Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23350 |
| ensemblid | ENSG00000163714.18 |
| hgncid | 30855 |
| symbol | U2SURP |
| name | U2 snRNP associated SURP domain containing |
| refseq_nuc | NM_001080415.2 |
| refseq_prot | NP_001073884.1 |
| ensembl_nuc | ENST00000473835.7 |
| ensembl_prot | ENSP00000418563.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 143001570 |
| end | 143060725 |
| strand | + |
| ver | v1.2 |
| region | chr3:143001570-143060725 |
| region5000 | chr3:142996570-143065725 |
| regionname0 | U2SURP_chr3_143001570_143060725 |
| regionname5000 | U2SURP_chr3_142996570_143065725 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1029 | 373 | 85 | 68 | 164 | 12 | 42 | 130 | U2SURP_chr3_142996570_143065725 | U2SURP | MADKT others(1024): Show |
chr3 | 142996570 | 143065725 |
| a0002 | 0/0 | 1029 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | MADKT others(1024): Show |
chr3 | 142996570 | 143065725 |
| a0003 | 0/0 | 1029 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | MADKT others(1024): Show |
chr3 | 142996570 | 143065725 |
| a0004 | 0/0 | 1029 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | MADKT others(1024): Show |
chr3 | 142996570 | 143065725 |
| a0005 | 0/0 | 1029 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | MADKT others(1024): Show |
chr3 | 142996570 | 143065725 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3087 | 358 | 74 | 65 | 164 | 12 | 41 | U2SURP_chr3_142996570_143065725 | U2SURP | ATGGC others(3082): Show |
chr3 | 142996570 | 143065725 | ||
| a0001c0002 | 0/0 | 3087 | 10 | 10 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | ATGGC others(3082): Show |
chr3 | 142996570 | 143065725 | ||
| a0001c0004 | 0/0 | 3087 | 2 | 1 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | ATGGC others(3082): Show |
chr3 | 142996570 | 143065725 | ||
| a0001c0005 | 0/0 | 3087 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | ATGGC others(3082): Show |
chr3 | 142996570 | 143065725 | ||
| a0001c0008 | 0/0 | 3087 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | ATGGC others(3082): Show |
chr3 | 142996570 | 143065725 | ||
| a0001c0010 | 0/0 | 3087 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | ATGGC others(3082): Show |
chr3 | 142996570 | 143065725 | ||
| a0002c0003 | 0/0 | 3087 | 2 | 2 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | ATGGC others(3082): Show |
chr3 | 142996570 | 143065725 | ||
| a0003c0009 | 0/0 | 3087 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | ATGGC others(3082): Show |
chr3 | 142996570 | 143065725 | ||
| a0004c0006 | 0/0 | 3087 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | ATGGC others(3082): Show |
chr3 | 142996570 | 143065725 | ||
| a0005c0007 | 0/0 | 3087 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | ATGGC others(3082): Show |
chr3 | 142996570 | 143065725 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7426 | 108 | 29 | 20 | 48 | 2 | 9 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0002 | 0/0 | 7426 | 83 | 4 | 18 | 48 | 4 | 9 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0003 | 1/1 | 7424 | 80 | 5 | 16 | 43 | 4 | 10 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7419): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0004 | 0/0 | 7426 | 21 | 11 | 0 | 10 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0005 | 0/0 | 7426 | 14 | 12 | 2 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0006 | 0/0 | 7424 | 9 | 2 | 1 | 1 | 0 | 5 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7419): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0007 | 0/0 | 7427 | 7 | 1 | 2 | 0 | 2 | 2 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7422): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0008 | 0/0 | 7426 | 7 | 0 | 3 | 0 | 0 | 4 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0009 | 0/0 | 7424 | 5 | 0 | 0 | 5 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7419): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0010 | 0/0 | 7424 | 4 | 0 | 0 | 3 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7419): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0011 | 0/0 | 7424 | 3 | 0 | 0 | 2 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7419): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0013 | 0/0 | 7426 | 2 | 1 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0014 | 0/0 | 7424 | 2 | 2 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7419): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0015 | 0/0 | 7424 | 2 | 2 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7419): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0016 | 0/0 | 7426 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0017 | 0/0 | 7424 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7419): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0018 | 0/0 | 7424 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7419): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0019 | 0/0 | 7425 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7420): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0020 | 0/0 | 7426 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0021 | 0/0 | 7426 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0022 | 0/0 | 7426 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0023 | 0/0 | 7426 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0024 | 0/0 | 7426 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0025 | 0/0 | 7476 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7471): Show |
chr3 | 142996570 | 143065725 |
| a0001c0001t0026 | 0/0 | 7424 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7419): Show |
chr3 | 142996570 | 143065725 |
| a0001c0002t0002 | 0/0 | 7426 | 9 | 9 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0001c0002t0011 | 0/0 | 7424 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7419): Show |
chr3 | 142996570 | 143065725 |
| a0001c0004t0012 | 0/0 | 7424 | 2 | 1 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7419): Show |
chr3 | 142996570 | 143065725 |
| a0001c0005t0001 | 0/0 | 7426 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0001c0008t0007 | 0/0 | 7427 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7422): Show |
chr3 | 142996570 | 143065725 |
| a0001c0010t0001 | 0/0 | 7426 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0002c0003t0004 | 0/0 | 7426 | 2 | 2 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0003c0009t0004 | 0/0 | 7426 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0004c0006t0002 | 0/0 | 7426 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| a0005c0007t0001 | 0/0 | 7426 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | CTTTC others(7421): Show |
chr3 | 142996570 | 143065725 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0302 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0320 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0003g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0005g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0006g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0006g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0006g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0006g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0006g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0006g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0006g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0006g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0007g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0007g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0007g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0007g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0007g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0008g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0008g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0008g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0008g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0008g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0008g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0009g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0009g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0009g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0009g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0010g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0010g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0010g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0010g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0011g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0011g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0011g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0013g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0013g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0014g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0014g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0015g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0015g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0016g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0017g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0018g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0019g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0020g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0021g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0022g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0023g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0024g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0025g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0001t0026g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0002t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0002t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0002t0011g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0004t0012g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0004t0012g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0005t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0008t0007g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0001c0010t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0002c0003t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0002c0003t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0003c0009t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0004c0006t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| a0005c0007t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0057 | EUR | GBR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0322 | EUR | GBR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | CHS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0331 | EAS | CHS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | CHS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00621 | hp1 | a0001 | c0001 | t0010 | g0214 | EAS | CHS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0317 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0314 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | CHS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00735 | hp1 | a0001 | c0004 | t0012 | g0018 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG00738 | hp2 | a0001 | c0001 | t0013 | g0256 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01069 | hp2 | a0001 | c0001 | t0019 | g0135 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0323 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0326 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01074 | hp1 | a0001 | c0001 | t0008 | g0030 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0281 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01099 | hp2 | a0001 | c0001 | t0007 | g0114 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0343 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0022 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0123 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01192 | hp1 | a0001 | c0005 | t0001 | g0011 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0282 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0131 | AMR | PUR | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01255 | hp1 | a0001 | c0001 | t0008 | g0029 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0327 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01257 | hp1 | a0001 | c0001 | t0017 | g0291 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0297 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0296 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0186 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0318 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0342 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0292 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0285 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0360 | EUR | IBS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01515 | hp2 | a0001 | c0001 | t0007 | g0113 | EUR | IBS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0086 | EUR | IBS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | IBS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01517 | hp1 | a0001 | c0001 | t0007 | g0112 | EUR | IBS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0087 | EUR | IBS | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0124 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0129 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01891 | hp2 | a0001 | c0001 | t0015 | g0019 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0287 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG01978 | hp2 | a0001 | c0008 | t0007 | g0232 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0294 | EAS | KHV | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | KHV | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0248 | EAS | KHV | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02080 | hp2 | a0001 | c0001 | t0006 | g0350 | EAS | KHV | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | KHV | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02145 | hp1 | a0001 | c0001 | t0018 | g0254 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0312 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0274 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CDX | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02155 | hp2 | a0001 | c0001 | t0010 | g0210 | EAS | CDX | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CDX | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | CDX | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02257 | hp1 | a0001 | c0001 | t0016 | g0128 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02257 | hp2 | a0001 | c0001 | t0014 | g0358 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0283 | AMR | PEL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02451 | hp2 | a0001 | c0001 | t0022 | g0193 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0357 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0348 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02615 | hp1 | a0001 | c0002 | t0011 | g0033 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0355 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0354 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0121 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0055 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0120 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0244 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02683 | hp1 | a0001 | c0001 | t0007 | g0115 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02698 | hp2 | a0001 | c0001 | t0006 | g0351 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0056 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0330 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02818 | hp1 | a0001 | c0004 | t0012 | g0017 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02896 | hp1 | a0002 | c0003 | t0004 | g0242 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02897 | hp1 | a0002 | c0003 | t0004 | g0014 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0094 | AFR | ESN | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0127 | AFR | ESN | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | ESN | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ESN | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0118 | AFR | ESN | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | ESN | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02976 | hp2 | a0001 | c0001 | t0026 | g0021 | AFR | ESN | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03041 | hp2 | a0001 | c0001 | t0024 | g0122 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0339 | AFR | MSL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0119 | AFR | ESN | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0235 | AFR | ESN | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0356 | AFR | ESN | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03239 | hp1 | a0001 | c0001 | t0007 | g0161 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03239 | hp2 | a0001 | c0001 | t0006 | g0352 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0264 | AFR | MSL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0337 | AFR | MSL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0130 | AFR | MSL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0251 | AFR | MSL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03490 | hp1 | a0001 | c0001 | t0008 | g0003 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03492 | hp2 | a0001 | c0001 | t0008 | g0003 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0084 | AFR | GWD | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0262 | AFR | MSL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03654 | hp1 | a0001 | c0001 | t0008 | g0027 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03669 | hp1 | a0001 | c0001 | t0010 | g0236 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03669 | hp2 | a0001 | c0001 | t0008 | g0026 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03704 | hp1 | a0001 | c0010 | t0001 | g0225 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0321 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0303 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03831 | hp1 | a0001 | c0001 | t0011 | g0095 | SAS | BEB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | BEB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0329 | SAS | BEB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0349 | SAS | BEB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | STU | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0332 | SAS | STU | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0082 | SAS | BEB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0328 | SAS | BEB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | STU | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0263 | SAS | STU | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0278 | SAS | STU | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0309 | SAS | STU | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG04228 | hp1 | a0001 | c0001 | t0006 | g0353 | SAS | STU | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0344 | SAS | STU | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | YRI | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | YRI | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | CHB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18906 | hp1 | a0001 | c0001 | t0014 | g0359 | AFR | YRI | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18943 | hp1 | a0001 | c0001 | t0009 | g0347 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18943 | hp2 | a0001 | c0001 | t0020 | g0109 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18952 | hp1 | a0001 | c0001 | t0025 | g0074 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18957 | hp1 | a0001 | c0001 | t0009 | g0346 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0333 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0334 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18980 | hp2 | a0001 | c0001 | t0023 | g0247 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18989 | hp1 | a0001 | c0001 | t0010 | g0177 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18991 | hp1 | a0001 | c0001 | t0011 | g0079 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19000 | hp1 | a0004 | c0006 | t0002 | g0110 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19011 | hp1 | a0001 | c0001 | t0009 | g0345 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0336 | AFR | LWK | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0104 | AFR | LWK | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19062 | hp1 | a0001 | c0001 | t0021 | g0034 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19078 | hp2 | a0001 | c0001 | t0011 | g0044 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19082 | hp1 | a0001 | c0001 | t0009 | g0015 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19086 | hp2 | a0005 | c0007 | t0001 | g0141 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19088 | hp1 | a0001 | c0001 | t0009 | g0015 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0239 | AFR | YRI | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ASW | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA20129 | hp2 | a0001 | c0001 | t0013 | g0255 | AFR | ASW | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | TSI | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0341 | EUR | TSI | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0319 | EUR | TSI | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0100 | EUR | TSI | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | GIH | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | GIH | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0238 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0249 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0246 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03471 | hp1 | a0003 | c0009 | t0004 | g0245 | AFR | MSL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0125 | AFR | USA | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | USA | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA20300 | hp1 | a0001 | c0001 | t0015 | g0020 | AFR | USA | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0184 | AFR | USA | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0069 | AFR | LWK | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | LWK | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0302 | REF | REF | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0320 | REF | REF | U2SURP_chr3_142996570_143065725 | U2SURP | chr3 | 142996570 | 143065725 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:143010830 | G | A | 1 | a0002 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.61G>A | p.Val21Ile | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 2/28 | 120/7424 | 61/3090 | 21/1029 | chr3 | 143010830 | |||
| chr3:143021490 | C | T | 1 | a0003 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.787C>T | p.Pro263Ser | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 10/28 | 846/7424 | 787/3090 | 263/1029 | chr3 | 143021490 | |||
| chr3:143034899 | A | G | 1 | a0005 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.1865A>G | p.Lys622Arg | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 19/28 | 1924/7424 | 1865/3090 | 622/1029 | chr3 | 143034899 | |||
| chr3:143055105 | C | G | 1 | a0004 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.2937C>G | p.Ser979Arg | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 27/28 | 2996/7424 | 2937/3090 | 979/1029 | chr3 | 143055105 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:143001646 | A | T | 1 | a0001c0010 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.18A>T | p.Pro6Pro | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/28 | 77/7424 | 18/3090 | 6/1029 | chr3 | 143001646 | |||
| chr3:143020683 | G | A | 1 | a0001c0005 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.723G>A | p.Gln241Gln | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 8/28 | 782/7424 | 723/3090 | 241/1029 | chr3 | 143020683 | |||
| chr3:143027179 | A | T | 1 | a0001c0008 | 1 | HG01978.hp2 | synonymous_variant | LOW | c.1305A>T | p.Ile435Ile | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 14/28 | 1364/7424 | 1305/3090 | 435/1029 | chr3 | 143027179 | |||
| chr3:143028388 | G | A | 1 | a0001c0004 | 2 | HG00735.hp1 HG02818.hp1 |
synonymous_variant | LOW | c.1428G>A | p.Lys476Lys | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 15/28 | 1487/7424 | 1428/3090 | 476/1029 | chr3 | 143028388 | |||
| chr3:143033315 | A | T | 1 | a0001c0002 | 10 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(7): Show |
synonymous_variant | LOW | c.1818A>T | p.Ser606Ser | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 18/28 | 1877/7424 | 1818/3090 | 606/1029 | chr3 | 143033315 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:143001601 | C | G | 3 | a0001c0001t0014 a0001c0001t0015 a0001c0001t0026 |
5 | HG01891.hp2 HG02257.hp2 HG02976.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-28C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/28 | 28 | chr3 | 143001601 | ||||||
| chr3:143056836 | G | A | 1 | a0001c0001t0016 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*386G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 386 | chr3 | 143056836 | ||||||
| chr3:143057309 | C | T | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(24): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*859C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 859 | chr3 | 143057309 | ||||||
| chr3:143057399 | T | TCC | 22 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(19): Show |
266 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*956_*957dupCC | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 958 | INFO_REALIGN_3_PRIME | chr3 | 143057399 | |||||
| chr3:143057484 | C | T | 1 | a0001c0001t0017 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1034C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 1034 | chr3 | 143057484 | ||||||
| chr3:143057565 | T | G | 2 | a0001c0001t0020 a0001c0001t0021 |
2 | NA18943.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1115T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 1115 | chr3 | 143057565 | ||||||
| chr3:143057887 | T | TG | 3 | a0001c0001t0007 a0001c0001t0019 a0001c0008t0007 |
9 | HG01069.hp2 HG01099.hp2 HG01261.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1438dupG | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 1439 | INFO_REALIGN_3_PRIME | chr3 | 143057887 | |||||
| chr3:143057936 | G | C | 1 | a0001c0004t0012 | 2 | HG00735.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1486G>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 1486 | chr3 | 143057936 | ||||||
| chr3:143057968 | T | C | 1 | a0001c0001t0014 | 2 | HG02257.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1518T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 1518 | chr3 | 143057968 | ||||||
| chr3:143058205 | G | A | 1 | a0001c0001t0022 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1755G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 1755 | chr3 | 143058205 | ||||||
| chr3:143058341 | C | T | 1 | a0001c0001t0026 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1891C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 1891 | chr3 | 143058341 | ||||||
| chr3:143058666 | C | A | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(24): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*2216C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 2216 | chr3 | 143058666 | ||||||
| chr3:143058669 | G | A | 1 | a0001c0001t0020 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2219G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 2219 | chr3 | 143058669 | ||||||
| chr3:143058873 | T | C | 2 | a0001c0001t0005 a0001c0001t0016 |
15 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2423T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 2423 | chr3 | 143058873 | ||||||
| chr3:143058876 | C | A | 1 | a0001c0004t0012 | 2 | HG00735.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2426C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 2426 | chr3 | 143058876 | ||||||
| chr3:143059472 | G | T | 1 | a0001c0001t0009 | 5 | NA18943.hp1 NA18957.hp1 NA19011.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3022G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 3022 | chr3 | 143059472 | ||||||
| chr3:143059513 | C | T | 9 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0011 others(6): Show |
107 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*3063C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 3063 | chr3 | 143059513 | ||||||
| chr3:143059563 | T | C | 1 | a0001c0001t0023 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3113T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 3113 | chr3 | 143059563 | ||||||
| chr3:143059824 | C | T | 32 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(29): Show |
292 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*3374C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 3374 | chr3 | 143059824 | ||||||
| chr3:143059920 | C | T | 1 | a0001c0001t0008 | 7 | HG01074.hp1 HG01169.hp2 HG01255.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3470C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 3470 | chr3 | 143059920 | ||||||
| chr3:143060190 | A | G | 18 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(15): Show |
232 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*3740A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 3740 | chr3 | 143060190 | ||||||
| chr3:143060248 | C | T | 1 | a0001c0001t0013 | 2 | HG00738.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3798C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 3798 | chr3 | 143060248 | ||||||
| chr3:143060452 | C | T | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(21): Show |
260 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*4002C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 4002 | chr3 | 143060452 | ||||||
| chr3:143060575 | A | ATTGTTTT others(43): Show |
1 | a0001c0001t0025 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4127_*4176dupTGTT others(46): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 4177 | INFO_REALIGN_3_PRIME | chr3 | 143060575 | |||||
| chr3:143060698 | A | G | 6 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0018 others(3): Show |
28 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4248A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 28/28 | 4248 | chr3 | 143060698 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:143001785 | C | G | 1 | a0001c0001t0003g0360 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.45+112C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143001785 | |||||||
| chr3:143001847 | A | G | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.45+174A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143001847 | |||||||
| chr3:143001884 | C | T | 2 | a0001c0002t0002g0356 a0001c0002t0002g0357 |
2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.45+211C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143001884 | |||||||
| chr3:143001888 | T | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(264): Show |
282 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(279): Show |
intron_variant | MODIFIER | c.45+215T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143001888 | |||||||
| chr3:143001894 | G | C | 1 | a0001c0001t0001g0016 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.45+221G>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143001894 | |||||||
| chr3:143001992 | C | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(259): Show |
277 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(274): Show |
intron_variant | MODIFIER | c.45+319C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143001992 | |||||||
| chr3:143001993 | C | T | 1 | a0001c0001t0004g0262 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.45+320C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143001993 | |||||||
| chr3:143002115 | C | T | 1 | a0001c0002t0002g0357 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.45+442C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143002115 | |||||||
| chr3:143002142 | T | A | 1 | a0001c0001t0004g0354 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.45+469T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143002142 | |||||||
| chr3:143002245 | A | G | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 |
3 | HG02055.hp2 HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.45+572A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143002245 | |||||||
| chr3:143002627 | A | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(270): Show |
288 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(285): Show |
intron_variant | MODIFIER | c.45+954A>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143002627 | |||||||
| chr3:143002766 | T | C | 104 | a0001c0001t0001g0093 a0001c0001t0002g0002 a0001c0001t0002g0004 others(101): Show |
112 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.45+1093T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143002766 | |||||||
| chr3:143002873 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.45+1200A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143002873 | |||||||
| chr3:143002898 | C | T | 4 | a0001c0001t0009g0015 a0001c0001t0009g0345 a0001c0001t0009g0346 others(1): Show |
5 | NA18943.hp1 NA18957.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+1225C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143002898 | |||||||
| chr3:143003022 | A | G | 27 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(24): Show |
28 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.45+1349A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143003022 | |||||||
| chr3:143003050 | TG | T | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 |
3 | HG02055.hp2 HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.45+1378delG | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143003050 | |||||||
| chr3:143003051 | G | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(156): Show |
166 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(163): Show |
intron_variant | MODIFIER | c.45+1378G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143003051 | |||||||
| chr3:143003195 | T | G | 1 | a0001c0001t0004g0237 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.45+1522T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143003195 | |||||||
| chr3:143003226 | T | G | 4 | a0001c0001t0007g0112 a0001c0001t0007g0113 a0001c0001t0007g0114 others(1): Show |
4 | HG01099.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+1553T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143003226 | |||||||
| chr3:143003385 | T | G | 2 | a0001c0001t0004g0238 a0001c0001t0004g0239 |
2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.45+1712T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143003385 | |||||||
| chr3:143003434 | A | G | 1 | a0001c0001t0004g0262 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.45+1761A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143003434 | |||||||
| chr3:143003582 | A | G | 1 | a0001c0001t0010g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.45+1909A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143003582 | |||||||
| chr3:143003677 | C | CT | 24 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0003g0328 others(21): Show |
24 | HG00438.hp2 HG01109.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.45+2028dupT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143003677 | ||||||
| chr3:143003677 | C | CTT | 80 | a0001c0001t0001g0093 a0001c0001t0002g0002 a0001c0001t0002g0004 others(77): Show |
88 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.45+2027_45+2028dup others(2): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143003677 | ||||||
| chr3:143003677 | C | CTTT | 18 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 others(15): Show |
18 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.45+2026_45+2028dup others(3): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143003677 | ||||||
| chr3:143003677 | CT | C | 6 | a0001c0001t0003g0263 a0001c0001t0006g0264 a0001c0001t0015g0019 others(3): Show |
6 | HG00735.hp1 HG01891.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+2028delT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143003677 | ||||||
| chr3:143003677 | CTT | C | 6 | a0001c0001t0006g0348 a0001c0001t0006g0349 a0001c0001t0006g0350 others(3): Show |
6 | HG02080.hp2 HG02602.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+2027_45+2028del others(2): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143003677 | ||||||
| chr3:143003677 | CTTTTTTT | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(108): Show |
116 | HG00438.hp1 HG00609.hp2 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.45+2022_45+2028del others(7): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143003677 | ||||||
| chr3:143003677 | CTTTTTTT others(1): Show |
C | 46 | a0001c0001t0001g0016 a0001c0001t0001g0116 a0001c0001t0001g0117 others(43): Show |
48 | HG00558.hp2 HG00738.hp2 HG01175.hp1 others(45): Show |
intron_variant | MODIFIER | c.45+2021_45+2028del others(8): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143003677 | ||||||
| chr3:143003878 | G | A | 3 | a0001c0001t0015g0019 a0001c0001t0015g0020 a0001c0001t0026g0021 |
3 | HG01891.hp2 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.45+2205G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143003878 | |||||||
| chr3:143004069 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(264): Show |
282 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(279): Show |
intron_variant | MODIFIER | c.45+2396A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143004069 | |||||||
| chr3:143004087 | T | A | 99 | a0001c0001t0001g0093 a0001c0001t0002g0002 a0001c0001t0002g0004 others(96): Show |
107 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.45+2414T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143004087 | |||||||
| chr3:143004155 | G | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(159): Show |
169 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(166): Show |
intron_variant | MODIFIER | c.45+2482G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143004155 | |||||||
| chr3:143004161 | A | C | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.45+2488A>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143004161 | |||||||
| chr3:143004198 | A | T | 1 | a0001c0001t0006g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.45+2525A>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143004198 | |||||||
| chr3:143004353 | G | GT | 8 | a0001c0001t0003g0325 a0001c0001t0003g0326 a0001c0001t0003g0339 others(5): Show |
8 | HG01071.hp1 HG01109.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+2708dupT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004353 | ||||||
| chr3:143004353 | GT | G | 80 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0075 others(77): Show |
83 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.45+2708delT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004353 | ||||||
| chr3:143004353 | GTT | G | 81 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(78): Show |
87 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.45+2707_45+2708del others(2): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004353 | ||||||
| chr3:143004353 | GTTTTTTT others(2): Show |
G | 6 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(3): Show |
6 | HG00738.hp1 HG03710.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+2700_45+2708del others(9): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004353 | ||||||
| chr3:143004353 | GTTTTTTT others(3): Show |
G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(147): Show |
157 | HG00438.hp1 HG00609.hp2 HG00621.hp1 others(154): Show |
intron_variant | MODIFIER | c.45+2699_45+2708del others(10): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004353 | ||||||
| chr3:143004353 | GTTTTTTT others(4): Show |
G | 5 | a0001c0001t0001g0116 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
5 | HG00558.hp2 HG01069.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+2698_45+2708del others(11): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004353 | ||||||
| chr3:143004371 | TTTTTTTT others(4): Show |
T | 1 | a0001c0001t0002g0137 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.45+2699_45+2709del others(11): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143004371 | |||||||
| chr3:143004413 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.45+2740G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143004413 | |||||||
| chr3:143004438 | A | G | 1 | a0001c0001t0004g0237 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.45+2765A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143004438 | |||||||
| chr3:143004502 | T | G | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.45+2829T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143004502 | |||||||
| chr3:143004558 | C | CCAGGCTG others(8): Show |
158 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
165 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(162): Show |
intron_variant | MODIFIER | c.45+2886_45+2887ins others(15): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004558 | ||||||
| chr3:143004558 | C | CCAGGCTG others(8): Show |
4 | a0001c0001t0004g0354 a0001c0001t0004g0355 a0001c0001t0013g0255 others(1): Show |
4 | HG00738.hp2 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+2886_45+2887ins others(15): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004558 | ||||||
| chr3:143004573 | A | AC | 82 | a0001c0001t0001g0093 a0001c0001t0002g0002 a0001c0001t0002g0005 others(79): Show |
87 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.45+2912dupC | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004573 | ||||||
| chr3:143004573 | A | ACC | 58 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(55): Show |
61 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.45+2911_45+2912dup others(2): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004573 | ||||||
| chr3:143004573 | A | ACCC | 27 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(24): Show |
28 | HG00735.hp1 HG00738.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.45+2910_45+2912dup others(3): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004573 | ||||||
| chr3:143004573 | A | ACCCCCCC others(3): Show |
8 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(5): Show |
8 | HG02055.hp1 HG02451.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+2903_45+2912dup others(10): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004573 | ||||||
| chr3:143004573 | A | ACCCCCCC others(4): Show |
3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0229 |
3 | HG02132.hp1 HG03540.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.45+2902_45+2912dup others(11): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004573 | ||||||
| chr3:143004573 | A | ACCCCCCC others(5): Show |
10 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(7): Show |
10 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+2901_45+2912dup others(12): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004573 | ||||||
| chr3:143004573 | A | ACCCCCCC others(6): Show |
7 | a0001c0001t0001g0016 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
7 | HG01934.hp2 HG02165.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+2912_45+2913ins others(13): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004573 | ||||||
| chr3:143004573 | A | ACCCCCCC others(7): Show |
11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG00735.hp2 HG01169.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+2912_45+2913ins others(14): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004573 | ||||||
| chr3:143004573 | A | ACCCCCCC others(8): Show |
9 | a0001c0001t0001g0134 a0001c0001t0001g0162 a0001c0001t0001g0163 others(6): Show |
9 | HG01069.hp2 HG01099.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+2912_45+2913ins others(15): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004573 | ||||||
| chr3:143004573 | A | ACCCCCCC others(9): Show |
13 | a0001c0001t0001g0116 a0001c0001t0001g0133 a0001c0001t0001g0152 others(10): Show |
13 | HG00558.hp2 HG00642.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.45+2912_45+2913ins others(16): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004573 | ||||||
| chr3:143004573 | A | ACCCCCCC others(10): Show |
4 | a0001c0001t0001g0011 a0001c0001t0001g0150 a0001c0001t0001g0151 others(1): Show |
4 | HG01192.hp1 HG01346.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+2912_45+2913ins others(17): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004573 | ||||||
| chr3:143004573 | A | ACCCCCCC others(11): Show |
8 | a0001c0001t0001g0010 a0001c0001t0001g0145 a0001c0001t0001g0146 others(5): Show |
9 | HG00609.hp2 HG00738.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+2912_45+2913ins others(18): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004573 | ||||||
| chr3:143004573 | A | ACCCCCCC others(13): Show |
3 | a0001c0001t0001g0117 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG01358.hp2 HG03195.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.45+2912_45+2913ins others(20): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004573 | ||||||
| chr3:143004573 | A | ACCCCCCC others(14): Show |
3 | a0001c0001t0001g0140 a0001c0001t0001g0142 a0005c0007t0001g0141 |
3 | NA18957.hp2 NA18979.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.45+2912_45+2913ins others(21): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004573 | ||||||
| chr3:143004573 | A | ACCCCCCC others(15): Show |
1 | a0001c0001t0001g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.45+2912_45+2913ins others(22): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004573 | ||||||
| chr3:143004573 | A | ACCCCCCC others(16): Show |
1 | a0001c0001t0001g0138 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.45+2912_45+2913ins others(23): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143004573 | ||||||
| chr3:143004577 | C | A | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.45+2904C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143004577 | |||||||
| chr3:143004581 | C | A | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.45+2908C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143004581 | |||||||
| chr3:143004679 | G | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0190 |
2 | HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.45+3006G>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143004679 | |||||||
| chr3:143004700 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.45+3027A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143004700 | |||||||
| chr3:143004767 | T | G | 6 | a0001c0001t0003g0269 a0001c0001t0003g0283 a0001c0001t0003g0284 others(3): Show |
6 | HG00639.hp2 HG01496.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+3094T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143004767 | |||||||
| chr3:143004808 | A | G | 1 | a0001c0001t0003g0316 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.45+3135A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143004808 | |||||||
| chr3:143005128 | T | G | 1 | a0001c0001t0010g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.45+3455T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143005128 | |||||||
| chr3:143005141 | C | CT | 8 | a0001c0001t0001g0160 a0001c0001t0002g0107 a0001c0001t0003g0263 others(5): Show |
8 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+3483dupT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143005141 | ||||||
| chr3:143005153 | T | C | 2 | a0001c0001t0002g0053 a0001c0001t0011g0095 |
2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.45+3480T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143005153 | |||||||
| chr3:143005166 | C | T | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.45+3493C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143005166 | |||||||
| chr3:143005203 | C | CAG | 267 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(264): Show |
282 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(279): Show |
intron_variant | MODIFIER | c.45+3531_45+3532ins others(2): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143005203 | ||||||
| chr3:143005450 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.45+3777A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143005450 | |||||||
| chr3:143005770 | C | T | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.45+4097C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143005770 | |||||||
| chr3:143005777 | G | A | 1 | a0001c0001t0003g0270 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.45+4104G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143005777 | |||||||
| chr3:143005798 | C | A | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.45+4125C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143005798 | |||||||
| chr3:143005925 | A | G | 1 | a0001c0010t0001g0225 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.45+4252A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143005925 | |||||||
| chr3:143005945 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.45+4272A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143005945 | |||||||
| chr3:143006142 | C | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0227 |
2 | HG00738.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.45+4469C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143006142 | |||||||
| chr3:143006407 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.46-4408C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143006407 | |||||||
| chr3:143006458 | T | A | 2 | a0001c0001t0015g0019 a0001c0001t0015g0020 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.46-4357T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143006458 | |||||||
| chr3:143006605 | A | G | 6 | a0001c0001t0006g0348 a0001c0001t0006g0349 a0001c0001t0006g0350 others(3): Show |
6 | HG02080.hp2 HG02602.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-4210A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143006605 | |||||||
| chr3:143006635 | G | A | 15 | a0001c0001t0005g0009 a0001c0001t0005g0118 a0001c0001t0005g0119 others(12): Show |
16 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.46-4180G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143006635 | |||||||
| chr3:143006883 | G | T | 5 | a0001c0001t0014g0358 a0001c0001t0014g0359 a0001c0001t0015g0019 others(2): Show |
5 | HG01891.hp2 HG02257.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-3932G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143006883 | |||||||
| chr3:143006886 | A | C | 1 | a0001c0001t0003g0310 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.46-3929A>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143006886 | |||||||
| chr3:143006894 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.46-3921C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143006894 | |||||||
| chr3:143006919 | C | T | 1 | a0001c0001t0003g0338 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.46-3896C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143006919 | |||||||
| chr3:143007293 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(216): Show |
232 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.46-3522T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143007293 | |||||||
| chr3:143007314 | G | T | 1 | a0001c0001t0026g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-3501G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143007314 | |||||||
| chr3:143007438 | C | G | 105 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(102): Show |
107 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.46-3377C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143007438 | |||||||
| chr3:143007444 | A | AT | 170 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0093 others(167): Show |
181 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.46-3352dupT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143007444 | ||||||
| chr3:143007444 | A | ATT | 75 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(72): Show |
78 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.46-3353_46-3352dup others(2): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143007444 | ||||||
| chr3:143007444 | A | ATTT | 18 | a0001c0001t0001g0144 a0001c0001t0001g0223 a0001c0001t0001g0224 others(15): Show |
19 | HG01175.hp1 HG01243.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.46-3354_46-3352dup others(3): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143007444 | ||||||
| chr3:143007727 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(213): Show |
229 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.46-3088G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143007727 | |||||||
| chr3:143007727 | G | C | 1 | a0001c0001t0001g0160 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.46-3088G>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143007727 | |||||||
| chr3:143007732 | C | T | 2 | a0001c0001t0006g0352 a0001c0001t0006g0353 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.46-3083C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143007732 | |||||||
| chr3:143008262 | T | TG | 260 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(257): Show |
275 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(272): Show |
intron_variant | MODIFIER | c.46-2551dupG | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 143008262 | ||||||
| chr3:143008411 | G | A | 15 | a0001c0001t0002g0007 a0001c0001t0002g0028 a0001c0001t0002g0076 others(12): Show |
17 | HG00639.hp1 HG01070.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.46-2404G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143008411 | |||||||
| chr3:143008492 | G | A | 27 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(24): Show |
28 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.46-2323G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143008492 | |||||||
| chr3:143008588 | TG | T | 4 | a0001c0001t0001g0145 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | HG00642.hp1 HG01169.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-2226delG | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143008588 | |||||||
| chr3:143008840 | A | G | 1 | a0001c0001t0009g0345 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.46-1975A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143008840 | |||||||
| chr3:143008865 | A | G | 1 | a0001c0001t0005g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.46-1950A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143008865 | |||||||
| chr3:143008973 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.46-1842C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143008973 | |||||||
| chr3:143009034 | C | G | 1 | a0001c0001t0003g0328 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.46-1781C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143009034 | |||||||
| chr3:143009145 | G | T | 1 | a0001c0001t0001g0258 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.46-1670G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143009145 | |||||||
| chr3:143009177 | G | T | 1 | a0001c0001t0001g0169 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.46-1638G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143009177 | |||||||
| chr3:143009325 | C | T | 6 | a0001c0001t0008g0003 a0001c0001t0008g0022 a0001c0001t0008g0026 others(3): Show |
7 | HG01074.hp1 HG01169.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-1490C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143009325 | |||||||
| chr3:143009329 | C | T | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 |
3 | HG02055.hp2 HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.46-1486C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143009329 | |||||||
| chr3:143009382 | G | A | 1 | a0001c0001t0003g0287 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.46-1433G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143009382 | |||||||
| chr3:143009552 | C | T | 1 | a0001c0001t0002g0081 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.46-1263C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143009552 | |||||||
| chr3:143009762 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(216): Show |
232 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.46-1053T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143009762 | |||||||
| chr3:143009772 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(216): Show |
232 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.46-1043A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143009772 | |||||||
| chr3:143009848 | A | C | 1 | a0001c0001t0001g0168 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.46-967A>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143009848 | |||||||
| chr3:143009983 | T | C | 1 | a0001c0001t0003g0322 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.46-832T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143009983 | |||||||
| chr3:143009992 | C | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.46-823C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143009992 | |||||||
| chr3:143010044 | A | G | 1 | a0001c0001t0026g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-771A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143010044 | |||||||
| chr3:143010293 | C | T | 1 | a0001c0001t0026g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-522C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143010293 | |||||||
| chr3:143010376 | G | A | 15 | a0001c0001t0005g0009 a0001c0001t0005g0118 a0001c0001t0005g0119 others(12): Show |
16 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.46-439G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143010376 | |||||||
| chr3:143010431 | C | T | 15 | a0001c0001t0005g0009 a0001c0001t0005g0118 a0001c0001t0005g0119 others(12): Show |
16 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.46-384C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143010431 | |||||||
| chr3:143010456 | G | A | 1 | a0001c0001t0004g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.46-359G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143010456 | |||||||
| chr3:143010509 | A | G | 99 | a0001c0001t0001g0093 a0001c0001t0002g0002 a0001c0001t0002g0004 others(96): Show |
107 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.46-306A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143010509 | |||||||
| chr3:143010591 | T | C | 99 | a0001c0001t0001g0093 a0001c0001t0002g0002 a0001c0001t0002g0004 others(96): Show |
107 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.46-224T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143010591 | |||||||
| chr3:143010741 | T | C | 27 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(24): Show |
28 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.46-74T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143010741 | |||||||
| chr3:143010806 | T | C | 1 | a0001c0001t0006g0327 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.46-9T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 1/27 | chr3 | 143010806 | |||||||
| chr3:143010923 | C | T | 6 | a0001c0001t0002g0023 a0001c0001t0002g0051 a0001c0001t0002g0070 others(3): Show |
6 | HG00673.hp2 NA18951.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+64C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 2/27 | chr3 | 143010923 | |||||||
| chr3:143010955 | A | G | 1 | a0001c0001t0006g0350 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.90+96A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 2/27 | chr3 | 143010955 | |||||||
| chr3:143011131 | T | C | 1 | a0001c0001t0007g0161 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.90+272T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 2/27 | chr3 | 143011131 | |||||||
| chr3:143011186 | T | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0190 |
2 | HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.90+327T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 2/27 | chr3 | 143011186 | |||||||
| chr3:143011285 | T | G | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.90+426T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 2/27 | chr3 | 143011285 | |||||||
| chr3:143011296 | G | A | 24 | a0001c0001t0003g0271 a0001c0001t0003g0272 a0001c0001t0003g0273 others(21): Show |
25 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.90+437G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 2/27 | chr3 | 143011296 | |||||||
| chr3:143011338 | A | G | 1 | a0003c0009t0004g0245 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.90+479A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 2/27 | chr3 | 143011338 | |||||||
| chr3:143011368 | A | G | 1 | a0001c0001t0004g0248 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.90+509A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 2/27 | chr3 | 143011368 | |||||||
| chr3:143011543 | A | G | 1 | a0001c0001t0019g0135 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.91-679A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 2/27 | chr3 | 143011543 | |||||||
| chr3:143011932 | T | G | 262 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(259): Show |
277 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(274): Show |
intron_variant | MODIFIER | c.91-290T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 2/27 | chr3 | 143011932 | |||||||
| chr3:143012009 | A | G | 28 | a0001c0001t0003g0309 a0001c0001t0004g0013 a0001c0001t0004g0014 others(25): Show |
29 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.91-213A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 2/27 | chr3 | 143012009 | |||||||
| chr3:143012040 | GA | G | 6 | a0001c0001t0006g0235 a0001c0001t0014g0358 a0001c0001t0014g0359 others(3): Show |
6 | HG01891.hp2 HG02257.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-178delA | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 143012040 | ||||||
| chr3:143012133 | A | G | 1 | a0001c0001t0006g0351 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.91-89A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 2/27 | chr3 | 143012133 | |||||||
| chr3:143012146 | C | T | 2 | a0001c0001t0002g0071 a0001c0001t0002g0072 |
2 | NA18951.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.91-76C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 2/27 | chr3 | 143012146 | |||||||
| chr3:143012412 | C | A | 1 | a0001c0001t0006g0350 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.222+59C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 3/27 | chr3 | 143012412 | |||||||
| chr3:143012601 | A | T | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.222+248A>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 3/27 | chr3 | 143012601 | |||||||
| chr3:143012949 | G | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(165): Show |
175 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(172): Show |
intron_variant | MODIFIER | c.222+596G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 3/27 | chr3 | 143012949 | |||||||
| chr3:143012997 | C | T | 27 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(24): Show |
28 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.222+644C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 3/27 | chr3 | 143012997 | |||||||
| chr3:143013607 | GTAAC | G | 3 | a0001c0001t0006g0264 a0001c0001t0015g0019 a0001c0001t0015g0020 |
3 | HG01891.hp2 HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.223-702_223-699del others(4): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr3 | 143013607 | ||||||
| chr3:143013849 | T | C | 27 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(24): Show |
28 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.223-462T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 3/27 | chr3 | 143013849 | |||||||
| chr3:143013864 | G | T | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.223-447G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 3/27 | chr3 | 143013864 | |||||||
| chr3:143013926 | G | A | 1 | a0003c0009t0004g0245 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.223-385G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 3/27 | chr3 | 143013926 | |||||||
| chr3:143013972 | A | G | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.223-339A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 3/27 | chr3 | 143013972 | |||||||
| chr3:143014058 | CT | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(169): Show |
179 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(176): Show |
intron_variant | MODIFIER | c.223-243delT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr3 | 143014058 | ||||||
| chr3:143014179 | C | G | 2 | a0001c0001t0015g0019 a0001c0001t0015g0020 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.223-132C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 3/27 | chr3 | 143014179 | |||||||
| chr3:143014212 | C | T | 2 | a0001c0001t0005g0129 a0001c0001t0005g0130 |
2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.223-99C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 3/27 | chr3 | 143014212 | |||||||
| chr3:143014215 | C | T | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.223-96C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 3/27 | chr3 | 143014215 | |||||||
| chr3:143014675 | G | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(162): Show |
172 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(169): Show |
intron_variant | MODIFIER | c.321+266G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 4/27 | chr3 | 143014675 | |||||||
| chr3:143014762 | G | A | 10 | a0001c0001t0001g0144 a0001c0001t0001g0146 a0001c0001t0001g0147 others(7): Show |
10 | HG00609.hp2 HG01358.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.321+353G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 4/27 | chr3 | 143014762 | |||||||
| chr3:143014882 | T | C | 99 | a0001c0001t0001g0093 a0001c0001t0002g0002 a0001c0001t0002g0004 others(96): Show |
107 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.321+473T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 4/27 | chr3 | 143014882 | |||||||
| chr3:143015004 | C | G | 6 | a0001c0001t0005g0121 a0001c0001t0005g0126 a0001c0001t0005g0127 others(3): Show |
6 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.321+595C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 4/27 | chr3 | 143015004 | |||||||
| chr3:143015047 | G | A | 2 | a0001c0001t0003g0265 a0001c0001t0003g0266 |
2 | HG00673.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.321+638G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 4/27 | chr3 | 143015047 | |||||||
| chr3:143015133 | C | T | 1 | a0001c0001t0026g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.321+724C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 4/27 | chr3 | 143015133 | |||||||
| chr3:143015253 | C | G | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.321+844C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 4/27 | chr3 | 143015253 | |||||||
| chr3:143015435 | G | GT | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.322-816dupT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr3 | 143015435 | ||||||
| chr3:143015732 | G | C | 27 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(24): Show |
28 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.322-525G>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 4/27 | chr3 | 143015732 | |||||||
| chr3:143015759 | A | G | 1 | a0001c0001t0003g0263 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.322-498A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 4/27 | chr3 | 143015759 | |||||||
| chr3:143015769 | AATATCAA others(20): Show |
A | 1 | a0001c0001t0003g0344 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.322-463_322-437del others(27): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr3 | 143015769 | ||||||
| chr3:143015786 | G | C | 1 | a0001c0001t0026g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.322-471G>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 4/27 | chr3 | 143015786 | |||||||
| chr3:143015966 | A | G | 2 | a0001c0001t0005g0009 a0001c0001t0005g0125 |
3 | HG02258.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.322-291A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 4/27 | chr3 | 143015966 | |||||||
| chr3:143016625 | C | T | 2 | a0001c0001t0015g0019 a0001c0001t0015g0020 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.437-217C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 5/27 | chr3 | 143016625 | |||||||
| chr3:143017155 | C | T | 1 | a0001c0001t0014g0358 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.570+180C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143017155 | |||||||
| chr3:143017156 | G | A | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.570+181G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143017156 | |||||||
| chr3:143017211 | A | G | 14 | a0001c0001t0005g0009 a0001c0001t0005g0118 a0001c0001t0005g0119 others(11): Show |
15 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.570+236A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143017211 | |||||||
| chr3:143017380 | C | T | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.570+405C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143017380 | |||||||
| chr3:143017421 | A | T | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.570+446A>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143017421 | |||||||
| chr3:143017583 | A | C | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.570+608A>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143017583 | |||||||
| chr3:143017584 | C | A | 2 | a0001c0001t0003g0296 a0001c0001t0003g0297 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.570+609C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143017584 | |||||||
| chr3:143017878 | C | T | 1 | a0001c0001t0003g0286 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.570+903C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143017878 | |||||||
| chr3:143017885 | A | C | 1 | a0001c0002t0002g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.570+910A>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143017885 | |||||||
| chr3:143017935 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.570+960C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143017935 | |||||||
| chr3:143018112 | G | T | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.570+1137G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143018112 | |||||||
| chr3:143018230 | G | A | 1 | a0001c0001t0002g0031 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.570+1255G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143018230 | |||||||
| chr3:143018322 | A | G | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.570+1347A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143018322 | |||||||
| chr3:143018515 | G | A | 27 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(24): Show |
28 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.571-1454G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143018515 | |||||||
| chr3:143018849 | C | T | 1 | a0001c0001t0026g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.571-1120C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143018849 | |||||||
| chr3:143018891 | C | T | 2 | a0001c0001t0003g0296 a0001c0001t0003g0297 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.571-1078C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143018891 | |||||||
| chr3:143019161 | G | A | 1 | a0001c0001t0005g0123 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.571-808G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143019161 | |||||||
| chr3:143019364 | A | T | 1 | a0001c0001t0014g0359 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.571-605A>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143019364 | |||||||
| chr3:143019548 | T | A | 1 | a0001c0001t0002g0054 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.571-421T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143019548 | |||||||
| chr3:143019563 | G | A | 2 | a0001c0001t0003g0267 a0001c0001t0003g0335 |
2 | NA18939.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.571-406G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143019563 | |||||||
| chr3:143019689 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.571-280T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143019689 | |||||||
| chr3:143019786 | A | G | 1 | a0001c0001t0003g0306 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.571-183A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143019786 | |||||||
| chr3:143019890 | T | C | 3 | a0001c0001t0003g0276 a0001c0001t0003g0298 a0001c0001t0003g0308 |
3 | NA18947.hp1 NA18967.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.571-79T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 6/27 | chr3 | 143019890 | |||||||
| chr3:143020261 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(167): Show |
177 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(174): Show |
intron_variant | MODIFIER | c.638+225C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 7/27 | chr3 | 143020261 | |||||||
| chr3:143020515 | T | G | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.639-84T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 7/27 | chr3 | 143020515 | |||||||
| chr3:143020753 | T | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0191 a0001c0001t0001g0204 |
3 | HG01516.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.733+60T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 8/27 | chr3 | 143020753 | |||||||
| chr3:143020788 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.733+95A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 8/27 | chr3 | 143020788 | |||||||
| chr3:143020890 | A | C | 11 | a0001c0001t0003g0275 a0001c0001t0003g0293 a0001c0001t0003g0294 others(8): Show |
12 | HG02071.hp2 HG02165.hp2 NA18943.hp1 others(9): Show |
intron_variant | MODIFIER | c.733+197A>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 8/27 | chr3 | 143020890 | |||||||
| chr3:143020968 | G | C | 4 | a0001c0001t0007g0112 a0001c0001t0007g0113 a0001c0001t0007g0114 others(1): Show |
4 | HG01099.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+275G>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 8/27 | chr3 | 143020968 | |||||||
| chr3:143020981 | C | G | 4 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0222 others(1): Show |
4 | HG00438.hp1 HG00621.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+288C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 8/27 | chr3 | 143020981 | |||||||
| chr3:143021170 | G | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(158): Show |
168 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(165): Show |
intron_variant | MODIFIER | c.734-180G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 8/27 | chr3 | 143021170 | |||||||
| chr3:143021219 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(153): Show |
163 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(160): Show |
intron_variant | MODIFIER | c.734-131G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 8/27 | chr3 | 143021219 | |||||||
| chr3:143021306 | T | A | 1 | a0001c0001t0006g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.734-44T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 8/27 | chr3 | 143021306 | |||||||
| chr3:143021324 | AATTGTCT others(3): Show |
A | 1 | a0001c0001t0001g0142 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.734-25_734-16delAT others(8): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 8/27 | chr3 | 143021324 | |||||||
| chr3:143021335 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.734-15T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 8/27 | chr3 | 143021335 | |||||||
| chr3:143021788 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.852+233A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 10/27 | chr3 | 143021788 | |||||||
| chr3:143022021 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.852+466A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 10/27 | chr3 | 143022021 | |||||||
| chr3:143022172 | C | G | 1 | a0001c0001t0002g0068 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.853-325C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 10/27 | chr3 | 143022172 | |||||||
| chr3:143022234 | A | T | 3 | a0001c0001t0007g0112 a0001c0001t0007g0113 a0001c0001t0007g0114 |
3 | HG01099.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.853-263A>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 10/27 | chr3 | 143022234 | |||||||
| chr3:143022277 | C | T | 15 | a0001c0001t0005g0009 a0001c0001t0005g0118 a0001c0001t0005g0119 others(12): Show |
16 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.853-220C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 10/27 | chr3 | 143022277 | |||||||
| chr3:143022344 | G | A | 1 | a0001c0001t0003g0270 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.853-153G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 10/27 | chr3 | 143022344 | |||||||
| chr3:143022361 | G | A | 1 | a0001c0001t0007g0115 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.853-136G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 10/27 | chr3 | 143022361 | |||||||
| chr3:143022481 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.853-16T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 10/27 | chr3 | 143022481 | |||||||
| chr3:143022686 | T | C | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1018+24T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 11/27 | chr3 | 143022686 | |||||||
| chr3:143023358 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1230+294C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 12/27 | chr3 | 143023358 | |||||||
| chr3:143023390 | G | A | 1 | a0001c0001t0003g0271 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1230+326G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 12/27 | chr3 | 143023390 | |||||||
| chr3:143023424 | T | C | 1 | a0001c0001t0005g0123 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1230+360T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 12/27 | chr3 | 143023424 | |||||||
| chr3:143023443 | A | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(274): Show |
292 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(289): Show |
intron_variant | MODIFIER | c.1230+379A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 12/27 | chr3 | 143023443 | |||||||
| chr3:143023570 | C | T | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1231-405C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 12/27 | chr3 | 143023570 | |||||||
| chr3:143023642 | G | A | 1 | a0001c0001t0008g0022 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1231-333G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 12/27 | chr3 | 143023642 | |||||||
| chr3:143023725 | AGTGCATT others(3): Show |
A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0218 |
3 | HG01952.hp2 NA18984.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1231-242_1231-233d others(12): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr3 | 143023725 | ||||||
| chr3:143024189 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0172 a0001c0001t0001g0173 others(5): Show |
11 | HG01516.hp2 HG02451.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1274+171A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143024189 | |||||||
| chr3:143024212 | G | C | 2 | a0001c0001t0015g0019 a0001c0001t0015g0020 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1274+194G>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143024212 | |||||||
| chr3:143024282 | T | C | 1 | a0001c0001t0002g0028 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1274+264T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143024282 | |||||||
| chr3:143024310 | G | A | 1 | a0001c0001t0026g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1274+292G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143024310 | |||||||
| chr3:143024335 | G | A | 2 | a0001c0001t0004g0246 a0001c0001t0004g0249 |
2 | HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1274+317G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143024335 | |||||||
| chr3:143024365 | C | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
7 | HG02451.hp1 HG02559.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1274+347C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143024365 | |||||||
| chr3:143024534 | T | A | 7 | a0001c0001t0001g0174 a0001c0001t0001g0181 a0001c0001t0001g0182 others(4): Show |
7 | HG02809.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1274+516T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143024534 | |||||||
| chr3:143024923 | A | G | 1 | a0001c0001t0003g0304 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1274+905A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143024923 | |||||||
| chr3:143025047 | G | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.1274+1029G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143025047 | |||||||
| chr3:143025137 | A | T | 1 | a0001c0001t0001g0183 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1274+1119A>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143025137 | |||||||
| chr3:143025141 | A | G | 1 | a0001c0001t0008g0030 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1274+1123A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143025141 | |||||||
| chr3:143025577 | T | C | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1274+1559T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143025577 | |||||||
| chr3:143025725 | T | C | 7 | a0001c0001t0006g0264 a0001c0001t0006g0348 a0001c0001t0006g0349 others(4): Show |
7 | HG02080.hp2 HG02602.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.1275-1424T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143025725 | |||||||
| chr3:143025935 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(216): Show |
232 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.1275-1214G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143025935 | |||||||
| chr3:143025944 | G | A | 5 | a0001c0001t0014g0358 a0001c0001t0014g0359 a0001c0001t0015g0019 others(2): Show |
5 | HG01891.hp2 HG02257.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1275-1205G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143025944 | |||||||
| chr3:143026026 | G | A | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1275-1123G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143026026 | |||||||
| chr3:143026042 | G | A | 1 | a0001c0001t0014g0358 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1275-1107G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143026042 | |||||||
| chr3:143026341 | C | T | 1 | a0001c0001t0002g0050 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1275-808C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143026341 | |||||||
| chr3:143026438 | T | A | 1 | a0001c0001t0001g0016 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1275-711T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143026438 | |||||||
| chr3:143026451 | A | G | 262 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(259): Show |
277 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(274): Show |
intron_variant | MODIFIER | c.1275-698A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143026451 | |||||||
| chr3:143026740 | A | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(259): Show |
277 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(274): Show |
intron_variant | MODIFIER | c.1275-409A>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143026740 | |||||||
| chr3:143026778 | C | T | 1 | a0001c0001t0006g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1275-371C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143026778 | |||||||
| chr3:143026874 | T | C | 1 | a0001c0001t0005g0126 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1275-275T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143026874 | |||||||
| chr3:143027004 | T | C | 4 | a0001c0001t0003g0277 a0001c0001t0003g0299 a0001c0001t0003g0305 others(1): Show |
4 | NA18989.hp2 NA18990.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1275-145T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143027004 | |||||||
| chr3:143027005 | G | A | 1 | a0001c0001t0014g0359 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1275-144G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 13/27 | chr3 | 143027005 | |||||||
| chr3:143027383 | C | T | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1379+130C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 14/27 | chr3 | 143027383 | |||||||
| chr3:143027418 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(244): Show |
261 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(258): Show |
intron_variant | MODIFIER | c.1379+165T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 14/27 | chr3 | 143027418 | |||||||
| chr3:143027462 | C | T | 5 | a0001c0001t0015g0019 a0001c0001t0015g0020 a0001c0001t0026g0021 others(2): Show |
5 | HG00735.hp1 HG01891.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1379+209C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 14/27 | chr3 | 143027462 | |||||||
| chr3:143027503 | T | A | 1 | a0001c0001t0003g0278 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1379+250T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 14/27 | chr3 | 143027503 | |||||||
| chr3:143027613 | C | T | 1 | a0001c0001t0006g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1379+360C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 14/27 | chr3 | 143027613 | |||||||
| chr3:143027677 | G | T | 4 | a0001c0001t0002g0049 a0001c0001t0002g0075 a0001c0001t0002g0080 others(1): Show |
4 | NA18952.hp1 NA18959.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.1379+424G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 14/27 | chr3 | 143027677 | |||||||
| chr3:143027745 | G | A | 4 | a0001c0001t0007g0112 a0001c0001t0007g0113 a0001c0001t0007g0114 others(1): Show |
4 | HG01099.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1379+492G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 14/27 | chr3 | 143027745 | |||||||
| chr3:143027765 | C | T | 1 | a0001c0001t0006g0351 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1379+512C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 14/27 | chr3 | 143027765 | |||||||
| chr3:143027814 | A | G | 15 | a0001c0001t0005g0009 a0001c0001t0005g0118 a0001c0001t0005g0119 others(12): Show |
16 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1380-526A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 14/27 | chr3 | 143027814 | |||||||
| chr3:143028034 | C | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(267): Show |
285 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(282): Show |
intron_variant | MODIFIER | c.1380-306C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 14/27 | chr3 | 143028034 | |||||||
| chr3:143028136 | G | A | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1380-204G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 14/27 | chr3 | 143028136 | |||||||
| chr3:143028146 | A | G | 262 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(259): Show |
277 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(274): Show |
intron_variant | MODIFIER | c.1380-194A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 14/27 | chr3 | 143028146 | |||||||
| chr3:143028197 | T | C | 1 | a0001c0001t0004g0262 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1380-143T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 14/27 | chr3 | 143028197 | |||||||
| chr3:143028261 | T | A | 1 | a0001c0001t0003g0272 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1380-79T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 14/27 | chr3 | 143028261 | |||||||
| chr3:143028655 | T | C | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1610+9T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143028655 | |||||||
| chr3:143028694 | T | C | 1 | a0001c0001t0014g0359 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1610+48T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143028694 | |||||||
| chr3:143028894 | T | G | 4 | a0001c0001t0007g0112 a0001c0001t0007g0113 a0001c0001t0007g0114 others(1): Show |
4 | HG01099.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1610+248T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143028894 | |||||||
| chr3:143029020 | A | G | 11 | a0001c0001t0002g0096 a0001c0001t0002g0100 a0001c0001t0002g0101 others(8): Show |
12 | HG00639.hp1 HG01070.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1610+374A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143029020 | |||||||
| chr3:143029095 | G | C | 3 | a0001c0001t0008g0003 a0001c0001t0008g0022 a0001c0001t0008g0026 |
4 | HG01169.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1610+449G>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143029095 | |||||||
| chr3:143029181 | A | C | 74 | a0001c0001t0001g0093 a0001c0001t0002g0002 a0001c0001t0002g0004 others(71): Show |
80 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1610+535A>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143029181 | |||||||
| chr3:143029193 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0191 |
2 | HG01516.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1610+547A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143029193 | |||||||
| chr3:143029307 | A | G | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1610+661A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143029307 | |||||||
| chr3:143029379 | A | G | 1 | a0001c0008t0007g0232 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1610+733A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143029379 | |||||||
| chr3:143029483 | C | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(259): Show |
277 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(274): Show |
intron_variant | MODIFIER | c.1610+837C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143029483 | |||||||
| chr3:143029492 | T | G | 2 | a0001c0001t0003g0288 a0001c0001t0003g0289 |
2 | NA18959.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1610+846T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143029492 | |||||||
| chr3:143029634 | G | T | 1 | a0001c0001t0002g0048 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1610+988G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143029634 | |||||||
| chr3:143029672 | G | A | 262 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(259): Show |
277 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(274): Show |
intron_variant | MODIFIER | c.1610+1026G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143029672 | |||||||
| chr3:143029750 | T | C | 3 | a0001c0001t0002g0035 a0001c0001t0020g0109 a0001c0001t0021g0034 |
3 | HG02083.hp1 NA18943.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1610+1104T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143029750 | |||||||
| chr3:143029876 | C | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(266): Show |
284 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(281): Show |
intron_variant | MODIFIER | c.1610+1230C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143029876 | |||||||
| chr3:143030017 | T | C | 1 | a0001c0001t0003g0312 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1610+1371T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143030017 | |||||||
| chr3:143030201 | G | A | 120 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(117): Show |
123 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.1610+1555G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143030201 | |||||||
| chr3:143030269 | T | A | 27 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(24): Show |
28 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.1610+1623T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143030269 | |||||||
| chr3:143030504 | T | C | 3 | a0001c0001t0015g0019 a0001c0001t0015g0020 a0001c0001t0026g0021 |
3 | HG01891.hp2 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1610+1858T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143030504 | |||||||
| chr3:143030553 | G | T | 6 | a0001c0001t0002g0023 a0001c0001t0002g0051 a0001c0001t0002g0070 others(3): Show |
6 | HG00673.hp2 NA18951.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1610+1907G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143030553 | |||||||
| chr3:143030591 | T | C | 1 | a0001c0001t0003g0336 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1610+1945T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143030591 | |||||||
| chr3:143030594 | C | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.1610+1948C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143030594 | |||||||
| chr3:143030658 | A | G | 1 | a0001c0001t0005g0009 | 2 | HG02258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1610+2012A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143030658 | |||||||
| chr3:143030717 | C | T | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1611-2067C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143030717 | |||||||
| chr3:143030873 | C | G | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1611-1911C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143030873 | |||||||
| chr3:143030915 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1611-1869G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143030915 | |||||||
| chr3:143030977 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(261): Show |
279 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(276): Show |
intron_variant | MODIFIER | c.1611-1807A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143030977 | |||||||
| chr3:143030993 | G | T | 8 | a0001c0002t0002g0025 a0001c0002t0002g0055 a0001c0002t0002g0056 others(5): Show |
8 | HG02615.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1611-1791G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143030993 | |||||||
| chr3:143031061 | G | A | 12 | a0001c0001t0005g0009 a0001c0001t0005g0120 a0001c0001t0005g0121 others(9): Show |
13 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1611-1723G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143031061 | |||||||
| chr3:143031237 | T | C | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1611-1547T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143031237 | |||||||
| chr3:143031246 | A | G | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1611-1538A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143031246 | |||||||
| chr3:143031367 | G | A | 15 | a0001c0001t0005g0009 a0001c0001t0005g0118 a0001c0001t0005g0119 others(12): Show |
16 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1611-1417G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143031367 | |||||||
| chr3:143031405 | C | CAACCTTC others(15): Show |
9 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0124 others(6): Show |
9 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1611-1362_1611-136 others(26): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr3 | 143031405 | ||||||
| chr3:143031405 | C | CAACCTTC others(37): Show |
21 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(18): Show |
22 | HG02080.hp1 HG02486.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.1611-1362_1611-136 others(48): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr3 | 143031405 | ||||||
| chr3:143031405 | C | CAACCTTC others(81): Show |
1 | a0001c0001t0004g0239 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1611-1362_1611-136 others(92): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr3 | 143031405 | ||||||
| chr3:143031405 | C | CAACCTTC others(15): Show |
2 | a0001c0001t0002g0065 a0001c0001t0002g0068 |
2 | HG02155.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1611-1361_1611-134 others(26): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr3 | 143031405 | ||||||
| chr3:143031405 | C | CAACCTTC others(59): Show |
1 | a0001c0001t0001g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1611-1378_1611-131 others(70): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr3 | 143031405 | ||||||
| chr3:143031405 | C | CAACCTTC others(81): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0206 a0001c0001t0001g0207 |
6 | HG02451.hp1 HG02559.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1611-1313_1611-131 others(92): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr3 | 143031405 | ||||||
| chr3:143031405 | C | CAACCTTC others(59): Show |
6 | a0001c0001t0001g0136 a0001c0001t0006g0348 a0001c0001t0006g0349 others(3): Show |
6 | HG02602.hp1 HG02698.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1611-1318_1611-131 others(70): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr3 | 143031405 | ||||||
| chr3:143031405 | CAACCTTC others(37): Show |
C | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1611-1361_1611-131 others(48): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr3 | 143031405 | ||||||
| chr3:143031422 | C | T | 1 | a0001c0001t0002g0106 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1611-1362C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143031422 | |||||||
| chr3:143031423 | G | A | 44 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(41): Show |
46 | HG00738.hp2 HG01175.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.1611-1361G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143031423 | |||||||
| chr3:143031423 | G | GCCCTAAC others(15): Show |
125 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(122): Show |
129 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(126): Show |
intron_variant | MODIFIER | c.1611-1334_1611-131 others(26): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr3 | 143031423 | ||||||
| chr3:143031423 | G | GCCCTAAC others(37): Show |
5 | a0001c0001t0001g0153 a0001c0001t0001g0162 a0001c0001t0001g0165 others(2): Show |
5 | HG00735.hp2 HG01106.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1611-1356_1611-131 others(48): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr3 | 143031423 | ||||||
| chr3:143031423 | G | GCCCTAAC others(59): Show |
7 | a0001c0001t0001g0117 a0001c0001t0001g0133 a0001c0001t0001g0138 others(4): Show |
7 | HG02056.hp1 HG02074.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1611-1313_1611-131 others(70): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr3 | 143031423 | ||||||
| chr3:143031423 | G | GCCCTAAC others(169): Show |
5 | a0001c0001t0002g0096 a0001c0001t0002g0100 a0001c0001t0002g0101 others(2): Show |
5 | HG00639.hp1 HG01070.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.1611-1313_1611-131 others(180): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr3 | 143031423 | ||||||
| chr3:143031423 | GCCCTAAC others(15): Show |
G | 10 | a0001c0001t0003g0281 a0001c0001t0003g0282 a0001c0001t0003g0296 others(7): Show |
10 | HG01099.hp1 HG01192.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1611-1334_1611-131 others(26): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr3 | 143031423 | ||||||
| chr3:143031523 | A | G | 15 | a0001c0001t0002g0007 a0001c0001t0002g0028 a0001c0001t0002g0076 others(12): Show |
17 | HG00639.hp1 HG01070.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1611-1261A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143031523 | |||||||
| chr3:143031643 | T | C | 1 | a0001c0001t0002g0100 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1611-1141T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143031643 | |||||||
| chr3:143031670 | G | C | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1611-1114G>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143031670 | |||||||
| chr3:143031797 | G | A | 2 | a0001c0001t0015g0019 a0001c0001t0015g0020 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1611-987G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143031797 | |||||||
| chr3:143031922 | G | A | 3 | a0001c0001t0015g0019 a0001c0001t0015g0020 a0001c0001t0026g0021 |
3 | HG01891.hp2 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1611-862G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143031922 | |||||||
| chr3:143031928 | A | C | 1 | a0001c0001t0002g0064 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1611-856A>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143031928 | |||||||
| chr3:143032066 | G | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(264): Show |
282 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(279): Show |
intron_variant | MODIFIER | c.1611-718G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143032066 | |||||||
| chr3:143032074 | T | G | 3 | a0001c0001t0003g0273 a0001c0001t0003g0290 a0001c0001t0003g0333 |
3 | NA18972.hp2 NA18986.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1611-710T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143032074 | |||||||
| chr3:143032197 | C | T | 1 | a0001c0001t0003g0312 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1611-587C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143032197 | |||||||
| chr3:143032198 | G | A | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1611-586G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143032198 | |||||||
| chr3:143032285 | A | G | 1 | a0001c0001t0002g0063 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1611-499A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143032285 | |||||||
| chr3:143032292 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.1611-492T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143032292 | |||||||
| chr3:143032314 | G | A | 1 | a0001c0001t0003g0328 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1611-470G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143032314 | |||||||
| chr3:143032414 | G | A | 1 | a0001c0001t0024g0122 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1611-370G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143032414 | |||||||
| chr3:143032464 | A | G | 1 | a0001c0001t0005g0123 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1611-320A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143032464 | |||||||
| chr3:143032478 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1611-306G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143032478 | |||||||
| chr3:143032530 | G | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(266): Show |
284 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(281): Show |
intron_variant | MODIFIER | c.1611-254G>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143032530 | |||||||
| chr3:143032624 | A | G | 15 | a0001c0001t0005g0009 a0001c0001t0005g0118 a0001c0001t0005g0119 others(12): Show |
16 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1611-160A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143032624 | |||||||
| chr3:143032677 | A | G | 3 | a0001c0001t0002g0064 a0001c0001t0002g0098 a0001c0001t0002g0107 |
3 | HG01074.hp2 HG01243.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.1611-107A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 16/27 | chr3 | 143032677 | |||||||
| chr3:143033139 | T | G | 7 | a0001c0001t0006g0264 a0001c0001t0006g0348 a0001c0001t0006g0349 others(4): Show |
7 | HG02080.hp2 HG02602.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.1774-132T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 17/27 | chr3 | 143033139 | |||||||
| chr3:143033451 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(261): Show |
279 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(276): Show |
intron_variant | MODIFIER | c.1853+101G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 18/27 | chr3 | 143033451 | |||||||
| chr3:143033454 | C | G | 1 | a0001c0001t0001g0224 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1853+104C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 18/27 | chr3 | 143033454 | |||||||
| chr3:143033667 | G | T | 2 | a0001c0001t0003g0265 a0001c0001t0003g0266 |
2 | HG00673.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.1853+317G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 18/27 | chr3 | 143033667 | |||||||
| chr3:143033738 | A | G | 2 | a0001c0001t0003g0275 a0001c0001t0003g0295 |
2 | NA18985.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1853+388A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 18/27 | chr3 | 143033738 | |||||||
| chr3:143033819 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1853+469A>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 18/27 | chr3 | 143033819 | |||||||
| chr3:143034016 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1853+666A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 18/27 | chr3 | 143034016 | |||||||
| chr3:143034209 | C | T | 11 | a0001c0001t0001g0171 a0001c0001t0001g0174 a0001c0001t0001g0181 others(8): Show |
11 | HG02451.hp2 HG02630.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1854-679C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 18/27 | chr3 | 143034209 | |||||||
| chr3:143034250 | AAAGATTA others(3): Show |
A | 1 | a0001c0001t0003g0336 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1854-637_1854-628d others(12): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 18/27 | chr3 | 143034250 | |||||||
| chr3:143034262 | G | A | 1 | a0001c0001t0003g0336 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1854-626G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 18/27 | chr3 | 143034262 | |||||||
| chr3:143034297 | G | A | 4 | a0001c0001t0002g0035 a0001c0001t0002g0057 a0001c0001t0020g0109 others(1): Show |
4 | HG00140.hp1 HG02083.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1854-591G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 18/27 | chr3 | 143034297 | |||||||
| chr3:143034336 | G | A | 3 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0010g0214 |
3 | HG00621.hp1 NA18948.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1854-552G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 18/27 | chr3 | 143034336 | |||||||
| chr3:143034359 | G | A | 1 | a0001c0001t0002g0005 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1854-529G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 18/27 | chr3 | 143034359 | |||||||
| chr3:143034390 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1854-498A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 18/27 | chr3 | 143034390 | |||||||
| chr3:143034402 | CA | C | 58 | a0001c0001t0003g0270 a0001c0001t0003g0323 a0001c0001t0004g0013 others(55): Show |
60 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.1854-474delA | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr3 | 143034402 | ||||||
| chr3:143034551 | GT | G | 7 | a0001c0001t0006g0264 a0001c0001t0006g0348 a0001c0001t0006g0349 others(4): Show |
7 | HG02080.hp2 HG02602.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.1854-330delT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr3 | 143034551 | ||||||
| chr3:143034553 | T | A | 7 | a0001c0001t0006g0264 a0001c0001t0006g0348 a0001c0001t0006g0349 others(4): Show |
7 | HG02080.hp2 HG02602.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.1854-335T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 18/27 | chr3 | 143034553 | |||||||
| chr3:143035004 | C | G | 1 | a0001c0001t0003g0334 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1941+29C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 19/27 | chr3 | 143035004 | |||||||
| chr3:143035193 | G | A | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1941+218G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 19/27 | chr3 | 143035193 | |||||||
| chr3:143035340 | C | T | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1941+365C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 19/27 | chr3 | 143035340 | |||||||
| chr3:143035384 | T | G | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0233 |
3 | NA18978.hp2 NA18987.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1941+409T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 19/27 | chr3 | 143035384 | |||||||
| chr3:143035394 | A | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(216): Show |
232 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.1941+419A>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 19/27 | chr3 | 143035394 | |||||||
| chr3:143035454 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.1941+479C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 19/27 | chr3 | 143035454 | |||||||
| chr3:143035699 | G | A | 1 | a0001c0001t0010g0210 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1942-283G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 19/27 | chr3 | 143035699 | |||||||
| chr3:143035714 | A | G | 1 | a0001c0001t0026g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1942-268A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 19/27 | chr3 | 143035714 | |||||||
| chr3:143035824 | A | T | 3 | a0001c0001t0002g0096 a0001c0001t0002g0100 a0001c0001t0003g0278 |
3 | HG00639.hp1 HG04204.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1942-158A>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 19/27 | chr3 | 143035824 | |||||||
| chr3:143035872 | AC | A | 5 | a0001c0001t0005g0121 a0001c0001t0005g0126 a0001c0001t0005g0127 others(2): Show |
5 | HG01891.hp1 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1942-109delC | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 19/27 | chr3 | 143035872 | |||||||
| chr3:143035938 | A | G | 1 | a0001c0001t0004g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1942-44A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 19/27 | chr3 | 143035938 | |||||||
| chr3:143036143 | G | A | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2064+39G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 20/27 | chr3 | 143036143 | |||||||
| chr3:143036375 | TAAGC | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(216): Show |
232 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.2064+275_2064+278d others(6): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 143036375 | ||||||
| chr3:143036664 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2065-515C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 20/27 | chr3 | 143036664 | |||||||
| chr3:143036673 | T | C | 1 | a0001c0001t0003g0275 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2065-506T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 20/27 | chr3 | 143036673 | |||||||
| chr3:143036713 | C | T | 24 | a0001c0001t0003g0271 a0001c0001t0003g0272 a0001c0001t0003g0273 others(21): Show |
25 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.2065-466C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 20/27 | chr3 | 143036713 | |||||||
| chr3:143036803 | T | TA | 15 | a0001c0001t0005g0009 a0001c0001t0005g0118 a0001c0001t0005g0119 others(12): Show |
16 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2065-375dupA | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 143036803 | ||||||
| chr3:143036808 | C | T | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2065-371C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 20/27 | chr3 | 143036808 | |||||||
| chr3:143036899 | G | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(260): Show |
278 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(275): Show |
intron_variant | MODIFIER | c.2065-280G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 20/27 | chr3 | 143036899 | |||||||
| chr3:143037088 | T | C | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2065-91T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 20/27 | chr3 | 143037088 | |||||||
| chr3:143037152 | A | G | 1 | a0001c0001t0003g0329 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2065-27A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 20/27 | chr3 | 143037152 | |||||||
| chr3:143037157 | A | G | 14 | a0001c0001t0003g0267 a0001c0001t0003g0269 a0001c0001t0003g0280 others(11): Show |
14 | HG00639.hp2 HG01496.hp1 HG02293.hp2 others(11): Show |
intron_variant | MODIFIER | c.2065-22A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 20/27 | chr3 | 143037157 | |||||||
| chr3:143037161 | T | G | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2065-18T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 20/27 | chr3 | 143037161 | |||||||
| chr3:143038060 | G | A | 4 | a0001c0001t0001g0136 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
4 | HG01109.hp2 HG01433.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2222-48G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 21/27 | chr3 | 143038060 | |||||||
| chr3:143038065 | A | G | 15 | a0001c0001t0002g0007 a0001c0001t0002g0028 a0001c0001t0002g0076 others(12): Show |
17 | HG00639.hp1 HG01070.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.2222-43A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 21/27 | chr3 | 143038065 | |||||||
| chr3:143038343 | T | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0228 |
2 | HG01884.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2317+140T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 22/27 | chr3 | 143038343 | |||||||
| chr3:143038376 | C | A | 3 | a0001c0001t0015g0019 a0001c0001t0015g0020 a0001c0001t0026g0021 |
3 | HG01891.hp2 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2317+173C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 22/27 | chr3 | 143038376 | |||||||
| chr3:143038510 | T | C | 2 | a0001c0001t0015g0019 a0001c0001t0015g0020 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2317+307T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 22/27 | chr3 | 143038510 | |||||||
| chr3:143038688 | C | T | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2318-206C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 22/27 | chr3 | 143038688 | |||||||
| chr3:143038998 | A | C | 1 | a0001c0001t0014g0358 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2384+38A>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143038998 | |||||||
| chr3:143039095 | C | T | 5 | a0001c0001t0001g0136 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
5 | HG01109.hp2 HG01433.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.2384+135C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143039095 | |||||||
| chr3:143039250 | C | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(266): Show |
284 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(281): Show |
intron_variant | MODIFIER | c.2384+290C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143039250 | |||||||
| chr3:143039412 | T | C | 1 | a0001c0001t0003g0265 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2384+452T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143039412 | |||||||
| chr3:143039563 | C | A | 1 | a0001c0001t0002g0083 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2384+603C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143039563 | |||||||
| chr3:143039574 | T | C | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2384+614T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143039574 | |||||||
| chr3:143039599 | A | AT | 11 | a0001c0001t0003g0274 a0001c0001t0003g0314 a0001c0001t0003g0324 others(8): Show |
11 | HG00642.hp2 HG02080.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.2384+660dupT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr3 | 143039599 | ||||||
| chr3:143039599 | AT | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(199): Show |
214 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.2384+660delT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr3 | 143039599 | ||||||
| chr3:143039599 | ATT | A | 61 | a0001c0001t0001g0145 a0001c0001t0001g0152 a0001c0001t0001g0153 others(58): Show |
64 | HG00558.hp1 HG00642.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.2384+659_2384+660d others(4): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr3 | 143039599 | ||||||
| chr3:143039718 | G | T | 6 | a0001c0001t0006g0348 a0001c0001t0006g0349 a0001c0001t0006g0350 others(3): Show |
6 | HG02080.hp2 HG02602.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.2384+758G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143039718 | |||||||
| chr3:143040222 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2384+1262A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143040222 | |||||||
| chr3:143040286 | A | G | 3 | a0001c0001t0003g0267 a0001c0001t0003g0301 a0001c0001t0003g0335 |
3 | NA18939.hp2 NA18983.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.2384+1326A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143040286 | |||||||
| chr3:143040330 | T | G | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2384+1370T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143040330 | |||||||
| chr3:143040386 | A | G | 1 | a0001c0001t0004g0248 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2384+1426A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143040386 | |||||||
| chr3:143040449 | A | G | 1 | a0001c0001t0006g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2384+1489A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143040449 | |||||||
| chr3:143040564 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.2384+1604A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143040564 | |||||||
| chr3:143040642 | A | C | 1 | a0001c0001t0002g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2384+1682A>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143040642 | |||||||
| chr3:143040746 | T | C | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2384+1786T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143040746 | |||||||
| chr3:143040756 | T | C | 27 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(24): Show |
28 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.2384+1796T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143040756 | |||||||
| chr3:143040937 | C | T | 27 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(24): Show |
28 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.2384+1977C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143040937 | |||||||
| chr3:143041065 | C | CA | 15 | a0001c0001t0005g0009 a0001c0001t0005g0118 a0001c0001t0005g0119 others(12): Show |
16 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2385-2043dupA | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr3 | 143041065 | ||||||
| chr3:143041238 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2385-1879A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143041238 | |||||||
| chr3:143041281 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2385-1836A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143041281 | |||||||
| chr3:143041292 | T | A | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2385-1825T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143041292 | |||||||
| chr3:143041322 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2385-1795C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143041322 | |||||||
| chr3:143041540 | T | A | 6 | a0001c0001t0006g0348 a0001c0001t0006g0349 a0001c0001t0006g0350 others(3): Show |
6 | HG02080.hp2 HG02602.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.2385-1577T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143041540 | |||||||
| chr3:143041848 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.2385-1269T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143041848 | |||||||
| chr3:143041969 | T | TAC | 18 | a0001c0001t0001g0133 a0001c0001t0001g0180 a0001c0001t0001g0228 others(15): Show |
18 | HG01978.hp2 HG02056.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2385-1126_2385-112 others(6): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr3 | 143041969 | ||||||
| chr3:143041969 | TAC | T | 47 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(44): Show |
49 | HG00738.hp2 HG01175.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.2385-1126_2385-112 others(6): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr3 | 143041969 | ||||||
| chr3:143042002 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2385-1115C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143042002 | |||||||
| chr3:143042003 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.2385-1114A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143042003 | |||||||
| chr3:143042174 | C | G | 1 | a0001c0001t0003g0307 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2385-943C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143042174 | |||||||
| chr3:143042472 | T | G | 3 | a0001c0001t0003g0276 a0001c0001t0003g0298 a0001c0001t0003g0308 |
3 | NA18947.hp1 NA18967.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.2385-645T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143042472 | |||||||
| chr3:143042503 | G | A | 1 | a0001c0001t0003g0271 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2385-614G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143042503 | |||||||
| chr3:143042511 | T | C | 1 | a0001c0001t0003g0328 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2385-606T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143042511 | |||||||
| chr3:143042586 | T | A | 1 | a0001c0001t0003g0310 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2385-531T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143042586 | |||||||
| chr3:143042601 | C | A | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2385-516C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143042601 | |||||||
| chr3:143042829 | A | G | 1 | a0001c0001t0002g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2385-288A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143042829 | |||||||
| chr3:143042878 | T | C | 1 | a0001c0001t0003g0301 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2385-239T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143042878 | |||||||
| chr3:143043073 | C | G | 27 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(24): Show |
28 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.2385-44C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 23/27 | chr3 | 143043073 | |||||||
| chr3:143043645 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.2544+369T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143043645 | |||||||
| chr3:143043668 | A | G | 263 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(260): Show |
278 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(275): Show |
intron_variant | MODIFIER | c.2544+392A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143043668 | |||||||
| chr3:143043669 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.2544+393C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143043669 | |||||||
| chr3:143043703 | T | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0187 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2544+427T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143043703 | |||||||
| chr3:143043717 | G | GTA | 8 | a0001c0001t0003g0269 a0001c0001t0003g0283 a0001c0001t0003g0284 others(5): Show |
8 | HG00639.hp2 HG01496.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2544+459_2544+460d others(4): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143043717 | ||||||
| chr3:143043717 | GTA | G | 100 | a0001c0001t0001g0016 a0001c0001t0001g0093 a0001c0001t0001g0132 others(97): Show |
106 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.2544+459_2544+460d others(4): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143043717 | ||||||
| chr3:143043717 | GTATA | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(160): Show |
172 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(169): Show |
intron_variant | MODIFIER | c.2544+457_2544+460d others(6): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143043717 | ||||||
| chr3:143043719 | A | G | 1 | a0001c0001t0014g0359 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2544+443A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143043719 | |||||||
| chr3:143043772 | A | AT | 25 | a0001c0001t0001g0150 a0001c0001t0003g0271 a0001c0001t0003g0272 others(22): Show |
25 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.2544+510dupT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143043772 | ||||||
| chr3:143043869 | C | T | 1 | a0001c0001t0004g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2544+593C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143043869 | |||||||
| chr3:143043954 | C | T | 1 | a0001c0001t0011g0079 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2544+678C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143043954 | |||||||
| chr3:143043988 | C | T | 1 | a0001c0001t0010g0210 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2544+712C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143043988 | |||||||
| chr3:143044065 | CATCTT | C | 3 | a0001c0001t0008g0003 a0001c0001t0008g0022 a0001c0001t0008g0026 |
4 | HG01169.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.2544+790_2544+794d others(7): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143044065 | |||||||
| chr3:143044068 | C | T | 266 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(263): Show |
280 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(277): Show |
intron_variant | MODIFIER | c.2544+792C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143044068 | |||||||
| chr3:143044079 | A | G | 15 | a0001c0001t0005g0009 a0001c0001t0005g0118 a0001c0001t0005g0119 others(12): Show |
16 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2544+803A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143044079 | |||||||
| chr3:143044088 | C | T | 264 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(261): Show |
279 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(276): Show |
intron_variant | MODIFIER | c.2544+812C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143044088 | |||||||
| chr3:143044238 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2544+962C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143044238 | |||||||
| chr3:143044255 | T | C | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2544+979T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143044255 | |||||||
| chr3:143044289 | C | CTTTTTTT others(2): Show |
10 | a0001c0001t0001g0165 a0001c0001t0001g0191 a0001c0001t0001g0201 others(7): Show |
10 | HG01169.hp1 HG01943.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2544+1022_2544+103 others(13): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143044289 | ||||||
| chr3:143044289 | C | CTTTTTTT others(3): Show |
166 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(163): Show |
177 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(174): Show |
intron_variant | MODIFIER | c.2544+1021_2544+103 others(14): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143044289 | ||||||
| chr3:143044289 | C | CTTTTTTT others(4): Show |
44 | a0001c0001t0001g0093 a0001c0001t0001g0147 a0001c0001t0001g0192 others(41): Show |
47 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.2544+1020_2544+103 others(15): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143044289 | ||||||
| chr3:143044289 | C | CTTTTTTT others(5): Show |
16 | a0001c0001t0001g0230 a0001c0001t0002g0076 a0001c0001t0002g0100 others(13): Show |
17 | HG01243.hp2 HG01884.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.2544+1019_2544+103 others(16): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143044289 | ||||||
| chr3:143044289 | C | CTTTTTTT others(6): Show |
19 | a0001c0001t0002g0028 a0001c0001t0002g0096 a0001c0001t0004g0014 others(16): Show |
19 | HG00639.hp1 HG00738.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.2544+1018_2544+103 others(17): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143044289 | ||||||
| chr3:143044289 | C | CTTTTTTT others(7): Show |
5 | a0001c0001t0004g0354 a0001c0001t0004g0355 a0001c0001t0015g0019 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2544+1017_2544+103 others(18): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143044289 | ||||||
| chr3:143044289 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0004g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2544+1016_2544+103 others(19): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143044289 | ||||||
| chr3:143044289 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0004g0262 a0001c0001t0014g0359 |
2 | HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2544+1015_2544+103 others(20): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143044289 | ||||||
| chr3:143044289 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0026g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2544+1014_2544+103 others(21): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143044289 | ||||||
| chr3:143044289 | CT | C | 89 | a0001c0001t0003g0263 a0001c0001t0003g0265 a0001c0001t0003g0266 others(86): Show |
90 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.2544+1030delT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143044289 | ||||||
| chr3:143044311 | C | T | 5 | a0001c0001t0014g0358 a0001c0001t0014g0359 a0001c0001t0015g0019 others(2): Show |
5 | HG01891.hp2 HG02257.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2544+1035C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143044311 | |||||||
| chr3:143044366 | G | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0218 |
3 | HG01952.hp2 NA18984.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2544+1090G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143044366 | |||||||
| chr3:143044450 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0190 |
2 | HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2544+1174G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143044450 | |||||||
| chr3:143044542 | A | G | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2544+1266A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143044542 | |||||||
| chr3:143044686 | T | C | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2544+1410T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143044686 | |||||||
| chr3:143044717 | T | A | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2544+1441T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143044717 | |||||||
| chr3:143044729 | C | T | 1 | a0001c0001t0003g0270 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2544+1453C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143044729 | |||||||
| chr3:143044829 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2544+1553A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143044829 | |||||||
| chr3:143045141 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(216): Show |
232 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.2544+1865C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143045141 | |||||||
| chr3:143045167 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(216): Show |
232 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.2544+1891G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143045167 | |||||||
| chr3:143045226 | G | A | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2544+1950G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143045226 | |||||||
| chr3:143045262 | A | G | 8 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0032 others(5): Show |
10 | HG00609.hp1 HG01361.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.2544+1986A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143045262 | |||||||
| chr3:143045360 | C | T | 102 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(99): Show |
104 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.2544+2084C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143045360 | |||||||
| chr3:143045366 | C | CA | 23 | a0001c0001t0003g0263 a0001c0001t0003g0268 a0001c0001t0003g0273 others(20): Show |
23 | HG01070.hp1 HG01071.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.2544+2113dupA | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143045366 | ||||||
| chr3:143045366 | CA | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(213): Show |
229 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.2544+2113delA | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143045366 | ||||||
| chr3:143045367 | A | C | 1 | a0001c0001t0026g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2544+2091A>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143045367 | |||||||
| chr3:143045394 | A | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(266): Show |
284 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(281): Show |
intron_variant | MODIFIER | c.2544+2118A>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143045394 | |||||||
| chr3:143045454 | T | TGTATTTT others(318): Show |
1 | a0001c0001t0002g0048 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2544+2188_2544+218 others(329): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143045454 | ||||||
| chr3:143045506 | T | C | 2 | a0001c0001t0003g0318 a0001c0001t0014g0358 |
2 | HG01346.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2544+2230T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143045506 | |||||||
| chr3:143045528 | A | G | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2544+2252A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143045528 | |||||||
| chr3:143045629 | C | A | 1 | a0001c0001t0008g0022 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2544+2353C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143045629 | |||||||
| chr3:143045736 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.2544+2460T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143045736 | |||||||
| chr3:143045768 | C | T | 21 | a0001c0001t0001g0010 a0001c0001t0001g0116 a0001c0001t0001g0134 others(18): Show |
22 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.2544+2492C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143045768 | |||||||
| chr3:143045809 | T | G | 1 | a0001c0001t0024g0122 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2544+2533T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143045809 | |||||||
| chr3:143045850 | G | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(266): Show |
284 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(281): Show |
intron_variant | MODIFIER | c.2544+2574G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143045850 | |||||||
| chr3:143046049 | C | G | 2 | a0001c0001t0005g0121 a0001c0001t0005g0126 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2544+2773C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046049 | |||||||
| chr3:143046185 | C | T | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2544+2909C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046185 | |||||||
| chr3:143046249 | G | A | 1 | a0001c0001t0003g0282 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2544+2973G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046249 | |||||||
| chr3:143046266 | C | CT | 14 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0198 others(11): Show |
14 | HG00558.hp1 HG00621.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.2544+3008dupT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143046266 | ||||||
| chr3:143046266 | CT | C | 19 | a0001c0001t0001g0136 a0001c0001t0001g0165 a0001c0001t0001g0179 others(16): Show |
19 | HG01070.hp1 HG01109.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.2544+3008delT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143046266 | ||||||
| chr3:143046278 | T | A | 1 | a0001c0001t0003g0304 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2544+3002T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046278 | |||||||
| chr3:143046291 | TTTTTTA | T | 73 | a0001c0001t0001g0093 a0001c0001t0002g0002 a0001c0001t0002g0004 others(70): Show |
79 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.2544+3021_2544+302 others(10): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143046291 | ||||||
| chr3:143046297 | A | AT | 170 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(167): Show |
178 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(175): Show |
intron_variant | MODIFIER | c.2544+3030dupT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143046297 | ||||||
| chr3:143046297 | A | T | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2544+3021A>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046297 | |||||||
| chr3:143046301 | T | TA | 31 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(28): Show |
32 | HG00735.hp1 HG00738.hp2 HG02080.hp1 others(29): Show |
intron_variant | MODIFIER | c.2544+3025_2544+302 others(5): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046301 | |||||||
| chr3:143046325 | T | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0154 |
2 | HG01358.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.2544+3049T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046325 | |||||||
| chr3:143046328 | A | T | 5 | a0001c0001t0001g0144 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG01358.hp2 HG02148.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.2544+3052A>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046328 | |||||||
| chr3:143046332 | T | A | 1 | a0001c0001t0006g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2544+3056T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046332 | |||||||
| chr3:143046405 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2544+3129G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046405 | |||||||
| chr3:143046473 | C | A | 1 | a0001c0001t0003g0278 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2544+3197C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046473 | |||||||
| chr3:143046473 | C | T | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2544+3197C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046473 | |||||||
| chr3:143046476 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(216): Show |
232 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.2544+3200C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046476 | |||||||
| chr3:143046477 | A | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(266): Show |
284 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(281): Show |
intron_variant | MODIFIER | c.2544+3201A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046477 | |||||||
| chr3:143046484 | T | G | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2544+3208T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046484 | |||||||
| chr3:143046517 | TGACTCTT others(3): Show |
T | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2544+3244_2544+325 others(14): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143046517 | ||||||
| chr3:143046542 | C | T | 1 | a0001c0001t0022g0193 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2544+3266C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046542 | |||||||
| chr3:143046688 | A | G | 1 | a0001c0001t0003g0289 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2544+3412A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046688 | |||||||
| chr3:143046776 | C | A | 1 | a0001c0001t0001g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2544+3500C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046776 | |||||||
| chr3:143046776 | C | G | 3 | a0001c0001t0007g0161 a0001c0001t0007g0184 a0001c0001t0019g0135 |
3 | HG01069.hp2 HG03239.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2544+3500C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046776 | |||||||
| chr3:143046907 | G | A | 1 | a0001c0001t0026g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2544+3631G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046907 | |||||||
| chr3:143046914 | ACCTCCCG others(366): Show |
A | 1 | a0001c0001t0004g0262 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2544+3678_2545-361 others(4): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143046914 | ||||||
| chr3:143046951 | A | AC | 213 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(210): Show |
226 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.2544+3677dupC | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143046951 | ||||||
| chr3:143046951 | A | ACC | 4 | a0001c0001t0001g0145 a0001c0001t0002g0028 a0001c0001t0002g0082 others(1): Show |
4 | HG02738.hp1 HG02738.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2544+3676_2544+367 others(6): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143046951 | ||||||
| chr3:143046952 | CCTCCCCC others(316): Show |
C | 26 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(23): Show |
27 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.2544+3678_2545-366 others(4): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143046952 | ||||||
| chr3:143046953 | CT | C | 3 | a0001c0001t0014g0358 a0001c0001t0014g0359 a0001c0001t0026g0021 |
3 | HG02257.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2544+3678delT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046953 | |||||||
| chr3:143046954 | T | A | 2 | a0001c0001t0015g0019 a0001c0001t0015g0020 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2544+3678T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046954 | |||||||
| chr3:143046954 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(241): Show |
258 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(255): Show |
intron_variant | MODIFIER | c.2544+3678T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046954 | |||||||
| chr3:143046991 | C | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2544+3715C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046991 | |||||||
| chr3:143046994 | G | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0221 |
2 | HG02273.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2544+3718G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143046994 | |||||||
| chr3:143047002 | CCCCCCCA others(41): Show |
C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0221 |
2 | HG02273.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2544+3733_2544+378 others(52): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047002 | ||||||
| chr3:143047023 | TGGGGCGG others(42): Show |
T | 2 | a0001c0001t0006g0352 a0001c0001t0006g0353 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2544+3761_2544+380 others(53): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047023 | ||||||
| chr3:143047052 | C | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0221 |
2 | HG02273.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2544+3776C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047052 | |||||||
| chr3:143047055 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(229): Show |
246 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(243): Show |
intron_variant | MODIFIER | c.2544+3779C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047055 | |||||||
| chr3:143047069 | T | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(229): Show |
246 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(243): Show |
intron_variant | MODIFIER | c.2544+3793T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047069 | |||||||
| chr3:143047073 | G | A | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2544+3797G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047073 | |||||||
| chr3:143047085 | C | T | 15 | a0001c0001t0005g0009 a0001c0001t0005g0118 a0001c0001t0005g0119 others(12): Show |
16 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2544+3809C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047085 | |||||||
| chr3:143047116 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0221 |
2 | HG02273.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2545-3823G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047116 | |||||||
| chr3:143047122 | C | T | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2545-3817C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047122 | |||||||
| chr3:143047159 | T | C | 3 | a0001c0001t0003g0288 a0001c0001t0003g0289 a0001c0001t0003g0305 |
3 | NA18959.hp1 NA18983.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.2545-3780T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047159 | |||||||
| chr3:143047164 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0221 |
2 | HG02273.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2545-3775A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047164 | |||||||
| chr3:143047177 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0221 |
2 | HG02273.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2545-3762A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047177 | |||||||
| chr3:143047177 | A | T | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2545-3762A>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047177 | |||||||
| chr3:143047177 | ATCCCCCC others(395): Show |
A | 1 | a0001c0001t0001g0222 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2545-3761_2545-336 others(4): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047177 | |||||||
| chr3:143047178 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(230): Show |
247 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(244): Show |
intron_variant | MODIFIER | c.2545-3761T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047178 | |||||||
| chr3:143047199 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0221 |
2 | HG02273.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2545-3740C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047199 | |||||||
| chr3:143047204 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2545-3735C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047204 | |||||||
| chr3:143047208 | C | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(230): Show |
247 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(244): Show |
intron_variant | MODIFIER | c.2545-3731C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047208 | |||||||
| chr3:143047213 | A | G | 14 | a0001c0001t0001g0142 a0001c0001t0001g0221 a0001c0001t0006g0264 others(11): Show |
14 | HG01891.hp2 HG02080.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.2545-3726A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047213 | |||||||
| chr3:143047213 | A | T | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2545-3726A>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047213 | |||||||
| chr3:143047214 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0221 |
2 | HG02273.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2545-3725G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047214 | |||||||
| chr3:143047216 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0221 |
2 | HG02273.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2545-3723C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047216 | |||||||
| chr3:143047227 | T | C | 16 | a0001c0001t0001g0142 a0001c0001t0001g0221 a0001c0001t0006g0264 others(13): Show |
16 | HG00735.hp1 HG01891.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.2545-3712T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047227 | |||||||
| chr3:143047255 | GCCGGCCT others(218): Show |
G | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2545-3682_2545-345 others(4): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047255 | ||||||
| chr3:143047257 | C | T | 14 | a0001c0001t0001g0142 a0001c0001t0001g0221 a0001c0001t0006g0264 others(11): Show |
14 | HG01891.hp2 HG02080.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.2545-3682C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047257 | |||||||
| chr3:143047262 | T | A | 14 | a0001c0001t0001g0142 a0001c0001t0001g0221 a0001c0001t0006g0264 others(11): Show |
14 | HG01891.hp2 HG02080.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.2545-3677T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047262 | |||||||
| chr3:143047264 | G | C | 2 | a0001c0001t0005g0009 a0001c0001t0005g0125 |
3 | HG02258.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2545-3675G>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047264 | |||||||
| chr3:143047266 | GGGGGGCT others(346): Show |
G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(211): Show |
227 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(224): Show |
intron_variant | MODIFIER | c.2545-3656_2545-330 others(4): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047266 | ||||||
| chr3:143047271 | G | T | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2545-3668G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047271 | |||||||
| chr3:143047275 | A | ACCCCCCC others(170): Show |
72 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(69): Show |
73 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.2545-3634_2545-363 others(181): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047275 | ||||||
| chr3:143047275 | A | ACCCCCCC others(171): Show |
3 | a0001c0001t0003g0283 a0001c0001t0003g0298 a0001c0001t0003g0313 |
3 | HG02293.hp2 NA18947.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2545-3634_2545-363 others(182): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047275 | ||||||
| chr3:143047275 | A | ACCCCCCC others(171): Show |
1 | a0001c0001t0003g0285 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2545-3634_2545-363 others(182): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047275 | ||||||
| chr3:143047275 | A | ACCCCCCC others(171): Show |
2 | a0001c0001t0003g0263 a0001c0001t0003g0329 |
2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2545-3634_2545-363 others(182): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047275 | ||||||
| chr3:143047275 | A | ACCCCCCC others(172): Show |
1 | a0001c0001t0003g0312 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2545-3634_2545-363 others(183): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047275 | ||||||
| chr3:143047275 | A | ACCCCCCC others(121): Show |
14 | a0001c0001t0005g0009 a0001c0001t0005g0118 a0001c0001t0005g0119 others(11): Show |
15 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.2545-3623_2545-362 others(132): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047275 | ||||||
| chr3:143047275 | A | ACCCCCCC others(122): Show |
1 | a0001c0001t0005g0126 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2545-3623_2545-362 others(133): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047275 | ||||||
| chr3:143047275 | A | ACCCCCCC others(121): Show |
1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2545-3623_2545-362 others(132): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047275 | ||||||
| chr3:143047275 | A | ACCCCCCC others(170): Show |
2 | a0001c0001t0003g0299 a0001c0001t0003g0306 |
2 | NA18989.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2545-3649_2545-364 others(181): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047275 | ||||||
| chr3:143047275 | A | ACCCCCCC others(171): Show |
1 | a0001c0001t0003g0271 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2545-3657_2545-365 others(182): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047275 | ||||||
| chr3:143047275 | A | ACCCCCCC others(173): Show |
1 | a0001c0001t0003g0282 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2545-3657_2545-365 others(184): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047275 | ||||||
| chr3:143047275 | A | ATCCCCCC others(170): Show |
9 | a0001c0001t0006g0264 a0001c0001t0006g0348 a0001c0001t0006g0349 others(6): Show |
9 | HG01891.hp2 HG02080.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.2545-3664_2545-366 others(181): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047275 | |||||||
| chr3:143047275 | A | ATCCCCCC others(170): Show |
1 | a0001c0001t0026g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2545-3664_2545-366 others(181): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047275 | |||||||
| chr3:143047276 | C | T | 4 | a0001c0001t0001g0142 a0001c0001t0001g0221 a0001c0001t0014g0358 others(1): Show |
4 | HG02257.hp2 HG02273.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2545-3663C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047276 | |||||||
| chr3:143047276 | CCCCCCCA others(345): Show |
C | 1 | a0001c0001t0002g0046 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2545-3656_2545-330 others(4): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047276 | ||||||
| chr3:143047283 | A | T | 1 | a0005c0007t0001g0141 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2545-3656A>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047283 | |||||||
| chr3:143047284 | CCTCCCTC others(345): Show |
C | 1 | a0005c0007t0001g0141 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2545-3653_2545-330 others(4): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047284 | ||||||
| chr3:143047306 | T | C | 5 | a0001c0001t0001g0142 a0001c0001t0001g0221 a0001c0001t0003g0314 others(2): Show |
5 | HG00642.hp2 HG02257.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.2545-3633T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047306 | |||||||
| chr3:143047308 | GCCGGGCA others(120): Show |
G | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2545-3624_2545-349 others(4): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047308 | ||||||
| chr3:143047311 | G | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0221 a0001c0001t0003g0314 |
3 | HG00642.hp2 HG02273.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2545-3628G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047311 | |||||||
| chr3:143047315 | A | G | 30 | a0001c0001t0001g0142 a0001c0001t0001g0221 a0001c0001t0003g0314 others(27): Show |
31 | HG00642.hp2 HG00738.hp2 HG02080.hp1 others(28): Show |
intron_variant | MODIFIER | c.2545-3624A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047315 | |||||||
| chr3:143047318 | G | T | 2 | a0001c0001t0003g0269 a0001c0001t0003g0286 |
2 | NA18962.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.2545-3621G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047318 | |||||||
| chr3:143047332 | T | A | 1 | a0001c0001t0003g0314 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2545-3607T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047332 | |||||||
| chr3:143047335 | C | T | 1 | a0001c0001t0003g0314 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2545-3604C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047335 | |||||||
| chr3:143047336 | CCCTCCCG others(297): Show |
C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0221 |
2 | HG02273.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2545-3588_2545-328 others(4): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047336 | ||||||
| chr3:143047351 | T | C | 43 | a0001c0001t0003g0314 a0001c0001t0004g0013 a0001c0001t0004g0014 others(40): Show |
45 | HG00642.hp2 HG00738.hp2 HG01175.hp1 others(42): Show |
intron_variant | MODIFIER | c.2545-3588T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047351 | |||||||
| chr3:143047390 | G | A | 27 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(24): Show |
28 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.2545-3549G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047390 | |||||||
| chr3:143047407 | G | A | 1 | a0001c0001t0003g0314 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2545-3532G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047407 | |||||||
| chr3:143047425 | T | G | 1 | a0001c0001t0003g0314 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2545-3514T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047425 | |||||||
| chr3:143047435 | A | G | 135 | a0001c0001t0003g0263 a0001c0001t0003g0265 a0001c0001t0003g0266 others(132): Show |
138 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.2545-3504A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047435 | |||||||
| chr3:143047438 | G | T | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2545-3501G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047438 | |||||||
| chr3:143047469 | T | C | 3 | a0001c0001t0003g0314 a0001c0001t0014g0358 a0001c0001t0014g0359 |
3 | HG00642.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2545-3470T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047469 | |||||||
| chr3:143047478 | C | CGGCTGGC others(42): Show |
1 | a0001c0001t0003g0314 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2545-3460_2545-345 others(53): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047478 | ||||||
| chr3:143047480 | A | G | 3 | a0001c0001t0003g0314 a0001c0001t0014g0358 a0001c0001t0014g0359 |
3 | HG00642.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2545-3459A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047480 | |||||||
| chr3:143047533 | A | C | 3 | a0001c0001t0003g0314 a0001c0001t0014g0358 a0001c0001t0014g0359 |
3 | HG00642.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2545-3406A>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047533 | |||||||
| chr3:143047534 | G | A | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2545-3405G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047534 | |||||||
| chr3:143047535 | C | T | 1 | a0001c0001t0005g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2545-3404C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047535 | |||||||
| chr3:143047537 | C | T | 2 | a0001c0001t0003g0299 a0001c0001t0003g0306 |
2 | NA18989.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2545-3402C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047537 | |||||||
| chr3:143047551 | C | T | 1 | a0001c0001t0005g0123 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2545-3388C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047551 | |||||||
| chr3:143047552 | G | T | 1 | a0001c0001t0003g0314 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2545-3387G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047552 | |||||||
| chr3:143047564 | T | C | 3 | a0001c0001t0003g0314 a0001c0001t0014g0358 a0001c0001t0014g0359 |
3 | HG00642.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2545-3375T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047564 | |||||||
| chr3:143047568 | C | T | 1 | a0001c0001t0003g0329 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2545-3371C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047568 | |||||||
| chr3:143047569 | GGGGGGCT others(43): Show |
G | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2545-3353_2545-330 others(54): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047569 | ||||||
| chr3:143047591 | C | CCCTCCTG others(71): Show |
1 | a0001c0001t0003g0314 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2545-3343_2545-334 others(82): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047591 | ||||||
| chr3:143047608 | GCTGGCCG others(169): Show |
G | 2 | a0001c0001t0004g0243 a0001c0001t0004g0248 |
2 | HG02080.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2545-3318_2545-314 others(4): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047608 | ||||||
| chr3:143047614 | C | T | 8 | a0001c0001t0003g0314 a0001c0001t0006g0264 a0001c0001t0006g0348 others(5): Show |
8 | HG00642.hp2 HG02080.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2545-3325C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047614 | |||||||
| chr3:143047615 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2545-3324G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047615 | |||||||
| chr3:143047619 | A | G | 2 | a0001c0001t0001g0222 a0001c0001t0003g0314 |
2 | HG00438.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.2545-3320A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047619 | |||||||
| chr3:143047619 | AG | A | 15 | a0001c0001t0005g0009 a0001c0001t0005g0118 a0001c0001t0005g0119 others(12): Show |
16 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2545-3315delG | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047619 | ||||||
| chr3:143047624 | G | T | 15 | a0001c0001t0005g0009 a0001c0001t0005g0118 a0001c0001t0005g0119 others(12): Show |
16 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2545-3315G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047624 | |||||||
| chr3:143047636 | T | A | 1 | a0001c0001t0003g0314 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2545-3303T>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047636 | |||||||
| chr3:143047639 | C | T | 1 | a0001c0001t0003g0314 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2545-3300C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047639 | |||||||
| chr3:143047640 | G | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(268): Show |
286 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(283): Show |
intron_variant | MODIFIER | c.2545-3299G>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047640 | |||||||
| chr3:143047655 | C | T | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2545-3284C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047655 | |||||||
| chr3:143047664 | G | A | 1 | a0001c0001t0023g0247 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2545-3275G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047664 | |||||||
| chr3:143047710 | C | A | 1 | a0001c0001t0004g0240 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2545-3229C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047710 | |||||||
| chr3:143047710 | C | T | 3 | a0001c0001t0003g0336 a0001c0001t0003g0337 a0001c0001t0003g0339 |
3 | HG03098.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2545-3229C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047710 | |||||||
| chr3:143047746 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2545-3193G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047746 | |||||||
| chr3:143047759 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.2545-3180T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047759 | |||||||
| chr3:143047764 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2545-3175C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047764 | |||||||
| chr3:143047775 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(212): Show |
227 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(224): Show |
intron_variant | MODIFIER | c.2545-3164A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047775 | |||||||
| chr3:143047826 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2545-3113C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047826 | |||||||
| chr3:143047837 | A | C | 2 | a0001c0001t0004g0243 a0001c0001t0004g0248 |
2 | HG02080.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2545-3102A>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047837 | |||||||
| chr3:143047855 | C | T | 2 | a0001c0002t0002g0356 a0001c0002t0002g0357 |
2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2545-3084C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047855 | |||||||
| chr3:143047856 | G | T | 2 | a0001c0001t0004g0243 a0001c0001t0004g0248 |
2 | HG02080.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2545-3083G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047856 | |||||||
| chr3:143047882 | A | AC | 223 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(220): Show |
237 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.2545-3049dupC | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047882 | ||||||
| chr3:143047882 | A | ACC | 36 | a0001c0001t0001g0133 a0001c0001t0001g0149 a0001c0001t0001g0230 others(33): Show |
37 | HG00544.hp2 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.2545-3050_2545-304 others(6): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143047882 | ||||||
| chr3:143047891 | A | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(260): Show |
278 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(275): Show |
intron_variant | MODIFIER | c.2545-3048A>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047891 | |||||||
| chr3:143047901 | C | T | 13 | a0001c0001t0004g0014 a0001c0001t0004g0244 a0001c0001t0004g0246 others(10): Show |
13 | HG00738.hp2 HG02145.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2545-3038C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047901 | |||||||
| chr3:143047902 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.2545-3037C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047902 | |||||||
| chr3:143047934 | C | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(243): Show |
260 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(257): Show |
intron_variant | MODIFIER | c.2545-3005C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143047934 | |||||||
| chr3:143048006 | A | G | 2 | a0001c0001t0015g0019 a0001c0001t0015g0020 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2545-2933A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143048006 | |||||||
| chr3:143048238 | T | G | 1 | a0001c0001t0002g0046 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2545-2701T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143048238 | |||||||
| chr3:143048430 | C | T | 1 | a0001c0001t0006g0353 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2545-2509C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143048430 | |||||||
| chr3:143048540 | C | A | 13 | a0001c0001t0001g0133 a0001c0001t0001g0167 a0001c0001t0001g0189 others(10): Show |
14 | HG02074.hp2 HG02080.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.2545-2399C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143048540 | |||||||
| chr3:143048794 | G | T | 2 | a0001c0001t0015g0019 a0001c0001t0015g0020 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2545-2145G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143048794 | |||||||
| chr3:143048824 | T | G | 1 | a0001c0001t0003g0329 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2545-2115T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143048824 | |||||||
| chr3:143048926 | G | A | 1 | a0001c0001t0014g0358 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2545-2013G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143048926 | |||||||
| chr3:143048985 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2545-1954C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143048985 | |||||||
| chr3:143048993 | T | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.2545-1946T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143048993 | |||||||
| chr3:143049022 | A | G | 6 | a0001c0001t0006g0348 a0001c0001t0006g0349 a0001c0001t0006g0350 others(3): Show |
6 | HG02080.hp2 HG02602.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.2545-1917A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143049022 | |||||||
| chr3:143049093 | T | TA | 75 | a0001c0001t0001g0093 a0001c0001t0002g0002 a0001c0001t0002g0004 others(72): Show |
81 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.2545-1829dupA | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143049093 | ||||||
| chr3:143049122 | T | C | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2545-1817T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143049122 | |||||||
| chr3:143049135 | G | A | 9 | a0001c0001t0005g0009 a0001c0001t0005g0118 a0001c0001t0005g0119 others(6): Show |
10 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2545-1804G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143049135 | |||||||
| chr3:143049139 | G | C | 7 | a0001c0001t0006g0264 a0001c0001t0006g0348 a0001c0001t0006g0349 others(4): Show |
7 | HG02080.hp2 HG02602.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.2545-1800G>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143049139 | |||||||
| chr3:143049172 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2545-1767G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143049172 | |||||||
| chr3:143049265 | C | CA | 15 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0268 others(12): Show |
15 | HG00673.hp1 HG00735.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.2545-1647dupA | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143049265 | ||||||
| chr3:143049265 | CA | C | 13 | a0001c0001t0003g0271 a0001c0001t0003g0272 a0001c0001t0003g0274 others(10): Show |
13 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(10): Show |
intron_variant | MODIFIER | c.2545-1647delA | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143049265 | ||||||
| chr3:143049265 | CAAAAAAA others(2): Show |
C | 15 | a0001c0001t0001g0010 a0001c0001t0001g0116 a0001c0001t0001g0140 others(12): Show |
16 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.2545-1655_2545-164 others(13): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143049265 | ||||||
| chr3:143049265 | CAAAAAAA others(3): Show |
C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(238): Show |
255 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(252): Show |
intron_variant | MODIFIER | c.2545-1656_2545-164 others(14): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143049265 | ||||||
| chr3:143049265 | CAAAAAAA others(4): Show |
C | 6 | a0001c0001t0001g0143 a0001c0001t0001g0173 a0001c0001t0001g0258 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2545-1657_2545-164 others(15): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143049265 | ||||||
| chr3:143049289 | A | G | 1 | a0001c0001t0026g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2545-1650A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143049289 | |||||||
| chr3:143049354 | T | TA | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.2545-1583dupA | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr3 | 143049354 | ||||||
| chr3:143049573 | C | A | 2 | a0001c0001t0015g0019 a0001c0001t0015g0020 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2545-1366C>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143049573 | |||||||
| chr3:143049857 | C | T | 1 | a0001c0001t0014g0358 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2545-1082C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143049857 | |||||||
| chr3:143049872 | T | C | 1 | a0001c0001t0004g0240 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2545-1067T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143049872 | |||||||
| chr3:143049954 | A | G | 27 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(24): Show |
28 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.2545-985A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143049954 | |||||||
| chr3:143050160 | G | A | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2545-779G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143050160 | |||||||
| chr3:143050166 | C | T | 1 | a0001c0001t0006g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2545-773C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143050166 | |||||||
| chr3:143050167 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2545-772G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143050167 | |||||||
| chr3:143050353 | G | A | 1 | a0001c0001t0003g0263 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2545-586G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143050353 | |||||||
| chr3:143050368 | C | T | 27 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(24): Show |
28 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.2545-571C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143050368 | |||||||
| chr3:143050369 | G | A | 2 | a0001c0002t0002g0356 a0001c0002t0002g0357 |
2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2545-570G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143050369 | |||||||
| chr3:143050617 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.2545-322T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143050617 | |||||||
| chr3:143050709 | A | G | 1 | a0001c0001t0004g0239 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2545-230A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 24/27 | chr3 | 143050709 | |||||||
| chr3:143051082 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2655+33T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143051082 | |||||||
| chr3:143051312 | A | G | 1 | a0001c0001t0003g0344 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2655+263A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143051312 | |||||||
| chr3:143051472 | G | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.2655+423G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143051472 | |||||||
| chr3:143051602 | C | CA | 20 | a0001c0001t0001g0145 a0001c0001t0001g0167 a0001c0001t0001g0189 others(17): Show |
21 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.2655+572dupA | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr3 | 143051602 | ||||||
| chr3:143051602 | C | CAA | 197 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(194): Show |
207 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.2655+571_2655+572d others(4): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr3 | 143051602 | ||||||
| chr3:143051602 | C | CAAA | 17 | a0001c0001t0001g0144 a0001c0001t0001g0173 a0001c0001t0001g0204 others(14): Show |
17 | HG01243.hp1 HG01358.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.2655+570_2655+572d others(5): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr3 | 143051602 | ||||||
| chr3:143051602 | CAAA | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
7 | HG02451.hp1 HG02559.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2655+570_2655+572d others(5): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr3 | 143051602 | ||||||
| chr3:143051602 | CAAAAA | C | 27 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0237 others(24): Show |
28 | HG00738.hp2 HG02080.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.2655+568_2655+572d others(7): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr3 | 143051602 | ||||||
| chr3:143051617 | A | G | 1 | a0001c0001t0003g0281 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2655+568A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143051617 | |||||||
| chr3:143051685 | T | C | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 |
3 | HG02055.hp2 HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2655+636T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143051685 | |||||||
| chr3:143051763 | C | T | 2 | a0001c0001t0003g0299 a0001c0001t0003g0306 |
2 | NA18989.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2655+714C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143051763 | |||||||
| chr3:143051803 | G | T | 1 | a0001c0001t0006g0327 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2655+754G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143051803 | |||||||
| chr3:143051828 | C | G | 1 | a0001c0002t0002g0025 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2655+779C>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143051828 | |||||||
| chr3:143051874 | G | T | 1 | a0001c0001t0007g0115 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2655+825G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143051874 | |||||||
| chr3:143051896 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2655+847G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143051896 | |||||||
| chr3:143052140 | A | G | 1 | a0001c0001t0002g0054 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2655+1091A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143052140 | |||||||
| chr3:143052168 | G | A | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2655+1119G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143052168 | |||||||
| chr3:143052290 | A | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0224 |
3 | NA18999.hp1 NA19001.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2655+1241A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143052290 | |||||||
| chr3:143052506 | A | G | 7 | a0001c0001t0006g0264 a0001c0001t0006g0348 a0001c0001t0006g0349 others(4): Show |
7 | HG02080.hp2 HG02602.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.2656-1170A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143052506 | |||||||
| chr3:143052621 | C | T | 1 | a0001c0001t0006g0327 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2656-1055C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143052621 | |||||||
| chr3:143052688 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2656-988G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143052688 | |||||||
| chr3:143052727 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.2656-949C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143052727 | |||||||
| chr3:143052950 | G | GT | 23 | a0001c0001t0002g0051 a0001c0001t0002g0086 a0001c0001t0003g0263 others(20): Show |
23 | HG00673.hp2 HG01496.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.2656-709dupT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr3 | 143052950 | ||||||
| chr3:143052950 | G | GTT | 233 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(230): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(245): Show |
intron_variant | MODIFIER | c.2656-710_2656-709d others(4): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr3 | 143052950 | ||||||
| chr3:143052950 | G | GTTT | 23 | a0001c0001t0001g0136 a0001c0001t0001g0148 a0001c0001t0001g0156 others(20): Show |
23 | HG00609.hp2 HG00735.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.2656-711_2656-709d others(5): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr3 | 143052950 | ||||||
| chr3:143053055 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2656-621C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143053055 | |||||||
| chr3:143053535 | A | AT | 249 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
263 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(260): Show |
intron_variant | MODIFIER | c.2656-128dupT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr3 | 143053535 | ||||||
| chr3:143053605 | T | C | 2 | a0001c0001t0015g0019 a0001c0001t0015g0020 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2656-71T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 25/27 | chr3 | 143053605 | |||||||
| chr3:143053943 | G | A | 105 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(102): Show |
107 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.2774+149G>A | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 26/27 | chr3 | 143053943 | |||||||
| chr3:143054220 | C | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(274): Show |
292 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(289): Show |
intron_variant | MODIFIER | c.2774+426C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 26/27 | chr3 | 143054220 | |||||||
| chr3:143054280 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2774+486G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 26/27 | chr3 | 143054280 | |||||||
| chr3:143054676 | CTTAA | C | 3 | a0001c0001t0004g0013 a0001c0001t0004g0237 a0001c0001t0004g0241 |
4 | NA18951.hp2 NA18994.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2775-263_2775-260d others(6): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr3 | 143054676 | ||||||
| chr3:143054714 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2775-229T>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 26/27 | chr3 | 143054714 | |||||||
| chr3:143054732 | A | G | 2 | a0001c0001t0014g0358 a0001c0001t0014g0359 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2775-211A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 26/27 | chr3 | 143054732 | |||||||
| chr3:143054896 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
276 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.2775-47C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 26/27 | chr3 | 143054896 | |||||||
| chr3:143055206 | A | AT | 10 | a0001c0001t0001g0117 a0001c0001t0004g0253 a0001c0001t0006g0235 others(7): Show |
10 | HG02080.hp2 HG02602.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.2951+102dupT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr3 | 143055206 | ||||||
| chr3:143055206 | AT | A | 20 | a0001c0001t0001g0197 a0001c0001t0001g0202 a0001c0001t0001g0226 others(17): Show |
21 | HG00735.hp1 HG01884.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2951+102delT | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr3 | 143055206 | ||||||
| chr3:143055371 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0116 a0001c0001t0001g0140 |
4 | HG00558.hp2 NA18952.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.2951+252G>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 27/27 | chr3 | 143055371 | |||||||
| chr3:143055389 | T | G | 7 | a0001c0001t0006g0264 a0001c0001t0006g0348 a0001c0001t0006g0349 others(4): Show |
7 | HG02080.hp2 HG02602.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.2951+270T>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 27/27 | chr3 | 143055389 | |||||||
| chr3:143055664 | C | T | 9 | a0001c0001t0002g0040 a0001c0001t0002g0047 a0001c0001t0002g0065 others(6): Show |
9 | HG00408.hp2 HG02155.hp1 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.2951+545C>T | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 27/27 | chr3 | 143055664 | |||||||
| chr3:143056020 | A | G | 3 | a0001c0001t0001g0133 a0001c0001t0001g0167 a0001c0001t0001g0189 |
3 | HG02074.hp2 HG02132.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.2952-292A>G | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 27/27 | chr3 | 143056020 | |||||||
| chr3:143056146 | C | CTG | 6 | a0001c0001t0002g0036 a0001c0001t0002g0039 a0001c0001t0002g0045 others(3): Show |
6 | HG00558.hp1 HG00621.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.2952-152_2952-151d others(4): Show |
U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr3 | 143056146 | ||||||
| chr3:143056148 | G | C | 2 | a0001c0004t0012g0017 a0001c0004t0012g0018 |
2 | HG00735.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2952-164G>C | U2SURP | ENSG00000163714.18 | transcript | ENST00000473835.7 | protein_coding | 27/27 | chr3 | 143056148 |