T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952074 | |||||||
chr8:21952226 | T | C | 2 | a0001c0002t0001g0271 a0001c0002t0001g0288 |
2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.19-14631T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952226 | |||||||
chr8:21952248 | G | T | 2 | a0001c0002t0001g0013 a0001c0002t0001g0014 |
4 | HG02109.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-14609G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952248 | |||||||
chr8:21952486 | C | G | 3 | a0001c0001t0002g0162 a0001c0001t0002g0247 a0001c0005t0002g0224 |
3 | HG02135.hp2 HG02155.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.19-14371C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952486 | |||||||
chr8:21952582 | T | G | 2 | a0001c0006t0005g0263 a0001c0006t0005g0268 |
2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.19-14275T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952582 | |||||||
chr8:21952689 | C | T | 1 | a0001c0003t0001g0032 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.19-14168C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952689 | |||||||
chr8:21952836 | G | C | 1 | a0001c0001t0002g0136 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.19-14021G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952836 | |||||||
chr8:21952866 | C | T | 180 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(177): Show |
192 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.19-13991C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952866 | |||||||
chr8:21952883 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.19-13974G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952883 | |||||||
chr8:21952997 | A | G | 2 | a0001c0001t0002g0147 a0001c0001t0002g0201 |
2 | HG01175.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.19-13860A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952997 | |||||||
chr8:21953092 | G | A | 92 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(89): Show |
100 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.19-13765G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953092 | |||||||
chr8:21953113 | C | T | 2 | a0001c0003t0001g0060 a0001c0003t0001g0061 |
2 | HG01167.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.19-13744C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953113 | |||||||
chr8:21953129 | G | T | 2 | a0001c0005t0002g0146 a0001c0005t0002g0151 |
2 | NA18975.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.19-13728G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953129 | |||||||
chr8:21953282 | C | G | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-13575C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953282 | |||||||
chr8:21953542 | G | A | 1 | a0001c0003t0001g0037 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.19-13315G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953542 | |||||||
chr8:21953644 | C | T | 1 | a0001c0002t0007g0010 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.19-13213C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953644 | |||||||
chr8:21953713 | T | G | 1 | a0001c0003t0012g0069 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.19-13144T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953713 | |||||||
chr8:21953778 | T | C | 1 | a0001c0001t0002g0128 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.19-13079T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953778 | |||||||
chr8:21953785 | G | C | 1 | a0001c0005t0002g0224 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.19-13072G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953785 | |||||||
chr8:21953844 | T | A | 1 | a0001c0002t0001g0253 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.19-13013T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953844 | |||||||
chr8:21954019 | C | G | 110 | a0001c0002t0001g0007 a0001c0002t0001g0046 a0001c0002t0001g0064 others(107): Show |
115 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.19-12838C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954019 | |||||||
chr8:21954200 | T | A | 2 | a0001c0005t0002g0146 a0001c0005t0002g0151 |
2 | NA18975.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.19-12657T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954200 | |||||||
chr8:21954206 | T | G | 2 | a0001c0002t0001g0228 a0001c0002t0001g0238 |
2 | NA18940.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.19-12651T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954206 | |||||||
chr8:21954264 | A | G | 2 | a0001c0002t0001g0228 a0001c0002t0001g0238 |
2 | NA18940.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.19-12593A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954264 | |||||||
chr8:21954482 | A | C | 93 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(90): Show |
101 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.19-12375A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954482 | |||||||
chr8:21954484 | A | G | 1 | a0001c0002t0001g0267 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.19-12373A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954484 | |||||||
chr8:21954489 | C | T | 4 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0251 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-12368C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954489 | |||||||
chr8:21954853 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.19-12004C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954853 | |||||||
chr8:21954872 | A | G | 1 | a0001c0001t0002g0126 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.19-11985A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954872 | |||||||
chr8:21955203 | T | C | 1 | a0001c0001t0002g0242 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.19-11654T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21955203 | |||||||
chr8:21955219 | A | AG | 111 | a0001c0002t0001g0007 a0001c0002t0001g0046 a0001c0002t0001g0064 others(108): Show |
116 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.19-11638_19-11637i others(3): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21955219 | |||||||
chr8:21955507 | A | G | 89 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(86): Show |
93 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.19-11350A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21955507 | |||||||
chr8:21955629 | C | T | 90 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(87): Show |
98 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.19-11228C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21955629 | |||||||
chr8:21955724 | C | CT | 14 | a0001c0001t0002g0012 a0001c0001t0002g0143 a0001c0001t0002g0144 others(11): Show |
15 | HG00438.hp2 HG00558.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.19-11110dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21955724 | ||||||
chr8:21955724 | C | CTT | 19 | a0001c0002t0001g0051 a0001c0002t0001g0124 a0001c0002t0001g0272 others(16): Show |
19 | HG01433.hp1 HG02056.hp2 HG02738.hp2 others(16): Show |
intron_variant | MODIFIER | c.19-11111_19-11110d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21955724 | ||||||
chr8:21955724 | C | CTTT | 16 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0251 others(13): Show |
18 | HG02451.hp2 HG02572.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.19-11112_19-11110d others(5): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21955724 | ||||||
chr8:21955724 | C | CTTTT | 33 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(30): Show |
37 | HG00733.hp2 HG01891.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.19-11113_19-11110d others(6): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21955724 | ||||||
chr8:21955724 | C | CTTTTT | 22 | a0001c0002t0001g0298 a0001c0002t0001g0299 a0001c0002t0001g0305 others(19): Show |
24 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.19-11114_19-11110d others(7): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21955724 | ||||||
chr8:21955724 | CTTTTTT | C | 86 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(83): Show |
90 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.19-11115_19-11110d others(8): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21955724 | ||||||
chr8:21955724 | CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.19-11120_19-11110d others(13): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21955724 | ||||||
chr8:21955925 | C | T | 1 | a0001c0002t0004g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.19-10932C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21955925 | |||||||
chr8:21956224 | C | T | 1 | a0001c0002t0001g0254 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.19-10633C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956224 | |||||||
chr8:21956300 | G | T | 1 | a0001c0002t0001g0283 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.19-10557G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956300 | |||||||
chr8:21956396 | T | C | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.19-10461T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956396 | |||||||
chr8:21956451 | A | G | 90 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(87): Show |
94 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.19-10406A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956451 | |||||||
chr8:21956477 | T | C | 1 | a0001c0001t0002g0185 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.19-10380T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956477 | |||||||
chr8:21956493 | A | G | 183 | a0001c0001t0002g0011 a0001c0002t0001g0003 a0001c0002t0001g0013 others(180): Show |
196 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.19-10364A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956493 | |||||||
chr8:21956546 | G | C | 2 | a0001c0002t0001g0258 a0001c0002t0001g0266 |
2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.19-10311G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956546 | |||||||
chr8:21956645 | CT | C | 180 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(177): Show |
192 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.19-10208delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21956645 | ||||||
chr8:21956652 | T | A | 2 | a0001c0002t0001g0251 a0003c0012t0001g0250 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.19-10205T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956652 | |||||||
chr8:21956952 | A | G | 1 | a0001c0002t0001g0307 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.19-9905A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956952 | |||||||
chr8:21957063 | T | C | 1 | a0001c0003t0001g0063 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.19-9794T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957063 | |||||||
chr8:21957104 | C | G | 6 | a0001c0002t0001g0003 a0001c0002t0001g0024 a0001c0002t0001g0025 others(3): Show |
7 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-9753C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957104 | |||||||
chr8:21957162 | G | T | 1 | a0001c0002t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.19-9695G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957162 | |||||||
chr8:21957210 | C | G | 2 | a0001c0002t0001g0258 a0001c0002t0001g0266 |
2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.19-9647C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957210 | |||||||
chr8:21957214 | T | G | 10 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(7): Show |
11 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.19-9643T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957214 | |||||||
chr8:21957221 | A | G | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.19-9636A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957221 | |||||||
chr8:21957227 | C | T | 1 | a0001c0002t0001g0311 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.19-9630C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957227 | |||||||
chr8:21957228 | C | T | 88 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(85): Show |
92 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.19-9629C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957228 | |||||||
chr8:21957233 | G | A | 3 | a0001c0002t0001g0261 a0001c0002t0001g0262 a0001c0002t0001g0267 |
3 | HG02055.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.19-9624G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957233 | |||||||
chr8:21957259 | G | C | 1 | a0001c0001t0002g0186 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.19-9598G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957259 | |||||||
chr8:21957498 | C | T | 46 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0156 others(43): Show |
51 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.19-9359C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957498 | |||||||
chr8:21957499 | C | T | 1 | a0001c0003t0001g0110 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.19-9358C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957499 | |||||||
chr8:21957527 | C | A | 1 | a0001c0001t0002g0206 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.19-9330C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957527 | |||||||
chr8:21957662 | T | A | 1 | a0001c0001t0002g0138 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.19-9195T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957662 | |||||||
chr8:21957693 | C | T | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-9164C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957693 | |||||||
chr8:21957803 | G | T | 21 | a0001c0002t0001g0051 a0001c0002t0001g0272 a0001c0002t0001g0273 others(18): Show |
23 | HG01433.hp1 HG02647.hp2 HG02738.hp2 others(20): Show |
intron_variant | MODIFIER | c.19-9054G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957803 | |||||||
chr8:21957815 | C | T | 2 | a0001c0002t0001g0228 a0001c0002t0001g0238 |
2 | NA18940.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.19-9042C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957815 | |||||||
chr8:21957867 | G | A | 87 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(84): Show |
95 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.19-8990G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957867 | |||||||
chr8:21957879 | G | GT | 8 | a0001c0001t0002g0218 a0001c0002t0001g0029 a0001c0002t0001g0245 others(5): Show |
8 | HG02056.hp1 HG02300.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-8968dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21957879 | ||||||
chr8:21957914 | T | G | 111 | a0001c0002t0001g0007 a0001c0002t0001g0046 a0001c0002t0001g0064 others(108): Show |
116 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.19-8943T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957914 | |||||||
chr8:21958022 | C | T | 1 | a0003c0012t0001g0250 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.19-8835C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958022 | |||||||
chr8:21958054 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.19-8803G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958054 | |||||||
chr8:21958174 | T | A | 2 | a0001c0003t0001g0063 a0001c0003t0001g0067 |
2 | HG00741.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.19-8683T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958174 | |||||||
chr8:21958277 | C | G | 2 | a0001c0002t0001g0156 a0001c0002t0001g0159 |
2 | HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.19-8580C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958277 | |||||||
chr8:21958289 | A | G | 4 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-8568A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958289 | |||||||
chr8:21958359 | C | A | 2 | a0001c0006t0005g0263 a0001c0006t0005g0268 |
2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.19-8498C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958359 | |||||||
chr8:21958430 | G | A | 1 | a0001c0002t0001g0252 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.19-8427G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958430 | |||||||
chr8:21958539 | A | C | 1 | a0001c0002t0001g0282 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.19-8318A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958539 | |||||||
chr8:21958540 | G | C | 1 | a0001c0002t0001g0282 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.19-8317G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958540 | |||||||
chr8:21958574 | C | T | 1 | a0001c0002t0008g0270 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.19-8283C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958574 | |||||||
chr8:21958602 | A | G | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-8255A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958602 | |||||||
chr8:21958610 | G | GA | 23 | a0001c0001t0002g0019 a0001c0001t0002g0165 a0001c0001t0002g0166 others(20): Show |
23 | HG00621.hp2 HG00735.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.19-8235dupA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21958610 | ||||||
chr8:21958643 | T | G | 1 | a0001c0002t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.19-8214T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958643 | |||||||
chr8:21958776 | A | G | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.19-8081A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958776 | |||||||
chr8:21958812 | C | G | 2 | a0001c0001t0002g0133 a0001c0001t0002g0177 |
2 | NA18983.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.19-8045C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958812 | |||||||
chr8:21958910 | G | A | 1 | a0001c0002t0001g0278 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.19-7947G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958910 | |||||||
chr8:21958961 | CA | C | 9 | a0001c0001t0002g0122 a0001c0002t0001g0013 a0001c0002t0001g0014 others(6): Show |
11 | HG01175.hp1 HG01934.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.19-7879delA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21958961 | ||||||
chr8:21958961 | CAA | C | 168 | a0001c0002t0001g0003 a0001c0002t0001g0023 a0001c0002t0001g0024 others(165): Show |
178 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.19-7880_19-7879del others(2): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21958961 | ||||||
chr8:21958973 | A | G | 1 | a0001c0003t0001g0112 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.19-7884A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958973 | |||||||
chr8:21959153 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.19-7704C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21959153 | |||||||
chr8:21959498 | C | G | 1 | a0001c0001t0002g0202 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.19-7359C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21959498 | |||||||
chr8:21959619 | T | A | 1 | a0001c0001t0002g0170 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.19-7238T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21959619 | |||||||
chr8:21959734 | C | T | 180 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(177): Show |
192 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.19-7123C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21959734 | |||||||
chr8:21959856 | A | C | 1 | a0001c0001t0002g0202 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.19-7001A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21959856 | |||||||
chr8:21959862 | A | G | 1 | a0001c0001t0002g0160 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.19-6995A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21959862 | |||||||
chr8:21959869 | C | T | 1 | a0001c0003t0001g0056 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.19-6988C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21959869 | |||||||
chr8:21959895 | G | A | 4 | a0001c0002t0001g0273 a0001c0002t0001g0282 a0001c0002t0001g0284 others(1): Show |
4 | NA18946.hp2 NA18955.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-6962G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21959895 | |||||||
chr8:21960104 | G | A | 313 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(310): Show |
331 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.19-6753G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960104 | |||||||
chr8:21960265 | C | A | 1 | a0001c0003t0001g0073 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.19-6592C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960265 | |||||||
chr8:21960295 | G | A | 17 | a0001c0002t0001g0051 a0001c0002t0001g0272 a0001c0002t0001g0273 others(14): Show |
19 | HG01433.hp1 HG02738.hp2 HG03704.hp1 others(16): Show |
intron_variant | MODIFIER | c.19-6562G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960295 | |||||||
chr8:21960296 | T | G | 1 | a0001c0001t0002g0187 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.19-6561T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960296 | |||||||
chr8:21960479 | C | G | 2 | a0001c0002t0004g0289 a0001c0002t0004g0290 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.19-6378C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960479 | |||||||
chr8:21960549 | A | G | 90 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(87): Show |
94 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.19-6308A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960549 | |||||||
chr8:21960660 | C | G | 1 | a0001c0001t0002g0197 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.19-6197C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960660 | |||||||
chr8:21960699 | G | A | 2 | a0001c0001t0002g0162 a0001c0005t0002g0224 |
2 | HG02155.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.19-6158G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960699 | |||||||
chr8:21960834 | A | C | 1 | a0001c0001t0002g0196 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.19-6023A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960834 | |||||||
chr8:21961204 | G | GT | 7 | a0001c0001t0002g0145 a0001c0001t0002g0214 a0001c0002t0001g0315 others(4): Show |
7 | HG01358.hp1 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-5638dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21961204 | ||||||
chr8:21961390 | A | G | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.19-5467A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961390 | |||||||
chr8:21961405 | G | A | 1 | a0001c0002t0005g0260 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.19-5452G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961405 | |||||||
chr8:21961412 | C | T | 1 | a0001c0002t0005g0260 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.19-5445C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961412 | |||||||
chr8:21961464 | C | T | 1 | a0001c0001t0002g0126 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.19-5393C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961464 | |||||||
chr8:21961687 | G | C | 1 | a0001c0001t0002g0129 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.19-5170G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961687 | |||||||
chr8:21961774 | G | A | 26 | a0001c0002t0001g0280 a0001c0002t0001g0283 a0001c0002t0001g0298 others(23): Show |
28 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.19-5083G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961774 | |||||||
chr8:21961854 | G | A | 3 | a0001c0001t0002g0164 a0001c0001t0002g0219 a0004c0011t0002g0163 |
3 | HG03041.hp1 HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.19-5003G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961854 | |||||||
chr8:21961855 | GT | G | 56 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(53): Show |
62 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.19-4999delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21961855 | ||||||
chr8:21961864 | C | T | 2 | a0001c0003t0001g0078 a0001c0003t0001g0079 |
2 | HG02165.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.19-4993C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961864 | |||||||
chr8:21961965 | A | G | 1 | a0001c0001t0002g0197 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.19-4892A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961965 | |||||||
chr8:21962084 | C | T | 1 | a0001c0003t0001g0109 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.19-4773C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962084 | |||||||
chr8:21962266 | C | T | 1 | a0001c0003t0001g0056 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.19-4591C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962266 | |||||||
chr8:21962470 | T | C | 1 | a0001c0001t0002g0202 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.19-4387T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962470 | |||||||
chr8:21962514 | G | A | 17 | a0001c0002t0001g0051 a0001c0002t0001g0272 a0001c0002t0001g0273 others(14): Show |
19 | HG01433.hp1 HG02738.hp2 HG03704.hp1 others(16): Show |
intron_variant | MODIFIER | c.19-4343G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962514 | |||||||
chr8:21962517 | G | C | 1 | a0001c0001t0002g0202 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.19-4340G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962517 | |||||||
chr8:21962531 | A | G | 1 | a0001c0001t0002g0182 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.19-4326A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962531 | |||||||
chr8:21962566 | C | A | 4 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0251 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-4291C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962566 | |||||||
chr8:21962602 | CA | C | 5 | a0001c0002t0005g0257 a0001c0002t0005g0260 a0001c0002t0005g0264 others(2): Show |
5 | HG02572.hp1 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-4254delA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962602 | |||||||
chr8:21962724 | T | G | 1 | a0001c0003t0002g0294 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.19-4133T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962724 | |||||||
chr8:21962968 | A | T | 87 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(84): Show |
91 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.19-3889A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962968 | |||||||
chr8:21963257 | G | T | 1 | a0001c0001t0002g0135 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.19-3600G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21963257 | |||||||
chr8:21963302 | C | A | 89 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(86): Show |
93 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.19-3555C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21963302 | |||||||
chr8:21963637 | G | T | 1 | a0001c0003t0001g0099 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.19-3220G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21963637 | |||||||
chr8:21963643 | C | T | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.19-3214C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21963643 | |||||||
chr8:21963694 | CA | C | 108 | a0001c0001t0002g0011 a0001c0002t0001g0046 a0001c0002t0001g0051 others(105): Show |
115 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.19-3147delA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21963694 | ||||||
chr8:21963694 | CAA | C | 69 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(66): Show |
75 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.19-3148_19-3147del others(2): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21963694 | ||||||
chr8:21963760 | C | T | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0009g0269 |
5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-3097C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21963760 | |||||||
chr8:21964147 | A | G | 1 | a0001c0002t0001g0299 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.19-2710A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964147 | |||||||
chr8:21964150 | G | A | 1 | a0001c0004t0001g0304 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.19-2707G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964150 | |||||||
chr8:21964220 | G | T | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.19-2637G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964220 | |||||||
chr8:21964267 | G | T | 87 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(84): Show |
95 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.19-2590G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964267 | |||||||
chr8:21964275 | G | T | 6 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(3): Show |
7 | HG02280.hp2 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-2582G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964275 | |||||||
chr8:21964338 | C | T | 1 | a0001c0002t0005g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-2519C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964338 | |||||||
chr8:21964514 | C | T | 3 | a0001c0002t0006g0317 a0001c0002t0006g0318 a0001c0002t0006g0319 |
3 | HG02818.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.19-2343C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964514 | |||||||
chr8:21964515 | G | A | 1 | a0001c0003t0001g0080 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.19-2342G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964515 | |||||||
chr8:21964539 | A | T | 1 | a0001c0001t0002g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.19-2318A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964539 | |||||||
chr8:21964562 | C | T | 2 | a0001c0002t0001g0298 a0001c0002t0001g0311 |
2 | HG03704.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.19-2295C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964562 | |||||||
chr8:21964613 | CA | C | 75 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(72): Show |
81 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.19-2232delA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21964613 | ||||||
chr8:21964613 | CAA | C | 6 | a0001c0002t0001g0051 a0001c0002t0001g0272 a0001c0002t0004g0001 others(3): Show |
8 | HG01433.hp1 HG04115.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-2233_19-2232del others(2): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21964613 | ||||||
chr8:21964667 | G | A | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.19-2190G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964667 | |||||||
chr8:21964853 | G | A | 2 | a0001c0001t0002g0161 a0001c0001t0002g0217 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.19-2004G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964853 | |||||||
chr8:21965119 | C | G | 8 | a0001c0002t0001g0292 a0001c0002t0005g0257 a0001c0002t0005g0260 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-1738C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965119 | |||||||
chr8:21965208 | C | T | 3 | a0001c0002t0001g0228 a0001c0002t0001g0229 a0001c0002t0001g0238 |
3 | NA18940.hp2 NA18950.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.19-1649C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965208 | |||||||
chr8:21965276 | A | G | 1 | a0001c0003t0001g0032 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.19-1581A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965276 | |||||||
chr8:21965391 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.19-1466A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965391 | |||||||
chr8:21965471 | G | T | 1 | a0001c0002t0009g0269 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.19-1386G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965471 | |||||||
chr8:21965514 | G | A | 89 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(86): Show |
93 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.19-1343G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965514 | |||||||
chr8:21965533 | A | G | 1 | a0001c0003t0003g0062 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.19-1324A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965533 | |||||||
chr8:21965556 | C | T | 2 | a0001c0001t0002g0135 a0001c0001t0002g0154 |
2 | NA18978.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.19-1301C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965556 | |||||||
chr8:21965603 | A | G | 1 | a0001c0003t0001g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.19-1254A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965603 | |||||||
chr8:21965638 | C | T | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.19-1219C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965638 | |||||||
chr8:21965662 | G | C | 88 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(85): Show |
96 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.19-1195G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965662 | |||||||
chr8:21965663 | T | C | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.19-1194T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965663 | |||||||
chr8:21965673 | A | G | 111 | a0001c0002t0001g0007 a0001c0002t0001g0046 a0001c0002t0001g0064 others(108): Show |
116 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.19-1184A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965673 | |||||||
chr8:21965695 | T | G | 111 | a0001c0002t0001g0007 a0001c0002t0001g0046 a0001c0002t0001g0064 others(108): Show |
116 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.19-1162T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965695 | |||||||
chr8:21965750 | C | T | 1 | a0001c0003t0001g0037 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.19-1107C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965750 | |||||||
chr8:21965758 | A | G | 1 | a0001c0002t0001g0244 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.19-1099A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965758 | |||||||
chr8:21965949 | A | G | 3 | a0001c0002t0001g0292 a0001c0006t0005g0263 a0001c0006t0005g0268 |
3 | HG02055.hp2 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.19-908A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965949 | |||||||
chr8:21965976 | C | T | 88 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(85): Show |
96 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.19-881C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965976 | |||||||
chr8:21965980 | C | CCACTT | 203 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0013 others(200): Show |
216 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.19-875_19-874insCT others(3): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21965980 | ||||||
chr8:21966136 | A | G | 1 | a0001c0002t0001g0252 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.19-721A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21966136 | |||||||
chr8:21966374 | C | T | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-483C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21966374 | |||||||
chr8:21966466 | G | A | 1 | a0001c0003t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.19-391G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21966466 | |||||||
chr8:21966552 | C | T | 1 | a0001c0002t0005g0293 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-305C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21966552 | |||||||
chr8:21966590 | G | A | 8 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0005g0257 others(5): Show |
10 | HG02109.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.19-267G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21966590 | |||||||
chr8:21966626 | A | G | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.19-231A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21966626 | |||||||
chr8:21966636 | AG | A | 10 | a0001c0002t0001g0003 a0001c0002t0001g0023 a0001c0002t0001g0024 others(7): Show |
11 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.19-220delG | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21966636 | |||||||
chr8:21966637 | GT | G | 169 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0030 others(166): Show |
180 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.19-218delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21966637 | ||||||
chr8:21966638 | T | A | 10 | a0001c0002t0001g0003 a0001c0002t0001g0023 a0001c0002t0001g0024 others(7): Show |
11 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.19-219T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21966638 | |||||||
chr8:21967036 | A | G | 185 | a0001c0001t0002g0011 a0001c0002t0001g0003 a0001c0002t0001g0013 others(182): Show |
198 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.165+33A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967036 | |||||||
chr8:21967087 | G | A | 1 | a0001c0002t0001g0280 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.165+84G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967087 | |||||||
chr8:21967246 | C | T | 2 | a0001c0002t0001g0298 a0001c0002t0001g0311 |
2 | HG03704.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.165+243C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967246 | |||||||
chr8:21967368 | T | C | 3 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 |
3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.165+365T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967368 | |||||||
chr8:21967629 | G | A | 1 | a0001c0002t0001g0256 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.165+626G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967629 | |||||||
chr8:21967768 | A | C | 1 | a0001c0009t0002g0074 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.165+765A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967768 | |||||||
chr8:21967852 | A | G | 1 | a0001c0003t0001g0063 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.165+849A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967852 | |||||||
chr8:21967892 | G | C | 3 | a0001c0001t0002g0155 a0001c0001t0002g0197 a0001c0001t0002g0200 |
3 | HG02040.hp2 HG02165.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.165+889G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967892 | |||||||
chr8:21967968 | G | C | 3 | a0001c0004t0001g0015 a0001c0004t0001g0295 a0001c0004t0001g0310 |
4 | HG01070.hp1 HG01071.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+965G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967968 | |||||||
chr8:21968064 | C | T | 4 | a0001c0002t0001g0051 a0001c0002t0004g0001 a0001c0002t0004g0049 others(1): Show |
6 | NA18947.hp2 NA18957.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+1061C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968064 | |||||||
chr8:21968246 | A | T | 1 | a0001c0001t0002g0129 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.166-1237A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968246 | |||||||
chr8:21968380 | G | A | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0009g0269 |
5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-1103G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968380 | |||||||
chr8:21968424 | A | C | 3 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 |
3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.166-1059A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968424 | |||||||
chr8:21968462 | C | G | 1 | a0001c0003t0001g0088 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.166-1021C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968462 | |||||||
chr8:21968507 | G | A | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.166-976G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968507 | |||||||
chr8:21968592 | A | C | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.166-891A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968592 | |||||||
chr8:21968786 | T | C | 7 | a0001c0003t0001g0033 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
7 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-697T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968786 | |||||||
chr8:21968838 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.166-645G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968838 | |||||||
chr8:21968910 | C | T | 179 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(176): Show |
191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.166-573C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968910 | |||||||
chr8:21969181 | A | G | 13 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(10): Show |
14 | HG02055.hp1 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.166-302A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21969181 | |||||||
chr8:21969210 | T | G | 1 | a0001c0002t0001g0252 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.166-273T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21969210 | |||||||
chr8:21969309 | TTATGC | T | 87 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(84): Show |
95 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.166-169_166-165del others(5): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 21969309 | ||||||
chr8:21969316 | A | G | 3 | a0001c0002t0001g0236 a0001c0002t0001g0258 a0001c0002t0001g0266 |
3 | HG01358.hp2 HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.166-167A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21969316 | |||||||
chr8:21969316 | A | T | 1 | a0001c0001t0002g0128 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.166-167A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21969316 | |||||||
chr8:21969428 | T | C | 3 | a0001c0004t0001g0016 a0001c0004t0001g0296 a0001c0004t0001g0312 |
4 | HG00323.hp1 HG01069.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-55T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21969428 | |||||||
chr8:21969598 | C | T | 11 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(8): Show |
12 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.259+22C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 3/27 | chr8 | 21969598 | |||||||
chr8:21969651 | C | T | 91 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(88): Show |
95 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.259+75C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 3/27 | chr8 | 21969651 | |||||||
chr8:21969722 | T | G | 1 | a0001c0002t0006g0317 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.259+146T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 3/27 | chr8 | 21969722 | |||||||
chr8:21969734 | A | G | 2 | a0001c0006t0005g0263 a0001c0006t0005g0268 |
2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.259+158A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 3/27 | chr8 | 21969734 | |||||||
chr8:21969880 | G | A | 86 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(83): Show |
94 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.260-264G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 3/27 | chr8 | 21969880 | |||||||
chr8:21969947 | A | G | 3 | a0001c0002t0001g0280 a0001c0002t0001g0283 a0001c0002t0002g0281 |
3 | HG03688.hp1 HG03927.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.260-197A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 3/27 | chr8 | 21969947 | |||||||
chr8:21970044 | A | T | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.260-100A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 3/27 | chr8 | 21970044 | |||||||
chr8:21970322 | A | G | 108 | a0001c0002t0001g0007 a0001c0002t0001g0153 a0001c0002t0001g0228 others(105): Show |
113 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.426+12A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21970322 | |||||||
chr8:21970364 | A | C | 1 | a0001c0001t0002g0176 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.426+54A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21970364 | |||||||
chr8:21970369 | A | AAC | 13 | a0001c0001t0002g0174 a0001c0001t0002g0181 a0001c0001t0002g0195 others(10): Show |
13 | HG00733.hp1 HG00735.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.426+81_426+82dupCA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr8 | 21970369 | ||||||
chr8:21970369 | A | AACAC | 102 | a0001c0002t0001g0007 a0001c0002t0001g0046 a0001c0002t0001g0064 others(99): Show |
105 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.426+79_426+82dupCA others(2): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr8 | 21970369 | ||||||
chr8:21970369 | A | AACACAC | 8 | a0001c0003t0001g0002 a0001c0003t0001g0054 a0001c0003t0001g0071 others(5): Show |
10 | HG02027.hp2 HG02083.hp1 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.426+77_426+82dupCA others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr8 | 21970369 | ||||||
chr8:21970661 | C | T | 3 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 |
3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.426+351C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21970661 | |||||||
chr8:21970715 | A | G | 1 | a0001c0001t0002g0324 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.426+405A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21970715 | |||||||
chr8:21970751 | G | A | 1 | a0001c0002t0001g0153 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.426+441G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21970751 | |||||||
chr8:21970784 | C | T | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0009g0269 |
5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.426+474C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21970784 | |||||||
chr8:21970795 | A | G | 1 | a0001c0002t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.426+485A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21970795 | |||||||
chr8:21970805 | G | GA | 7 | a0001c0002t0005g0257 a0001c0002t0005g0260 a0001c0002t0005g0264 others(4): Show |
7 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.426+503dupA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr8 | 21970805 | ||||||
chr8:21970932 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.426+622C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21970932 | |||||||
chr8:21971007 | G | C | 6 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(3): Show |
7 | HG02280.hp2 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.426+697G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971007 | |||||||
chr8:21971036 | A | T | 1 | a0001c0002t0001g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.426+726A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971036 | |||||||
chr8:21971111 | T | C | 1 | a0001c0002t0001g0259 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.427-765T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971111 | |||||||
chr8:21971133 | G | A | 3 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 |
3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.427-743G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971133 | |||||||
chr8:21971270 | G | A | 2 | a0001c0001t0002g0212 a0001c0001t0002g0214 |
2 | NA19000.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.427-606G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971270 | |||||||
chr8:21971347 | C | T | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.427-529C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971347 | |||||||
chr8:21971477 | G | A | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.427-399G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971477 | |||||||
chr8:21971574 | C | G | 2 | a0001c0002t0001g0251 a0003c0012t0001g0250 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.427-302C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971574 | |||||||
chr8:21971712 | T | C | 1 | a0001c0002t0001g0320 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.427-164T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971712 | |||||||
chr8:21971822 | G | A | 1 | a0001c0003t0001g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.427-54G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971822 | |||||||
chr8:21972176 | C | CT | 21 | a0001c0002t0001g0003 a0001c0002t0001g0023 a0001c0002t0001g0024 others(18): Show |
23 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.492+247dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr8 | 21972176 | ||||||
chr8:21972304 | C | G | 1 | a0001c0002t0001g0251 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.492+363C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21972304 | |||||||
chr8:21972360 | TC | T | 3 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 |
3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.492+422delC | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr8 | 21972360 | ||||||
chr8:21972437 | G | A | 184 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(181): Show |
196 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.492+496G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21972437 | |||||||
chr8:21972525 | A | C | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.492+584A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21972525 | |||||||
chr8:21972579 | T | C | 1 | a0001c0002t0005g0257 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.492+638T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21972579 | |||||||
chr8:21972647 | T | C | 186 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(183): Show |
198 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.492+706T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21972647 | |||||||
chr8:21972686 | A | G | 3 | a0001c0002t0001g0158 a0001c0002t0001g0216 a0001c0002t0007g0010 |
4 | HG02280.hp2 HG02572.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.492+745A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21972686 | |||||||
chr8:21972784 | A | G | 96 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(93): Show |
104 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.492+843A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21972784 | |||||||
chr8:21972867 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.492+926G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21972867 | |||||||
chr8:21973019 | A | T | 2 | a0001c0001t0002g0182 a0001c0001t0002g0183 |
2 | HG01934.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.492+1078A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973019 | |||||||
chr8:21973027 | C | A | 2 | a0001c0003t0001g0060 a0001c0003t0001g0061 |
2 | HG01167.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.492+1086C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973027 | |||||||
chr8:21973033 | A | AG | 5 | a0001c0001t0002g0011 a0001c0001t0002g0165 a0001c0001t0002g0218 others(2): Show |
6 | HG00738.hp1 HG01099.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.492+1094dupG | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr8 | 21973033 | ||||||
chr8:21973291 | A | G | 1 | a0001c0003t0001g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.492+1350A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973291 | |||||||
chr8:21973621 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.493-1049G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973621 | |||||||
chr8:21973634 | T | G | 3 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 |
3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.493-1036T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973634 | |||||||
chr8:21973738 | A | C | 2 | a0001c0003t0001g0086 a0001c0003t0001g0107 |
2 | HG00735.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.493-932A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973738 | |||||||
chr8:21973865 | G | A | 45 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0156 others(42): Show |
50 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.493-805G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973865 | |||||||
chr8:21973874 | A | G | 86 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(83): Show |
90 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.493-796A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973874 | |||||||
chr8:21973972 | C | A | 1 | a0001c0001t0002g0139 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.493-698C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973972 | |||||||
chr8:21973993 | CTT | C | 3 | a0001c0002t0005g0257 a0001c0002t0005g0264 a0001c0002t0005g0293 |
3 | HG03195.hp1 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.493-676_493-675del others(2): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973993 | |||||||
chr8:21973999 | C | A | 45 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0156 others(42): Show |
50 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.493-671C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973999 | |||||||
chr8:21974087 | G | GACAGGAT others(3): Show |
204 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0013 others(201): Show |
217 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.493-581_493-580ins others(10): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr8 | 21974087 | ||||||
chr8:21974107 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.493-563A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21974107 | |||||||
chr8:21974208 | T | G | 1 | a0001c0003t0001g0054 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.493-462T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21974208 | |||||||
chr8:21974231 | T | TG | 102 | a0001c0002t0001g0007 a0001c0002t0001g0153 a0001c0002t0001g0228 others(99): Show |
107 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.493-433dupG | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr8 | 21974231 | ||||||
chr8:21974554 | G | T | 1 | a0001c0003t0001g0056 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.493-116G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21974554 | |||||||
chr8:21974983 | A | C | 210 | a0001c0001t0002g0162 a0001c0001t0002g0247 a0001c0002t0001g0003 others(207): Show |
223 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.597+209A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 6/27 | chr8 | 21974983 | |||||||
chr8:21975305 | T | G | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.597+531T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 6/27 | chr8 | 21975305 | |||||||
chr8:21975430 | C | G | 1 | a0001c0002t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.597+656C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 6/27 | chr8 | 21975430 | |||||||
chr8:21975467 | A | G | 1 | a0001c0002t0005g0260 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.597+693A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 6/27 | chr8 | 21975467 | |||||||
chr8:21975575 | C | T | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.598-781C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 6/27 | chr8 | 21975575 | |||||||
chr8:21975729 | C | G | 13 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(10): Show |
14 | HG02055.hp1 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.598-627C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 6/27 | chr8 | 21975729 | |||||||
chr8:21975863 | G | C | 93 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(90): Show |
101 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.598-493G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 6/27 | chr8 | 21975863 | |||||||
chr8:21976336 | T | C | 1 | a0001c0006t0005g0263 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.598-20T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 6/27 | chr8 | 21976336 | |||||||
chr8:21976532 | T | C | 1 | a0001c0003t0001g0109 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.763+11T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21976532 | |||||||
chr8:21976855 | A | C | 186 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(183): Show |
198 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.763+334A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21976855 | |||||||
chr8:21976893 | A | C | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.763+372A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21976893 | |||||||
chr8:21976895 | G | C | 1 | a0001c0002t0001g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.763+374G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21976895 | |||||||
chr8:21976932 | T | G | 1 | a0001c0003t0001g0068 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.763+411T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21976932 | |||||||
chr8:21976945 | C | G | 96 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(93): Show |
104 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.763+424C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21976945 | |||||||
chr8:21977004 | C | T | 1 | a0001c0001t0002g0020 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.763+483C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21977004 | |||||||
chr8:21977056 | A | G | 86 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(83): Show |
90 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.763+535A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21977056 | |||||||
chr8:21977070 | T | C | 189 | a0001c0001t0002g0011 a0001c0002t0001g0003 a0001c0002t0001g0013 others(186): Show |
202 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.763+549T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21977070 | |||||||
chr8:21977303 | G | A | 31 | a0001c0002t0001g0025 a0001c0002t0001g0298 a0001c0002t0001g0299 others(28): Show |
33 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.764-467G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21977303 | |||||||
chr8:21977490 | A | G | 1 | a0001c0002t0001g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.764-280A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21977490 | |||||||
chr8:21977567 | A | C | 1 | a0001c0002t0005g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.764-203A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21977567 | |||||||
chr8:21977706 | G | A | 1 | a0001c0002t0005g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.764-64G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21977706 | |||||||
chr8:21977859 | C | T | 2 | a0001c0002t0001g0258 a0001c0002t0001g0266 |
2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.837+16C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21977859 | |||||||
chr8:21977930 | A | G | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.837+87A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21977930 | |||||||
chr8:21977954 | A | G | 86 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(83): Show |
90 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.837+111A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21977954 | |||||||
chr8:21978041 | C | T | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.837+198C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978041 | |||||||
chr8:21978043 | G | T | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.837+200G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978043 | |||||||
chr8:21978074 | C | CT | 96 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(93): Show |
104 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.837+232dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr8 | 21978074 | ||||||
chr8:21978117 | A | G | 86 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(83): Show |
90 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.837+274A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978117 | |||||||
chr8:21978307 | T | C | 3 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 |
3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.837+464T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978307 | |||||||
chr8:21978396 | G | A | 95 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(92): Show |
103 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.837+553G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978396 | |||||||
chr8:21978509 | A | G | 53 | a0001c0003t0001g0005 a0001c0003t0001g0071 a0001c0003t0001g0073 others(50): Show |
54 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.837+666A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978509 | |||||||
chr8:21978838 | G | A | 2 | a0001c0002t0001g0252 a0001c0002t0001g0253 |
2 | HG00733.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.837+995G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978838 | |||||||
chr8:21978873 | C | G | 88 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0003t0001g0002 others(85): Show |
92 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.837+1030C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978873 | |||||||
chr8:21978875 | A | T | 1 | a0001c0002t0004g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.837+1032A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978875 | |||||||
chr8:21979203 | G | A | 2 | a0001c0002t0001g0258 a0001c0002t0001g0266 |
2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.838-881G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21979203 | |||||||
chr8:21979217 | A | G | 186 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(183): Show |
198 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.838-867A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21979217 | |||||||
chr8:21979382 | ATTTCTTT others(4): Show |
A | 1 | a0001c0001t0002g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.838-687_838-677del others(11): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr8 | 21979382 | ||||||
chr8:21979397 | C | CT | 9 | a0001c0002t0001g0278 a0001c0002t0001g0279 a0001c0002t0001g0280 others(6): Show |
9 | HG02738.hp2 HG03688.hp1 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.838-676dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr8 | 21979397 | ||||||
chr8:21979397 | C | T | 1 | a0001c0002t0001g0245 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.838-687C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21979397 | |||||||
chr8:21979410 | G | GT | 10 | a0001c0001t0002g0133 a0001c0001t0002g0144 a0001c0001t0002g0205 others(7): Show |
10 | HG00738.hp2 HG02056.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.838-665dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr8 | 21979410 | ||||||
chr8:21979712 | G | A | 2 | a0001c0001t0002g0150 a0001c0001t0002g0211 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.838-372G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21979712 | |||||||
chr8:21980290 | G | A | 2 | a0001c0002t0001g0252 a0001c0002t0001g0253 |
2 | HG00733.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.957+87G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980290 | |||||||
chr8:21980367 | A | C | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0009g0269 |
5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.957+164A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980367 | |||||||
chr8:21980410 | A | G | 1 | a0001c0002t0001g0320 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.957+207A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980410 | |||||||
chr8:21980483 | C | G | 93 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(90): Show |
101 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.957+280C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980483 | |||||||
chr8:21980638 | G | A | 2 | a0001c0002t0004g0289 a0001c0002t0004g0290 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.957+435G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980638 | |||||||
chr8:21980769 | C | T | 2 | a0001c0002t0001g0046 a0001c0002t0001g0065 |
2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.957+566C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980769 | |||||||
chr8:21980774 | C | CA | 8 | a0001c0002t0001g0245 a0001c0002t0001g0286 a0001c0002t0002g0249 others(5): Show |
8 | HG02056.hp2 HG02071.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.957+587dupA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr8 | 21980774 | ||||||
chr8:21980778 | A | G | 2 | a0001c0002t0004g0289 a0001c0002t0004g0290 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.957+575A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980778 | |||||||
chr8:21980831 | A | C | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.957+628A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980831 | |||||||
chr8:21980870 | G | A | 3 | a0001c0002t0001g0158 a0001c0002t0001g0216 a0001c0002t0007g0010 |
4 | HG02280.hp2 HG02572.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.957+667G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980870 | |||||||
chr8:21980999 | C | CA | 111 | a0001c0002t0001g0007 a0001c0002t0001g0046 a0001c0002t0001g0064 others(108): Show |
116 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.958-731dupA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr8 | 21980999 | ||||||
chr8:21981159 | T | A | 208 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0013 others(205): Show |
221 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.958-572T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981159 | |||||||
chr8:21981220 | T | C | 2 | a0001c0002t0004g0289 a0001c0002t0004g0290 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.958-511T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981220 | |||||||
chr8:21981274 | T | C | 1 | a0001c0002t0005g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.958-457T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981274 | |||||||
chr8:21981278 | T | C | 95 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(92): Show |
103 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.958-453T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981278 | |||||||
chr8:21981327 | C | T | 2 | a0001c0002t0001g0014 a0001c0003t0001g0091 |
3 | HG02109.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.958-404C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981327 | |||||||
chr8:21981357 | T | G | 10 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(7): Show |
10 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.958-374T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981357 | |||||||
chr8:21981468 | C | G | 3 | a0001c0002t0001g0261 a0001c0002t0001g0262 a0001c0002t0001g0267 |
3 | HG02055.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.958-263C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981468 | |||||||
chr8:21981509 | T | C | 95 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(92): Show |
103 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.958-222T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981509 | |||||||
chr8:21981524 | A | G | 6 | a0001c0002t0005g0257 a0001c0002t0005g0264 a0001c0002t0005g0265 others(3): Show |
6 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.958-207A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981524 | |||||||
chr8:21981582 | T | G | 95 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(92): Show |
103 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.958-149T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981582 | |||||||
chr8:21981589 | G | A | 2 | a0001c0002t0004g0289 a0001c0002t0004g0290 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.958-142G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981589 | |||||||
chr8:21981603 | C | T | 3 | a0001c0002t0006g0317 a0001c0002t0006g0318 a0001c0002t0006g0319 |
3 | HG02818.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.958-128C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981603 | |||||||
chr8:21981662 | A | C | 1 | a0001c0002t0004g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.958-69A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981662 | |||||||
chr8:21982157 | G | A | 93 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(90): Show |
101 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.1104+280G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982157 | |||||||
chr8:21982213 | T | C | 1 | a0001c0002t0001g0259 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1104+336T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982213 | |||||||
chr8:21982254 | A | C | 1 | a0001c0001t0002g0128 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1104+377A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982254 | |||||||
chr8:21982368 | A | G | 1 | a0001c0003t0001g0035 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1105-272A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982368 | |||||||
chr8:21982400 | T | C | 4 | a0001c0002t0001g0157 a0001c0002t0001g0158 a0001c0002t0001g0216 others(1): Show |
5 | HG02280.hp2 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1105-240T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982400 | |||||||
chr8:21982410 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1105-230T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982410 | |||||||
chr8:21982486 | A | G | 2 | a0001c0001t0002g0182 a0001c0001t0002g0183 |
2 | HG01934.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1105-154A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982486 | |||||||
chr8:21982541 | T | A | 1 | a0001c0003t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1105-99T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982541 | |||||||
chr8:21982541 | T | TA | 108 | a0001c0002t0001g0007 a0001c0002t0001g0046 a0001c0002t0001g0064 others(105): Show |
113 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1105-91dupA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr8 | 21982541 | ||||||
chr8:21982542 | A | T | 1 | a0001c0002t0001g0262 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1105-98A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982542 | |||||||
chr8:21982568 | C | G | 1 | a0001c0002t0001g0308 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1105-72C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982568 | |||||||
chr8:21982858 | T | C | 1 | a0001c0003t0001g0103 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1277+46T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21982858 | |||||||
chr8:21982899 | A | G | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1277+87A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21982899 | |||||||
chr8:21982908 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1277+96G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21982908 | |||||||
chr8:21983023 | A | G | 114 | a0001c0002t0001g0007 a0001c0002t0001g0030 a0001c0002t0001g0031 others(111): Show |
119 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1277+211A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983023 | |||||||
chr8:21983212 | G | A | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1277+400G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983212 | |||||||
chr8:21983327 | C | T | 1 | a0003c0012t0001g0250 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1277+515C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983327 | |||||||
chr8:21983397 | A | G | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1277+585A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983397 | |||||||
chr8:21983504 | A | G | 1 | a0001c0002t0001g0245 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1277+692A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983504 | |||||||
chr8:21983586 | T | G | 1 | a0001c0009t0002g0074 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1277+774T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983586 | |||||||
chr8:21983587 | T | C | 1 | a0001c0009t0002g0074 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1277+775T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983587 | |||||||
chr8:21983666 | T | C | 2 | a0001c0006t0005g0263 a0001c0006t0005g0268 |
2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1277+854T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983666 | |||||||
chr8:21983682 | C | T | 1 | a0001c0003t0001g0078 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1277+870C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983682 | |||||||
chr8:21983844 | GTGCTGCT others(11): Show |
G | 1 | a0001c0004t0001g0295 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1278-791_1278-774d others(20): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr8 | 21983844 | ||||||
chr8:21983852 | GCTC | G | 3 | a0001c0002t0006g0317 a0001c0002t0006g0318 a0001c0002t0006g0319 |
3 | HG02818.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1278-791_1278-789d others(5): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr8 | 21983852 | ||||||
chr8:21983855 | CCTGCTG | C | 50 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(47): Show |
56 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1278-777_1278-772d others(8): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr8 | 21983855 | ||||||
chr8:21983861 | G | C | 3 | a0001c0002t0006g0317 a0001c0002t0006g0318 a0001c0002t0006g0319 |
3 | HG02818.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1278-785G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983861 | |||||||
chr8:21983885 | T | C | 209 | a0001c0001t0002g0011 a0001c0002t0001g0003 a0001c0002t0001g0007 others(206): Show |
223 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.1278-761T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983885 | |||||||
chr8:21983965 | C | A | 1 | a0001c0002t0001g0245 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1278-681C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983965 | |||||||
chr8:21984037 | A | G | 4 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0251 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1278-609A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984037 | |||||||
chr8:21984065 | C | T | 2 | a0001c0002t0001g0023 a0001c0002t0001g0029 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1278-581C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984065 | |||||||
chr8:21984099 | A | T | 1 | a0001c0002t0001g0245 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1278-547A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984099 | |||||||
chr8:21984110 | T | C | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1278-536T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984110 | |||||||
chr8:21984153 | G | T | 2 | a0001c0002t0004g0289 a0001c0002t0004g0290 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1278-493G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984153 | |||||||
chr8:21984186 | G | C | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1278-460G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984186 | |||||||
chr8:21984203 | A | G | 1 | a0001c0001t0002g0203 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1278-443A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984203 | |||||||
chr8:21984352 | C | G | 186 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(183): Show |
198 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.1278-294C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984352 | |||||||
chr8:21984512 | T | G | 320 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(317): Show |
338 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(335): Show |
intron_variant | MODIFIER | c.1278-134T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984512 | |||||||
chr8:21984513 | T | A | 321 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(318): Show |
339 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.1278-133T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984513 | |||||||
chr8:21984552 | T | C | 111 | a0001c0002t0001g0007 a0001c0002t0001g0046 a0001c0002t0001g0064 others(108): Show |
116 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1278-94T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984552 | |||||||
chr8:21984628 | T | C | 1 | a0001c0003t0001g0043 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1278-18T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984628 | |||||||
chr8:21984882 | T | C | 3 | a0001c0002t0001g0274 a0001c0002t0001g0276 a0001c0002t0001g0287 |
3 | NA18612.hp1 NA19000.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1471+43T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 12/27 | chr8 | 21984882 | |||||||
chr8:21984974 | A | T | 3 | a0001c0001t0002g0169 a0001c0001t0002g0215 a0001c0001t0010g0142 |
3 | NA18984.hp2 NA18997.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1471+135A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 12/27 | chr8 | 21984974 | |||||||
chr8:21985074 | G | GC | 206 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0013 others(203): Show |
219 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.1471+237dupC | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr8 | 21985074 | ||||||
chr8:21985079 | G | A | 1 | a0001c0003t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1471+240G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 12/27 | chr8 | 21985079 | |||||||
chr8:21985217 | G | C | 95 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(92): Show |
103 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.1472-369G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 12/27 | chr8 | 21985217 | |||||||
chr8:21985240 | G | C | 208 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0013 others(205): Show |
221 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.1472-346G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 12/27 | chr8 | 21985240 | |||||||
chr8:21985564 | C | G | 3 | a0001c0002t0001g0271 a0001c0002t0001g0288 a0001c0002t0008g0270 |
3 | HG04115.hp1 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1472-22C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 12/27 | chr8 | 21985564 | |||||||
chr8:21985781 | T | G | 1 | a0001c0001t0002g0222 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1577+90T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21985781 | |||||||
chr8:21986134 | A | T | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1577+443A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986134 | |||||||
chr8:21986135 | C | CT | 10 | a0001c0001t0002g0019 a0001c0002t0001g0046 a0001c0002t0001g0065 others(7): Show |
10 | HG01169.hp2 HG02300.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1577+463dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr8 | 21986135 | ||||||
chr8:21986135 | CT | C | 23 | a0001c0001t0002g0129 a0001c0002t0001g0051 a0001c0002t0001g0156 others(20): Show |
26 | HG01433.hp1 HG02055.hp1 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.1577+463delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr8 | 21986135 | ||||||
chr8:21986135 | CTT | C | 14 | a0001c0002t0001g0273 a0001c0002t0001g0274 a0001c0002t0001g0275 others(11): Show |
14 | HG02738.hp2 HG03688.hp1 HG03927.hp2 others(11): Show |
intron_variant | MODIFIER | c.1577+462_1577+463d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr8 | 21986135 | ||||||
chr8:21986178 | C | T | 1 | a0001c0002t0001g0274 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1577+487C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986178 | |||||||
chr8:21986224 | G | A | 1 | a0001c0003t0001g0063 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1577+533G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986224 | |||||||
chr8:21986463 | A | T | 3 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 |
3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1578-678A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986463 | |||||||
chr8:21986484 | T | G | 1 | a0001c0001t0002g0208 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1578-657T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986484 | |||||||
chr8:21986585 | T | C | 22 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0032 others(19): Show |
25 | HG00323.hp2 HG01109.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1578-556T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986585 | |||||||
chr8:21986663 | G | A | 1 | a0001c0002t0005g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1578-478G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986663 | |||||||
chr8:21986754 | A | G | 187 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(184): Show |
199 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1578-387A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986754 | |||||||
chr8:21986971 | T | C | 1 | a0001c0004t0001g0303 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1578-170T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986971 | |||||||
chr8:21987022 | G | C | 1 | a0001c0002t0009g0269 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1578-119G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21987022 | |||||||
chr8:21987032 | G | C | 1 | a0001c0001t0002g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1578-109G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21987032 | |||||||
chr8:21987066 | G | A | 4 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578-75G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21987066 | |||||||
chr8:21987353 | G | C | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1713+77G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 14/27 | chr8 | 21987353 | |||||||
chr8:21987380 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1713+104C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 14/27 | chr8 | 21987380 | |||||||
chr8:21987391 | A | G | 9 | a0001c0003t0001g0073 a0001c0003t0001g0075 a0001c0003t0001g0077 others(6): Show |
9 | NA18747.hp1 NA18944.hp1 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.1713+115A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 14/27 | chr8 | 21987391 | |||||||
chr8:21987917 | T | C | 205 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0013 others(202): Show |
218 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.1787+60T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 15/27 | chr8 | 21987917 | |||||||
chr8:21988108 | G | T | 93 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(90): Show |
101 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.1787+251G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 15/27 | chr8 | 21988108 | |||||||
chr8:21988226 | G | T | 2 | a0001c0003t0003g0085 a0001c0003t0003g0102 |
2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1787+369G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 15/27 | chr8 | 21988226 | |||||||
chr8:21988237 | G | A | 1 | a0001c0001t0002g0006 | 2 | NA18959.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1787+380G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 15/27 | chr8 | 21988237 | |||||||
chr8:21988344 | G | A | 26 | a0001c0002t0001g0051 a0001c0002t0001g0124 a0001c0002t0001g0271 others(23): Show |
28 | HG01433.hp1 HG02056.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.1787+487G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 15/27 | chr8 | 21988344 | |||||||
chr8:21988385 | A | T | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1787+528A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 15/27 | chr8 | 21988385 | |||||||
chr8:21989275 | G | A | 1 | a0001c0003t0001g0094 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1868+192G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989275 | |||||||
chr8:21989356 | A | G | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1868+273A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989356 | |||||||
chr8:21989477 | A | T | 1 | a0001c0001t0002g0012 | 2 | HG00438.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1868+394A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989477 | |||||||
chr8:21989492 | C | G | 7 | a0001c0001t0002g0009 a0001c0001t0002g0022 a0001c0001t0002g0141 others(4): Show |
8 | HG01257.hp2 HG01258.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1868+409C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989492 | |||||||
chr8:21989514 | A | G | 1 | a0001c0003t0001g0094 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1868+431A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989514 | |||||||
chr8:21989724 | T | C | 206 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0013 others(203): Show |
219 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.1869-620T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989724 | |||||||
chr8:21989820 | C | G | 206 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0013 others(203): Show |
219 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.1869-524C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989820 | |||||||
chr8:21989821 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0002g0171 a0001c0001t0002g0173 |
2 | HG04115.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1869-486_1869-477d others(12): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0002g0128 a0001c0001t0002g0130 |
2 | NA18982.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1869-488_1869-477d others(14): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | C | CTTTTTTT others(7): Show |
1 | a0001c0003t0001g0061 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1869-490_1869-477d others(16): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0002g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1869-491_1869-477d others(17): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0002g0121 a0001c0003t0001g0034 |
2 | HG01361.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1869-492_1869-477d others(18): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | C | CTTTTTTT others(10): Show |
1 | a0001c0003t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1869-493_1869-477d others(19): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CT | C | 6 | a0001c0002t0001g0153 a0001c0002t0001g0238 a0001c0002t0001g0241 others(3): Show |
6 | HG01255.hp2 NA18962.hp1 NA19057.hp2 others(3): Show |
intron_variant | MODIFIER | c.1869-477delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTT | C | 10 | a0001c0001t0002g0144 a0001c0001t0002g0192 a0001c0001t0002g0199 others(7): Show |
10 | HG00621.hp2 HG01928.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1869-478_1869-477d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTT | C | 24 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0161 others(21): Show |
24 | HG00423.hp2 HG00558.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1869-479_1869-477d others(5): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTT | C | 29 | a0001c0001t0002g0012 a0001c0001t0002g0018 a0001c0001t0002g0019 others(26): Show |
31 | HG00438.hp2 HG00621.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869-480_1869-477d others(6): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTT | C | 42 | a0001c0001t0002g0017 a0001c0001t0002g0020 a0001c0001t0002g0021 others(39): Show |
43 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1869-481_1869-477d others(7): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTT | C | 36 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0011 others(33): Show |
39 | HG00423.hp1 HG00735.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1869-482_1869-477d others(8): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTTT | C | 10 | a0001c0001t0002g0160 a0001c0001t0002g0195 a0001c0003t0001g0040 others(7): Show |
10 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1869-483_1869-477d others(9): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0002g0209 a0001c0003t0001g0036 a0001c0003t0001g0063 |
3 | HG00741.hp1 HG01346.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1869-486_1869-477d others(12): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0002g0006 a0001c0003t0001g0055 |
3 | NA18959.hp1 NA18962.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1869-487_1869-477d others(13): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTTT others(6): Show |
C | 1 | a0001c0003t0001g0052 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1869-489_1869-477d others(15): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTTT others(7): Show |
C | 4 | a0001c0001t0011g0246 a0001c0003t0001g0004 a0001c0003t0001g0039 others(1): Show |
5 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1869-490_1869-477d others(16): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTTT others(8): Show |
C | 1 | a0001c0003t0001g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1869-491_1869-477d others(17): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTTT others(11): Show |
C | 4 | a0001c0002t0001g0231 a0001c0003t0001g0033 a0001c0003t0001g0053 others(1): Show |
4 | HG00438.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1869-494_1869-477d others(20): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTTT others(12): Show |
C | 1 | a0001c0003t0001g0114 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1869-495_1869-477d others(21): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTTT others(13): Show |
C | 2 | a0001c0002t0004g0289 a0001c0003t0012g0069 |
2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1869-496_1869-477d others(22): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0002g0176 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1869-497_1869-477d others(23): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTTT others(15): Show |
C | 2 | a0001c0001t0002g0204 a0001c0001t0002g0220 |
2 | HG02155.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.1869-498_1869-477d others(24): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTTT others(18): Show |
C | 5 | a0001c0003t0001g0002 a0001c0003t0001g0032 a0001c0003t0001g0054 others(2): Show |
7 | HG02027.hp2 HG02083.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.1869-501_1869-477d others(27): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTTT others(19): Show |
C | 2 | a0001c0002t0001g0283 a0001c0002t0001g0286 |
2 | HG02056.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1869-502_1869-477d others(28): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTTT others(20): Show |
C | 33 | a0001c0002t0001g0051 a0001c0002t0001g0124 a0001c0002t0001g0157 others(30): Show |
36 | HG01358.hp1 HG01433.hp1 HG01928.hp1 others(33): Show |
intron_variant | MODIFIER | c.1869-503_1869-477d others(29): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTTT others(21): Show |
C | 61 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(58): Show |
66 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.1869-504_1869-477d others(30): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTTT others(22): Show |
C | 1 | a0001c0001t0002g0316 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1869-505_1869-477d others(31): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989821 | CTTTTTTT others(24): Show |
C | 1 | a0001c0003t0001g0116 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1869-507_1869-477d others(33): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | ||||||
chr8:21989887 | T | C | 29 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0051 others(26): Show |
31 | HG01433.hp1 HG02056.hp2 HG02451.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869-457T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989887 | |||||||
chr8:21989905 | A | G | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1869-439A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989905 | |||||||
chr8:21989913 | G | A | 95 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(92): Show |
103 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.1869-431G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989913 | |||||||
chr8:21989932 | C | T | 4 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0004g0290 others(1): Show |
6 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1869-412C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989932 | |||||||
chr8:21990085 | G | C | 2 | a0001c0003t0001g0097 a0001c0003t0001g0098 |
2 | NA18747.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1869-259G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21990085 | |||||||
chr8:21990144 | C | T | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1869-200C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21990144 | |||||||
chr8:21990235 | T | A | 1 | a0001c0003t0001g0114 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1869-109T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21990235 | |||||||
chr8:21990236 | A | T | 4 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0004g0290 others(1): Show |
6 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1869-108A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21990236 | |||||||
chr8:21990301 | G | A | 2 | a0001c0002t0001g0251 a0003c0012t0001g0250 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1869-43G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21990301 | |||||||
chr8:21990464 | C | T | 2 | a0001c0002t0001g0258 a0001c0002t0001g0266 |
2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1932+57C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 17/27 | chr8 | 21990464 | |||||||
chr8:21990538 | A | G | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1932+131A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 17/27 | chr8 | 21990538 | |||||||
chr8:21990558 | C | T | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0009g0269 |
5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1932+151C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 17/27 | chr8 | 21990558 | |||||||
chr8:21990583 | C | G | 1 | a0001c0002t0005g0257 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1932+176C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 17/27 | chr8 | 21990583 | |||||||
chr8:21990621 | C | T | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1933-190C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 17/27 | chr8 | 21990621 | |||||||
chr8:21990739 | C | G | 1 | a0001c0001t0002g0172 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1933-72C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 17/27 | chr8 | 21990739 | |||||||
chr8:21991009 | C | G | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0009g0269 |
5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+90C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991009 | |||||||
chr8:21991018 | T | C | 1 | a0001c0003t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2041+99T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991018 | |||||||
chr8:21991108 | T | G | 1 | a0001c0002t0005g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2041+189T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991108 | |||||||
chr8:21991116 | T | C | 1 | a0001c0002t0005g0257 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2041+197T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991116 | |||||||
chr8:21991119 | TCCTGAAG others(8): Show |
T | 1 | a0001c0003t0003g0092 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2041+201_2041+215d others(17): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991119 | |||||||
chr8:21991133 | T | C | 1 | a0001c0001t0002g0128 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2041+214T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991133 | |||||||
chr8:21991173 | G | T | 1 | a0001c0001t0002g0206 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2041+254G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991173 | |||||||
chr8:21991224 | A | G | 1 | a0001c0002t0001g0277 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2041+305A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991224 | |||||||
chr8:21991237 | C | A | 1 | a0001c0003t0001g0060 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2041+318C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991237 | |||||||
chr8:21991303 | G | A | 1 | a0001c0001t0002g0316 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2041+384G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991303 | |||||||
chr8:21991321 | T | A | 207 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0013 others(204): Show |
220 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.2041+402T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991321 | |||||||
chr8:21991347 | T | C | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2041+428T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991347 | |||||||
chr8:21991372 | A | T | 3 | a0001c0002t0001g0292 a0001c0006t0005g0263 a0001c0006t0005g0268 |
3 | HG02055.hp2 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2041+453A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991372 | |||||||
chr8:21991497 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2042-371G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991497 | |||||||
chr8:21991689 | T | G | 3 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 |
3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2042-179T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991689 | |||||||
chr8:21992006 | G | C | 2 | a0001c0003t0003g0092 a0001c0003t0003g0111 |
2 | NA18965.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.2148+32G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21992006 | |||||||
chr8:21992055 | C | T | 74 | a0001c0002t0001g0007 a0001c0002t0001g0153 a0001c0002t0001g0228 others(71): Show |
76 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.2148+81C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21992055 | |||||||
chr8:21992205 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2148+231T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21992205 | |||||||
chr8:21992386 | T | A | 3 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 |
3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2148+412T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21992386 | |||||||
chr8:21992451 | T | C | 108 | a0001c0002t0001g0007 a0001c0002t0001g0153 a0001c0002t0001g0228 others(105): Show |
113 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2148+477T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21992451 | |||||||
chr8:21992605 | A | G | 209 | a0001c0001t0002g0011 a0001c0002t0001g0003 a0001c0002t0001g0007 others(206): Show |
223 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.2148+631A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21992605 | |||||||
chr8:21992958 | A | G | 1 | a0001c0002t0001g0233 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2148+984A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21992958 | |||||||
chr8:21993019 | A | G | 1 | a0001c0003t0001g0082 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2148+1045A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21993019 | |||||||
chr8:21993145 | A | G | 94 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(91): Show |
102 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.2148+1171A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21993145 | |||||||
chr8:21993147 | CTT | C | 23 | a0001c0002t0001g0298 a0001c0002t0001g0299 a0001c0002t0001g0305 others(20): Show |
25 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.2148+1175_2148+117 others(6): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr8 | 21993147 | ||||||
chr8:21993176 | G | A | 106 | a0001c0002t0001g0007 a0001c0002t0001g0153 a0001c0002t0001g0228 others(103): Show |
111 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.2149-1187G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21993176 | |||||||
chr8:21993194 | G | T | 1 | a0001c0003t0001g0119 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2149-1169G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21993194 | |||||||
chr8:21993201 | A | C | 1 | a0001c0001t0002g0185 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2149-1162A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21993201 | |||||||
chr8:21993590 | G | A | 5 | a0001c0002t0005g0257 a0001c0002t0005g0260 a0001c0002t0005g0264 others(2): Show |
5 | HG02572.hp1 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2149-773G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21993590 | |||||||
chr8:21993616 | T | C | 1 | a0001c0003t0001g0032 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2149-747T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21993616 | |||||||
chr8:21993915 | G | GTC | 58 | a0001c0001t0002g0316 a0001c0002t0001g0003 a0001c0002t0001g0023 others(55): Show |
62 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.2149-424_2149-423d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr8 | 21993915 | ||||||
chr8:21993915 | G | GTCTC | 9 | a0001c0001t0002g0011 a0001c0002t0001g0013 a0001c0002t0001g0014 others(6): Show |
12 | HG00738.hp1 HG01099.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2149-426_2149-423d others(6): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr8 | 21993915 | ||||||
chr8:21993915 | G | GTCTCTC | 3 | a0001c0002t0001g0266 a0001c0002t0001g0284 a0001c0002t0001g0285 |
3 | HG02258.hp1 NA18955.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.2149-428_2149-423d others(8): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr8 | 21993915 | ||||||
chr8:21993997 | G | A | 1 | a0001c0004t0001g0295 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2149-366G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21993997 | |||||||
chr8:21994016 | C | T | 3 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 |
3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2149-347C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21994016 | |||||||
chr8:21994064 | C | G | 1 | a0001c0002t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2149-299C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21994064 | |||||||
chr8:21994283 | A | C | 1 | a0001c0003t0012g0069 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2149-80A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21994283 | |||||||
chr8:21994322 | T | A | 1 | a0001c0003t0003g0092 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2149-41T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21994322 | |||||||
chr8:21994738 | G | C | 1 | a0001c0001t0002g0170 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2237+287G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | chr8 | 21994738 | |||||||
chr8:21995064 | AAATAAT | A | 94 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(91): Show |
102 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.2238-410_2238-405d others(8): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 21995064 | ||||||
chr8:21995070 | T | A | 1 | a0001c0002t0005g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2238-422T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | chr8 | 21995070 | |||||||
chr8:21995122 | G | A | 1 | a0001c0003t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2238-370G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | chr8 | 21995122 | |||||||
chr8:21995176 | T | C | 4 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0251 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2238-316T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | chr8 | 21995176 | |||||||
chr8:21995200 | T | C | 1 | a0001c0001t0002g0202 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2238-292T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | chr8 | 21995200 | |||||||
chr8:21995206 | A | T | 1 | a0001c0002t0001g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2238-286A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | chr8 | 21995206 | |||||||
chr8:21995300 | C | G | 8 | a0001c0002t0001g0230 a0001c0002t0001g0231 a0001c0002t0001g0232 others(5): Show |
8 | NA18949.hp2 NA18970.hp2 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.2238-192C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | chr8 | 21995300 | |||||||
chr8:21995368 | A | C | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2238-124A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | chr8 | 21995368 | |||||||
chr8:21995780 | T | C | 1 | a0001c0001t0002g0184 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2345+181T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21995780 | |||||||
chr8:21995917 | G | A | 2 | a0001c0002t0001g0251 a0003c0012t0001g0250 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2345+318G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21995917 | |||||||
chr8:21995940 | G | A | 2 | a0001c0002t0001g0256 a0001c0003t0001g0044 |
2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2345+341G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21995940 | |||||||
chr8:21996109 | C | T | 4 | a0001c0002t0001g0305 a0001c0002t0001g0306 a0001c0002t0001g0307 others(1): Show |
4 | HG01358.hp1 HG01928.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.2345+510C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21996109 | |||||||
chr8:21996222 | T | C | 83 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(80): Show |
87 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.2345+623T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21996222 | |||||||
chr8:21996559 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2345+960T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21996559 | |||||||
chr8:21996677 | T | A | 177 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(174): Show |
189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.2345+1078T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21996677 | |||||||
chr8:21996966 | G | A | 83 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(80): Show |
87 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.2345+1367G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21996966 | |||||||
chr8:21997014 | G | T | 1 | a0001c0002t0001g0236 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2345+1415G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997014 | |||||||
chr8:21997061 | G | T | 1 | a0001c0002t0001g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2345+1462G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997061 | |||||||
chr8:21997149 | T | C | 3 | a0001c0002t0006g0317 a0001c0002t0006g0318 a0001c0002t0006g0319 |
3 | HG02818.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2345+1550T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997149 | |||||||
chr8:21997203 | A | C | 1 | a0001c0002t0001g0286 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2346-1552A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997203 | |||||||
chr8:21997208 | A | C | 1 | a0001c0003t0003g0092 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2346-1547A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997208 | |||||||
chr8:21997384 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2346-1371G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997384 | |||||||
chr8:21997613 | C | G | 2 | a0001c0006t0005g0263 a0001c0006t0005g0268 |
2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2346-1142C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997613 | |||||||
chr8:21997784 | G | C | 1 | a0001c0001t0002g0247 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2346-971G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997784 | |||||||
chr8:21997846 | G | T | 1 | a0001c0002t0001g0245 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2346-909G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997846 | |||||||
chr8:21997847 | G | C | 4 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0004g0289 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2346-908G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997847 | |||||||
chr8:21997889 | C | A | 1 | a0001c0001t0002g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2346-866C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997889 | |||||||
chr8:21998042 | A | G | 1 | a0001c0002t0005g0260 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2346-713A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21998042 | |||||||
chr8:21998169 | C | T | 10 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 others(7): Show |
11 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2346-586C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21998169 | |||||||
chr8:21998213 | G | A | 1 | a0001c0005t0002g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2346-542G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21998213 | |||||||
chr8:21998269 | A | G | 206 | a0001c0001t0002g0011 a0001c0002t0001g0003 a0001c0002t0001g0007 others(203): Show |
220 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.2346-486A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21998269 | |||||||
chr8:21998309 | C | T | 2 | a0001c0001t0002g0195 a0001c0001t0002g0210 |
2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.2346-446C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21998309 | |||||||
chr8:21998310 | G | A | 2 | a0001c0001t0002g0161 a0001c0001t0002g0217 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2346-445G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21998310 | |||||||
chr8:21998398 | G | A | 1 | a0001c0001t0002g0170 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2346-357G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21998398 | |||||||
chr8:21998752 | C | T | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | splice_region_variant&intron_variant | LOW | c.2346-3C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21998752 | |||||||
chr8:21998866 | G | T | 3 | a0001c0002t0005g0257 a0001c0002t0005g0264 a0001c0002t0005g0293 |
3 | HG03195.hp1 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2428+29G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 22/27 | chr8 | 21998866 | |||||||
chr8:21998894 | T | C | 3 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0004g0289 |
3 | HG02451.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2428+57T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 22/27 | chr8 | 21998894 | |||||||
chr8:21999043 | G | C | 5 | a0001c0003t0003g0070 a0001c0003t0003g0085 a0001c0003t0003g0092 others(2): Show |
5 | NA18942.hp1 NA18950.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2429-48G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 22/27 | chr8 | 21999043 | |||||||
chr8:21999046 | C | T | 4 | a0001c0001t0002g0122 a0001c0001t0002g0212 a0001c0001t0002g0213 others(1): Show |
4 | NA19000.hp1 NA19005.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.2429-45C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 22/27 | chr8 | 21999046 | |||||||
chr8:21999052 | T | C | 5 | a0001c0003t0003g0070 a0001c0003t0003g0085 a0001c0003t0003g0092 others(2): Show |
5 | NA18942.hp1 NA18950.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2429-39T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 22/27 | chr8 | 21999052 | |||||||
chr8:21999500 | G | C | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2644-36G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 23/27 | chr8 | 21999500 | |||||||
chr8:21999756 | G | A | 104 | a0001c0002t0001g0007 a0001c0002t0001g0153 a0001c0002t0001g0228 others(101): Show |
109 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.2782+82G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 21999756 | |||||||
chr8:21999872 | T | A | 1 | a0001c0007t0001g0314 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2782+198T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 21999872 | |||||||
chr8:22000068 | A | G | 2 | a0001c0006t0005g0263 a0001c0006t0005g0268 |
2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2782+394A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000068 | |||||||
chr8:22000097 | G | A | 1 | a0001c0002t0001g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2782+423G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000097 | |||||||
chr8:22000104 | A | G | 1 | a0001c0002t0005g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2782+430A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000104 | |||||||
chr8:22000276 | G | A | 105 | a0001c0002t0001g0007 a0001c0002t0001g0153 a0001c0002t0001g0228 others(102): Show |
110 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.2782+602G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000276 | |||||||
chr8:22000280 | A | C | 1 | a0001c0002t0006g0319 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2782+606A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000280 | |||||||
chr8:22000386 | A | G | 1 | a0001c0003t0001g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2782+712A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000386 | |||||||
chr8:22000440 | C | T | 2 | a0001c0002t0001g0251 a0003c0012t0001g0250 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2782+766C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000440 | |||||||
chr8:22000453 | A | AT | 74 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(71): Show |
80 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.2782+798dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr8 | 22000453 | ||||||
chr8:22000453 | A | ATT | 99 | a0001c0002t0001g0007 a0001c0002t0001g0153 a0001c0002t0001g0228 others(96): Show |
104 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.2782+797_2782+798d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr8 | 22000453 | ||||||
chr8:22000483 | C | A | 5 | a0001c0003t0001g0043 a0001c0003t0001g0044 a0001c0003t0001g0045 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2782+809C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000483 | |||||||
chr8:22000565 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2782+891G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000565 | |||||||
chr8:22000805 | A | C | 4 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0251 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2782+1131A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000805 | |||||||
chr8:22000829 | G | A | 321 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(318): Show |
339 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.2782+1155G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000829 | |||||||
chr8:22001108 | C | T | 202 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0013 others(199): Show |
215 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.2783-1004C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001108 | |||||||
chr8:22001164 | G | C | 1 | a0001c0001t0002g0131 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2783-948G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001164 | |||||||
chr8:22001284 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2783-828G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001284 | |||||||
chr8:22001287 | C | T | 5 | a0001c0002t0005g0257 a0001c0002t0005g0260 a0001c0002t0005g0264 others(2): Show |
5 | HG02572.hp1 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2783-825C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001287 | |||||||
chr8:22001343 | G | A | 3 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 |
3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2783-769G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001343 | |||||||
chr8:22001360 | A | G | 1 | a0001c0003t0002g0294 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2783-752A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001360 | |||||||
chr8:22001378 | A | G | 3 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 |
3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2783-734A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001378 | |||||||
chr8:22001455 | G | A | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2783-657G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001455 | |||||||
chr8:22001532 | T | C | 1 | a0001c0002t0004g0049 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2783-580T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001532 | |||||||
chr8:22001557 | A | G | 1 | a0001c0003t0001g0036 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2783-555A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001557 | |||||||
chr8:22001573 | G | A | 203 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0013 others(200): Show |
216 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.2783-539G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001573 | |||||||
chr8:22001583 | A | T | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2783-529A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001583 | |||||||
chr8:22001606 | C | G | 1 | a0001c0002t0002g0249 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2783-506C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001606 | |||||||
chr8:22001695 | T | C | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2783-417T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001695 | |||||||
chr8:22001705 | C | CTCCTAAT | 2 | a0001c0001t0002g0011 a0001c0001t0002g0165 |
3 | HG00738.hp1 HG01099.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2783-404_2783-398d others(9): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr8 | 22001705 | ||||||
chr8:22001804 | C | T | 204 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0013 others(201): Show |
217 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.2783-308C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001804 | |||||||
chr8:22001934 | A | T | 3 | a0001c0003t0001g0048 a0001c0003t0001g0056 a0001c0003t0001g0057 |
3 | HG01109.hp1 HG01261.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.2783-178A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001934 | |||||||
chr8:22001974 | G | A | 105 | a0001c0002t0001g0007 a0001c0002t0001g0153 a0001c0002t0001g0228 others(102): Show |
110 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.2783-138G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001974 | |||||||
chr8:22002044 | A | G | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0009g0269 |
5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2783-68A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22002044 | |||||||
chr8:22002088 | T | A | 1 | a0001c0005t0002g0146 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2783-24T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22002088 | |||||||
chr8:22002313 | G | A | 2 | a0001c0002t0001g0251 a0003c0012t0001g0250 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2943+41G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002313 | |||||||
chr8:22002396 | G | A | 4 | a0001c0003t0001g0033 a0001c0003t0001g0034 a0001c0003t0001g0035 others(1): Show |
4 | HG00323.hp2 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2943+124G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002396 | |||||||
chr8:22002477 | C | A | 1 | a0001c0003t0001g0115 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2943+205C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002477 | |||||||
chr8:22002480 | C | T | 105 | a0001c0002t0001g0007 a0001c0002t0001g0153 a0001c0002t0001g0228 others(102): Show |
110 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.2943+208C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002480 | |||||||
chr8:22002488 | C | T | 3 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 |
3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2943+216C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002488 | |||||||
chr8:22002496 | T | C | 203 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0013 others(200): Show |
216 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.2943+224T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002496 | |||||||
chr8:22002539 | G | T | 1 | a0001c0002t0001g0282 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2943+267G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002539 | |||||||
chr8:22002574 | G | A | 1 | a0001c0003t0001g0115 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2943+302G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002574 | |||||||
chr8:22002631 | GGAA | G | 5 | a0001c0003t0001g0043 a0001c0003t0001g0044 a0001c0003t0001g0045 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2943+366_2943+368d others(5): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr8 | 22002631 | ||||||
chr8:22002797 | T | TAA | 95 | a0001c0001t0002g0225 a0001c0002t0001g0003 a0001c0002t0001g0013 others(92): Show |
103 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.2944-421_2944-420i others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr8 | 22002797 | ||||||
chr8:22002914 | T | A | 105 | a0001c0002t0001g0007 a0001c0002t0001g0153 a0001c0002t0001g0228 others(102): Show |
110 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.2944-305T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002914 | |||||||
chr8:22002922 | A | C | 1 | a0001c0001t0002g0196 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2944-297A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002922 | |||||||
chr8:22002922 | A | G | 1 | a0001c0001t0002g0125 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2944-297A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002922 | |||||||
chr8:22003135 | A | G | 1 | a0001c0002t0004g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2944-84A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22003135 | |||||||
chr8:22003160 | T | G | 3 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 |
3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2944-59T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22003160 | |||||||
chr8:22003335 | C | T | 1 | a0001c0002t0001g0277 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3042+18C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 26/27 | chr8 | 22003335 | |||||||
chr8:22003383 | G | A | 1 | a0001c0001t0002g0129 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3042+66G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 26/27 | chr8 | 22003383 | |||||||
chr8:22003392 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3042+75G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 26/27 | chr8 | 22003392 | |||||||
chr8:22003701 | A | G | 1 | a0001c0003t0001g0116 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3043-202A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 26/27 | chr8 | 22003701 | |||||||
chr8:22004152 | G | C | 199 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0013 others(196): Show |
212 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.3170+122G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004152 | |||||||
chr8:22004376 | T | C | 8 | a0001c0002t0001g0003 a0001c0002t0001g0023 a0001c0002t0001g0024 others(5): Show |
9 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.3170+346T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004376 | |||||||
chr8:22004430 | A | T | 1 | a0001c0003t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3170+400A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004430 | |||||||
chr8:22004511 | A | C | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3170+481A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004511 | |||||||
chr8:22004621 | G | A | 1 | a0001c0002t0001g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3171-374G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004621 | |||||||
chr8:22004637 | G | A | 1 | a0001c0002t0005g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3171-358G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004637 | |||||||
chr8:22004640 | G | C | 7 | a0001c0002t0005g0257 a0001c0002t0005g0260 a0001c0002t0005g0264 others(4): Show |
7 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3171-355G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004640 | |||||||
chr8:22004733 | G | A | 1 | a0001c0002t0001g0252 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3171-262G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004733 | |||||||
chr8:22004919 | TA | T | 103 | a0001c0001t0002g0166 a0001c0001t0002g0199 a0001c0002t0001g0007 others(100): Show |
108 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.3171-58delA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr8 | 22004919 | ||||||
chr8:22004919 | TAA | T | 6 | a0001c0002t0001g0046 a0001c0002t0001g0064 a0001c0002t0001g0065 others(3): Show |
6 | HG00735.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3171-59_3171-58del others(2): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr8 | 22004919 | ||||||
chr8:22004945 | A | G | 1 | a0001c0001t0002g0129 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3171-50A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004945 | |||||||
chr8:22004957 | C | G | 1 | a0001c0001t0002g0022 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3171-38C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004957 | |||||||
chr8:22004969 | C | G | 2 | a0001c0001t0002g0148 a0001c0001t0002g0198 |
2 | HG00621.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.3171-26C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004969 |