Item | Value |
---|---|
geneid | 58155 |
ensemblid | ENSG00000117569.20 |
hgncid | 17662 |
symbol | PTBP2 |
name | polypyrimidine tract binding protein 2 |
refseq_nuc | NM_021190.4 |
refseq_prot | NP_067013.1 |
ensembl_nuc | ENST00000674951.1 |
ensembl_prot | ENSP00000502818.1 |
mane_status | MANE Select |
chr | chr1 |
start | 96721784 |
end | 96815049 |
strand | + |
ver | v1.2 |
region | chr1:96721784-96815049 |
region5000 | chr1:96716784-96820049 |
regionname0 | PTBP2_chr1_96721784_96815049 |
regionname5000 | PTBP2_chr1_96716784_96820049 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1593 | 253 | 39 | 53 | 122 | 7 | 31 | PTBP2_chr1_96716784_96820049 | PTBP2 | ATGGA others(1588): Show |
chr1 | 96716784 | 96820049 | ||
a0001c0002 | 0/1 | 1593 | 108 | 45 | 11 | 40 | 7 | 4 | PTBP2_chr1_96716784_96820049 | PTBP2 | ATGGA others(1588): Show |
chr1 | 96716784 | 96820049 | ||
a0001c0003 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | ATGGA others(1588): Show |
chr1 | 96716784 | 96820049 | ||
a0001c0004 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | ATGGA others(1588): Show |
chr1 | 96716784 | 96820049 | ||
a0001c0005 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | ATGGA others(1588): Show |
chr1 | 96716784 | 96820049 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3321 | 10 | 8 | 0 | 2 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3316): Show |
chr1 | 96716784 | 96820049 |
a0001c0001t0002 | 0/0 | 3316 | 89 | 2 | 17 | 58 | 3 | 9 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3311): Show |
chr1 | 96716784 | 96820049 |
a0001c0001t0003 | 0/0 | 3322 | 88 | 16 | 19 | 38 | 4 | 11 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3317): Show |
chr1 | 96716784 | 96820049 |
a0001c0001t0004 | 0/0 | 3323 | 29 | 2 | 10 | 16 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3318): Show |
chr1 | 96716784 | 96820049 |
a0001c0001t0006 | 1/0 | 3321 | 12 | 0 | 3 | 3 | 0 | 5 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3316): Show |
chr1 | 96716784 | 96820049 |
a0001c0001t0007 | 0/0 | 3323 | 10 | 8 | 2 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3318): Show |
chr1 | 96716784 | 96820049 |
a0001c0001t0008 | 0/0 | 3322 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3317): Show |
chr1 | 96716784 | 96820049 |
a0001c0001t0009 | 0/0 | 3316 | 3 | 1 | 0 | 2 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3311): Show |
chr1 | 96716784 | 96820049 |
a0001c0001t0010 | 0/0 | 3316 | 3 | 0 | 1 | 0 | 0 | 2 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3311): Show |
chr1 | 96716784 | 96820049 |
a0001c0001t0011 | 0/0 | 3316 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3311): Show |
chr1 | 96716784 | 96820049 |
a0001c0001t0013 | 0/0 | 3316 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3311): Show |
chr1 | 96716784 | 96820049 |
a0001c0001t0014 | 0/0 | 3316 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3311): Show |
chr1 | 96716784 | 96820049 |
a0001c0001t0015 | 0/0 | 3321 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3316): Show |
chr1 | 96716784 | 96820049 |
a0001c0001t0016 | 0/0 | 3337 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3332): Show |
chr1 | 96716784 | 96820049 |
a0001c0001t0017 | 0/0 | 3316 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3311): Show |
chr1 | 96716784 | 96820049 |
a0001c0001t0018 | 0/0 | 3316 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3311): Show |
chr1 | 96716784 | 96820049 |
a0001c0001t0019 | 0/0 | 3322 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | GGCCG others(3317): Show |
chr1 | 96716784 | 96820049 |
a0001c0002t0001 | 0/1 | 3321 | 86 | 30 | 9 | 37 | 6 | 3 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3316): Show |
chr1 | 96716784 | 96820049 |
a0001c0002t0005 | 0/0 | 3322 | 14 | 13 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3317): Show |
chr1 | 96716784 | 96820049 |
a0001c0002t0008 | 0/0 | 3322 | 8 | 2 | 2 | 3 | 1 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3317): Show |
chr1 | 96716784 | 96820049 |
a0001c0003t0001 | 0/0 | 3321 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3316): Show |
chr1 | 96716784 | 96820049 |
a0001c0004t0004 | 0/0 | 3323 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3318): Show |
chr1 | 96716784 | 96820049 |
a0001c0005t0012 | 0/0 | 3323 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | AGCCG others(3318): Show |
chr1 | 96716784 | 96820049 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0006g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0006g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0006g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0006g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0006g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0006g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0006g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0007g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0007g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0009g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0009g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0009g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0010g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0010g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0010g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0011g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0013g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0014g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0015g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0016g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0017g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0018g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0001t0019g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0005g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0008g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0008g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0008g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0008g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0008g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0008g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0008g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0002t0008g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0004t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
a0001c0005t0012g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0270 | EUR | GBR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0210 | EUR | GBR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00140 | hp1 | a0001 | c0002 | t0008 | g0345 | EUR | GBR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0060 | EUR | GBR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0277 | EUR | FIN | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0173 | EUR | FIN | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | CHS | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | CHS | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | CHS | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00438 | hp2 | a0001 | c0001 | t0006 | g0135 | EAS | CHS | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0329 | EAS | CHS | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | CHS | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | CHS | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0339 | EAS | CHS | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0334 | EAS | CHS | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | CHS | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | CHS | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00642 | hp1 | a0001 | c0001 | t0010 | g0205 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00642 | hp2 | a0001 | c0001 | t0006 | g0133 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00735 | hp1 | a0001 | c0001 | t0007 | g0013 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00735 | hp2 | a0001 | c0001 | t0007 | g0016 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0030 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0106 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0281 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0280 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0286 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0306 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0122 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01099 | hp2 | a0001 | c0002 | t0008 | g0293 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0298 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0134 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0308 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0075 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0330 | AMR | PUR | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | CLM | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | CLM | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0103 | AMR | CLM | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01346 | hp1 | a0001 | c0001 | t0006 | g0131 | AMR | CLM | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | CLM | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0288 | AMR | CLM | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0305 | AMR | CLM | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | CLM | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0294 | EUR | IBS | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0116 | EUR | IBS | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0307 | EUR | IBS | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0124 | EUR | IBS | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0357 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0314 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0031 | AMR | PEL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0049 | AMR | PEL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0079 | AMR | PEL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PEL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0037 | AMR | PEL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0129 | AMR | PEL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0110 | AMR | PEL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | PEL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02004 | hp1 | a0001 | c0001 | t0013 | g0222 | AMR | PEL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02004 | hp2 | a0001 | c0001 | t0006 | g0093 | AMR | PEL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | KHV | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02027 | hp2 | a0001 | c0002 | t0008 | g0265 | EAS | KHV | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | KHV | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | KHV | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0340 | EAS | KHV | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02129 | hp2 | a0001 | c0001 | t0006 | g0108 | EAS | KHV | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0271 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PEL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02148 | hp2 | a0001 | c0002 | t0008 | g0289 | AMR | PEL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | CDX | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0267 | EAS | CDX | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02257 | hp2 | a0001 | c0002 | t0008 | g0287 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0132 | AMR | PEL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0136 | AMR | PEL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02572 | hp1 | a0001 | c0004 | t0004 | g0022 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02572 | hp2 | a0001 | c0002 | t0005 | g0259 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02602 | hp1 | a0001 | c0001 | t0006 | g0024 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02602 | hp2 | a0001 | c0005 | t0012 | g0077 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0317 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02630 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02647 | hp2 | a0001 | c0002 | t0005 | g0253 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0086 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0073 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02698 | hp2 | a0001 | c0001 | t0010 | g0204 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0342 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02723 | hp1 | a0001 | c0002 | t0005 | g0257 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0315 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0347 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0343 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0344 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02886 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0318 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0321 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0316 | AFR | ESN | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0299 | AFR | ESN | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02965 | hp1 | a0001 | c0002 | t0005 | g0258 | AFR | ESN | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02965 | hp2 | a0001 | c0002 | t0005 | g0255 | AFR | ESN | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | ESN | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02970 | hp2 | a0001 | c0001 | t0008 | g0166 | AFR | ESN | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | ESN | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0153 | AFR | ESN | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0112 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03017 | hp2 | a0001 | c0001 | t0016 | g0120 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0268 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03041 | hp2 | a0001 | c0002 | t0005 | g0260 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0346 | AFR | MSL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0311 | AFR | MSL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0084 | AFR | ESN | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | ESN | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0300 | AFR | MSL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03209 | hp2 | a0001 | c0002 | t0005 | g0002 | AFR | MSL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03225 | hp2 | a0001 | c0002 | t0005 | g0254 | AFR | MSL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03239 | hp1 | a0001 | c0002 | t0005 | g0274 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03453 | hp1 | a0001 | c0002 | t0005 | g0261 | AFR | MSL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0309 | AFR | MSL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0320 | AFR | MSL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03486 | hp2 | a0001 | c0001 | t0019 | g0018 | AFR | MSL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03490 | hp1 | a0001 | c0001 | t0006 | g0027 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03490 | hp2 | a0001 | c0001 | t0006 | g0072 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03491 | hp1 | a0001 | c0001 | t0006 | g0115 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0029 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03516 | hp1 | a0001 | c0002 | t0008 | g0322 | AFR | ESN | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | ESN | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0296 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03540 | hp2 | a0001 | c0002 | t0005 | g0256 | AFR | GWD | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03579 | hp1 | a0001 | c0002 | t0005 | g0251 | AFR | MSL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0297 | AFR | MSL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | STU | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0125 | SAS | STU | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0117 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0295 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0121 | SAS | PJL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | BEB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | BEB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0147 | SAS | BEB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0269 | SAS | BEB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0332 | SAS | BEB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | BEB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG04184 | hp1 | a0001 | c0001 | t0015 | g0151 | SAS | BEB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | BEB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0033 | SAS | STU | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | STU | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | STU | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG04204 | hp2 | a0001 | c0001 | t0010 | g0150 | SAS | STU | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0119 | SAS | STU | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG04228 | hp2 | a0001 | c0001 | t0014 | g0157 | SAS | STU | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | CHB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | CHB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0263 | AFR | YRI | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0312 | AFR | YRI | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0350 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0337 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0351 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18960 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18965 | hp1 | a0001 | c0001 | t0009 | g0040 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0336 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18967 | hp2 | a0001 | c0002 | t0008 | g0290 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0353 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18978 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0349 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18979 | hp2 | a0001 | c0001 | t0011 | g0186 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0361 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18991 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0354 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18995 | hp2 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19002 | hp1 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19002 | hp2 | a0001 | c0001 | t0017 | g0230 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19006 | hp2 | a0001 | c0001 | t0009 | g0054 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19011 | hp2 | a0001 | c0001 | t0018 | g0234 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0319 | AFR | LWK | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0301 | AFR | LWK | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19054 | hp1 | a0001 | c0002 | t0008 | g0279 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19060 | hp2 | a0001 | c0001 | t0006 | g0065 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0341 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0335 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0328 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19085 | hp2 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0338 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0348 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19240 | hp1 | a0001 | c0002 | t0005 | g0002 | AFR | YRI | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0313 | AFR | YRI | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0324 | AFR | ASW | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ASW | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0201 | EUR | TSI | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0284 | EUR | TSI | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0098 | EUR | TSI | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0282 | EUR | TSI | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0046 | SAS | GIH | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0164 | SAS | GIH | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0302 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0323 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0310 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | ACB | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | MSL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG03471 | hp2 | a0001 | c0002 | t0005 | g0252 | AFR | MSL | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG06807 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | USA | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0262 | AFR | USA | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | USA | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | USA | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA21309 | hp1 | a0001 | c0001 | t0009 | g0113 | AFR | LWK | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0352 | AFR | LWK | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0149 | REF | REF | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0097 | REF | REF | PTBP2_chr1_96716784_96820049 | PTBP2 | chr1 | 96716784 | 96820049 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:96769734 | A | G | 1 | a0001c0005 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.147A>G | p.Gly49Gly | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 4/14 | 228/3321 | 147/1596 | 49/531 | chr1 | 96769734 | |||
chr1:96770842 | A | G | 1 | a0001c0004 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.423A>G | p.Thr141Thr | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/14 | 504/3321 | 423/1596 | 141/531 | chr1 | 96770842 | |||
chr1:96785184 | A | G | 1 | a0001c0003 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.834A>G | p.Pro278Pro | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/14 | 915/3321 | 834/1596 | 278/531 | chr1 | 96785184 | |||
chr1:96806900 | A | G | 2 | a0001c0002 a0001c0003 |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
synonymous_variant | LOW | c.1113A>G | p.Leu371Leu | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/14 | 1194/3321 | 1113/1596 | 371/531 | chr1 | 96806900 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:96721784 | A | G | 1 | a0001c0001t0019 | 1 | HG03486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-81A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 1/14 | 81 | chr1 | 96721784 | ||||||
chr1:96721859 | T | G | 1 | a0001c0001t0011 | 1 | NA18979.hp2 | 5_prime_UTR_variant | MODIFIER | c.-6T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 1/14 | 6 | chr1 | 96721859 | ||||||
chr1:96813416 | A | G | 1 | a0001c0001t0018 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 14/14 | 11 | chr1 | 96813416 | ||||||
chr1:96813523 | C | CT | 1 | a0001c0002t0005 | 14 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*128dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 14/14 | 129 | INFO_REALIGN_3_PRIME | chr1 | 96813523 | |||||
chr1:96813575 | A | C | 1 | a0001c0001t0017 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*170A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 14/14 | 170 | chr1 | 96813575 | ||||||
chr1:96813653 | T | C | 1 | a0001c0005t0012 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*248T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 14/14 | 248 | chr1 | 96813653 | ||||||
chr1:96813661 | C | CT | 5 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0016 others(2): Show |
99 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*277dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 14/14 | 278 | INFO_REALIGN_3_PRIME | chr1 | 96813661 | |||||
chr1:96813661 | C | CTT | 4 | a0001c0001t0004 a0001c0001t0007 a0001c0004t0004 others(1): Show |
41 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*276_*277dupTT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 14/14 | 278 | INFO_REALIGN_3_PRIME | chr1 | 96813661 | |||||
chr1:96813661 | CTTTTT | C | 8 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0010 others(5): Show |
100 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*273_*277delTTTTT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 14/14 | 273 | INFO_REALIGN_3_PRIME | chr1 | 96813661 | |||||
chr1:96813984 | T | C | 1 | a0001c0001t0013 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*579T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 14/14 | 579 | chr1 | 96813984 | ||||||
chr1:96814136 | C | T | 15 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(12): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*731C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 14/14 | 731 | chr1 | 96814136 | ||||||
chr1:96814365 | T | C | 1 | a0001c0001t0014 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*960T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 14/14 | 960 | chr1 | 96814365 | ||||||
chr1:96814576 | A | T | 2 | a0001c0001t0010 a0001c0001t0015 |
4 | HG00642.hp1 HG02698.hp2 HG04184.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1171A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 14/14 | 1171 | chr1 | 96814576 | ||||||
chr1:96814590 | T | TTGTCAAT others(8): Show |
1 | a0001c0001t0016 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1187_*1201dupGTCA others(11): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 14/14 | 1202 | INFO_REALIGN_3_PRIME | chr1 | 96814590 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:96721905 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.8+33G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 1/13 | chr1 | 96721905 | |||||||
chr1:96721915 | T | C | 1 | a0001c0002t0001g0004 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.8+43T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 1/13 | chr1 | 96721915 | |||||||
chr1:96722357 | C | G | 2 | a0001c0001t0002g0361 a0001c0001t0002g0362 |
2 | NA18947.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.8+485C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 1/13 | chr1 | 96722357 | |||||||
chr1:96722403 | G | C | 3 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 |
3 | HG02647.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.8+531G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 1/13 | chr1 | 96722403 | |||||||
chr1:96722447 | G | A | 9 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0010 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.8+575G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 1/13 | chr1 | 96722447 | |||||||
chr1:96722802 | G | C | 1 | a0001c0001t0002g0017 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.9-762G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 1/13 | chr1 | 96722802 | |||||||
chr1:96722838 | G | T | 226 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.9-726G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 1/13 | chr1 | 96722838 | |||||||
chr1:96722939 | A | G | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.9-625A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 1/13 | chr1 | 96722939 | |||||||
chr1:96723003 | C | A | 243 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(240): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.9-561C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 1/13 | chr1 | 96723003 | |||||||
chr1:96723032 | T | C | 2 | a0001c0001t0010g0150 a0001c0001t0015g0151 |
2 | HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.9-532T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 1/13 | chr1 | 96723032 | |||||||
chr1:96723227 | T | C | 1 | a0001c0002t0001g0152 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.9-337T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 1/13 | chr1 | 96723227 | |||||||
chr1:96723450 | T | C | 1 | a0001c0001t0019g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.9-114T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 1/13 | chr1 | 96723450 | |||||||
chr1:96723519 | T | G | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.9-45T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 1/13 | chr1 | 96723519 | |||||||
chr1:96723535 | G | A | 226 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.9-29G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 1/13 | chr1 | 96723535 | |||||||
chr1:96723732 | T | A | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.39+138T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96723732 | |||||||
chr1:96723771 | C | G | 2 | a0001c0002t0001g0353 a0001c0002t0001g0354 |
2 | NA18970.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.39+177C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96723771 | |||||||
chr1:96724013 | C | T | 1 | a0001c0001t0002g0250 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.39+419C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96724013 | |||||||
chr1:96724139 | G | T | 1 | a0001c0002t0001g0352 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.39+545G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96724139 | |||||||
chr1:96724167 | A | G | 95 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.39+573A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96724167 | |||||||
chr1:96724174 | G | A | 1 | a0001c0001t0003g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.39+580G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96724174 | |||||||
chr1:96724174 | G | T | 95 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.39+580G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96724174 | |||||||
chr1:96724248 | TTTTTTTG | T | 102 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(99): Show |
102 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.39+668_39+674delGT others(5): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96724248 | ||||||
chr1:96724285 | T | A | 1 | a0001c0001t0003g0020 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.39+691T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96724285 | |||||||
chr1:96724302 | A | G | 1 | a0001c0001t0003g0148 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.39+708A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96724302 | |||||||
chr1:96724313 | C | T | 1 | a0001c0002t0001g0351 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.39+719C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96724313 | |||||||
chr1:96724323 | C | T | 1 | a0001c0001t0003g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.39+729C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96724323 | |||||||
chr1:96724339 | C | T | 4 | a0001c0001t0002g0247 a0001c0001t0002g0248 a0001c0001t0002g0249 others(1): Show |
4 | NA18994.hp2 NA18995.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+745C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96724339 | |||||||
chr1:96724663 | A | T | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.39+1069A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96724663 | |||||||
chr1:96724727 | G | A | 1 | a0001c0001t0004g0021 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.39+1133G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96724727 | |||||||
chr1:96724775 | G | A | 95 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.39+1181G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96724775 | |||||||
chr1:96724800 | T | C | 1 | a0001c0002t0001g0353 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.39+1206T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96724800 | |||||||
chr1:96724860 | G | A | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.39+1266G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96724860 | |||||||
chr1:96724972 | T | C | 2 | a0001c0001t0002g0154 a0001c0001t0002g0155 |
2 | HG03239.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.39+1378T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96724972 | |||||||
chr1:96725013 | G | C | 1 | a0001c0004t0004g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.39+1419G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96725013 | |||||||
chr1:96725301 | G | GT | 119 | a0001c0001t0001g0163 a0001c0001t0001g0359 a0001c0001t0001g0360 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.39+1725dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96725301 | ||||||
chr1:96725301 | G | GTT | 39 | a0001c0001t0001g0220 a0001c0001t0001g0229 a0001c0001t0002g0215 others(36): Show |
39 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.39+1724_39+1725dup others(2): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96725301 | ||||||
chr1:96725301 | G | GTTT | 9 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0242 others(6): Show |
9 | HG00544.hp2 HG02080.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.39+1723_39+1725dup others(3): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96725301 | ||||||
chr1:96725302 | T | G | 1 | a0001c0001t0003g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.39+1708T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96725302 | |||||||
chr1:96725404 | A | C | 1 | a0001c0001t0002g0246 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.39+1810A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96725404 | |||||||
chr1:96725515 | G | C | 1 | a0001c0001t0002g0215 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.39+1921G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96725515 | |||||||
chr1:96725588 | TA | T | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.39+2003delA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96725588 | ||||||
chr1:96725658 | T | C | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+2064T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96725658 | |||||||
chr1:96725768 | C | T | 121 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(118): Show |
121 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.39+2174C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96725768 | |||||||
chr1:96725801 | C | T | 17 | a0001c0002t0001g0310 a0001c0002t0001g0311 a0001c0002t0001g0312 others(14): Show |
17 | HG01884.hp2 HG02109.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.39+2207C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96725801 | |||||||
chr1:96725802 | G | A | 3 | a0001c0001t0002g0156 a0001c0001t0003g0023 a0001c0001t0006g0024 |
3 | HG02602.hp1 HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.39+2208G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96725802 | |||||||
chr1:96725808 | G | A | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+2214G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96725808 | |||||||
chr1:96726035 | A | G | 1 | a0001c0001t0003g0122 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.39+2441A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726035 | |||||||
chr1:96726074 | C | CA | 56 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0007 others(53): Show |
57 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.39+2517dupA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96726074 | ||||||
chr1:96726074 | C | CAA | 27 | a0001c0001t0003g0019 a0001c0001t0003g0032 a0001c0001t0003g0033 others(24): Show |
27 | HG00733.hp1 HG00741.hp1 HG01943.hp1 others(24): Show |
intron_variant | MODIFIER | c.39+2516_39+2517dup others(2): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96726074 | ||||||
chr1:96726074 | C | CAAA | 10 | a0001c0001t0003g0005 a0001c0001t0003g0023 a0001c0001t0003g0026 others(7): Show |
10 | HG01433.hp2 HG01517.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.39+2515_39+2517dup others(3): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96726074 | ||||||
chr1:96726074 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0003g0123 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.39+2507_39+2517dup others(11): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96726074 | ||||||
chr1:96726074 | CA | C | 7 | a0001c0001t0003g0114 a0001c0001t0003g0116 a0001c0001t0003g0117 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.39+2517delA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96726074 | ||||||
chr1:96726074 | CAAAAAAA others(3): Show |
C | 32 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0358 others(29): Show |
32 | HG00099.hp1 HG00544.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.39+2508_39+2517del others(10): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96726074 | ||||||
chr1:96726074 | CAAAAAAA others(4): Show |
C | 73 | a0001c0001t0001g0003 a0001c0001t0002g0247 a0001c0001t0002g0248 others(70): Show |
74 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.39+2507_39+2517del others(11): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96726074 | ||||||
chr1:96726074 | CAAAAAAA others(5): Show |
C | 36 | a0001c0001t0001g0220 a0001c0001t0002g0158 a0001c0001t0002g0159 others(33): Show |
36 | HG00423.hp2 HG00544.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.39+2506_39+2517del others(12): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96726074 | ||||||
chr1:96726074 | CAAAAAAA others(6): Show |
C | 81 | a0001c0001t0001g0163 a0001c0001t0001g0229 a0001c0001t0002g0017 others(78): Show |
81 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.39+2505_39+2517del others(13): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96726074 | ||||||
chr1:96726074 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0002g0214 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.39+2504_39+2517del others(14): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96726074 | ||||||
chr1:96726074 | CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0003g0121 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.39+2499_39+2517del others(19): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96726074 | ||||||
chr1:96726093 | A | T | 1 | a0001c0001t0016g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.39+2499A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726093 | |||||||
chr1:96726101 | A | T | 1 | a0001c0001t0016g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.39+2507A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726101 | |||||||
chr1:96726236 | G | A | 1 | a0001c0001t0003g0023 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.39+2642G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726236 | |||||||
chr1:96726275 | C | CT | 23 | a0001c0001t0002g0155 a0001c0001t0002g0161 a0001c0001t0002g0213 others(20): Show |
23 | HG00423.hp2 HG00733.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.39+2697dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96726275 | ||||||
chr1:96726275 | C | CTTTTTTT others(59): Show |
1 | a0001c0001t0003g0087 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.39+2697_39+2698ins others(66): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96726275 | ||||||
chr1:96726291 | T | G | 1 | a0001c0001t0009g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.39+2697T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726291 | |||||||
chr1:96726295 | T | A | 1 | a0001c0001t0003g0087 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.39+2701T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726295 | |||||||
chr1:96726305 | C | G | 1 | a0001c0001t0003g0087 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.39+2711C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726305 | |||||||
chr1:96726313 | A | C | 1 | a0001c0001t0003g0087 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.39+2719A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726313 | |||||||
chr1:96726314 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.39+2720T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726314 | |||||||
chr1:96726332 | G | T | 1 | a0001c0001t0003g0087 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.39+2738G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726332 | |||||||
chr1:96726334 | A | G | 1 | a0001c0001t0003g0087 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.39+2740A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726334 | |||||||
chr1:96726335 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.39+2741T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726335 | |||||||
chr1:96726342 | G | T | 1 | a0001c0001t0003g0087 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.39+2748G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726342 | |||||||
chr1:96726346 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.39+2752T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726346 | |||||||
chr1:96726439 | AT | A | 46 | a0001c0001t0002g0243 a0001c0001t0003g0047 a0001c0002t0001g0004 others(43): Show |
46 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.39+2860delT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96726439 | ||||||
chr1:96726454 | T | C | 5 | a0001c0001t0001g0163 a0001c0001t0002g0162 a0001c0001t0002g0227 others(2): Show |
5 | HG00621.hp2 HG01433.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+2860T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726454 | |||||||
chr1:96726469 | G | T | 1 | a0001c0001t0006g0027 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.39+2875G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726469 | |||||||
chr1:96726711 | A | C | 8 | a0001c0001t0003g0028 a0001c0001t0003g0047 a0001c0001t0003g0086 others(5): Show |
8 | HG00733.hp1 HG01433.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.39+3117A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726711 | |||||||
chr1:96726733 | A | G | 1 | a0001c0002t0001g0329 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.39+3139A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726733 | |||||||
chr1:96726829 | C | T | 95 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.39+3235C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726829 | |||||||
chr1:96726878 | C | T | 9 | a0001c0002t0001g0323 a0001c0002t0005g0002 a0001c0002t0005g0251 others(6): Show |
10 | HG02109.hp2 HG02647.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.39+3284C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726878 | |||||||
chr1:96726995 | G | A | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.39+3401G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96726995 | |||||||
chr1:96727075 | C | G | 1 | a0001c0002t0001g0352 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.39+3481C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96727075 | |||||||
chr1:96727154 | G | A | 1 | a0001c0002t0001g0339 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.39+3560G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96727154 | |||||||
chr1:96727357 | ATTACTGT others(24): Show |
A | 1 | a0001c0001t0002g0214 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.39+3766_39+3796del others(31): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96727357 | ||||||
chr1:96727465 | G | A | 2 | a0001c0001t0002g0164 a0001c0001t0002g0213 |
2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.39+3871G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96727465 | |||||||
chr1:96727533 | T | G | 1 | a0001c0001t0004g0030 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.39+3939T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96727533 | |||||||
chr1:96727589 | A | G | 128 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(125): Show |
129 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.39+3995A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96727589 | |||||||
chr1:96727642 | C | T | 1 | a0001c0001t0004g0136 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.39+4048C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96727642 | |||||||
chr1:96727794 | C | T | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.39+4200C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96727794 | |||||||
chr1:96727833 | T | C | 2 | a0001c0001t0002g0240 a0001c0001t0002g0244 |
2 | NA18948.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.39+4239T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96727833 | |||||||
chr1:96727865 | T | C | 2 | a0001c0002t0001g0310 a0001c0002t0001g0324 |
2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.39+4271T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96727865 | |||||||
chr1:96728130 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.39+4536G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96728130 | |||||||
chr1:96728320 | G | A | 1 | a0001c0001t0008g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.39+4726G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96728320 | |||||||
chr1:96728756 | G | A | 2 | a0001c0002t0001g0312 a0001c0002t0001g0313 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.39+5162G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96728756 | |||||||
chr1:96728815 | A | AT | 12 | a0001c0001t0001g0003 a0001c0001t0004g0111 a0001c0002t0001g0004 others(9): Show |
12 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.39+5237dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96728815 | ||||||
chr1:96728815 | A | ATTG | 9 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0010 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.39+5223_39+5224ins others(3): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96728815 | ||||||
chr1:96728815 | AT | A | 60 | a0001c0001t0003g0019 a0001c0001t0003g0032 a0001c0001t0003g0048 others(57): Show |
60 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.39+5237delT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96728815 | ||||||
chr1:96728816 | T | TTG | 10 | a0001c0001t0001g0163 a0001c0001t0002g0209 a0001c0001t0002g0210 others(7): Show |
10 | HG00099.hp2 HG01109.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.39+5223_39+5224ins others(2): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96728816 | ||||||
chr1:96728817 | T | TG | 102 | a0001c0001t0001g0220 a0001c0001t0001g0229 a0001c0001t0002g0017 others(99): Show |
102 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.39+5223_39+5224ins others(1): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96728817 | |||||||
chr1:96728869 | C | A | 1 | a0001c0002t0008g0293 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.39+5275C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96728869 | |||||||
chr1:96729097 | A | G | 1 | a0001c0002t0001g0309 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.39+5503A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96729097 | |||||||
chr1:96729525 | C | G | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+5931C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96729525 | |||||||
chr1:96729559 | T | G | 2 | a0001c0001t0004g0051 a0001c0001t0004g0091 |
2 | NA19010.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.39+5965T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96729559 | |||||||
chr1:96729609 | T | C | 1 | a0001c0001t0008g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.39+6015T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96729609 | |||||||
chr1:96729636 | C | A | 1 | a0001c0001t0002g0209 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.39+6042C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96729636 | |||||||
chr1:96729732 | A | AT | 12 | a0001c0001t0003g0007 a0001c0001t0003g0042 a0001c0001t0003g0082 others(9): Show |
12 | HG01981.hp1 HG02148.hp1 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.39+6160dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96729732 | ||||||
chr1:96729732 | AT | A | 116 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(113): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.39+6160delT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96729732 | ||||||
chr1:96729732 | ATT | A | 8 | a0001c0001t0001g0003 a0001c0001t0002g0164 a0001c0001t0002g0225 others(5): Show |
8 | HG01099.hp2 HG01515.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.39+6159_39+6160del others(2): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96729732 | ||||||
chr1:96729732 | ATTT | A | 107 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(104): Show |
107 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.39+6158_39+6160del others(3): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96729732 | ||||||
chr1:96729812 | A | G | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.39+6218A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96729812 | |||||||
chr1:96729877 | C | T | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.39+6283C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96729877 | |||||||
chr1:96729988 | A | G | 1 | a0001c0001t0003g0083 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.39+6394A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96729988 | |||||||
chr1:96729989 | A | G | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.39+6395A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96729989 | |||||||
chr1:96730061 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.39+6467G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96730061 | |||||||
chr1:96730082 | T | C | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.39+6488T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96730082 | |||||||
chr1:96730094 | G | A | 226 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.39+6500G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96730094 | |||||||
chr1:96730222 | A | ATTTCTGC others(19): Show |
1 | a0001c0002t0001g0295 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.39+6632_39+6657dup others(26): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96730222 | ||||||
chr1:96730325 | T | C | 1 | a0001c0002t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.39+6731T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96730325 | |||||||
chr1:96730438 | G | A | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+6844G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96730438 | |||||||
chr1:96730502 | C | T | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.39+6908C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96730502 | |||||||
chr1:96730808 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.39+7214C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96730808 | |||||||
chr1:96730928 | G | T | 219 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.39+7334G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96730928 | |||||||
chr1:96731010 | T | G | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.39+7416T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96731010 | |||||||
chr1:96731122 | C | T | 95 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.39+7528C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96731122 | |||||||
chr1:96731143 | C | T | 2 | a0001c0001t0004g0051 a0001c0001t0004g0091 |
2 | NA19010.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.39+7549C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96731143 | |||||||
chr1:96731330 | C | A | 1 | a0001c0004t0004g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.39+7736C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96731330 | |||||||
chr1:96731483 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.39+7889A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96731483 | |||||||
chr1:96731511 | T | C | 121 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(118): Show |
121 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.39+7917T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96731511 | |||||||
chr1:96731537 | A | G | 1 | a0001c0001t0004g0110 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.39+7943A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96731537 | |||||||
chr1:96731548 | G | T | 1 | a0001c0002t0001g0338 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.39+7954G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96731548 | |||||||
chr1:96731552 | C | G | 1 | a0001c0002t0001g0292 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.39+7958C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96731552 | |||||||
chr1:96731754 | A | G | 1 | a0001c0001t0003g0032 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.39+8160A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96731754 | |||||||
chr1:96731766 | A | G | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+8172A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96731766 | |||||||
chr1:96731790 | A | C | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+8196A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96731790 | |||||||
chr1:96732397 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.39+8803G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96732397 | |||||||
chr1:96732446 | G | C | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+8852G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96732446 | |||||||
chr1:96732591 | T | C | 7 | a0001c0002t0001g0296 a0001c0002t0001g0297 a0001c0002t0001g0298 others(4): Show |
7 | HG01109.hp1 HG02109.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.39+8997T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96732591 | |||||||
chr1:96732716 | G | A | 1 | a0001c0001t0002g0164 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.39+9122G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96732716 | |||||||
chr1:96732775 | G | T | 219 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.39+9181G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96732775 | |||||||
chr1:96732874 | A | G | 1 | a0001c0001t0009g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.39+9280A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96732874 | |||||||
chr1:96732986 | C | G | 1 | a0001c0001t0002g0017 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.39+9392C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96732986 | |||||||
chr1:96733004 | C | T | 121 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(118): Show |
121 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.39+9410C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733004 | |||||||
chr1:96733021 | C | CT | 132 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.39+9442dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96733021 | ||||||
chr1:96733052 | T | A | 7 | a0001c0002t0001g0311 a0001c0002t0001g0314 a0001c0002t0001g0315 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.39+9458T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733052 | |||||||
chr1:96733086 | T | C | 1 | a0001c0002t0005g0002 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.39+9492T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733086 | |||||||
chr1:96733194 | A | T | 9 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0010 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.39+9600A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733194 | |||||||
chr1:96733196 | CTT | C | 9 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0010 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.39+9603_39+9604del others(2): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733196 | |||||||
chr1:96733199 | C | G | 1 | a0001c0001t0002g0160 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.39+9605C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733199 | |||||||
chr1:96733201 | TCTTCAAA others(12): Show |
T | 9 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0010 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.39+9608_39+9626del others(19): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733201 | |||||||
chr1:96733205 | C | T | 6 | a0001c0001t0003g0028 a0001c0001t0003g0086 a0001c0001t0003g0125 others(3): Show |
6 | HG00733.hp1 HG01433.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+9611C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733205 | |||||||
chr1:96733221 | A | T | 9 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0010 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.39+9627A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733221 | |||||||
chr1:96733243 | C | T | 1 | a0001c0001t0002g0167 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.39+9649C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733243 | |||||||
chr1:96733281 | T | TA | 19 | a0001c0002t0001g0263 a0001c0002t0001g0268 a0001c0002t0001g0269 others(16): Show |
19 | HG00558.hp2 HG01109.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.39+9688dupA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96733281 | ||||||
chr1:96733296 | ATTACAAT others(3): Show |
A | 3 | a0001c0001t0003g0026 a0001c0001t0003g0043 a0001c0001t0004g0025 |
3 | HG03471.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.39+9703_39+9712del others(10): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733296 | |||||||
chr1:96733302 | A | G | 1 | a0001c0001t0002g0207 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.39+9708A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733302 | |||||||
chr1:96733315 | C | T | 3 | a0001c0001t0003g0026 a0001c0001t0003g0043 a0001c0001t0004g0025 |
3 | HG03471.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.39+9721C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733315 | |||||||
chr1:96733319 | A | G | 1 | a0001c0002t0001g0352 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.39+9725A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733319 | |||||||
chr1:96733642 | G | T | 1 | a0001c0001t0002g0155 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.39+10048G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733642 | |||||||
chr1:96733724 | A | G | 1 | a0001c0001t0007g0153 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.39+10130A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733724 | |||||||
chr1:96733767 | C | T | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.39+10173C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733767 | |||||||
chr1:96733799 | C | T | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.39+10205C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733799 | |||||||
chr1:96733821 | G | A | 1 | a0001c0001t0003g0137 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.39+10227G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733821 | |||||||
chr1:96733977 | A | G | 12 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(9): Show |
13 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.39+10383A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96733977 | |||||||
chr1:96734017 | C | G | 44 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0264 others(41): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.39+10423C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96734017 | |||||||
chr1:96734159 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.39+10565G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96734159 | |||||||
chr1:96734341 | T | C | 5 | a0001c0001t0003g0044 a0001c0001t0003g0083 a0001c0001t0003g0090 others(2): Show |
5 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+10747T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96734341 | |||||||
chr1:96734464 | G | GT | 10 | a0001c0001t0002g0225 a0001c0001t0002g0240 a0001c0001t0003g0109 others(7): Show |
10 | HG00544.hp1 HG00735.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.39+10881dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96734464 | ||||||
chr1:96734466 | T | A | 1 | a0001c0001t0002g0210 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+10872T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96734466 | |||||||
chr1:96734524 | C | T | 2 | a0001c0001t0002g0208 a0001c0001t0002g0215 |
2 | NA18962.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.39+10930C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96734524 | |||||||
chr1:96734539 | A | G | 1 | a0001c0002t0008g0290 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.39+10945A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96734539 | |||||||
chr1:96734628 | C | G | 1 | a0001c0001t0007g0153 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.39+11034C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96734628 | |||||||
chr1:96734649 | T | G | 3 | a0001c0002t0005g0251 a0001c0002t0005g0254 a0001c0002t0005g0260 |
3 | HG03041.hp2 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.39+11055T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96734649 | |||||||
chr1:96734903 | CTT | C | 18 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(15): Show |
18 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.39+11327_39+11328d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96734903 | ||||||
chr1:96734903 | CTTT | C | 98 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(95): Show |
98 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.39+11326_39+11328d others(5): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96734903 | ||||||
chr1:96734906 | T | G | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.39+11312T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96734906 | |||||||
chr1:96734911 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.39+11317T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96734911 | |||||||
chr1:96734917 | T | C | 43 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0264 others(40): Show |
43 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.39+11323T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96734917 | |||||||
chr1:96735021 | G | C | 1 | a0001c0002t0005g0002 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.39+11427G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96735021 | |||||||
chr1:96735176 | C | A | 6 | a0001c0001t0003g0020 a0001c0001t0003g0128 a0001c0001t0003g0130 others(3): Show |
6 | HG00733.hp2 HG01074.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+11582C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96735176 | |||||||
chr1:96735268 | A | G | 1 | a0001c0001t0003g0146 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.39+11674A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96735268 | |||||||
chr1:96735276 | A | G | 2 | a0001c0001t0002g0210 a0001c0001t0002g0211 |
2 | HG00099.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.39+11682A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96735276 | |||||||
chr1:96735501 | T | C | 5 | a0001c0001t0007g0008 a0001c0001t0007g0011 a0001c0001t0007g0012 others(2): Show |
5 | HG00735.hp1 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+11907T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96735501 | |||||||
chr1:96735509 | A | G | 4 | a0001c0002t0001g0311 a0001c0002t0001g0315 a0001c0002t0001g0316 others(1): Show |
4 | HG02622.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+11915A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96735509 | |||||||
chr1:96735583 | CTT | C | 70 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(67): Show |
70 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.39+11992_39+11993d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96735583 | ||||||
chr1:96735626 | C | T | 3 | a0001c0002t0005g0252 a0001c0002t0005g0253 a0001c0002t0005g0255 |
3 | HG02647.hp2 HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.39+12032C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96735626 | |||||||
chr1:96735743 | C | T | 6 | a0001c0001t0007g0008 a0001c0001t0007g0011 a0001c0001t0007g0012 others(3): Show |
6 | HG00735.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+12149C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96735743 | |||||||
chr1:96735794 | C | A | 113 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(110): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.39+12200C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96735794 | |||||||
chr1:96735871 | A | C | 113 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(110): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.39+12277A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96735871 | |||||||
chr1:96736105 | C | G | 1 | a0001c0001t0002g0213 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.39+12511C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96736105 | |||||||
chr1:96736220 | A | C | 1 | a0001c0001t0003g0045 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.39+12626A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96736220 | |||||||
chr1:96736231 | C | A | 1 | a0001c0002t0001g0352 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.39+12637C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96736231 | |||||||
chr1:96736251 | C | A | 1 | a0001c0001t0018g0234 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.39+12657C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96736251 | |||||||
chr1:96736326 | C | T | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+12732C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96736326 | |||||||
chr1:96736343 | G | A | 3 | a0001c0002t0001g0311 a0001c0002t0001g0315 a0001c0002t0001g0316 |
3 | HG02723.hp2 HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.39+12749G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96736343 | |||||||
chr1:96736725 | C | T | 1 | a0001c0002t0001g0353 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.39+13131C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96736725 | |||||||
chr1:96736839 | G | T | 1 | a0001c0001t0003g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.39+13245G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96736839 | |||||||
chr1:96736976 | T | TTTTC | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+13394_39+13397d others(6): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96736976 | ||||||
chr1:96736976 | TTTTC | T | 101 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(98): Show |
101 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.39+13394_39+13397d others(6): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96736976 | ||||||
chr1:96737098 | G | A | 2 | a0001c0001t0002g0240 a0001c0001t0002g0244 |
2 | NA18948.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.39+13504G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96737098 | |||||||
chr1:96737104 | C | G | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.39+13510C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96737104 | |||||||
chr1:96737128 | T | G | 1 | a0001c0001t0003g0090 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.39+13534T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96737128 | |||||||
chr1:96737137 | A | G | 1 | a0001c0001t0003g0090 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.39+13543A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96737137 | |||||||
chr1:96737141 | G | A | 1 | a0001c0001t0003g0090 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.39+13547G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96737141 | |||||||
chr1:96737146 | A | G | 1 | a0001c0001t0004g0021 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.39+13552A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96737146 | |||||||
chr1:96737188 | G | A | 1 | a0001c0002t0001g0325 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.39+13594G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96737188 | |||||||
chr1:96737204 | G | A | 1 | a0001c0001t0010g0204 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.39+13610G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96737204 | |||||||
chr1:96737216 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.39+13622C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96737216 | |||||||
chr1:96737279 | T | C | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+13685T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96737279 | |||||||
chr1:96737285 | T | A | 61 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0264 others(58): Show |
61 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.39+13691T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96737285 | |||||||
chr1:96737300 | T | C | 120 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(117): Show |
121 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.39+13706T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96737300 | |||||||
chr1:96737579 | G | T | 1 | a0001c0001t0002g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.40-13846G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96737579 | |||||||
chr1:96737591 | G | A | 34 | a0001c0002t0001g0263 a0001c0002t0001g0267 a0001c0002t0001g0268 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.40-13834G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96737591 | |||||||
chr1:96737746 | G | A | 2 | a0001c0001t0003g0092 a0001c0001t0003g0123 |
2 | NA18967.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.40-13679G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96737746 | |||||||
chr1:96737816 | G | C | 1 | a0001c0001t0002g0169 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.40-13609G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96737816 | |||||||
chr1:96738001 | AG | A | 7 | a0001c0002t0001g0296 a0001c0002t0001g0297 a0001c0002t0001g0298 others(4): Show |
7 | HG01109.hp1 HG02109.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.40-13423delG | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96738001 | |||||||
chr1:96738234 | GTA | G | 119 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(116): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.40-13178_40-13177d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96738234 | ||||||
chr1:96738243 | T | C | 1 | a0001c0001t0002g0209 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.40-13182T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96738243 | |||||||
chr1:96738336 | C | T | 19 | a0001c0002t0001g0263 a0001c0002t0001g0268 a0001c0002t0001g0269 others(16): Show |
19 | HG00558.hp2 HG01109.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.40-13089C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96738336 | |||||||
chr1:96738460 | A | C | 1 | a0001c0002t0001g0330 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.40-12965A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96738460 | |||||||
chr1:96738475 | G | A | 119 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(116): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.40-12950G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96738475 | |||||||
chr1:96738476 | T | TGTTAGCC others(1): Show |
11 | a0001c0002t0001g0267 a0001c0002t0001g0270 a0001c0002t0001g0294 others(8): Show |
11 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.40-12947_40-12940d others(10): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96738476 | ||||||
chr1:96738647 | T | C | 219 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.40-12778T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96738647 | |||||||
chr1:96738735 | A | G | 20 | a0001c0001t0001g0220 a0001c0001t0002g0017 a0001c0001t0002g0154 others(17): Show |
20 | HG00099.hp2 HG01099.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.40-12690A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96738735 | |||||||
chr1:96738921 | G | A | 1 | a0001c0002t0001g0303 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.40-12504G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96738921 | |||||||
chr1:96738983 | A | C | 1 | a0001c0002t0001g0313 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.40-12442A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96738983 | |||||||
chr1:96739019 | T | A | 119 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(116): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.40-12406T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96739019 | |||||||
chr1:96739058 | A | G | 2 | a0001c0002t0001g0288 a0001c0002t0008g0289 |
2 | HG01433.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.40-12367A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96739058 | |||||||
chr1:96739369 | A | G | 1 | a0001c0001t0003g0087 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.40-12056A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96739369 | |||||||
chr1:96739379 | G | A | 6 | a0001c0001t0003g0019 a0001c0001t0003g0128 a0001c0001t0003g0130 others(3): Show |
6 | HG00733.hp2 HG01074.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-12046G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96739379 | |||||||
chr1:96739546 | T | C | 1 | a0001c0002t0001g0309 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.40-11879T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96739546 | |||||||
chr1:96739617 | T | TG | 28 | a0001c0001t0001g0220 a0001c0001t0002g0155 a0001c0001t0002g0158 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.40-11807dupG | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96739617 | ||||||
chr1:96739618 | G | GT | 33 | a0001c0001t0003g0007 a0001c0001t0003g0019 a0001c0001t0003g0020 others(30): Show |
33 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.40-11781dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96739618 | ||||||
chr1:96739618 | GT | G | 99 | a0001c0001t0001g0003 a0001c0001t0002g0170 a0001c0001t0002g0171 others(96): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.40-11781delT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96739618 | ||||||
chr1:96739618 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0007g0016 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.40-11790_40-11781d others(12): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96739618 | ||||||
chr1:96739619 | T | G | 68 | a0001c0001t0001g0163 a0001c0001t0001g0229 a0001c0001t0002g0017 others(65): Show |
68 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.40-11806T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96739619 | |||||||
chr1:96739620 | T | G | 14 | a0001c0001t0002g0170 a0001c0001t0002g0171 a0001c0001t0002g0172 others(11): Show |
14 | HG00642.hp1 HG00735.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.40-11805T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96739620 | |||||||
chr1:96739629 | T | G | 1 | a0001c0001t0007g0016 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.40-11796T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96739629 | |||||||
chr1:96739650 | G | A | 1 | a0001c0001t0007g0015 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.40-11775G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96739650 | |||||||
chr1:96739690 | G | A | 102 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(99): Show |
102 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.40-11735G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96739690 | |||||||
chr1:96739799 | A | T | 1 | a0001c0001t0002g0176 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.40-11626A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96739799 | |||||||
chr1:96739801 | A | T | 225 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(222): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.40-11624A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96739801 | |||||||
chr1:96739919 | T | C | 119 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(116): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.40-11506T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96739919 | |||||||
chr1:96740089 | A | G | 17 | a0001c0002t0001g0310 a0001c0002t0001g0311 a0001c0002t0001g0312 others(14): Show |
17 | HG01884.hp2 HG02109.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.40-11336A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96740089 | |||||||
chr1:96740152 | A | G | 1 | a0001c0002t0001g0354 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.40-11273A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96740152 | |||||||
chr1:96740219 | A | G | 119 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(116): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.40-11206A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96740219 | |||||||
chr1:96740255 | G | A | 15 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(12): Show |
15 | HG00733.hp1 HG01433.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.40-11170G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96740255 | |||||||
chr1:96740298 | G | C | 1 | a0001c0003t0001g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.40-11127G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96740298 | |||||||
chr1:96740322 | A | C | 5 | a0001c0001t0003g0038 a0001c0001t0003g0081 a0001c0001t0003g0085 others(2): Show |
5 | HG00438.hp2 HG02129.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-11103A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96740322 | |||||||
chr1:96740369 | C | T | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.40-11056C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96740369 | |||||||
chr1:96740556 | G | C | 119 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(116): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.40-10869G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96740556 | |||||||
chr1:96740558 | G | C | 119 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(116): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.40-10867G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96740558 | |||||||
chr1:96740570 | C | T | 1 | a0001c0001t0010g0204 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.40-10855C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96740570 | |||||||
chr1:96740676 | A | G | 1 | a0001c0002t0001g0284 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.40-10749A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96740676 | |||||||
chr1:96740785 | T | TTA | 7 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(4): Show |
7 | HG00558.hp1 HG01884.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-10626_40-10625d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96740785 | ||||||
chr1:96740900 | A | G | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-10525A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96740900 | |||||||
chr1:96740940 | A | C | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.40-10485A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96740940 | |||||||
chr1:96740941 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.40-10484C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96740941 | |||||||
chr1:96741040 | G | A | 1 | a0001c0001t0006g0093 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.40-10385G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96741040 | |||||||
chr1:96741151 | A | G | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.40-10274A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96741151 | |||||||
chr1:96741165 | C | CA | 11 | a0001c0001t0001g0003 a0001c0001t0003g0028 a0001c0001t0003g0033 others(8): Show |
11 | HG01433.hp2 HG02572.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.40-10247dupA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96741165 | ||||||
chr1:96741165 | CA | C | 10 | a0001c0001t0001g0163 a0001c0001t0002g0162 a0001c0001t0002g0167 others(7): Show |
10 | HG00639.hp2 HG06807.hp2 NA18940.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-10247delA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96741165 | ||||||
chr1:96741182 | T | C | 1 | a0001c0001t0018g0234 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.40-10243T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96741182 | |||||||
chr1:96741296 | G | A | 119 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(116): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.40-10129G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96741296 | |||||||
chr1:96741435 | A | G | 1 | a0001c0001t0003g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.40-9990A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96741435 | |||||||
chr1:96741484 | A | G | 119 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(116): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.40-9941A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96741484 | |||||||
chr1:96741598 | CCT | C | 6 | a0001c0001t0003g0076 a0001c0001t0004g0030 a0001c0001t0004g0037 others(3): Show |
6 | HG00639.hp1 HG00741.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-9820_40-9819del others(2): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96741598 | ||||||
chr1:96742003 | G | T | 2 | a0001c0001t0003g0042 a0001c0001t0003g0074 |
2 | NA18944.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.40-9422G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96742003 | |||||||
chr1:96742065 | C | G | 1 | a0001c0001t0019g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.40-9360C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96742065 | |||||||
chr1:96742167 | T | C | 1 | a0001c0002t0001g0268 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.40-9258T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96742167 | |||||||
chr1:96742198 | A | G | 12 | a0001c0001t0001g0229 a0001c0001t0002g0160 a0001c0001t0002g0174 others(9): Show |
12 | HG00423.hp2 HG02027.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.40-9227A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96742198 | |||||||
chr1:96742468 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.40-8957C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96742468 | |||||||
chr1:96742662 | C | CT | 13 | a0001c0001t0002g0156 a0001c0001t0003g0044 a0001c0001t0003g0083 others(10): Show |
14 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.40-8746dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96742662 | ||||||
chr1:96742662 | CT | C | 34 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0194 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.40-8746delT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96742662 | ||||||
chr1:96742948 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.40-8477C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96742948 | |||||||
chr1:96743130 | C | T | 1 | a0001c0005t0012g0077 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.40-8295C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96743130 | |||||||
chr1:96743147 | C | T | 1 | a0001c0001t0004g0046 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.40-8278C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96743147 | |||||||
chr1:96743186 | C | G | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.40-8239C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96743186 | |||||||
chr1:96743267 | A | ACTC | 128 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(125): Show |
129 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.40-8156_40-8154dup others(3): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96743267 | ||||||
chr1:96743276 | T | TA | 219 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.40-8133dupA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96743276 | ||||||
chr1:96743304 | G | A | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.40-8121G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96743304 | |||||||
chr1:96743322 | C | T | 21 | a0001c0001t0002g0221 a0001c0001t0002g0223 a0001c0001t0002g0224 others(18): Show |
21 | HG00544.hp2 HG00621.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.40-8103C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96743322 | |||||||
chr1:96743553 | ATTC | A | 5 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(2): Show |
5 | HG01943.hp1 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-7869_40-7867del others(3): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96743553 | ||||||
chr1:96743639 | G | C | 2 | a0001c0001t0003g0023 a0001c0001t0006g0024 |
2 | HG02602.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.40-7786G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96743639 | |||||||
chr1:96743651 | T | C | 1 | a0001c0001t0003g0139 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.40-7774T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96743651 | |||||||
chr1:96743689 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.40-7736A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96743689 | |||||||
chr1:96743783 | A | G | 4 | a0001c0001t0003g0044 a0001c0001t0003g0083 a0001c0001t0003g0090 others(1): Show |
4 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-7642A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96743783 | |||||||
chr1:96743783 | A | T | 6 | a0001c0001t0007g0008 a0001c0001t0007g0011 a0001c0001t0007g0012 others(3): Show |
6 | HG00735.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-7642A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96743783 | |||||||
chr1:96743819 | T | G | 1 | a0001c0001t0004g0126 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-7606T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96743819 | |||||||
chr1:96743915 | A | C | 128 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(125): Show |
129 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.40-7510A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96743915 | |||||||
chr1:96744000 | A | C | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.40-7425A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96744000 | |||||||
chr1:96744148 | C | T | 1 | a0001c0005t0012g0077 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.40-7277C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96744148 | |||||||
chr1:96744173 | G | A | 1 | a0001c0001t0002g0191 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.40-7252G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96744173 | |||||||
chr1:96744267 | T | C | 1 | a0001c0001t0003g0146 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.40-7158T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96744267 | |||||||
chr1:96744322 | A | AT | 3 | a0001c0001t0001g0163 a0001c0001t0002g0162 a0001c0001t0002g0169 |
3 | NA18940.hp2 NA18949.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.40-7102dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96744322 | ||||||
chr1:96744324 | A | T | 128 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(125): Show |
129 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.40-7101A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96744324 | |||||||
chr1:96744326 | T | A | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-7099T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96744326 | |||||||
chr1:96744507 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.40-6918C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96744507 | |||||||
chr1:96744557 | A | G | 43 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0264 others(40): Show |
43 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.40-6868A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96744557 | |||||||
chr1:96744962 | C | T | 7 | a0001c0001t0003g0033 a0001c0001t0003g0073 a0001c0001t0003g0122 others(4): Show |
7 | HG00741.hp2 HG01081.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.40-6463C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96744962 | |||||||
chr1:96745017 | T | C | 1 | a0001c0001t0004g0025 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.40-6408T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96745017 | |||||||
chr1:96745173 | C | CT | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.40-6240dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96745173 | ||||||
chr1:96745173 | CT | C | 111 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(108): Show |
111 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.40-6240delT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96745173 | ||||||
chr1:96745208 | G | T | 1 | a0001c0001t0008g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.40-6217G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96745208 | |||||||
chr1:96745493 | T | G | 1 | a0001c0001t0002g0226 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.40-5932T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96745493 | |||||||
chr1:96745554 | A | G | 1 | a0001c0002t0001g0305 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.40-5871A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96745554 | |||||||
chr1:96745575 | T | A | 15 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(12): Show |
15 | HG00733.hp1 HG01433.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.40-5850T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96745575 | |||||||
chr1:96745727 | T | A | 1 | a0001c0001t0003g0107 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.40-5698T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96745727 | |||||||
chr1:96746071 | C | A | 1 | a0001c0001t0002g0176 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.40-5354C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746071 | |||||||
chr1:96746071 | C | CA | 124 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.40-5351dupA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746071 | ||||||
chr1:96746075 | C | A | 234 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.40-5350C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746075 | |||||||
chr1:96746199 | T | C | 6 | a0001c0001t0007g0008 a0001c0001t0007g0011 a0001c0001t0007g0012 others(3): Show |
6 | HG00735.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-5226T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746199 | |||||||
chr1:96746405 | A | G | 1 | a0001c0001t0004g0105 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.40-5020A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746405 | |||||||
chr1:96746453 | G | A | 14 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(11): Show |
14 | HG00733.hp1 HG01433.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.40-4972G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746453 | |||||||
chr1:96746702 | G | GA | 142 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.40-4705dupA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746702 | ||||||
chr1:96746702 | GA | G | 23 | a0001c0001t0003g0085 a0001c0001t0003g0104 a0001c0001t0004g0111 others(20): Show |
23 | HG01256.hp2 HG01884.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.40-4705delA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746702 | ||||||
chr1:96746767 | T | C | 1 | a0001c0001t0003g0123 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.40-4658T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746767 | |||||||
chr1:96746800 | C | T | 1 | a0001c0003t0001g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.40-4625C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746800 | |||||||
chr1:96746817 | TTGTC | T | 3 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0002t0001g0285 |
3 | HG00099.hp2 HG01109.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.40-4590_40-4587del others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746817 | ||||||
chr1:96746817 | TTGTCTGT others(1): Show |
T | 8 | a0001c0001t0003g0146 a0001c0002t0005g0002 a0001c0002t0005g0251 others(5): Show |
9 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.40-4594_40-4587del others(8): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746817 | ||||||
chr1:96746831 | G | C | 110 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(107): Show |
110 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.40-4594G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746831 | |||||||
chr1:96746832 | T | C | 110 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(107): Show |
110 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.40-4593T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746832 | |||||||
chr1:96746835 | G | C | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.40-4590G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746835 | |||||||
chr1:96746836 | T | C | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.40-4589T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746836 | |||||||
chr1:96746848 | C | T | 108 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.40-4577C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746848 | |||||||
chr1:96746850 | T | C | 108 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.40-4575T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746850 | |||||||
chr1:96746852 | C | CCTCT | 95 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.40-4572_40-4571ins others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746852 | ||||||
chr1:96746852 | C | T | 110 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(107): Show |
110 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.40-4573C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746852 | |||||||
chr1:96746854 | C | T | 13 | a0001c0001t0003g0146 a0001c0002t0005g0002 a0001c0002t0005g0251 others(10): Show |
14 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.40-4571C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746854 | |||||||
chr1:96746863 | G | C | 13 | a0001c0001t0003g0146 a0001c0002t0005g0002 a0001c0002t0005g0251 others(10): Show |
14 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.40-4562G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746863 | |||||||
chr1:96746867 | G | C | 8 | a0001c0001t0003g0146 a0001c0002t0005g0002 a0001c0002t0005g0251 others(5): Show |
9 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.40-4558G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746867 | |||||||
chr1:96746867 | GTCTGTCC others(1): Show |
G | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-4555_40-4548del others(8): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746867 | ||||||
chr1:96746870 | T | C | 8 | a0001c0001t0003g0146 a0001c0002t0005g0002 a0001c0002t0005g0251 others(5): Show |
9 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.40-4555T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746870 | |||||||
chr1:96746871 | GTCCCTCC others(5): Show |
G | 5 | a0001c0001t0003g0023 a0001c0001t0003g0076 a0001c0001t0004g0030 others(2): Show |
5 | HG00639.hp1 HG00741.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-4520_40-4509del others(12): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746871 | ||||||
chr1:96746871 | GTCCCTCC others(9): Show |
G | 1 | a0001c0001t0016g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.40-4524_40-4509del others(16): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746871 | ||||||
chr1:96746875 | C | G | 8 | a0001c0001t0003g0146 a0001c0002t0005g0002 a0001c0002t0005g0251 others(5): Show |
9 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.40-4550C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746875 | |||||||
chr1:96746878 | C | T | 52 | a0001c0001t0003g0146 a0001c0002t0001g0004 a0001c0002t0001g0152 others(49): Show |
53 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.40-4547C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746878 | |||||||
chr1:96746879 | C | G | 13 | a0001c0001t0003g0146 a0001c0002t0005g0002 a0001c0002t0005g0251 others(10): Show |
14 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.40-4546C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746879 | |||||||
chr1:96746882 | C | T | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-4543C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746882 | |||||||
chr1:96746883 | C | G | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-4542C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746883 | |||||||
chr1:96746889 | CCCTCCCT others(25): Show |
C | 1 | a0001c0001t0002g0217 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.40-4532_40-4501del others(32): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746889 | ||||||
chr1:96746893 | CCCTCCCT others(21): Show |
C | 3 | a0001c0001t0001g0229 a0001c0001t0002g0185 a0001c0001t0002g0206 |
3 | HG00597.hp1 NA18999.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.40-4528_40-4501del others(28): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746893 | ||||||
chr1:96746893 | CCCTCCCT others(33): Show |
C | 1 | a0001c0002t0001g0341 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.40-4528_40-4489del others(40): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746893 | ||||||
chr1:96746901 | CCCTCCCT others(13): Show |
C | 3 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0016 |
3 | HG00735.hp2 HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.40-4520_40-4501del others(20): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746901 | ||||||
chr1:96746901 | CCCTCCCT others(25): Show |
C | 2 | a0001c0002t0001g0267 a0001c0002t0001g0270 |
2 | HG00099.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.40-4520_40-4489del others(32): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746901 | ||||||
chr1:96746905 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.40-4520C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746905 | |||||||
chr1:96746905 | CCCTCCCT others(9): Show |
C | 1 | a0001c0001t0002g0175 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.40-4516_40-4501del others(16): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746905 | ||||||
chr1:96746905 | CCCTCCCT others(13): Show |
C | 1 | a0001c0001t0007g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.40-4516_40-4497del others(20): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746905 | ||||||
chr1:96746909 | C | CCCTT | 15 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(12): Show |
15 | HG00733.hp1 HG01433.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.40-4513_40-4512ins others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746909 | ||||||
chr1:96746909 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0355 a0001c0001t0001g0356 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.40-4516C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746909 | |||||||
chr1:96746909 | CCCTCCCT others(5): Show |
C | 88 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0002g0017 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.40-4512_40-4501del others(12): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746909 | ||||||
chr1:96746909 | CCCTCCCT others(9): Show |
C | 5 | a0001c0001t0007g0008 a0001c0001t0007g0011 a0001c0001t0007g0012 others(2): Show |
5 | HG00735.hp1 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-4512_40-4497del others(16): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746909 | ||||||
chr1:96746909 | CCCTCCCT others(17): Show |
C | 63 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(60): Show |
63 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.40-4512_40-4489del others(24): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746909 | ||||||
chr1:96746913 | C | CCCTT | 27 | a0001c0001t0003g0047 a0001c0001t0003g0049 a0001c0001t0003g0112 others(24): Show |
27 | HG01175.hp1 HG01243.hp1 HG01943.hp2 others(24): Show |
intron_variant | MODIFIER | c.40-4484_40-4481dup others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746913 | ||||||
chr1:96746913 | C | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0355 a0001c0001t0001g0356 others(109): Show |
113 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.40-4512C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746913 | |||||||
chr1:96746913 | CCCTT | C | 3 | a0001c0001t0003g0146 a0001c0001t0007g0153 a0001c0001t0011g0186 |
3 | HG02976.hp2 NA18979.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.40-4484_40-4481del others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746913 | ||||||
chr1:96746913 | CCCTTCCT others(1): Show |
C | 15 | a0001c0001t0002g0167 a0001c0001t0002g0171 a0001c0001t0002g0182 others(12): Show |
16 | HG02647.hp2 HG02965.hp2 HG02970.hp2 others(13): Show |
intron_variant | MODIFIER | c.40-4488_40-4481del others(8): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746913 | ||||||
chr1:96746913 | CCCTTCCT others(9): Show |
C | 3 | a0001c0002t0001g0344 a0001c0002t0001g0346 a0001c0002t0001g0347 |
3 | HG02809.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.40-4496_40-4481del others(16): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746913 | ||||||
chr1:96746913 | CCCTTCCT others(13): Show |
C | 26 | a0001c0002t0001g0275 a0001c0002t0001g0283 a0001c0002t0001g0294 others(23): Show |
26 | HG00140.hp1 HG01099.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.40-4500_40-4481del others(20): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96746913 | ||||||
chr1:96746917 | T | C | 1 | a0001c0001t0002g0161 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.40-4508T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746917 | |||||||
chr1:96746921 | T | C | 3 | a0001c0001t0002g0161 a0001c0001t0003g0146 a0001c0001t0011g0186 |
3 | NA18979.hp2 NA19006.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.40-4504T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746921 | |||||||
chr1:96746933 | T | C | 3 | a0001c0002t0001g0344 a0001c0002t0001g0346 a0001c0002t0001g0347 |
3 | HG02809.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.40-4492T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96746933 | |||||||
chr1:96747120 | C | A | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.40-4305C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96747120 | |||||||
chr1:96747156 | T | C | 1 | a0001c0001t0003g0104 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.40-4269T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96747156 | |||||||
chr1:96747207 | T | A | 113 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(110): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.40-4218T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96747207 | |||||||
chr1:96747231 | T | G | 1 | a0001c0002t0001g0339 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.40-4194T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96747231 | |||||||
chr1:96747260 | T | C | 2 | a0001c0002t0005g0251 a0001c0002t0005g0254 |
2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.40-4165T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96747260 | |||||||
chr1:96747512 | A | C | 1 | a0001c0001t0002g0187 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.40-3913A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96747512 | |||||||
chr1:96747551 | CAATT | C | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-3871_40-3868del others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96747551 | ||||||
chr1:96747785 | T | TCC | 5 | a0001c0001t0001g0229 a0001c0001t0002g0174 a0001c0001t0002g0217 others(2): Show |
5 | HG02027.hp1 NA18978.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-3638_40-3637dup others(2): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96747785 | ||||||
chr1:96747911 | G | A | 2 | a0001c0001t0004g0134 a0001c0001t0006g0072 |
2 | HG01175.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.40-3514G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96747911 | |||||||
chr1:96748075 | G | A | 1 | a0001c0002t0005g0254 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.40-3350G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96748075 | |||||||
chr1:96748154 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.40-3271G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96748154 | |||||||
chr1:96748161 | T | A | 113 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(110): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.40-3264T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96748161 | |||||||
chr1:96748367 | T | C | 1 | a0001c0001t0001g0355 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.40-3058T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96748367 | |||||||
chr1:96748436 | A | AT | 113 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(110): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.40-2980dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96748436 | ||||||
chr1:96748465 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.40-2960C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96748465 | |||||||
chr1:96748925 | G | A | 1 | a0001c0001t0002g0215 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.40-2500G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96748925 | |||||||
chr1:96748948 | A | C | 1 | a0001c0001t0002g0188 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.40-2477A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96748948 | |||||||
chr1:96749203 | CTTT | C | 113 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(110): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.40-2220_40-2218del others(3): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96749203 | ||||||
chr1:96749208 | C | A | 113 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(110): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.40-2217C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96749208 | |||||||
chr1:96749209 | T | A | 113 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(110): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.40-2216T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96749209 | |||||||
chr1:96749250 | A | G | 1 | a0001c0001t0002g0235 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-2175A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96749250 | |||||||
chr1:96749404 | G | A | 1 | a0001c0002t0005g0252 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.40-2021G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96749404 | |||||||
chr1:96749707 | A | G | 4 | a0001c0001t0003g0044 a0001c0001t0003g0083 a0001c0001t0003g0090 others(1): Show |
4 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-1718A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96749707 | |||||||
chr1:96749904 | T | G | 1 | a0001c0001t0002g0213 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.40-1521T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96749904 | |||||||
chr1:96749934 | T | C | 6 | a0001c0001t0007g0008 a0001c0001t0007g0011 a0001c0001t0007g0012 others(3): Show |
6 | HG00735.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-1491T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96749934 | |||||||
chr1:96750069 | T | C | 15 | a0001c0002t0001g0267 a0001c0002t0001g0270 a0001c0002t0001g0294 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.40-1356T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96750069 | |||||||
chr1:96750077 | A | G | 1 | a0001c0001t0007g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.40-1348A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96750077 | |||||||
chr1:96750204 | G | C | 119 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(116): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.40-1221G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96750204 | |||||||
chr1:96750392 | G | GT | 16 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0003g0041 others(13): Show |
16 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.40-1022dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96750392 | ||||||
chr1:96750392 | GT | G | 13 | a0001c0002t0001g0338 a0001c0002t0005g0002 a0001c0002t0005g0251 others(10): Show |
14 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.40-1022delT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 96750392 | ||||||
chr1:96750480 | C | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(224): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.40-945C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96750480 | |||||||
chr1:96750571 | T | C | 113 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(110): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.40-854T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96750571 | |||||||
chr1:96750597 | C | G | 1 | a0001c0001t0003g0023 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.40-828C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96750597 | |||||||
chr1:96750780 | G | A | 227 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(224): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.40-645G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96750780 | |||||||
chr1:96750794 | C | A | 1 | a0001c0001t0001g0220 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.40-631C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96750794 | |||||||
chr1:96750810 | T | C | 1 | a0001c0001t0018g0234 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.40-615T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96750810 | |||||||
chr1:96750926 | A | G | 1 | a0001c0002t0001g0266 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.40-499A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96750926 | |||||||
chr1:96751006 | T | C | 1 | a0001c0001t0002g0209 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.40-419T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96751006 | |||||||
chr1:96751094 | C | G | 1 | a0001c0001t0002g0248 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.40-331C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96751094 | |||||||
chr1:96751392 | A | G | 3 | a0001c0001t0003g0026 a0001c0001t0003g0043 a0001c0001t0004g0025 |
3 | HG03471.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.40-33A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96751392 | |||||||
chr1:96751419 | T | C | 9 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0010 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG02280.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.40-6T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 2/13 | chr1 | 96751419 | |||||||
chr1:96751513 | C | A | 1 | a0001c0001t0006g0029 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.115+13C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96751513 | |||||||
chr1:96751658 | G | GA | 125 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(122): Show |
126 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.115+172dupA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96751658 | ||||||
chr1:96751658 | G | GAA | 9 | a0001c0001t0002g0161 a0001c0001t0002g0180 a0001c0001t0002g0216 others(6): Show |
9 | HG00735.hp2 HG03579.hp1 HG04199.hp2 others(6): Show |
intron_variant | MODIFIER | c.115+171_115+172dup others(2): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96751658 | ||||||
chr1:96751658 | GA | G | 90 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(87): Show |
90 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.115+172delA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96751658 | ||||||
chr1:96751930 | T | C | 8 | a0001c0001t0002g0158 a0001c0001t0002g0171 a0001c0001t0002g0178 others(5): Show |
8 | NA18943.hp1 NA18954.hp2 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+430T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96751930 | |||||||
chr1:96751938 | A | G | 1 | a0001c0002t0001g0325 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.115+438A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96751938 | |||||||
chr1:96751961 | G | T | 1 | a0001c0001t0002g0161 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.115+461G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96751961 | |||||||
chr1:96752037 | A | G | 1 | a0001c0001t0001g0360 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.115+537A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96752037 | |||||||
chr1:96752150 | AT | A | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+659delT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96752150 | ||||||
chr1:96752262 | A | G | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+762A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96752262 | |||||||
chr1:96752346 | T | C | 1 | a0001c0001t0003g0039 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.115+846T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96752346 | |||||||
chr1:96752462 | C | T | 1 | a0001c0003t0001g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.115+962C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96752462 | |||||||
chr1:96752598 | A | G | 6 | a0001c0001t0003g0076 a0001c0001t0004g0030 a0001c0001t0004g0037 others(3): Show |
6 | HG00639.hp1 HG00741.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.115+1098A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96752598 | |||||||
chr1:96752722 | C | A | 3 | a0001c0001t0003g0026 a0001c0001t0003g0043 a0001c0001t0004g0025 |
3 | HG03471.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.115+1222C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96752722 | |||||||
chr1:96752787 | CA | C | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+1291delA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96752787 | ||||||
chr1:96752792 | C | T | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+1292C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96752792 | |||||||
chr1:96752887 | C | T | 7 | a0001c0002t0001g0311 a0001c0002t0001g0314 a0001c0002t0001g0315 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+1387C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96752887 | |||||||
chr1:96752897 | G | A | 2 | a0001c0001t0003g0095 a0001c0001t0003g0114 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.115+1397G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96752897 | |||||||
chr1:96753011 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.115+1511G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96753011 | |||||||
chr1:96753073 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.115+1573G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96753073 | |||||||
chr1:96753075 | G | T | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.115+1575G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96753075 | |||||||
chr1:96753110 | G | A | 1 | a0001c0001t0006g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.115+1610G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96753110 | |||||||
chr1:96753225 | G | A | 22 | a0001c0001t0001g0163 a0001c0001t0002g0158 a0001c0001t0002g0162 others(19): Show |
22 | HG00621.hp2 HG00639.hp2 NA18939.hp2 others(19): Show |
intron_variant | MODIFIER | c.115+1725G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96753225 | |||||||
chr1:96753729 | T | G | 1 | a0001c0001t0002g0162 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.115+2229T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96753729 | |||||||
chr1:96753746 | AGC | A | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+2247_115+2248d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96753746 | |||||||
chr1:96753750 | T | C | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+2250T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96753750 | |||||||
chr1:96753765 | A | G | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+2265A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96753765 | |||||||
chr1:96753783 | T | A | 4 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(1): Show |
4 | HG02717.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+2283T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96753783 | |||||||
chr1:96753799 | G | A | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+2299G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96753799 | |||||||
chr1:96754125 | C | T | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+2625C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96754125 | |||||||
chr1:96754315 | A | G | 48 | a0001c0001t0001g0163 a0001c0001t0002g0162 a0001c0001t0002g0169 others(45): Show |
48 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.115+2815A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96754315 | |||||||
chr1:96754559 | A | T | 1 | a0001c0001t0002g0235 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.115+3059A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96754559 | |||||||
chr1:96754801 | C | T | 95 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.115+3301C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96754801 | |||||||
chr1:96754930 | A | T | 1 | a0001c0001t0002g0201 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.115+3430A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96754930 | |||||||
chr1:96755121 | A | G | 7 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0194 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+3621A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96755121 | |||||||
chr1:96755215 | C | T | 226 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.115+3715C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96755215 | |||||||
chr1:96755415 | A | G | 1 | a0001c0002t0001g0351 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.115+3915A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96755415 | |||||||
chr1:96755585 | C | T | 1 | a0001c0001t0003g0103 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.115+4085C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96755585 | |||||||
chr1:96755860 | ACAGGAAA others(3): Show |
A | 1 | a0001c0001t0003g0146 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.115+4362_115+4371d others(12): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96755860 | ||||||
chr1:96755895 | T | C | 1 | a0001c0002t0001g0312 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.115+4395T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96755895 | |||||||
chr1:96755982 | G | A | 1 | a0001c0001t0004g0106 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.115+4482G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96755982 | |||||||
chr1:96756060 | T | C | 1 | a0001c0002t0001g0313 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.115+4560T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96756060 | |||||||
chr1:96756116 | C | T | 5 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(2): Show |
5 | HG01943.hp1 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.115+4616C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96756116 | |||||||
chr1:96756136 | C | T | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+4636C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96756136 | |||||||
chr1:96756173 | C | T | 9 | a0001c0002t0001g0353 a0001c0002t0001g0354 a0001c0002t0005g0002 others(6): Show |
10 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.115+4673C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96756173 | |||||||
chr1:96756355 | C | T | 1 | a0001c0001t0007g0013 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.115+4855C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96756355 | |||||||
chr1:96756531 | C | A | 4 | a0001c0001t0003g0044 a0001c0001t0003g0083 a0001c0001t0003g0090 others(1): Show |
4 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+5031C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96756531 | |||||||
chr1:96756611 | CACT | C | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+5113_115+5115d others(5): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96756611 | ||||||
chr1:96756615 | A | T | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+5115A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96756615 | |||||||
chr1:96756616 | A | G | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+5116A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96756616 | |||||||
chr1:96756775 | A | C | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+5275A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96756775 | |||||||
chr1:96757110 | C | T | 1 | a0001c0001t0003g0052 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.115+5610C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96757110 | |||||||
chr1:96757140 | T | C | 1 | a0001c0002t0001g0269 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.115+5640T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96757140 | |||||||
chr1:96757324 | C | CAG | 12 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(9): Show |
13 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.115+5826_115+5827d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96757324 | ||||||
chr1:96757350 | A | G | 2 | a0001c0001t0002g0199 a0001c0001t0002g0232 |
2 | HG01168.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.115+5850A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96757350 | |||||||
chr1:96757548 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.115+6048C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96757548 | |||||||
chr1:96757637 | A | T | 1 | a0001c0001t0003g0032 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.115+6137A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96757637 | |||||||
chr1:96757715 | T | A | 1 | a0001c0001t0003g0082 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.115+6215T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96757715 | |||||||
chr1:96757740 | A | G | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+6240A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96757740 | |||||||
chr1:96757873 | T | C | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+6373T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96757873 | |||||||
chr1:96758068 | T | C | 6 | a0001c0001t0007g0008 a0001c0001t0007g0011 a0001c0001t0007g0012 others(3): Show |
6 | HG00735.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.115+6568T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96758068 | |||||||
chr1:96758180 | C | T | 1 | a0001c0001t0004g0134 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.115+6680C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96758180 | |||||||
chr1:96758219 | C | CT | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+6721dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96758219 | ||||||
chr1:96758436 | A | C | 12 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(9): Show |
13 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.115+6936A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96758436 | |||||||
chr1:96758864 | T | C | 3 | a0001c0001t0003g0140 a0001c0001t0003g0141 a0001c0001t0003g0143 |
3 | NA18964.hp1 NA18973.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.115+7364T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96758864 | |||||||
chr1:96758883 | T | G | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+7383T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96758883 | |||||||
chr1:96759089 | T | C | 1 | a0001c0001t0003g0078 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.115+7589T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96759089 | |||||||
chr1:96759405 | C | T | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+7905C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96759405 | |||||||
chr1:96759470 | C | T | 1 | a0001c0002t0001g0331 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.115+7970C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96759470 | |||||||
chr1:96759664 | A | G | 103 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(100): Show |
103 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.115+8164A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96759664 | |||||||
chr1:96759703 | C | A | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+8203C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96759703 | |||||||
chr1:96759726 | T | C | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+8226T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96759726 | |||||||
chr1:96759768 | T | C | 7 | a0001c0001t0003g0028 a0001c0001t0003g0086 a0001c0001t0003g0112 others(4): Show |
7 | HG00733.hp1 HG01433.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+8268T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96759768 | |||||||
chr1:96759779 | G | A | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+8279G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96759779 | |||||||
chr1:96759827 | C | T | 1 | a0001c0001t0017g0230 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.115+8327C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96759827 | |||||||
chr1:96759843 | A | G | 1 | a0001c0001t0002g0215 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.115+8343A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96759843 | |||||||
chr1:96759881 | A | G | 2 | a0001c0002t0001g0300 a0001c0002t0001g0301 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.115+8381A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96759881 | |||||||
chr1:96759978 | G | A | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+8478G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96759978 | |||||||
chr1:96760145 | A | G | 1 | a0001c0001t0002g0243 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.115+8645A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96760145 | |||||||
chr1:96760173 | T | TA | 8 | a0001c0001t0009g0054 a0001c0002t0005g0002 a0001c0002t0005g0251 others(5): Show |
9 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.115+8683dupA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96760173 | ||||||
chr1:96760279 | T | G | 1 | a0001c0001t0017g0230 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.115+8779T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96760279 | |||||||
chr1:96760333 | A | G | 3 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0003g0146 |
3 | HG00544.hp2 HG02080.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.115+8833A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96760333 | |||||||
chr1:96760365 | T | C | 235 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.115+8865T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96760365 | |||||||
chr1:96760440 | C | CT | 32 | a0001c0001t0001g0003 a0001c0001t0001g0358 a0001c0001t0002g0183 others(29): Show |
32 | HG00140.hp1 HG00621.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.115+8964dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96760440 | ||||||
chr1:96760440 | C | CTT | 8 | a0001c0001t0009g0113 a0001c0002t0005g0002 a0001c0002t0005g0251 others(5): Show |
9 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.115+8963_115+8964d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96760440 | ||||||
chr1:96760440 | CT | C | 30 | a0001c0001t0002g0200 a0001c0001t0003g0039 a0001c0001t0003g0056 others(27): Show |
30 | HG00558.hp2 HG01109.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.115+8964delT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96760440 | ||||||
chr1:96760520 | A | G | 1 | a0001c0001t0003g0103 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.115+9020A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96760520 | |||||||
chr1:96760587 | A | T | 1 | a0001c0003t0001g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.115+9087A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96760587 | |||||||
chr1:96760603 | A | G | 1 | a0001c0001t0004g0031 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.116-9100A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96760603 | |||||||
chr1:96760606 | C | T | 6 | a0001c0001t0003g0038 a0001c0001t0003g0081 a0001c0001t0003g0085 others(3): Show |
6 | HG00438.hp2 HG02004.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-9097C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96760606 | |||||||
chr1:96760611 | A | G | 1 | a0001c0001t0004g0030 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.116-9092A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96760611 | |||||||
chr1:96760726 | T | G | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-8977T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96760726 | |||||||
chr1:96760764 | G | A | 1 | a0001c0001t0004g0134 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.116-8939G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96760764 | |||||||
chr1:96760841 | A | G | 2 | a0001c0001t0003g0137 a0001c0001t0004g0110 |
2 | HG01981.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.116-8862A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96760841 | |||||||
chr1:96760873 | T | C | 1 | a0001c0001t0003g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.116-8830T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96760873 | |||||||
chr1:96760992 | C | T | 1 | a0001c0002t0001g0270 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.116-8711C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96760992 | |||||||
chr1:96761063 | G | A | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-8640G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96761063 | |||||||
chr1:96761119 | A | G | 44 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0264 others(41): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.116-8584A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96761119 | |||||||
chr1:96761131 | A | G | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-8572A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96761131 | |||||||
chr1:96761176 | C | T | 1 | a0001c0002t0005g0257 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.116-8527C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96761176 | |||||||
chr1:96761182 | A | G | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-8521A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96761182 | |||||||
chr1:96761217 | G | T | 235 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.116-8486G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96761217 | |||||||
chr1:96761264 | G | T | 1 | a0001c0001t0008g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.116-8439G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96761264 | |||||||
chr1:96761324 | A | C | 1 | a0001c0002t0001g0263 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.116-8379A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96761324 | |||||||
chr1:96761346 | A | ATG | 48 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(45): Show |
48 | HG00423.hp1 HG00733.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.116-8315_116-8314d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761346 | A | ATGTG | 72 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0229 others(69): Show |
72 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.116-8317_116-8314d others(6): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761346 | A | ATGTGTG | 16 | a0001c0001t0002g0168 a0001c0001t0002g0172 a0001c0001t0002g0180 others(13): Show |
16 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.116-8319_116-8314d others(8): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761346 | A | ATGTGTGT others(1): Show |
16 | a0001c0001t0001g0220 a0001c0001t0002g0171 a0001c0001t0002g0182 others(13): Show |
16 | HG00099.hp2 HG00544.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.116-8321_116-8314d others(10): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761346 | A | ATGTGTGT others(3): Show |
1 | a0001c0002t0005g0259 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.116-8323_116-8314d others(12): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761346 | A | ATGTGTGT others(5): Show |
2 | a0001c0001t0002g0178 a0001c0002t0005g0257 |
2 | HG02723.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.116-8325_116-8314d others(14): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761346 | A | ATGTGTGT others(7): Show |
1 | a0001c0002t0005g0261 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.116-8327_116-8314d others(16): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761346 | A | ATGTGTGT others(11): Show |
1 | a0001c0002t0005g0258 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.116-8331_116-8314d others(20): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761346 | A | ATGTGTGT others(15): Show |
1 | a0001c0002t0005g0256 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.116-8335_116-8314d others(24): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761346 | ATG | A | 13 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(10): Show |
14 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.116-8315_116-8314d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761346 | ATGTG | A | 8 | a0001c0001t0003g0107 a0001c0001t0003g0128 a0001c0001t0003g0130 others(5): Show |
8 | HG00733.hp2 HG01074.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-8317_116-8314d others(6): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761346 | ATGTGTG | A | 28 | a0001c0002t0001g0152 a0001c0002t0001g0266 a0001c0002t0001g0267 others(25): Show |
28 | HG00558.hp2 HG01109.hp1 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.116-8319_116-8314d others(8): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761346 | ATGTGTGT others(1): Show |
A | 63 | a0001c0002t0001g0004 a0001c0002t0001g0263 a0001c0002t0001g0264 others(60): Show |
63 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.116-8321_116-8314d others(10): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761346 | ATGTGTGT others(3): Show |
A | 3 | a0001c0002t0001g0310 a0001c0002t0001g0324 a0001c0002t0001g0354 |
3 | HG02486.hp2 NA18991.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.116-8323_116-8314d others(12): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761346 | ATGTGTGT others(5): Show |
A | 1 | a0001c0002t0005g0002 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.116-8325_116-8314d others(14): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761346 | ATGTGTGT others(7): Show |
A | 6 | a0001c0002t0005g0251 a0001c0002t0005g0252 a0001c0002t0005g0253 others(3): Show |
6 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-8327_116-8314d others(16): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761346 | ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0002g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.116-8329_116-8314d others(18): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761346 | ATGTGTGT others(13): Show |
A | 1 | a0001c0001t0004g0111 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.116-8333_116-8314d others(22): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761346 | ||||||
chr1:96761479 | A | G | 17 | a0001c0002t0001g0310 a0001c0002t0001g0311 a0001c0002t0001g0312 others(14): Show |
17 | HG01884.hp2 HG02109.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.116-8224A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96761479 | |||||||
chr1:96761535 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.116-8168G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96761535 | |||||||
chr1:96761550 | A | AAT | 262 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(259): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.116-8152_116-8151d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761550 | ||||||
chr1:96761651 | A | G | 1 | a0001c0002t0005g0002 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.116-8052A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96761651 | |||||||
chr1:96761724 | G | GT | 6 | a0001c0001t0006g0093 a0001c0002t0005g0256 a0001c0002t0005g0257 others(3): Show |
6 | HG02004.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-7970dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761724 | ||||||
chr1:96761730 | T | G | 1 | a0001c0001t0002g0164 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.116-7973T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96761730 | |||||||
chr1:96761730 | TTTTG | T | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-7965_116-7962d others(6): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96761730 | ||||||
chr1:96761887 | A | C | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-7816A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96761887 | |||||||
chr1:96761968 | C | A | 43 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0264 others(40): Show |
43 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.116-7735C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96761968 | |||||||
chr1:96761969 | T | C | 43 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0264 others(40): Show |
43 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.116-7734T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96761969 | |||||||
chr1:96762056 | G | A | 4 | a0001c0001t0003g0044 a0001c0001t0003g0083 a0001c0001t0003g0090 others(1): Show |
4 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-7647G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762056 | |||||||
chr1:96762068 | A | G | 1 | a0001c0001t0003g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.116-7635A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762068 | |||||||
chr1:96762265 | GTGGCCGG others(305): Show |
G | 1 | a0001c0002t0005g0002 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.116-7376_116-7065d others(2): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96762265 | ||||||
chr1:96762266 | TGGCCGGG others(30): Show |
T | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-7423_116-7387d others(39): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96762266 | ||||||
chr1:96762271 | G | A | 3 | a0001c0002t0001g0311 a0001c0002t0001g0315 a0001c0002t0001g0316 |
3 | HG02723.hp2 HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.116-7432G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762271 | |||||||
chr1:96762280 | G | C | 17 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(14): Show |
18 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.116-7423G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762280 | |||||||
chr1:96762283 | T | C | 17 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(14): Show |
18 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.116-7420T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762283 | |||||||
chr1:96762291 | T | C | 17 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(14): Show |
18 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.116-7412T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762291 | |||||||
chr1:96762318 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.116-7385G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762318 | |||||||
chr1:96762341 | A | G | 234 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(231): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.116-7362A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762341 | |||||||
chr1:96762344 | C | T | 1 | a0001c0002t0001g0354 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.116-7359C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762344 | |||||||
chr1:96762378 | GGCTGGCC others(42): Show |
G | 3 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0016 |
3 | HG00735.hp2 HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.116-7282_116-7234d others(51): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96762378 | ||||||
chr1:96762421 | T | C | 2 | a0001c0002t0001g0310 a0001c0002t0001g0324 |
2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.116-7282T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762421 | |||||||
chr1:96762427 | A | G | 61 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0264 others(58): Show |
61 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.116-7276A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762427 | |||||||
chr1:96762439 | GGGGGGCT others(42): Show |
G | 4 | a0001c0001t0003g0048 a0001c0001t0003g0050 a0001c0001t0003g0088 others(1): Show |
4 | NA18942.hp1 NA18954.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-7249_116-7201d others(51): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96762439 | ||||||
chr1:96762453 | CCCACCTC others(43): Show |
C | 1 | a0001c0001t0002g0227 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.116-7200_116-7151d others(52): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96762453 | ||||||
chr1:96762464 | C | G | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-7239C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762464 | |||||||
chr1:96762470 | C | T | 2 | a0001c0001t0004g0075 a0001c0005t0012g0077 |
2 | HG01243.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.116-7233C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762470 | |||||||
chr1:96762502 | CG | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(223): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.116-7200delG | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762502 | |||||||
chr1:96762503 | G | A | 1 | a0001c0001t0003g0104 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.116-7200G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762503 | |||||||
chr1:96762503 | G | C | 7 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-7200G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762503 | |||||||
chr1:96762517 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.116-7186G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762517 | |||||||
chr1:96762548 | C | G | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-7155C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762548 | |||||||
chr1:96762551 | C | G | 43 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0264 others(40): Show |
43 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.116-7152C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762551 | |||||||
chr1:96762566 | G | A | 1 | a0001c0001t0003g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.116-7137G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762566 | |||||||
chr1:96762569 | C | T | 2 | a0001c0001t0002g0180 a0001c0001t0003g0122 |
2 | HG01081.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.116-7134C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762569 | |||||||
chr1:96762575 | G | A | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | NA19074.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.116-7128G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762575 | |||||||
chr1:96762660 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.116-7043C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762660 | |||||||
chr1:96762674 | A | AC | 11 | a0001c0001t0002g0170 a0001c0001t0002g0179 a0001c0002t0001g0308 others(8): Show |
12 | HG01192.hp2 HG02647.hp2 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.116-7022dupC | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96762674 | ||||||
chr1:96762785 | C | T | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-6918C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762785 | |||||||
chr1:96762794 | C | T | 2 | a0001c0002t0001g0319 a0001c0002t0001g0320 |
2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.116-6909C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762794 | |||||||
chr1:96762805 | G | T | 4 | a0001c0002t0001g0280 a0001c0002t0001g0281 a0001c0002t0001g0282 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-6898G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762805 | |||||||
chr1:96762891 | CTCCCAGA others(33): Show |
C | 1 | a0001c0001t0004g0136 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.116-6799_116-6760d others(42): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96762891 | ||||||
chr1:96762912 | G | A | 2 | a0001c0001t0002g0198 a0001c0001t0003g0023 |
2 | HG01358.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.116-6791G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762912 | |||||||
chr1:96762977 | G | A | 1 | a0001c0002t0001g0311 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.116-6726G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96762977 | |||||||
chr1:96763023 | C | T | 6 | a0001c0001t0007g0008 a0001c0001t0007g0011 a0001c0001t0007g0012 others(3): Show |
6 | HG00735.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-6680C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763023 | |||||||
chr1:96763037 | C | T | 3 | a0001c0001t0003g0026 a0001c0001t0003g0043 a0001c0001t0004g0025 |
3 | HG03471.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.116-6666C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763037 | |||||||
chr1:96763127 | C | T | 34 | a0001c0002t0001g0263 a0001c0002t0001g0267 a0001c0002t0001g0268 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.116-6576C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763127 | |||||||
chr1:96763139 | G | A | 6 | a0001c0001t0003g0076 a0001c0001t0004g0030 a0001c0001t0004g0037 others(3): Show |
6 | HG00639.hp1 HG00741.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-6564G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763139 | |||||||
chr1:96763170 | C | CG | 14 | a0001c0001t0002g0196 a0001c0001t0002g0211 a0001c0001t0002g0212 others(11): Show |
14 | HG01081.hp1 HG01109.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.116-6529dupG | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96763170 | ||||||
chr1:96763171 | G | A | 1 | a0001c0002t0001g0328 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.116-6532G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763171 | |||||||
chr1:96763173 | G | T | 2 | a0001c0001t0003g0116 a0001c0001t0003g0118 |
2 | HG01167.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.116-6530G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763173 | |||||||
chr1:96763179 | G | A | 1 | a0001c0001t0003g0104 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.116-6524G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763179 | |||||||
chr1:96763197 | A | G | 4 | a0001c0001t0003g0076 a0001c0001t0004g0030 a0001c0001t0004g0037 others(1): Show |
4 | HG00639.hp1 HG00741.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-6506A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763197 | |||||||
chr1:96763208 | T | A | 1 | a0001c0001t0002g0213 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.116-6495T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763208 | |||||||
chr1:96763262 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.116-6441C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763262 | |||||||
chr1:96763314 | G | A | 1 | a0001c0002t0005g0002 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.116-6389G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763314 | |||||||
chr1:96763360 | G | C | 1 | a0001c0002t0001g0333 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.116-6343G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763360 | |||||||
chr1:96763362 | G | A | 5 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(2): Show |
5 | HG01943.hp1 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.116-6341G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763362 | |||||||
chr1:96763439 | G | A | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-6264G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763439 | |||||||
chr1:96763548 | G | C | 1 | a0001c0001t0002g0173 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.116-6155G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763548 | |||||||
chr1:96763599 | G | GGAGGGA | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-6102_116-6097d others(8): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96763599 | ||||||
chr1:96763601 | A | AGGGAGG | 7 | a0001c0001t0003g0066 a0001c0001t0011g0186 a0001c0002t0001g0318 others(4): Show |
7 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.116-6076_116-6071d others(8): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96763601 | ||||||
chr1:96763601 | A | AGGGAGGG others(5): Show |
1 | a0001c0002t0008g0279 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.116-6082_116-6071d others(14): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96763601 | ||||||
chr1:96763601 | AGGGAGG | A | 13 | a0001c0001t0003g0023 a0001c0001t0003g0032 a0001c0001t0004g0030 others(10): Show |
13 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.116-6076_116-6071d others(8): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96763601 | ||||||
chr1:96763611 | A | G | 1 | a0001c0001t0001g0358 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.116-6092A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763611 | |||||||
chr1:96763617 | A | G | 1 | a0001c0001t0002g0176 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.116-6086A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763617 | |||||||
chr1:96763634 | T | A | 1 | a0001c0002t0001g0303 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.116-6069T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96763634 | |||||||
chr1:96764014 | T | C | 2 | a0001c0001t0004g0096 a0001c0001t0011g0186 |
2 | NA18979.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.116-5689T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96764014 | |||||||
chr1:96764333 | A | G | 113 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(110): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.116-5370A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96764333 | |||||||
chr1:96764404 | A | G | 2 | a0001c0001t0002g0241 a0001c0001t0003g0146 |
2 | HG02080.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.116-5299A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96764404 | |||||||
chr1:96764600 | A | G | 61 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0264 others(58): Show |
61 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.116-5103A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96764600 | |||||||
chr1:96764615 | C | G | 1 | a0001c0001t0006g0024 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.116-5088C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96764615 | |||||||
chr1:96764757 | T | C | 2 | a0001c0001t0002g0154 a0001c0001t0002g0155 |
2 | HG03239.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.116-4946T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96764757 | |||||||
chr1:96764839 | T | C | 1 | a0001c0002t0001g0329 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.116-4864T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96764839 | |||||||
chr1:96765110 | T | C | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-4593T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96765110 | |||||||
chr1:96765242 | A | G | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-4461A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96765242 | |||||||
chr1:96765264 | G | C | 1 | a0001c0002t0001g0270 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.116-4439G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96765264 | |||||||
chr1:96765270 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.116-4433G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96765270 | |||||||
chr1:96765343 | C | T | 1 | a0001c0001t0006g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.116-4360C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96765343 | |||||||
chr1:96765508 | C | T | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-4195C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96765508 | |||||||
chr1:96765529 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.116-4174G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96765529 | |||||||
chr1:96765578 | G | A | 2 | a0001c0002t0005g0256 a0001c0002t0005g0257 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.116-4125G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96765578 | |||||||
chr1:96765708 | T | A | 2 | a0001c0001t0002g0221 a0001c0001t0002g0223 |
2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.116-3995T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96765708 | |||||||
chr1:96765708 | T | TTAGA | 141 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(138): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.116-3956_116-3953d others(6): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96765708 | ||||||
chr1:96765708 | T | TTAGATAG others(1): Show |
54 | a0001c0001t0001g0357 a0001c0001t0001g0360 a0001c0001t0002g0160 others(51): Show |
54 | HG00140.hp2 HG00544.hp2 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.116-3960_116-3953d others(10): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96765708 | ||||||
chr1:96765708 | T | TTAGATAG others(5): Show |
35 | a0001c0001t0001g0003 a0001c0001t0002g0172 a0001c0001t0002g0180 others(32): Show |
35 | HG00423.hp2 HG00621.hp2 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.116-3964_116-3953d others(14): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96765708 | ||||||
chr1:96765708 | T | TTAGATAG others(9): Show |
4 | a0001c0001t0002g0246 a0001c0001t0004g0025 a0001c0001t0013g0222 others(1): Show |
4 | HG02004.hp1 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3968_116-3953d others(18): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96765708 | ||||||
chr1:96765708 | TTAGA | T | 13 | a0001c0001t0002g0236 a0001c0001t0003g0038 a0001c0001t0004g0037 others(10): Show |
13 | HG00597.hp2 HG01952.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.116-3956_116-3953d others(6): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96765708 | ||||||
chr1:96765708 | TTAGATAG others(1): Show |
T | 5 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0253 others(2): Show |
6 | HG02647.hp2 HG02965.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-3960_116-3953d others(10): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96765708 | ||||||
chr1:96765752 | T | A | 19 | a0001c0002t0001g0263 a0001c0002t0001g0268 a0001c0002t0001g0269 others(16): Show |
19 | HG00558.hp2 HG01109.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.116-3951T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96765752 | |||||||
chr1:96765913 | A | G | 2 | a0001c0002t0001g0339 a0001c0002t0001g0349 |
2 | HG00558.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.116-3790A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96765913 | |||||||
chr1:96765948 | G | C | 4 | a0001c0002t0001g0280 a0001c0002t0001g0281 a0001c0002t0001g0282 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-3755G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96765948 | |||||||
chr1:96765959 | T | A | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-3744T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96765959 | |||||||
chr1:96766141 | G | C | 17 | a0001c0002t0001g0310 a0001c0002t0001g0311 a0001c0002t0001g0312 others(14): Show |
17 | HG01884.hp2 HG02109.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.116-3562G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96766141 | |||||||
chr1:96766292 | C | T | 1 | a0001c0001t0004g0031 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.116-3411C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96766292 | |||||||
chr1:96766506 | T | G | 17 | a0001c0002t0001g0310 a0001c0002t0001g0311 a0001c0002t0001g0312 others(14): Show |
17 | HG01884.hp2 HG02109.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.116-3197T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96766506 | |||||||
chr1:96766653 | A | G | 1 | a0001c0001t0008g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.116-3050A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96766653 | |||||||
chr1:96767177 | G | A | 3 | a0001c0001t0001g0220 a0001c0001t0002g0017 a0001c0001t0002g0168 |
3 | HG02257.hp1 HG02615.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.116-2526G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96767177 | |||||||
chr1:96767270 | G | A | 1 | a0001c0001t0004g0031 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.116-2433G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96767270 | |||||||
chr1:96767327 | A | G | 1 | a0001c0001t0004g0031 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.116-2376A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96767327 | |||||||
chr1:96767609 | A | G | 95 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.116-2094A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96767609 | |||||||
chr1:96767792 | G | T | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-1911G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96767792 | |||||||
chr1:96767819 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.116-1884C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96767819 | |||||||
chr1:96767932 | C | A | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-1771C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96767932 | |||||||
chr1:96768001 | G | A | 1 | a0001c0001t0007g0153 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.116-1702G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96768001 | |||||||
chr1:96768048 | A | G | 34 | a0001c0002t0001g0263 a0001c0002t0001g0267 a0001c0002t0001g0268 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.116-1655A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96768048 | |||||||
chr1:96768091 | C | T | 4 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(1): Show |
4 | HG02717.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-1612C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96768091 | |||||||
chr1:96768152 | C | T | 95 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.116-1551C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96768152 | |||||||
chr1:96768274 | A | T | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-1429A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96768274 | |||||||
chr1:96768282 | A | G | 1 | a0001c0002t0005g0254 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.116-1421A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96768282 | |||||||
chr1:96768582 | A | T | 1 | a0001c0001t0002g0247 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.116-1121A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96768582 | |||||||
chr1:96768688 | A | T | 121 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(118): Show |
121 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.116-1015A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96768688 | |||||||
chr1:96768708 | A | T | 12 | a0001c0002t0001g0263 a0001c0002t0001g0268 a0001c0002t0001g0269 others(9): Show |
12 | HG00558.hp2 HG02015.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.116-995A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96768708 | |||||||
chr1:96768815 | G | A | 1 | a0001c0002t0001g0270 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.116-888G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96768815 | |||||||
chr1:96768974 | T | C | 1 | a0001c0001t0007g0015 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.116-729T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96768974 | |||||||
chr1:96769051 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.116-652T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96769051 | |||||||
chr1:96769283 | G | A | 19 | a0001c0002t0001g0263 a0001c0002t0001g0268 a0001c0002t0001g0269 others(16): Show |
19 | HG00558.hp2 HG01109.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.116-420G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96769283 | |||||||
chr1:96769437 | G | C | 3 | a0001c0001t0003g0026 a0001c0001t0003g0043 a0001c0001t0004g0025 |
3 | HG03471.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.116-266G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96769437 | |||||||
chr1:96769488 | A | C | 2 | a0001c0001t0007g0008 a0001c0001t0007g0011 |
2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.116-215A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96769488 | |||||||
chr1:96769492 | T | C | 2 | a0001c0001t0007g0008 a0001c0001t0007g0011 |
2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.116-211T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96769492 | |||||||
chr1:96769548 | GA | G | 12 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(9): Show |
13 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.116-152delA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 96769548 | ||||||
chr1:96769656 | A | T | 1 | a0001c0001t0003g0128 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.116-47A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 3/13 | chr1 | 96769656 | |||||||
chr1:96769883 | T | C | 12 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(9): Show |
13 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.288+8T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 4/13 | chr1 | 96769883 | |||||||
chr1:96770196 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.288+321C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 4/13 | chr1 | 96770196 | |||||||
chr1:96770255 | C | T | 1 | a0001c0001t0006g0072 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.288+380C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 4/13 | chr1 | 96770255 | |||||||
chr1:96770295 | A | G | 1 | a0001c0001t0007g0015 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.289-413A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 4/13 | chr1 | 96770295 | |||||||
chr1:96770498 | A | G | 1 | a0001c0002t0001g0270 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.289-210A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 4/13 | chr1 | 96770498 | |||||||
chr1:96770504 | G | A | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.289-204G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 4/13 | chr1 | 96770504 | |||||||
chr1:96770574 | G | A | 226 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.289-134G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 4/13 | chr1 | 96770574 | |||||||
chr1:96770647 | G | T | 1 | a0001c0002t0005g0255 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.289-61G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 4/13 | chr1 | 96770647 | |||||||
chr1:96771131 | A | C | 1 | a0001c0001t0003g0047 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.432+280A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96771131 | |||||||
chr1:96771430 | T | C | 121 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(118): Show |
121 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.432+579T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96771430 | |||||||
chr1:96771605 | T | A | 1 | a0001c0002t0005g0256 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.432+754T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96771605 | |||||||
chr1:96771862 | T | C | 1 | a0001c0002t0001g0333 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.432+1011T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96771862 | |||||||
chr1:96771969 | T | C | 1 | a0001c0001t0003g0104 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.432+1118T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96771969 | |||||||
chr1:96771989 | A | G | 1 | a0001c0001t0003g0076 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.432+1138A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96771989 | |||||||
chr1:96772098 | C | T | 1 | a0001c0001t0007g0153 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.432+1247C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96772098 | |||||||
chr1:96772109 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.432+1258G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96772109 | |||||||
chr1:96772186 | C | G | 4 | a0001c0001t0003g0044 a0001c0001t0003g0083 a0001c0001t0003g0090 others(1): Show |
4 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+1335C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96772186 | |||||||
chr1:96772419 | C | A | 1 | a0001c0002t0001g0302 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.432+1568C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96772419 | |||||||
chr1:96772617 | A | C | 110 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(107): Show |
110 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.432+1766A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96772617 | |||||||
chr1:96772618 | C | G | 3 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0016 |
3 | HG00735.hp2 HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.432+1767C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96772618 | |||||||
chr1:96772706 | A | T | 2 | a0001c0002t0001g0323 a0001c0002t0008g0322 |
2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.432+1855A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96772706 | |||||||
chr1:96772894 | C | T | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+2043C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96772894 | |||||||
chr1:96772958 | C | CA | 15 | a0001c0001t0001g0003 a0001c0001t0001g0220 a0001c0001t0002g0017 others(12): Show |
16 | HG01099.hp1 HG01175.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.432+2122dupA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 96772958 | ||||||
chr1:96773049 | G | T | 1 | a0001c0001t0003g0146 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.432+2198G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96773049 | |||||||
chr1:96773123 | C | CA | 58 | a0001c0001t0003g0038 a0001c0001t0003g0076 a0001c0001t0003g0092 others(55): Show |
58 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.432+2295dupA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 96773123 | ||||||
chr1:96773123 | C | CAA | 24 | a0001c0001t0003g0140 a0001c0001t0004g0030 a0001c0002t0001g0280 others(21): Show |
24 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.432+2294_432+2295d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 96773123 | ||||||
chr1:96773123 | C | T | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.432+2272C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96773123 | |||||||
chr1:96773123 | CA | C | 16 | a0001c0001t0003g0005 a0001c0001t0003g0116 a0001c0001t0003g0121 others(13): Show |
17 | HG00099.hp1 HG01243.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.432+2295delA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 96773123 | ||||||
chr1:96773123 | CAAAAA | C | 108 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(105): Show |
108 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.432+2291_432+2295d others(7): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 96773123 | ||||||
chr1:96773149 | G | A | 107 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(104): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.432+2298G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96773149 | |||||||
chr1:96773314 | G | GA | 4 | a0001c0001t0003g0049 a0001c0001t0003g0137 a0001c0001t0004g0110 others(1): Show |
4 | HG01943.hp2 HG01981.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+2470dupA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 96773314 | ||||||
chr1:96773621 | C | T | 8 | a0001c0001t0001g0003 a0001c0002t0005g0002 a0001c0002t0005g0251 others(5): Show |
9 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.432+2770C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96773621 | |||||||
chr1:96773699 | G | T | 2 | a0001c0002t0001g0306 a0001c0002t0001g0308 |
2 | HG01081.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.432+2848G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96773699 | |||||||
chr1:96773700 | T | G | 235 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.432+2849T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96773700 | |||||||
chr1:96773704 | T | C | 2 | a0001c0001t0002g0221 a0001c0001t0002g0223 |
2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.432+2853T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96773704 | |||||||
chr1:96773792 | G | A | 1 | a0001c0005t0012g0077 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.432+2941G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96773792 | |||||||
chr1:96773801 | A | G | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+2950A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96773801 | |||||||
chr1:96773819 | T | C | 1 | a0001c0001t0007g0153 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.432+2968T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96773819 | |||||||
chr1:96773831 | C | T | 357 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(354): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.432+2980C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96773831 | |||||||
chr1:96773917 | C | T | 1 | a0001c0001t0003g0055 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.432+3066C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96773917 | |||||||
chr1:96773918 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.432+3067G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96773918 | |||||||
chr1:96773962 | C | CA | 120 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(117): Show |
120 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.432+3129dupA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 96773962 | ||||||
chr1:96773962 | C | CAA | 10 | a0001c0001t0002g0183 a0001c0001t0002g0196 a0001c0001t0002g0197 others(7): Show |
10 | HG00423.hp2 HG01168.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.432+3128_432+3129d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 96773962 | ||||||
chr1:96773962 | CA | C | 6 | a0001c0001t0003g0020 a0001c0001t0003g0049 a0001c0001t0003g0118 others(3): Show |
6 | HG00558.hp1 HG01069.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.432+3129delA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 96773962 | ||||||
chr1:96774017 | C | G | 19 | a0001c0001t0003g0038 a0001c0001t0003g0042 a0001c0001t0003g0045 others(16): Show |
19 | HG00423.hp1 HG00438.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.432+3166C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96774017 | |||||||
chr1:96774120 | T | TA | 115 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(112): Show |
115 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.432+3282dupA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 96774120 | ||||||
chr1:96774262 | C | G | 102 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(99): Show |
102 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.433-3323C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96774262 | |||||||
chr1:96774266 | T | C | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.433-3319T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96774266 | |||||||
chr1:96774276 | C | T | 23 | a0001c0001t0003g0049 a0001c0001t0003g0137 a0001c0001t0004g0021 others(20): Show |
23 | HG01943.hp2 HG01981.hp1 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.433-3309C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96774276 | |||||||
chr1:96774413 | ATAAAAT | A | 10 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0010 others(7): Show |
10 | HG00735.hp1 HG00735.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-3169_433-3164d others(8): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 96774413 | ||||||
chr1:96774453 | A | C | 5 | a0001c0001t0002g0167 a0001c0001t0002g0191 a0001c0001t0002g0192 others(2): Show |
5 | NA18944.hp2 NA18960.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-3132A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96774453 | |||||||
chr1:96774471 | A | G | 34 | a0001c0002t0001g0263 a0001c0002t0001g0267 a0001c0002t0001g0268 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.433-3114A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96774471 | |||||||
chr1:96774516 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.433-3069C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96774516 | |||||||
chr1:96774672 | T | G | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.433-2913T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96774672 | |||||||
chr1:96774787 | G | A | 14 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(11): Show |
14 | HG00733.hp1 HG01433.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.433-2798G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96774787 | |||||||
chr1:96774793 | G | A | 1 | a0001c0001t0003g0098 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.433-2792G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96774793 | |||||||
chr1:96774962 | T | C | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | NA19074.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.433-2623T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96774962 | |||||||
chr1:96775073 | T | TCTTCTCC others(12): Show |
1 | a0001c0001t0003g0103 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.433-2510_433-2492d others(21): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 96775073 | ||||||
chr1:96775189 | A | C | 1 | a0001c0001t0002g0212 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.433-2396A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96775189 | |||||||
chr1:96775198 | A | C | 8 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(5): Show |
9 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.433-2387A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96775198 | |||||||
chr1:96775295 | T | C | 1 | a0001c0002t0001g0354 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.433-2290T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96775295 | |||||||
chr1:96775812 | G | A | 1 | a0001c0001t0003g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.433-1773G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96775812 | |||||||
chr1:96775868 | A | G | 1 | a0001c0001t0008g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.433-1717A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96775868 | |||||||
chr1:96776097 | A | G | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-1488A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96776097 | |||||||
chr1:96776168 | T | C | 2 | a0001c0002t0001g0288 a0001c0002t0008g0289 |
2 | HG01433.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.433-1417T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96776168 | |||||||
chr1:96776293 | C | T | 44 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0264 others(41): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.433-1292C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96776293 | |||||||
chr1:96776365 | CTA | C | 95 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.433-1218_433-1217d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 96776365 | ||||||
chr1:96776397 | G | A | 2 | a0001c0002t0001g0310 a0001c0002t0001g0324 |
2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.433-1188G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96776397 | |||||||
chr1:96776410 | A | G | 233 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(230): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.433-1175A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96776410 | |||||||
chr1:96776588 | T | C | 1 | a0001c0001t0013g0222 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.433-997T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96776588 | |||||||
chr1:96776602 | T | G | 2 | a0001c0001t0002g0361 a0001c0001t0002g0362 |
2 | NA18947.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.433-983T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96776602 | |||||||
chr1:96776897 | A | G | 43 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0264 others(40): Show |
43 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.433-688A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96776897 | |||||||
chr1:96777047 | C | T | 1 | a0001c0001t0003g0049 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.433-538C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96777047 | |||||||
chr1:96777191 | C | T | 3 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0016 |
3 | HG00735.hp2 HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.433-394C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96777191 | |||||||
chr1:96777328 | A | G | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.433-257A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96777328 | |||||||
chr1:96777393 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.433-192A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96777393 | |||||||
chr1:96777467 | A | G | 39 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(36): Show |
39 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.433-118A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 5/13 | chr1 | 96777467 | |||||||
chr1:96778142 | C | T | 2 | a0001c0001t0003g0124 a0001c0001t0016g0120 |
2 | HG01517.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.708+196C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96778142 | |||||||
chr1:96778167 | CT | C | 18 | a0001c0001t0002g0170 a0001c0001t0002g0208 a0001c0001t0002g0236 others(15): Show |
18 | HG01069.hp1 HG01081.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.708+238delT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 96778167 | ||||||
chr1:96778167 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0010g0150 a0001c0001t0010g0204 a0001c0001t0010g0205 others(1): Show |
4 | HG00642.hp1 HG02698.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.708+229_708+238del others(10): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 96778167 | ||||||
chr1:96778368 | A | G | 1 | a0001c0001t0002g0243 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.708+422A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96778368 | |||||||
chr1:96778386 | C | CT | 224 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.708+448dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 96778386 | ||||||
chr1:96778598 | T | G | 1 | a0001c0002t0001g0344 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.708+652T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96778598 | |||||||
chr1:96778635 | T | C | 1 | a0001c0001t0003g0070 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.708+689T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96778635 | |||||||
chr1:96778671 | G | A | 2 | a0001c0001t0002g0199 a0001c0001t0002g0232 |
2 | HG01168.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.708+725G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96778671 | |||||||
chr1:96778739 | T | A | 8 | a0001c0001t0002g0158 a0001c0001t0002g0171 a0001c0001t0002g0178 others(5): Show |
8 | NA18943.hp1 NA18954.hp2 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.708+793T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96778739 | |||||||
chr1:96778972 | A | G | 3 | a0001c0002t0001g0264 a0001c0002t0001g0285 a0001c0002t0001g0336 |
3 | NA18966.hp1 NA19012.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.708+1026A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96778972 | |||||||
chr1:96779138 | T | G | 1 | a0001c0002t0001g0296 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.708+1192T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96779138 | |||||||
chr1:96779205 | A | T | 1 | a0001c0001t0004g0071 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.708+1259A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96779205 | |||||||
chr1:96779320 | A | T | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.708+1374A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96779320 | |||||||
chr1:96779361 | T | C | 1 | a0001c0002t0005g0251 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.708+1415T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96779361 | |||||||
chr1:96779464 | T | C | 1 | a0001c0002t0005g0251 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.708+1518T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96779464 | |||||||
chr1:96779490 | A | G | 6 | a0001c0001t0003g0076 a0001c0001t0004g0030 a0001c0001t0004g0037 others(3): Show |
6 | HG00639.hp1 HG00741.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.708+1544A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96779490 | |||||||
chr1:96779583 | A | T | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.708+1637A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96779583 | |||||||
chr1:96779591 | A | G | 1 | a0001c0002t0001g0353 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.708+1645A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96779591 | |||||||
chr1:96779644 | T | G | 95 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.708+1698T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96779644 | |||||||
chr1:96779712 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.708+1766C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96779712 | |||||||
chr1:96779742 | C | T | 1 | a0001c0001t0006g0027 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.708+1796C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96779742 | |||||||
chr1:96779863 | CATAAT | C | 34 | a0001c0002t0001g0263 a0001c0002t0001g0267 a0001c0002t0001g0268 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.708+1920_708+1924d others(7): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 96779863 | ||||||
chr1:96779870 | T | C | 1 | a0001c0001t0007g0010 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.708+1924T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96779870 | |||||||
chr1:96779901 | ATC | A | 15 | a0001c0002t0001g0267 a0001c0002t0001g0270 a0001c0002t0001g0294 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.708+1956_708+1957d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96779901 | |||||||
chr1:96779910 | C | T | 2 | a0001c0001t0002g0240 a0001c0001t0002g0244 |
2 | NA18948.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.708+1964C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96779910 | |||||||
chr1:96780189 | G | A | 1 | a0001c0001t0003g0067 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.708+2243G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96780189 | |||||||
chr1:96780338 | G | A | 226 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.708+2392G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96780338 | |||||||
chr1:96780363 | T | G | 1 | a0001c0001t0002g0167 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.708+2417T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96780363 | |||||||
chr1:96780501 | A | G | 5 | a0001c0002t0001g0318 a0001c0002t0001g0319 a0001c0002t0001g0320 others(2): Show |
5 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.708+2555A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96780501 | |||||||
chr1:96780617 | C | T | 1 | a0001c0001t0010g0205 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.708+2671C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96780617 | |||||||
chr1:96780660 | A | G | 1 | a0001c0001t0003g0139 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.708+2714A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96780660 | |||||||
chr1:96780712 | CT | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.708+2768delT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 96780712 | ||||||
chr1:96780809 | C | T | 1 | a0001c0001t0002g0212 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.708+2863C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96780809 | |||||||
chr1:96780844 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.708+2898G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96780844 | |||||||
chr1:96780910 | T | C | 17 | a0001c0002t0001g0310 a0001c0002t0001g0311 a0001c0002t0001g0312 others(14): Show |
17 | HG01884.hp2 HG02109.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.708+2964T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96780910 | |||||||
chr1:96781167 | C | T | 1 | a0001c0001t0003g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.708+3221C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96781167 | |||||||
chr1:96781168 | G | A | 1 | a0001c0001t0002g0187 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.708+3222G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96781168 | |||||||
chr1:96781310 | C | T | 1 | a0001c0002t0001g0284 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.708+3364C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96781310 | |||||||
chr1:96781324 | G | C | 10 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0010 others(7): Show |
10 | HG00735.hp1 HG00735.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.708+3378G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96781324 | |||||||
chr1:96781669 | G | A | 1 | a0001c0001t0003g0124 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.709-3390G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96781669 | |||||||
chr1:96782205 | G | T | 43 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0264 others(40): Show |
43 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.709-2854G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96782205 | |||||||
chr1:96782639 | T | G | 1 | a0001c0001t0007g0153 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.709-2420T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96782639 | |||||||
chr1:96782680 | A | G | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.709-2379A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96782680 | |||||||
chr1:96782690 | T | C | 111 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(108): Show |
111 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.709-2369T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96782690 | |||||||
chr1:96783448 | G | T | 34 | a0001c0002t0001g0263 a0001c0002t0001g0267 a0001c0002t0001g0268 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.709-1611G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96783448 | |||||||
chr1:96783517 | T | C | 1 | a0001c0001t0006g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.709-1542T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96783517 | |||||||
chr1:96783700 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.709-1359C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96783700 | |||||||
chr1:96783913 | C | T | 1 | a0001c0001t0003g0127 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.709-1146C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96783913 | |||||||
chr1:96783997 | T | C | 1 | a0001c0001t0003g0068 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.709-1062T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96783997 | |||||||
chr1:96783998 | C | T | 11 | a0001c0002t0001g0267 a0001c0002t0001g0270 a0001c0002t0001g0294 others(8): Show |
11 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.709-1061C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96783998 | |||||||
chr1:96784067 | A | G | 1 | a0001c0002t0001g0277 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.709-992A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96784067 | |||||||
chr1:96784101 | G | A | 3 | a0001c0001t0001g0220 a0001c0001t0002g0017 a0001c0001t0002g0168 |
3 | HG02257.hp1 HG02615.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.709-958G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96784101 | |||||||
chr1:96784240 | G | A | 44 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0264 others(41): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.709-819G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96784240 | |||||||
chr1:96784301 | C | CCCTTGAA others(8): Show |
1 | a0001c0002t0001g0295 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.709-757_709-743dup others(15): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 96784301 | ||||||
chr1:96784301 | C | T | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.709-758C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96784301 | |||||||
chr1:96784304 | T | TG | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.709-755_709-754ins others(1): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96784304 | |||||||
chr1:96784396 | G | T | 107 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(104): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.709-663G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96784396 | |||||||
chr1:96784466 | A | G | 121 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(118): Show |
121 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.709-593A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96784466 | |||||||
chr1:96784645 | T | C | 4 | a0001c0002t0001g0280 a0001c0002t0001g0281 a0001c0002t0001g0282 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.709-414T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96784645 | |||||||
chr1:96784896 | A | G | 2 | a0001c0001t0003g0033 a0001c0001t0003g0073 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.709-163A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96784896 | |||||||
chr1:96784964 | G | A | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.709-95G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96784964 | |||||||
chr1:96784964 | G | T | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.709-95G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 7/13 | chr1 | 96784964 | |||||||
chr1:96785335 | T | C | 2 | a0001c0001t0002g0154 a0001c0001t0002g0155 |
2 | HG03239.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.904+81T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96785335 | |||||||
chr1:96785732 | A | G | 2 | a0001c0002t0001g0323 a0001c0002t0008g0322 |
2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.904+478A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96785732 | |||||||
chr1:96785876 | G | A | 1 | a0001c0002t0001g0318 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.904+622G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96785876 | |||||||
chr1:96786058 | G | C | 1 | a0001c0001t0002g0209 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.904+804G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96786058 | |||||||
chr1:96786182 | C | A | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.904+928C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96786182 | |||||||
chr1:96786193 | A | C | 113 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(110): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.904+939A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96786193 | |||||||
chr1:96786289 | A | C | 228 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.904+1035A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96786289 | |||||||
chr1:96786520 | A | G | 103 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(100): Show |
103 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.904+1266A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96786520 | |||||||
chr1:96786557 | A | G | 1 | a0001c0001t0002g0218 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.904+1303A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96786557 | |||||||
chr1:96786566 | A | G | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.904+1312A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96786566 | |||||||
chr1:96786628 | G | A | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.904+1374G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96786628 | |||||||
chr1:96786639 | G | A | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.904+1385G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96786639 | |||||||
chr1:96786645 | T | C | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.904+1391T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96786645 | |||||||
chr1:96786725 | G | C | 1 | a0001c0001t0002g0155 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.904+1471G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96786725 | |||||||
chr1:96786907 | C | A | 1 | a0001c0002t0001g0295 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.904+1653C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96786907 | |||||||
chr1:96786943 | G | C | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.904+1689G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96786943 | |||||||
chr1:96787082 | G | A | 6 | a0001c0001t0007g0008 a0001c0001t0007g0011 a0001c0001t0007g0012 others(3): Show |
6 | HG00735.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.904+1828G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96787082 | |||||||
chr1:96787089 | C | T | 5 | a0001c0001t0003g0038 a0001c0001t0003g0081 a0001c0001t0003g0085 others(2): Show |
5 | HG00438.hp2 HG02129.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.904+1835C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96787089 | |||||||
chr1:96787283 | A | C | 100 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(97): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.904+2029A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96787283 | |||||||
chr1:96787385 | G | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(224): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.904+2131G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96787385 | |||||||
chr1:96787437 | T | G | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.904+2183T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96787437 | |||||||
chr1:96787514 | T | C | 2 | a0001c0001t0002g0154 a0001c0001t0002g0155 |
2 | HG03239.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.904+2260T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96787514 | |||||||
chr1:96787555 | A | T | 1 | a0001c0001t0003g0127 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.904+2301A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96787555 | |||||||
chr1:96787697 | G | A | 16 | a0001c0002t0001g0310 a0001c0002t0001g0311 a0001c0002t0001g0313 others(13): Show |
16 | HG01884.hp2 HG02109.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.904+2443G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96787697 | |||||||
chr1:96787913 | A | G | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.904+2659A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96787913 | |||||||
chr1:96788020 | T | C | 9 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0010 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.904+2766T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96788020 | |||||||
chr1:96788254 | A | T | 1 | a0001c0001t0017g0230 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.904+3000A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96788254 | |||||||
chr1:96788458 | T | C | 107 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(104): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.904+3204T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96788458 | |||||||
chr1:96788470 | A | G | 1 | a0001c0001t0002g0165 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.904+3216A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96788470 | |||||||
chr1:96788480 | A | G | 2 | a0001c0001t0002g0178 a0001c0001t0002g0183 |
2 | NA18965.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.904+3226A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96788480 | |||||||
chr1:96788560 | G | T | 25 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0272 others(22): Show |
25 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.904+3306G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96788560 | |||||||
chr1:96789102 | A | G | 3 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0016 |
3 | HG00735.hp2 HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.904+3848A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96789102 | |||||||
chr1:96789116 | G | A | 2 | a0001c0001t0003g0092 a0001c0001t0003g0123 |
2 | NA18967.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.904+3862G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96789116 | |||||||
chr1:96789172 | CAA | C | 4 | a0001c0002t0001g0294 a0001c0002t0001g0306 a0001c0002t0001g0307 others(1): Show |
4 | HG01081.hp1 HG01192.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.904+3920_904+3921d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96789172 | ||||||
chr1:96789227 | CTCA | C | 11 | a0001c0002t0001g0267 a0001c0002t0001g0270 a0001c0002t0001g0294 others(8): Show |
11 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.904+3978_904+3980d others(5): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96789227 | ||||||
chr1:96789728 | T | C | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.904+4474T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96789728 | |||||||
chr1:96789815 | C | A | 1 | a0001c0001t0002g0174 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.904+4561C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96789815 | |||||||
chr1:96789984 | G | A | 1 | a0001c0001t0003g0047 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.904+4730G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96789984 | |||||||
chr1:96790216 | T | C | 235 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.904+4962T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96790216 | |||||||
chr1:96790378 | T | A | 1 | a0001c0002t0001g0268 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.904+5124T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96790378 | |||||||
chr1:96790410 | C | T | 1 | a0001c0002t0001g0352 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.904+5156C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96790410 | |||||||
chr1:96790438 | A | T | 1 | a0001c0001t0009g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.904+5184A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96790438 | |||||||
chr1:96790491 | T | C | 1 | a0001c0001t0002g0214 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.904+5237T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96790491 | |||||||
chr1:96790505 | CT | C | 21 | a0001c0001t0003g0147 a0001c0001t0004g0021 a0001c0001t0004g0034 others(18): Show |
21 | HG02293.hp1 HG03927.hp1 NA18960.hp1 others(18): Show |
intron_variant | MODIFIER | c.904+5252delT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96790505 | |||||||
chr1:96790730 | G | C | 17 | a0001c0002t0001g0310 a0001c0002t0001g0311 a0001c0002t0001g0312 others(14): Show |
17 | HG01884.hp2 HG02109.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.904+5476G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96790730 | |||||||
chr1:96790958 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.904+5704G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96790958 | |||||||
chr1:96791016 | GA | G | 274 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(271): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.904+5773delA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791016 | ||||||
chr1:96791035 | G | T | 8 | a0001c0001t0002g0158 a0001c0001t0002g0171 a0001c0001t0002g0178 others(5): Show |
8 | NA18943.hp1 NA18954.hp2 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.904+5781G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96791035 | |||||||
chr1:96791062 | G | A | 1 | a0001c0002t0001g0351 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.904+5808G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96791062 | |||||||
chr1:96791319 | C | T | 1 | a0001c0001t0011g0186 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.904+6065C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96791319 | |||||||
chr1:96791587 | GAGGGGTT others(5): Show |
G | 1 | a0001c0001t0003g0078 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.904+6334_904+6345d others(14): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96791587 | |||||||
chr1:96791600 | G | T | 1 | a0001c0001t0003g0078 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.904+6346G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96791600 | |||||||
chr1:96791631 | C | G | 1 | a0001c0002t0008g0289 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.904+6377C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96791631 | |||||||
chr1:96791826 | C | CT | 18 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(15): Show |
18 | HG00642.hp2 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.904+6595dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791826 | ||||||
chr1:96791826 | C | CTTTTTTT others(2): Show |
33 | a0001c0001t0002g0168 a0001c0001t0002g0174 a0001c0001t0002g0176 others(30): Show |
33 | HG00544.hp2 HG00621.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.904+6580_904+6581i others(11): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791826 | ||||||
chr1:96791826 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0163 a0001c0001t0002g0169 a0001c0001t0002g0191 others(1): Show |
4 | NA18940.hp2 NA18949.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.904+6580_904+6581i others(12): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791826 | ||||||
chr1:96791826 | C | CTTTTTTT others(3): Show |
6 | a0001c0001t0002g0207 a0001c0001t0002g0215 a0001c0001t0002g0237 others(3): Show |
6 | HG00621.hp1 HG02015.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.904+6580_904+6581i others(12): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791826 | ||||||
chr1:96791826 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0002g0240 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.904+6580_904+6581i others(13): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791826 | ||||||
chr1:96791826 | C | CTTTTTTT others(13): Show |
35 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0266 others(32): Show |
35 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.904+6580_904+6581i others(22): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791826 | ||||||
chr1:96791826 | C | CTTTTTTT others(14): Show |
12 | a0001c0002t0001g0276 a0001c0002t0001g0285 a0001c0002t0001g0292 others(9): Show |
12 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.904+6580_904+6581i others(23): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791826 | ||||||
chr1:96791826 | C | CTTTTTTT others(15): Show |
2 | a0001c0002t0001g0264 a0001c0002t0001g0354 |
2 | NA18991.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.904+6580_904+6581i others(24): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791826 | ||||||
chr1:96791826 | C | CTTTTTTT others(14): Show |
16 | a0001c0002t0001g0267 a0001c0002t0001g0269 a0001c0002t0001g0270 others(13): Show |
16 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.904+6580_904+6581i others(23): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791826 | ||||||
chr1:96791826 | C | CTTTTTTT others(15): Show |
3 | a0001c0002t0001g0303 a0001c0002t0001g0330 a0001c0002t0001g0349 |
3 | HG01243.hp2 HG02015.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.904+6580_904+6581i others(24): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791826 | ||||||
chr1:96791826 | C | CTTTTTTT others(16): Show |
2 | a0001c0002t0001g0304 a0001c0002t0001g0309 |
2 | HG03453.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.904+6580_904+6581i others(25): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791826 | ||||||
chr1:96791826 | C | CTTTTTTT others(15): Show |
1 | a0001c0002t0001g0340 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.904+6580_904+6581i others(24): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791826 | ||||||
chr1:96791826 | CT | C | 11 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(8): Show |
11 | HG01256.hp2 HG01257.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.904+6595delT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791826 | ||||||
chr1:96791827 | T | TTTTTTTT others(1): Show |
52 | a0001c0001t0001g0220 a0001c0001t0001g0229 a0001c0001t0002g0017 others(49): Show |
52 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.904+6580_904+6581i others(10): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791827 | ||||||
chr1:96791827 | T | TTTTTTTT others(12): Show |
17 | a0001c0002t0001g0310 a0001c0002t0001g0312 a0001c0002t0001g0313 others(14): Show |
18 | HG02109.hp2 HG02486.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.904+6580_904+6581i others(21): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791827 | ||||||
chr1:96791827 | T | TTTTTTTT others(13): Show |
13 | a0001c0002t0001g0263 a0001c0002t0001g0268 a0001c0002t0001g0271 others(10): Show |
13 | HG01109.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.904+6580_904+6581i others(22): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791827 | ||||||
chr1:96791827 | T | TTTTTTTT others(12): Show |
1 | a0001c0002t0005g0260 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.904+6591_904+6592i others(21): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791827 | ||||||
chr1:96791828 | T | TTTTTTTG others(11): Show |
5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.904+6580_904+6581i others(20): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791828 | ||||||
chr1:96791830 | T | TTTTTG | 9 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0010 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.904+6580_904+6581i others(7): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96791830 | ||||||
chr1:96791847 | T | G | 1 | a0001c0002t0008g0265 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.904+6593T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96791847 | |||||||
chr1:96791978 | C | T | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.904+6724C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96791978 | |||||||
chr1:96791983 | G | A | 1 | a0001c0001t0003g0061 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.904+6729G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96791983 | |||||||
chr1:96791990 | C | T | 1 | a0001c0001t0018g0234 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.904+6736C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96791990 | |||||||
chr1:96792128 | C | T | 1 | a0001c0002t0001g0273 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.904+6874C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96792128 | |||||||
chr1:96792320 | C | T | 1 | a0001c0002t0001g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.904+7066C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96792320 | |||||||
chr1:96792333 | C | A | 1 | a0001c0001t0008g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.904+7079C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96792333 | |||||||
chr1:96792373 | C | G | 1 | a0001c0002t0001g0353 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.904+7119C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96792373 | |||||||
chr1:96792405 | T | C | 1 | a0001c0001t0003g0121 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.904+7151T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96792405 | |||||||
chr1:96792408 | A | T | 1 | a0001c0002t0001g0353 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.904+7154A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96792408 | |||||||
chr1:96792451 | A | T | 1 | a0001c0001t0003g0023 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.904+7197A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96792451 | |||||||
chr1:96792515 | C | T | 1 | a0001c0001t0003g0069 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.904+7261C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96792515 | |||||||
chr1:96792558 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.904+7304A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96792558 | |||||||
chr1:96792631 | G | A | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.904+7377G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96792631 | |||||||
chr1:96792720 | C | CAG | 228 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.904+7466_904+7467i others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96792720 | |||||||
chr1:96792912 | G | A | 107 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(104): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.904+7658G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96792912 | |||||||
chr1:96793020 | C | T | 34 | a0001c0002t0001g0263 a0001c0002t0001g0267 a0001c0002t0001g0268 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.904+7766C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96793020 | |||||||
chr1:96793104 | A | G | 1 | a0001c0001t0003g0068 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.904+7850A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96793104 | |||||||
chr1:96793134 | C | T | 1 | a0001c0001t0002g0227 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.904+7880C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96793134 | |||||||
chr1:96793273 | A | G | 2 | a0001c0001t0003g0023 a0001c0001t0006g0024 |
2 | HG02602.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.904+8019A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96793273 | |||||||
chr1:96793448 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.904+8194C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96793448 | |||||||
chr1:96793562 | A | G | 235 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.904+8308A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96793562 | |||||||
chr1:96793572 | C | T | 1 | a0001c0001t0003g0057 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.904+8318C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96793572 | |||||||
chr1:96793573 | G | T | 61 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0264 others(58): Show |
61 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.904+8319G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96793573 | |||||||
chr1:96793828 | G | A | 8 | a0001c0002t0001g0269 a0001c0002t0001g0303 a0001c0002t0001g0304 others(5): Show |
8 | HG00558.hp2 HG02015.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.904+8574G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96793828 | |||||||
chr1:96793948 | A | T | 2 | a0001c0002t0001g0288 a0001c0002t0008g0289 |
2 | HG01433.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.904+8694A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96793948 | |||||||
chr1:96794222 | C | T | 1 | a0001c0001t0010g0150 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.904+8968C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96794222 | |||||||
chr1:96794500 | A | C | 1 | a0001c0002t0001g0329 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.904+9246A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96794500 | |||||||
chr1:96794537 | G | C | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.904+9283G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96794537 | |||||||
chr1:96794628 | T | G | 1 | a0001c0001t0006g0135 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.904+9374T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96794628 | |||||||
chr1:96794766 | T | C | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.904+9512T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96794766 | |||||||
chr1:96794916 | C | T | 110 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(107): Show |
110 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.904+9662C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96794916 | |||||||
chr1:96794958 | C | T | 107 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(104): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.904+9704C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96794958 | |||||||
chr1:96795094 | G | C | 1 | a0001c0001t0004g0030 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.905-9706G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96795094 | |||||||
chr1:96795334 | T | C | 1 | a0001c0001t0004g0075 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.905-9466T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96795334 | |||||||
chr1:96795348 | G | A | 1 | a0001c0002t0001g0338 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.905-9452G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96795348 | |||||||
chr1:96795375 | T | C | 4 | a0001c0001t0003g0081 a0001c0001t0003g0085 a0001c0001t0006g0108 others(1): Show |
4 | HG00438.hp2 HG02129.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-9425T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96795375 | |||||||
chr1:96795511 | C | G | 1 | a0001c0003t0001g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.905-9289C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96795511 | |||||||
chr1:96795590 | C | T | 2 | a0001c0002t0001g0305 a0001c0002t0001g0330 |
2 | HG01243.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.905-9210C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96795590 | |||||||
chr1:96795706 | C | T | 7 | a0001c0002t0001g0296 a0001c0002t0001g0297 a0001c0002t0001g0298 others(4): Show |
7 | HG01109.hp1 HG02109.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.905-9094C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96795706 | |||||||
chr1:96795800 | G | C | 1 | a0001c0001t0002g0224 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.905-9000G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96795800 | |||||||
chr1:96795808 | A | G | 18 | a0001c0001t0003g0038 a0001c0001t0003g0042 a0001c0001t0003g0045 others(15): Show |
18 | HG00423.hp1 HG00438.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.905-8992A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96795808 | |||||||
chr1:96796052 | A | C | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-8748A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96796052 | |||||||
chr1:96796198 | A | G | 15 | a0001c0002t0001g0267 a0001c0002t0001g0270 a0001c0002t0001g0294 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.905-8602A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96796198 | |||||||
chr1:96796288 | A | G | 1 | a0001c0002t0001g0268 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.905-8512A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96796288 | |||||||
chr1:96796290 | C | CA | 115 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(112): Show |
115 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.905-8494dupA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96796290 | ||||||
chr1:96796485 | C | T | 100 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(97): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.905-8315C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96796485 | |||||||
chr1:96796650 | G | A | 1 | a0001c0002t0001g0347 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.905-8150G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96796650 | |||||||
chr1:96796715 | A | T | 1 | a0001c0001t0003g0088 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.905-8085A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96796715 | |||||||
chr1:96796790 | C | A | 4 | a0001c0001t0003g0044 a0001c0001t0003g0083 a0001c0001t0003g0090 others(1): Show |
4 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-8010C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96796790 | |||||||
chr1:96796835 | T | G | 2 | a0001c0001t0002g0221 a0001c0001t0002g0223 |
2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.905-7965T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96796835 | |||||||
chr1:96796944 | T | C | 1 | a0001c0001t0003g0026 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.905-7856T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96796944 | |||||||
chr1:96796945 | G | A | 1 | a0001c0002t0001g0313 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.905-7855G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96796945 | |||||||
chr1:96797160 | C | T | 95 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.905-7640C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96797160 | |||||||
chr1:96797628 | G | A | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.905-7172G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96797628 | |||||||
chr1:96797671 | G | T | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.905-7129G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96797671 | |||||||
chr1:96797850 | C | T | 1 | a0001c0001t0003g0090 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.905-6950C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96797850 | |||||||
chr1:96797998 | C | A | 1 | a0001c0001t0003g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.905-6802C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96797998 | |||||||
chr1:96798001 | G | A | 6 | a0001c0001t0003g0076 a0001c0001t0004g0030 a0001c0001t0004g0037 others(3): Show |
6 | HG00639.hp1 HG00741.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-6799G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96798001 | |||||||
chr1:96798076 | T | TA | 6 | a0001c0001t0002g0240 a0001c0001t0004g0136 a0001c0002t0001g0330 others(3): Show |
6 | HG01243.hp2 HG02293.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-6706dupA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96798076 | ||||||
chr1:96798120 | T | G | 236 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.905-6680T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96798120 | |||||||
chr1:96798130 | A | G | 3 | a0001c0002t0005g0251 a0001c0002t0005g0254 a0001c0002t0005g0260 |
3 | HG03041.hp2 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.905-6670A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96798130 | |||||||
chr1:96798237 | C | G | 107 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(104): Show |
107 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.905-6563C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96798237 | |||||||
chr1:96798248 | A | G | 1 | a0001c0001t0008g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.905-6552A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96798248 | |||||||
chr1:96798272 | G | A | 1 | a0001c0001t0016g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.905-6528G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96798272 | |||||||
chr1:96798724 | T | C | 1 | a0001c0002t0001g0282 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.905-6076T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96798724 | |||||||
chr1:96798826 | A | G | 111 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(108): Show |
111 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.905-5974A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96798826 | |||||||
chr1:96798828 | A | G | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.905-5972A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96798828 | |||||||
chr1:96799294 | C | CT | 147 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(144): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.905-5487dupT | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTT | 9 | a0001c0001t0002g0176 a0001c0001t0002g0185 a0001c0001t0002g0208 others(6): Show |
9 | HG00597.hp1 HG03942.hp2 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.905-5488_905-5487d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTT | 6 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(3): Show |
6 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-5491_905-5487d others(7): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(2): Show |
5 | a0001c0002t0005g0002 a0001c0002t0005g0252 a0001c0002t0005g0253 others(2): Show |
6 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.905-5495_905-5487d others(11): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(3): Show |
1 | a0001c0002t0005g0254 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.905-5496_905-5487d others(12): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(4): Show |
1 | a0001c0002t0005g0251 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.905-5497_905-5487d others(13): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(8): Show |
1 | a0001c0002t0001g0329 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.905-5501_905-5487d others(17): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(10): Show |
1 | a0001c0002t0001g0351 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.905-5503_905-5487d others(19): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(11): Show |
4 | a0001c0002t0001g0318 a0001c0002t0001g0324 a0001c0002t0001g0347 others(1): Show |
4 | HG02809.hp1 HG02896.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-5504_905-5487d others(20): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(12): Show |
2 | a0001c0002t0001g0321 a0001c0002t0008g0265 |
2 | HG02027.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.905-5505_905-5487d others(21): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(13): Show |
6 | a0001c0002t0001g0310 a0001c0002t0001g0313 a0001c0002t0001g0319 others(3): Show |
6 | HG02486.hp2 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-5487_905-5486i others(22): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(14): Show |
5 | a0001c0002t0001g0268 a0001c0002t0001g0312 a0001c0002t0001g0320 others(2): Show |
5 | HG00558.hp2 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.905-5487_905-5486i others(23): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(15): Show |
3 | a0001c0002t0001g0278 a0001c0002t0001g0303 a0001c0002t0001g0304 |
3 | HG02015.hp2 NA18983.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.905-5487_905-5486i others(24): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(16): Show |
8 | a0001c0002t0001g0267 a0001c0002t0001g0271 a0001c0002t0001g0314 others(5): Show |
8 | HG01884.hp2 HG02145.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-5487_905-5486i others(25): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(17): Show |
3 | a0001c0002t0001g0269 a0001c0002t0001g0292 a0001c0002t0001g0348 |
3 | HG03927.hp2 NA18943.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.905-5487_905-5486i others(26): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(18): Show |
2 | a0001c0002t0001g0299 a0001c0002t0001g0307 |
2 | HG01517.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.905-5487_905-5486i others(27): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(19): Show |
4 | a0001c0002t0001g0294 a0001c0002t0001g0296 a0001c0002t0001g0297 others(1): Show |
4 | HG01515.hp1 HG03453.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-5487_905-5486i others(28): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(20): Show |
2 | a0001c0002t0001g0272 a0001c0002t0008g0345 |
2 | HG00140.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.905-5487_905-5486i others(29): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(21): Show |
3 | a0001c0002t0001g0277 a0001c0002t0001g0326 a0001c0002t0008g0322 |
3 | HG00280.hp1 HG03516.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.905-5487_905-5486i others(30): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(22): Show |
6 | a0001c0002t0001g0276 a0001c0002t0001g0291 a0001c0002t0001g0333 others(3): Show |
6 | HG00438.hp1 HG02083.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.905-5487_905-5486i others(31): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(23): Show |
8 | a0001c0002t0001g0263 a0001c0002t0001g0266 a0001c0002t0001g0273 others(5): Show |
8 | HG00558.hp1 HG00597.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-5487_905-5486i others(32): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(24): Show |
2 | a0001c0002t0001g0284 a0001c0002t0001g0330 |
2 | HG01243.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.905-5487_905-5486i others(33): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(25): Show |
3 | a0001c0002t0001g0298 a0001c0002t0001g0331 a0001c0002t0008g0293 |
3 | HG01099.hp2 HG01109.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.905-5487_905-5486i others(34): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(26): Show |
1 | a0001c0002t0001g0295 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.905-5487_905-5486i others(35): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(27): Show |
2 | a0001c0002t0001g0323 a0001c0002t0001g0336 |
2 | HG02109.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.905-5487_905-5486i others(36): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(28): Show |
3 | a0001c0002t0001g0264 a0001c0002t0001g0328 a0001c0002t0005g0274 |
3 | HG03239.hp1 NA19012.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.905-5487_905-5486i others(37): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(29): Show |
4 | a0001c0002t0001g0332 a0001c0002t0001g0337 a0001c0002t0001g0350 others(1): Show |
4 | HG02257.hp2 HG03942.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-5487_905-5486i others(38): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(30): Show |
1 | a0001c0002t0001g0152 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.905-5487_905-5486i others(39): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(31): Show |
5 | a0001c0002t0001g0004 a0001c0002t0001g0280 a0001c0002t0001g0281 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.905-5487_905-5486i others(40): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(32): Show |
2 | a0001c0002t0001g0275 a0001c0002t0001g0302 |
2 | HG02109.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.905-5487_905-5486i others(41): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(34): Show |
1 | a0001c0002t0001g0285 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.905-5487_905-5486i others(43): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(35): Show |
2 | a0001c0002t0001g0305 a0001c0002t0008g0290 |
2 | HG01496.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.905-5487_905-5486i others(44): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(39): Show |
1 | a0001c0002t0001g0270 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.905-5487_905-5486i others(48): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799294 | C | CTTTTTTT others(41): Show |
1 | a0001c0002t0001g0288 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.905-5487_905-5486i others(50): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96799294 | ||||||
chr1:96799333 | T | C | 1 | a0001c0001t0008g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.905-5467T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96799333 | |||||||
chr1:96799352 | A | G | 1 | a0001c0001t0014g0157 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.905-5448A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96799352 | |||||||
chr1:96799430 | C | A | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-5370C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96799430 | |||||||
chr1:96799430 | C | G | 100 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(97): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.905-5370C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96799430 | |||||||
chr1:96799507 | A | G | 43 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0264 others(40): Show |
43 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.905-5293A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96799507 | |||||||
chr1:96799527 | A | C | 1 | a0001c0001t0003g0078 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.905-5273A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96799527 | |||||||
chr1:96799527 | A | T | 1 | a0001c0001t0008g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.905-5273A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96799527 | |||||||
chr1:96799541 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.905-5259C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96799541 | |||||||
chr1:96799543 | A | G | 1 | a0001c0002t0001g0268 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.905-5257A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96799543 | |||||||
chr1:96799587 | T | C | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-5213T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96799587 | |||||||
chr1:96799906 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.905-4894G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96799906 | |||||||
chr1:96799907 | T | G | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-4893T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96799907 | |||||||
chr1:96800136 | G | A | 15 | a0001c0002t0001g0267 a0001c0002t0001g0270 a0001c0002t0001g0294 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.905-4664G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96800136 | |||||||
chr1:96800185 | T | C | 121 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(118): Show |
121 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.905-4615T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96800185 | |||||||
chr1:96800395 | CTT | C | 143 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(140): Show |
144 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.905-4387_905-4386d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96800395 | ||||||
chr1:96800395 | CTTT | C | 91 | a0001c0001t0001g0003 a0001c0001t0002g0161 a0001c0001t0002g0244 others(88): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.905-4388_905-4386d others(5): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96800395 | ||||||
chr1:96800451 | A | G | 236 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.905-4349A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96800451 | |||||||
chr1:96800520 | C | T | 1 | a0001c0001t0003g0124 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.905-4280C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96800520 | |||||||
chr1:96800586 | T | C | 1 | a0001c0001t0008g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.905-4214T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96800586 | |||||||
chr1:96800684 | T | C | 2 | a0001c0001t0002g0182 a0001c0001t0002g0216 |
2 | NA18954.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.905-4116T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96800684 | |||||||
chr1:96800784 | C | A | 1 | a0001c0001t0003g0107 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.905-4016C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96800784 | |||||||
chr1:96800811 | TAATTACT others(9): Show |
T | 11 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0059 others(8): Show |
12 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.905-3981_905-3966d others(18): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96800811 | ||||||
chr1:96800829 | A | G | 1 | a0001c0001t0003g0026 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.905-3971A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96800829 | |||||||
chr1:96800893 | C | T | 1 | a0001c0002t0005g0257 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.905-3907C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96800893 | |||||||
chr1:96800913 | GA | G | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.905-3877delA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96800913 | ||||||
chr1:96801241 | A | G | 1 | a0001c0001t0003g0049 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.905-3559A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96801241 | |||||||
chr1:96801266 | CAT | C | 11 | a0001c0001t0003g0076 a0001c0001t0004g0030 a0001c0001t0004g0037 others(8): Show |
11 | HG00639.hp1 HG00741.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.905-3533_905-3532d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96801266 | |||||||
chr1:96801322 | T | A | 1 | a0001c0001t0003g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.905-3478T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96801322 | |||||||
chr1:96801817 | C | T | 1 | a0001c0001t0003g0117 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.905-2983C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96801817 | |||||||
chr1:96801829 | C | T | 1 | a0001c0001t0003g0033 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.905-2971C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96801829 | |||||||
chr1:96801861 | C | CA | 94 | a0001c0001t0001g0229 a0001c0001t0002g0158 a0001c0001t0002g0159 others(91): Show |
94 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.905-2921dupA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96801861 | ||||||
chr1:96801861 | CA | C | 14 | a0001c0001t0001g0356 a0001c0001t0003g0026 a0001c0001t0003g0032 others(11): Show |
15 | HG01167.hp1 HG02451.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.905-2921delA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96801861 | ||||||
chr1:96802039 | G | A | 1 | a0001c0001t0003g0026 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.905-2761G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96802039 | |||||||
chr1:96802100 | A | G | 1 | a0001c0001t0009g0054 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.905-2700A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96802100 | |||||||
chr1:96802103 | T | C | 3 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 |
3 | HG02647.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.905-2697T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96802103 | |||||||
chr1:96802142 | C | T | 2 | a0001c0001t0004g0071 a0001c0001t0004g0102 |
2 | NA19066.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.905-2658C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96802142 | |||||||
chr1:96802197 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.905-2603C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96802197 | |||||||
chr1:96802210 | C | CG | 11 | a0001c0002t0005g0002 a0001c0002t0005g0252 a0001c0002t0005g0253 others(8): Show |
12 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.905-2589dupG | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96802210 | ||||||
chr1:96802211 | G | GA | 38 | a0001c0001t0001g0003 a0001c0001t0002g0215 a0001c0001t0003g0001 others(35): Show |
39 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.905-2567dupA | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96802211 | ||||||
chr1:96802211 | G | GAA | 96 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(93): Show |
96 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.905-2568_905-2567d others(4): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96802211 | ||||||
chr1:96802211 | G | GAAA | 21 | a0001c0001t0001g0355 a0001c0001t0001g0359 a0001c0001t0002g0159 others(18): Show |
21 | HG00735.hp2 HG00741.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.905-2569_905-2567d others(5): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96802211 | ||||||
chr1:96802211 | G | GAAAA | 7 | a0001c0001t0002g0185 a0001c0001t0007g0008 a0001c0001t0007g0010 others(4): Show |
7 | HG00597.hp1 HG00735.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.905-2570_905-2567d others(6): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96802211 | ||||||
chr1:96802212 | A | G | 1 | a0001c0002t0001g0278 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.905-2588A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96802212 | |||||||
chr1:96802237 | C | G | 107 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(104): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.905-2563C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96802237 | |||||||
chr1:96802358 | A | G | 1 | a0001c0002t0005g0261 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.905-2442A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96802358 | |||||||
chr1:96802445 | T | C | 1 | a0001c0001t0003g0070 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.905-2355T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96802445 | |||||||
chr1:96802450 | A | G | 1 | a0001c0001t0002g0243 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.905-2350A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96802450 | |||||||
chr1:96802602 | A | C | 1 | a0001c0001t0008g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.905-2198A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96802602 | |||||||
chr1:96802664 | T | G | 1 | a0001c0002t0005g0259 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.905-2136T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96802664 | |||||||
chr1:96803021 | A | G | 1 | a0001c0001t0003g0127 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.905-1779A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96803021 | |||||||
chr1:96803109 | A | C | 1 | a0001c0001t0003g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.905-1691A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96803109 | |||||||
chr1:96803390 | G | A | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.905-1410G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96803390 | |||||||
chr1:96803496 | A | G | 1 | a0001c0001t0002g0217 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.905-1304A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96803496 | |||||||
chr1:96803559 | G | GGGAAAGT others(327): Show |
1 | a0001c0001t0003g0047 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.905-1231_905-1230i others(336): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96803559 | ||||||
chr1:96803594 | T | A | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.905-1206T>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96803594 | |||||||
chr1:96803785 | C | G | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.905-1015C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96803785 | |||||||
chr1:96803989 | G | T | 3 | a0001c0001t0002g0170 a0001c0001t0002g0177 a0001c0001t0002g0179 |
3 | NA18939.hp2 NA18942.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.905-811G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96803989 | |||||||
chr1:96803994 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.905-806C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96803994 | |||||||
chr1:96804051 | A | G | 9 | a0001c0001t0001g0163 a0001c0001t0002g0162 a0001c0001t0002g0167 others(6): Show |
9 | HG00639.hp2 NA18940.hp2 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-749A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96804051 | |||||||
chr1:96804054 | G | A | 1 | a0001c0001t0003g0138 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.905-746G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96804054 | |||||||
chr1:96804420 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.905-380C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96804420 | |||||||
chr1:96804424 | A | AGTGATAC others(114): Show |
1 | a0001c0001t0003g0023 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.905-363_905-362ins others(121): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96804424 | ||||||
chr1:96804424 | A | AGTGATAC others(129): Show |
1 | a0001c0001t0006g0024 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.905-363_905-362ins others(136): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 96804424 | ||||||
chr1:96804461 | C | T | 10 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0010 others(7): Show |
10 | HG00735.hp1 HG00735.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.905-339C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96804461 | |||||||
chr1:96804700 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.905-100G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 8/13 | chr1 | 96804700 | |||||||
chr1:96805071 | C | G | 5 | a0001c0001t0002g0167 a0001c0001t0002g0191 a0001c0001t0002g0192 others(2): Show |
5 | NA18944.hp2 NA18960.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044+132C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 9/13 | chr1 | 96805071 | |||||||
chr1:96805286 | C | G | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1044+347C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 9/13 | chr1 | 96805286 | |||||||
chr1:96805338 | G | C | 2 | a0001c0001t0003g0055 a0001c0001t0003g0099 |
2 | NA18612.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1044+399G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 9/13 | chr1 | 96805338 | |||||||
chr1:96805619 | G | A | 1 | a0001c0001t0003g0052 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1044+680G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 9/13 | chr1 | 96805619 | |||||||
chr1:96806454 | T | G | 1 | a0001c0001t0002g0184 | 1 | NA19003.hp1 | splice_donor_variant&intron_variant | HIGH | c.1078+2T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 10/13 | chr1 | 96806454 | |||||||
chr1:96806597 | C | T | 1 | a0001c0002t0001g0334 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1078+145C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 10/13 | chr1 | 96806597 | |||||||
chr1:96806658 | A | C | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1078+206A>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 10/13 | chr1 | 96806658 | |||||||
chr1:96807430 | T | C | 7 | a0001c0001t0003g0028 a0001c0001t0003g0086 a0001c0001t0003g0112 others(4): Show |
7 | HG00733.hp1 HG01433.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.1171+472T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96807430 | |||||||
chr1:96807494 | C | T | 1 | a0001c0001t0007g0153 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1171+536C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96807494 | |||||||
chr1:96807748 | A | G | 1 | a0001c0001t0002g0164 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1171+790A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96807748 | |||||||
chr1:96807757 | A | T | 112 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1171+799A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96807757 | |||||||
chr1:96807776 | G | A | 102 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(99): Show |
102 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1171+818G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96807776 | |||||||
chr1:96807834 | A | G | 1 | a0001c0002t0001g0278 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1171+876A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96807834 | |||||||
chr1:96807882 | A | G | 1 | a0001c0001t0003g0086 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1171+924A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96807882 | |||||||
chr1:96808103 | A | T | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1171+1145A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96808103 | |||||||
chr1:96808363 | C | T | 10 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0059 others(7): Show |
11 | HG00140.hp2 HG01069.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1171+1405C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96808363 | |||||||
chr1:96808405 | G | T | 1 | a0001c0001t0002g0218 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1171+1447G>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96808405 | |||||||
chr1:96808502 | T | G | 1 | a0001c0001t0003g0144 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1171+1544T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96808502 | |||||||
chr1:96808769 | A | G | 6 | a0001c0001t0007g0008 a0001c0001t0007g0011 a0001c0001t0007g0012 others(3): Show |
6 | HG00735.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1171+1811A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96808769 | |||||||
chr1:96808810 | AACAC | A | 5 | a0001c0001t0002g0203 a0001c0001t0003g0076 a0001c0001t0004g0030 others(2): Show |
5 | HG00639.hp1 HG00741.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.1171+1865_1171+186 others(8): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 96808810 | ||||||
chr1:96808851 | A | T | 2 | a0001c0002t0001g0294 a0001c0002t0001g0307 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1171+1893A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96808851 | |||||||
chr1:96808919 | A | T | 1 | a0001c0003t0001g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1171+1961A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96808919 | |||||||
chr1:96809027 | T | C | 1 | a0001c0001t0014g0157 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1171+2069T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96809027 | |||||||
chr1:96809393 | A | G | 1 | a0001c0001t0007g0015 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1171+2435A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96809393 | |||||||
chr1:96809508 | AGTTT | A | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1171+2567_1171+257 others(8): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 96809508 | ||||||
chr1:96809547 | C | G | 1 | a0001c0001t0009g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1171+2589C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96809547 | |||||||
chr1:96809577 | A | G | 7 | a0001c0002t0001g0296 a0001c0002t0001g0297 a0001c0002t0001g0298 others(4): Show |
7 | HG01109.hp1 HG02109.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1171+2619A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96809577 | |||||||
chr1:96809637 | A | G | 142 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(139): Show |
142 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1171+2679A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96809637 | |||||||
chr1:96809922 | G | A | 3 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0016 |
3 | HG00735.hp2 HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1172-2790G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96809922 | |||||||
chr1:96810087 | CACT | C | 100 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(97): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.1172-2623_1172-262 others(7): Show |
PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 96810087 | ||||||
chr1:96810137 | A | G | 122 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(119): Show |
122 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1172-2575A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96810137 | |||||||
chr1:96810138 | A | T | 122 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(119): Show |
122 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1172-2574A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96810138 | |||||||
chr1:96810245 | C | T | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1172-2467C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96810245 | |||||||
chr1:96810356 | C | T | 2 | a0001c0001t0003g0064 a0001c0001t0003g0100 |
2 | NA18962.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1172-2356C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96810356 | |||||||
chr1:96810496 | G | A | 1 | a0001c0002t0005g0002 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1172-2216G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96810496 | |||||||
chr1:96810550 | C | G | 8 | a0001c0001t0002g0158 a0001c0001t0002g0171 a0001c0001t0002g0178 others(5): Show |
8 | NA18943.hp1 NA18954.hp2 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1172-2162C>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96810550 | |||||||
chr1:96810583 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1172-2129G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96810583 | |||||||
chr1:96810634 | G | A | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1172-2078G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96810634 | |||||||
chr1:96810744 | A | G | 107 | a0001c0002t0001g0004 a0001c0002t0001g0152 a0001c0002t0001g0263 others(104): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1172-1968A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96810744 | |||||||
chr1:96810779 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1172-1933C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96810779 | |||||||
chr1:96810950 | A | T | 1 | a0001c0001t0007g0153 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1172-1762A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96810950 | |||||||
chr1:96811132 | T | C | 122 | a0001c0001t0001g0163 a0001c0001t0001g0220 a0001c0001t0001g0229 others(119): Show |
122 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1172-1580T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96811132 | |||||||
chr1:96811345 | A | G | 7 | a0001c0002t0005g0002 a0001c0002t0005g0251 a0001c0002t0005g0252 others(4): Show |
8 | HG02647.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1172-1367A>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96811345 | |||||||
chr1:96811415 | G | A | 1 | a0001c0002t0001g0318 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1172-1297G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96811415 | |||||||
chr1:96811485 | T | TC | 5 | a0001c0002t0005g0256 a0001c0002t0005g0257 a0001c0002t0005g0258 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1172-1226dupC | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 96811485 | ||||||
chr1:96811599 | T | G | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1172-1113T>G | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96811599 | |||||||
chr1:96811637 | G | A | 10 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0010 others(7): Show |
10 | HG00735.hp1 HG00735.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1172-1075G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96811637 | |||||||
chr1:96811655 | A | T | 1 | a0001c0001t0003g0042 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1172-1057A>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96811655 | |||||||
chr1:96811707 | C | T | 3 | a0001c0002t0005g0251 a0001c0002t0005g0254 a0001c0002t0005g0260 |
3 | HG03041.hp2 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1172-1005C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96811707 | |||||||
chr1:96811996 | C | T | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1172-716C>T | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96811996 | |||||||
chr1:96812192 | C | A | 1 | a0001c0002t0005g0002 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1172-520C>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96812192 | |||||||
chr1:96812574 | T | C | 5 | a0001c0001t0003g0038 a0001c0001t0003g0081 a0001c0001t0003g0085 others(2): Show |
5 | HG00438.hp2 HG02129.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1172-138T>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 11/13 | chr1 | 96812574 | |||||||
chr1:96813115 | G | C | 2 | a0001c0001t0003g0033 a0001c0001t0003g0073 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1466+9G>C | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 13/13 | chr1 | 96813115 | |||||||
chr1:96813248 | G | A | 226 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0220 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1467-28G>A | PTBP2 | ENSG00000117569.20 | transcript | ENST00000674951.1 | protein_coding | 13/13 | chr1 | 96813248 |