Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5782 |
| ensemblid | ENSG00000127947.16 |
| hgncid | 9645 |
| symbol | PTPN12 |
| name | protein tyrosine phosphatase non-receptor type 12 |
| refseq_nuc | NM_002835.4 |
| refseq_prot | NP_002826.3 |
| ensembl_nuc | ENST00000248594.11 |
| ensembl_prot | ENSP00000248594.6 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 77537295 |
| end | 77640069 |
| strand | + |
| ver | v1.2 |
| region | chr7:77537295-77640069 |
| region5000 | chr7:77532295-77645069 |
| regionname0 | PTPN12_chr7_77537295_77640069 |
| regionname5000 | PTPN12_chr7_77532295_77645069 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 780 | 124 | 53 | 14 | 41 | 7 | 8 | 30 | PTPN12_chr7_77532295_77645069 | PTPN12 | MEQVE others(775): Show |
chr7 | 77532295 | 77645069 |
| a0002 | 0/0 | 780 | 112 | 21 | 24 | 51 | 3 | 13 | 42 | PTPN12_chr7_77532295_77645069 | PTPN12 | MEQVE others(775): Show |
chr7 | 77532295 | 77645069 |
| a0003 | 1/0 | 780 | 66 | 12 | 17 | 18 | 5 | 13 | 14 | PTPN12_chr7_77532295_77645069 | PTPN12 | MEQVE others(775): Show |
chr7 | 77532295 | 77645069 |
| a0004 | 0/0 | 780 | 6 | 0 | 3 | 0 | 1 | 2 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | MEQVE others(775): Show |
chr7 | 77532295 | 77645069 |
| a0005 | 0/0 | 780 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | MEQVE others(775): Show |
chr7 | 77532295 | 77645069 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2340 | 123 | 52 | 14 | 41 | 7 | 8 | PTPN12_chr7_77532295_77645069 | PTPN12 | ATGGA others(2335): Show |
chr7 | 77532295 | 77645069 | ||
| a0001c0007 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | ATGGA others(2335): Show |
chr7 | 77532295 | 77645069 | ||
| a0002c0002 | 0/0 | 2340 | 112 | 21 | 24 | 51 | 3 | 13 | PTPN12_chr7_77532295_77645069 | PTPN12 | ATGGA others(2335): Show |
chr7 | 77532295 | 77645069 | ||
| a0003c0003 | 1/0 | 2340 | 65 | 12 | 16 | 18 | 5 | 13 | PTPN12_chr7_77532295_77645069 | PTPN12 | ATGGA others(2335): Show |
chr7 | 77532295 | 77645069 | ||
| a0003c0006 | 0/0 | 2340 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | ATGGA others(2335): Show |
chr7 | 77532295 | 77645069 | ||
| a0004c0004 | 0/0 | 2340 | 6 | 0 | 3 | 0 | 1 | 2 | PTPN12_chr7_77532295_77645069 | PTPN12 | ATGGA others(2335): Show |
chr7 | 77532295 | 77645069 | ||
| a0005c0005 | 0/0 | 2340 | 2 | 0 | 2 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | ATGGA others(2335): Show |
chr7 | 77532295 | 77645069 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3384 | 121 | 51 | 14 | 41 | 7 | 8 | PTPN12_chr7_77532295_77645069 | PTPN12 | GCTAG others(3379): Show |
chr7 | 77532295 | 77645069 |
| a0001c0001t0003 | 0/1 | 3385 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | GCTAG others(3380): Show |
chr7 | 77532295 | 77645069 |
| a0001c0001t0004 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | GCTAG others(3379): Show |
chr7 | 77532295 | 77645069 |
| a0001c0007t0001 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | GCTAG others(3379): Show |
chr7 | 77532295 | 77645069 |
| a0002c0002t0001 | 0/0 | 3384 | 111 | 21 | 24 | 51 | 3 | 12 | PTPN12_chr7_77532295_77645069 | PTPN12 | GCTAG others(3379): Show |
chr7 | 77532295 | 77645069 |
| a0002c0002t0005 | 0/0 | 3384 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | GCTAG others(3379): Show |
chr7 | 77532295 | 77645069 |
| a0003c0003t0001 | 1/0 | 3384 | 62 | 10 | 15 | 18 | 5 | 13 | PTPN12_chr7_77532295_77645069 | PTPN12 | GCTAG others(3379): Show |
chr7 | 77532295 | 77645069 |
| a0003c0003t0002 | 0/0 | 3384 | 3 | 2 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | GCTAG others(3379): Show |
chr7 | 77532295 | 77645069 |
| a0003c0006t0001 | 0/0 | 3384 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | GCTAG others(3379): Show |
chr7 | 77532295 | 77645069 |
| a0004c0004t0001 | 0/0 | 3384 | 6 | 0 | 3 | 0 | 1 | 2 | PTPN12_chr7_77532295_77645069 | PTPN12 | GCTAG others(3379): Show |
chr7 | 77532295 | 77645069 |
| a0005c0005t0001 | 0/0 | 3384 | 2 | 0 | 2 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | GCTAG others(3379): Show |
chr7 | 77532295 | 77645069 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0003g0304 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0001c0007t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0002c0002t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0200 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0003t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0003c0006t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0004c0004t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0004c0004t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0004c0004t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0004c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0004c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0004c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0005c0005t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| a0005c0005t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0001 | g0188 | EUR | GBR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00099 | hp2 | a0004 | c0004 | t0001 | g0270 | EUR | GBR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0095 | EUR | GBR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0302 | EUR | GBR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | FIN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | FIN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00323 | hp1 | a0003 | c0003 | t0001 | g0185 | EUR | FIN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | FIN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00408 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00423 | hp2 | a0003 | c0003 | t0001 | g0177 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00438 | hp1 | a0003 | c0003 | t0001 | g0176 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0128 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00642 | hp1 | a0003 | c0003 | t0001 | g0194 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00642 | hp2 | a0004 | c0004 | t0001 | g0265 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | CHS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00733 | hp2 | a0003 | c0003 | t0001 | g0199 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00735 | hp2 | a0003 | c0003 | t0001 | g0206 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00738 | hp1 | a0003 | c0003 | t0001 | g0204 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00738 | hp2 | a0005 | c0005 | t0001 | g0053 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00741 | hp1 | a0004 | c0004 | t0001 | g0266 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0051 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01070 | hp1 | a0003 | c0003 | t0001 | g0210 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0107 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01071 | hp2 | a0003 | c0003 | t0001 | g0299 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01074 | hp2 | a0003 | c0003 | t0001 | g0300 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0057 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01081 | hp2 | a0003 | c0003 | t0001 | g0187 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0084 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0072 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0189 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0184 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0034 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0059 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01243 | hp1 | a0003 | c0003 | t0002 | g0161 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0023 | AMR | PUR | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01255 | hp1 | a0003 | c0003 | t0001 | g0203 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01256 | hp1 | a0003 | c0003 | t0001 | g0303 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0104 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01257 | hp1 | a0005 | c0005 | t0001 | g0050 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0106 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01261 | hp1 | a0003 | c0003 | t0001 | g0191 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0083 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01346 | hp2 | a0003 | c0006 | t0001 | g0190 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0048 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0192 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01361 | hp2 | a0003 | c0003 | t0001 | g0209 | AMR | CLM | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01516 | hp1 | a0003 | c0003 | t0001 | g0193 | EUR | IBS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0056 | EUR | IBS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | IBS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0055 | EUR | IBS | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0088 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0098 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0101 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0102 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0064 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG01993 | hp2 | a0004 | c0004 | t0001 | g0267 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0073 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02015 | hp2 | a0003 | c0003 | t0001 | g0169 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0168 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CDX | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | CDX | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02257 | hp1 | a0003 | c0003 | t0001 | g0202 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | PEL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02451 | hp2 | a0003 | c0003 | t0001 | g0286 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02572 | hp1 | a0003 | c0003 | t0001 | g0113 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0306 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02683 | hp2 | a0004 | c0004 | t0001 | g0269 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02698 | hp2 | a0003 | c0003 | t0001 | g0205 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02717 | hp1 | a0003 | c0003 | t0002 | g0159 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02735 | hp1 | a0003 | c0003 | t0001 | g0207 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0045 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02738 | hp2 | a0003 | c0003 | t0001 | g0224 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02896 | hp1 | a0003 | c0003 | t0001 | g0133 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0090 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02976 | hp2 | a0003 | c0003 | t0001 | g0115 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0015 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0195 | AFR | GWD | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03130 | hp1 | a0003 | c0003 | t0002 | g0160 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03195 | hp2 | a0001 | c0007 | t0001 | g0227 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0087 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03239 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0020 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0086 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03453 | hp2 | a0003 | c0003 | t0001 | g0214 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03516 | hp1 | a0003 | c0003 | t0001 | g0116 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0091 | AFR | ESN | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0097 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03654 | hp2 | a0004 | c0004 | t0001 | g0268 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | STU | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0283 | SAS | STU | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03704 | hp2 | a0003 | c0003 | t0001 | g0186 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03710 | hp1 | a0003 | c0003 | t0001 | g0222 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03710 | hp2 | a0002 | c0002 | t0005 | g0054 | SAS | PJL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0212 | SAS | BEB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03831 | hp2 | a0003 | c0003 | t0001 | g0174 | SAS | BEB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0213 | SAS | BEB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0036 | SAS | BEB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03942 | hp2 | a0003 | c0003 | t0001 | g0208 | SAS | BEB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG04184 | hp1 | a0003 | c0003 | t0001 | g0201 | SAS | BEB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0079 | SAS | BEB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG04199 | hp1 | a0003 | c0003 | t0001 | g0183 | SAS | STU | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0062 | SAS | STU | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0028 | SAS | STU | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | STU | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | CHB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18942 | hp2 | a0003 | c0003 | t0001 | g0127 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18957 | hp2 | a0003 | c0003 | t0001 | g0173 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18964 | hp2 | a0003 | c0003 | t0001 | g0180 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18971 | hp2 | a0003 | c0003 | t0001 | g0196 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18984 | hp1 | a0003 | c0003 | t0001 | g0175 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18992 | hp2 | a0003 | c0003 | t0001 | g0178 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18993 | hp1 | a0003 | c0003 | t0001 | g0197 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19005 | hp2 | a0003 | c0003 | t0001 | g0181 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | LWK | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | LWK | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0093 | AFR | LWK | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19054 | hp2 | a0003 | c0003 | t0001 | g0221 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19060 | hp1 | a0003 | c0003 | t0001 | g0179 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19064 | hp1 | a0003 | c0003 | t0001 | g0172 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19072 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19082 | hp2 | a0003 | c0003 | t0001 | g0182 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19090 | hp2 | a0003 | c0003 | t0001 | g0171 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19091 | hp2 | a0003 | c0003 | t0001 | g0170 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | YRI | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | YRI | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0105 | AFR | ASW | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | ASW | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | TSI | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | TSI | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | TSI | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20805 | hp2 | a0003 | c0003 | t0001 | g0301 | EUR | TSI | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0071 | SAS | GIH | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0198 | SAS | GIH | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0112 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | ACB | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0037 | AFR | USA | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | USA | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | USA | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | USA | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | LWK | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | LWK | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0304 | REF | REF | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0200 | REF | REF | PTPN12_chr7_77532295_77645069 | PTPN12 | chr7 | 77532295 | 77645069 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77618504 | G | A | 4 | a0001 a0002 a0004 others(1): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
missense_variant | MODERATE | c.964G>A | p.Val322Ile | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/18 | 1216/3384 | 964/2343 | 322/780 | chr7 | 77618504 | |||
| chr7:77627090 | A | G | 1 | a0005 | 2 | HG00738.hp2 HG01257.hp1 |
missense_variant | MODERATE | c.1411A>G | p.Ile471Val | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/18 | 1663/3384 | 1411/2343 | 471/780 | chr7 | 77627090 | |||
| chr7:77627396 | A | G | 2 | a0002 a0005 |
114 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(111): Show |
missense_variant | MODERATE | c.1717A>G | p.Thr573Ala | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/18 | 1969/3384 | 1717/2343 | 573/780 | chr7 | 77627396 | |||
| chr7:77635823 | G | A | 1 | a0004 | 6 | HG00099.hp2 HG00642.hp2 HG00741.hp1 others(3): Show |
missense_variant | MODERATE | c.2116G>A | p.Glu706Lys | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/18 | 2368/3384 | 2116/2343 | 706/780 | chr7 | 77635823 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77610785 | T | C | 1 | a0003c0006 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.783T>C | p.Asn261Asn | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 10/18 | 1035/3384 | 783/2343 | 261/780 | chr7 | 77610785 | |||
| chr7:77627002 | C | T | 1 | a0001c0007 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.1323C>T | p.Val441Val | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/18 | 1575/3384 | 1323/2343 | 441/780 | chr7 | 77627002 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77537386 | G | C | 1 | a0001c0001t0004 | 1 | HG03471.hp1 | 5_prime_UTR_variant | MODIFIER | c.-161G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/18 | 161 | chr7 | 77537386 | ||||||
| chr7:77639602 | A | G | 1 | a0003c0003t0002 | 3 | HG01243.hp1 HG02717.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*322A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 18/18 | 322 | chr7 | 77639602 | ||||||
| chr7:77639840 | G | A | 1 | a0002c0002t0005 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*560G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 18/18 | 560 | chr7 | 77639840 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77537675 | C | G | 2 | a0002c0002t0001g0309 a0002c0002t0001g0310 |
2 | NA18983.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.99+30C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77537675 | |||||||
| chr7:77537706 | C | A | 1 | a0003c0003t0001g0001 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.99+61C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77537706 | |||||||
| chr7:77537760 | G | T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.99+115G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77537760 | |||||||
| chr7:77537827 | G | A | 1 | a0002c0002t0001g0002 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.99+182G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77537827 | |||||||
| chr7:77537899 | C | G | 1 | a0002c0002t0001g0306 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.99+254C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77537899 | |||||||
| chr7:77537958 | T | G | 125 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(122): Show |
125 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.99+313T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77537958 | |||||||
| chr7:77537978 | C | CG | 59 | a0001c0001t0001g0135 a0001c0001t0001g0142 a0001c0001t0001g0223 others(56): Show |
59 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.99+344dupG | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77537978 | ||||||
| chr7:77537978 | CG | C | 168 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(165): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.99+344delG | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77537978 | ||||||
| chr7:77537983 | G | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99+338G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77537983 | |||||||
| chr7:77538054 | C | T | 3 | a0003c0003t0001g0301 a0003c0003t0001g0302 a0003c0003t0001g0303 |
3 | HG00140.hp2 HG01256.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.99+409C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538054 | |||||||
| chr7:77538247 | T | C | 120 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(117): Show |
120 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.99+602T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538247 | |||||||
| chr7:77538269 | C | G | 1 | a0002c0002t0001g0118 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.99+624C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538269 | |||||||
| chr7:77538323 | A | G | 2 | a0003c0003t0001g0299 a0003c0003t0001g0300 |
2 | HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.99+678A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538323 | |||||||
| chr7:77538477 | G | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | NA18980.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.99+832G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538477 | |||||||
| chr7:77538691 | A | G | 10 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 others(7): Show |
10 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+1046A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538691 | |||||||
| chr7:77538708 | A | G | 1 | a0003c0003t0001g0300 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.99+1063A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538708 | |||||||
| chr7:77538709 | C | A | 1 | a0003c0003t0001g0300 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.99+1064C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538709 | |||||||
| chr7:77538862 | A | G | 3 | a0003c0003t0001g0301 a0003c0003t0001g0302 a0003c0003t0001g0303 |
3 | HG00140.hp2 HG01256.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.99+1217A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538862 | |||||||
| chr7:77538875 | G | C | 1 | a0003c0003t0001g0127 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.99+1230G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538875 | |||||||
| chr7:77538924 | A | G | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+1279A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538924 | |||||||
| chr7:77538960 | A | G | 74 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0001g0120 others(71): Show |
74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.99+1315A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77538960 | |||||||
| chr7:77539040 | A | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02132.hp1 HG02523.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.99+1395A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539040 | |||||||
| chr7:77539068 | G | A | 174 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(171): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.99+1423G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539068 | |||||||
| chr7:77539218 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99+1573C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539218 | |||||||
| chr7:77539231 | G | C | 3 | a0003c0003t0001g0301 a0003c0003t0001g0302 a0003c0003t0001g0303 |
3 | HG00140.hp2 HG01256.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.99+1586G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539231 | |||||||
| chr7:77539243 | C | T | 1 | a0003c0003t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.99+1598C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539243 | |||||||
| chr7:77539301 | G | A | 114 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(111): Show |
114 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.99+1656G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539301 | |||||||
| chr7:77539347 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.99+1702T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539347 | |||||||
| chr7:77539576 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99+1931G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539576 | |||||||
| chr7:77539609 | T | TTTGG | 3 | a0003c0003t0001g0301 a0003c0003t0001g0302 a0003c0003t0001g0303 |
3 | HG00140.hp2 HG01256.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.99+1983_99+1986dup others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77539609 | ||||||
| chr7:77539629 | G | GT | 6 | a0001c0001t0001g0110 a0002c0002t0001g0109 a0002c0002t0001g0111 others(3): Show |
6 | HG02135.hp1 HG02451.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+1994dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77539629 | ||||||
| chr7:77539805 | G | C | 3 | a0003c0003t0001g0301 a0003c0003t0001g0302 a0003c0003t0001g0303 |
3 | HG00140.hp2 HG01256.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.99+2160G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77539805 | |||||||
| chr7:77540197 | A | G | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+2552A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540197 | |||||||
| chr7:77540219 | A | ATTTC | 3 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0116 |
3 | HG02559.hp1 HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.99+2598_99+2601dup others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77540219 | ||||||
| chr7:77540239 | C | CT | 47 | a0001c0001t0001g0114 a0001c0001t0001g0134 a0001c0001t0001g0135 others(44): Show |
47 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.99+2597dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77540239 | ||||||
| chr7:77540243 | C | T | 249 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(246): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.99+2598C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540243 | |||||||
| chr7:77540465 | C | G | 158 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0027 others(155): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.99+2820C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540465 | |||||||
| chr7:77540490 | C | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG00609.hp1 NA19003.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.99+2845C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540490 | |||||||
| chr7:77540537 | A | G | 1 | a0002c0002t0001g0109 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99+2892A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540537 | |||||||
| chr7:77540538 | G | T | 1 | a0002c0002t0001g0109 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99+2893G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540538 | |||||||
| chr7:77540539 | T | G | 1 | a0002c0002t0001g0109 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99+2894T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540539 | |||||||
| chr7:77540609 | A | G | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+2964A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540609 | |||||||
| chr7:77540647 | CT | C | 38 | a0001c0001t0001g0017 a0001c0001t0001g0114 a0001c0001t0001g0139 others(35): Show |
38 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.99+3015delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77540647 | ||||||
| chr7:77540933 | A | G | 1 | a0003c0003t0001g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.99+3288A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77540933 | |||||||
| chr7:77541015 | G | A | 4 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(1): Show |
4 | HG02559.hp1 HG02572.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+3370G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541015 | |||||||
| chr7:77541080 | G | C | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+3435G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541080 | |||||||
| chr7:77541280 | C | T | 112 | a0001c0001t0001g0027 a0002c0002t0001g0002 a0002c0002t0001g0006 others(109): Show |
112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.99+3635C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541280 | |||||||
| chr7:77541385 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+3740C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541385 | |||||||
| chr7:77541422 | T | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+3777T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541422 | |||||||
| chr7:77541465 | G | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0023 |
3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.99+3820G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541465 | |||||||
| chr7:77541556 | C | T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.99+3911C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541556 | |||||||
| chr7:77541566 | C | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG00609.hp1 NA19003.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.99+3921C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541566 | |||||||
| chr7:77541603 | C | G | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+3958C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541603 | |||||||
| chr7:77541686 | G | C | 1 | a0003c0003t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+4041G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541686 | |||||||
| chr7:77541745 | A | G | 6 | a0002c0002t0001g0018 a0002c0002t0001g0104 a0002c0002t0001g0105 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+4100A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77541745 | |||||||
| chr7:77542013 | TA | T | 258 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(255): Show |
258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.99+4370delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77542013 | ||||||
| chr7:77542030 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+4385C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542030 | |||||||
| chr7:77542155 | T | G | 7 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(4): Show |
7 | HG01243.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+4510T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542155 | |||||||
| chr7:77542300 | T | C | 258 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(255): Show |
258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.99+4655T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542300 | |||||||
| chr7:77542318 | G | A | 7 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(4): Show |
7 | HG01243.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+4673G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542318 | |||||||
| chr7:77542417 | T | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+4772T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542417 | |||||||
| chr7:77542497 | G | A | 1 | a0003c0003t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+4852G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542497 | |||||||
| chr7:77542612 | G | A | 1 | a0002c0002t0001g0024 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99+4967G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542612 | |||||||
| chr7:77542637 | G | A | 267 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(264): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.99+4992G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542637 | |||||||
| chr7:77542646 | C | T | 1 | a0002c0002t0001g0016 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.99+5001C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542646 | |||||||
| chr7:77542660 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+5015C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542660 | |||||||
| chr7:77542692 | A | G | 8 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(5): Show |
8 | HG01891.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+5047A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542692 | |||||||
| chr7:77542818 | G | C | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+5173G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542818 | |||||||
| chr7:77542823 | A | C | 1 | a0001c0001t0001g0219 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.99+5178A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542823 | |||||||
| chr7:77542959 | G | C | 3 | a0003c0003t0001g0183 a0003c0003t0001g0224 a0003c0003t0001g0283 |
3 | HG02738.hp2 HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.99+5314G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542959 | |||||||
| chr7:77542987 | A | C | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+5342A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77542987 | |||||||
| chr7:77543039 | C | G | 6 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0116 others(3): Show |
6 | HG01243.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+5394C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543039 | |||||||
| chr7:77543078 | A | G | 6 | a0002c0002t0001g0098 a0002c0002t0001g0099 a0002c0002t0001g0100 others(3): Show |
6 | HG01952.hp1 HG01975.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+5433A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543078 | |||||||
| chr7:77543133 | G | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+5488G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543133 | |||||||
| chr7:77543266 | A | AT | 236 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(233): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.99+5629dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77543266 | ||||||
| chr7:77543344 | CT | C | 152 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0130 others(149): Show |
152 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.99+5715delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77543344 | ||||||
| chr7:77543344 | CTT | C | 87 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(84): Show |
87 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.99+5714_99+5715del others(2): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77543344 | ||||||
| chr7:77543360 | T | A | 1 | a0003c0003t0001g0207 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.99+5715T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543360 | |||||||
| chr7:77543482 | C | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.99+5837C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543482 | |||||||
| chr7:77543557 | T | G | 1 | a0002c0002t0001g0028 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.99+5912T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543557 | |||||||
| chr7:77543566 | G | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+5921G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543566 | |||||||
| chr7:77543650 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+6005C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543650 | |||||||
| chr7:77543698 | C | T | 1 | a0002c0002t0001g0015 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.99+6053C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543698 | |||||||
| chr7:77543885 | G | A | 42 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(39): Show |
42 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.99+6240G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543885 | |||||||
| chr7:77543889 | C | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+6244C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543889 | |||||||
| chr7:77543956 | G | A | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.99+6311G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543956 | |||||||
| chr7:77543966 | G | A | 252 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(249): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.99+6321G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77543966 | |||||||
| chr7:77544149 | G | C | 236 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(233): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.99+6504G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77544149 | |||||||
| chr7:77544392 | C | T | 11 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(8): Show |
11 | HG00609.hp1 HG00735.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+6747C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77544392 | |||||||
| chr7:77544633 | G | T | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+6988G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77544633 | |||||||
| chr7:77544804 | G | A | 156 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(153): Show |
156 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.99+7159G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77544804 | |||||||
| chr7:77544819 | A | T | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+7174A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77544819 | |||||||
| chr7:77544928 | T | C | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+7283T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77544928 | |||||||
| chr7:77545031 | T | C | 46 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(43): Show |
46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.99+7386T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77545031 | |||||||
| chr7:77545102 | T | C | 2 | a0002c0002t0001g0029 a0002c0002t0001g0030 |
2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.99+7457T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77545102 | |||||||
| chr7:77545180 | T | G | 46 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(43): Show |
46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.99+7535T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77545180 | |||||||
| chr7:77545498 | TATG | T | 4 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
4 | HG02615.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+7856_99+7858del others(3): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77545498 | ||||||
| chr7:77545564 | A | AT | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+7921dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77545564 | ||||||
| chr7:77545580 | C | G | 1 | a0003c0003t0001g0210 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.99+7935C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77545580 | |||||||
| chr7:77545632 | T | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+7987T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77545632 | |||||||
| chr7:77545967 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.99+8322T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77545967 | |||||||
| chr7:77545988 | G | A | 3 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0002g0161 |
3 | HG01243.hp1 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.99+8343G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77545988 | |||||||
| chr7:77546017 | C | T | 1 | a0002c0002t0001g0095 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.99+8372C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546017 | |||||||
| chr7:77546030 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.99+8385C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546030 | |||||||
| chr7:77546049 | G | A | 1 | a0002c0002t0001g0031 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.99+8404G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546049 | |||||||
| chr7:77546235 | A | G | 1 | a0002c0002t0001g0094 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.99+8590A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546235 | |||||||
| chr7:77546251 | A | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+8606A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546251 | |||||||
| chr7:77546257 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+8612C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546257 | |||||||
| chr7:77546487 | A | C | 1 | a0002c0002t0001g0014 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.99+8842A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546487 | |||||||
| chr7:77546575 | G | T | 1 | a0003c0003t0001g0303 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.99+8930G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546575 | |||||||
| chr7:77546577 | A | G | 1 | a0003c0003t0001g0303 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.99+8932A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546577 | |||||||
| chr7:77546662 | G | A | 111 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(108): Show |
111 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.99+9017G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546662 | |||||||
| chr7:77546693 | C | T | 1 | a0003c0003t0001g0209 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.99+9048C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546693 | |||||||
| chr7:77546770 | T | TA | 9 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0229 others(6): Show |
9 | HG02818.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+9126dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77546770 | ||||||
| chr7:77546904 | T | C | 246 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(243): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.99+9259T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77546904 | |||||||
| chr7:77547015 | G | A | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+9370G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77547015 | |||||||
| chr7:77547073 | A | G | 81 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(78): Show |
81 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.99+9428A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77547073 | |||||||
| chr7:77547128 | TGTCTCTG others(13): Show |
T | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+9510_99+9529del others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77547128 | ||||||
| chr7:77547269 | T | C | 6 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(3): Show |
6 | NA18946.hp1 NA18981.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+9624T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77547269 | |||||||
| chr7:77547558 | T | C | 2 | a0002c0002t0001g0284 a0002c0002t0001g0285 |
2 | HG00423.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.99+9913T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77547558 | |||||||
| chr7:77548056 | A | G | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+10411A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77548056 | |||||||
| chr7:77548706 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+11061T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77548706 | |||||||
| chr7:77548939 | A | G | 1 | a0002c0002t0001g0118 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.99+11294A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77548939 | |||||||
| chr7:77549199 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99+11554G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77549199 | |||||||
| chr7:77549586 | T | G | 17 | a0001c0001t0001g0117 a0001c0001t0001g0130 a0001c0001t0001g0131 others(14): Show |
17 | HG00639.hp1 HG01243.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+11941T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77549586 | |||||||
| chr7:77549590 | T | G | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0004g0132 others(1): Show |
4 | HG02572.hp2 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+11945T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77549590 | |||||||
| chr7:77549704 | G | C | 7 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(4): Show |
7 | HG01243.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+12059G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77549704 | |||||||
| chr7:77549806 | C | T | 1 | a0002c0002t0001g0111 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.99+12161C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77549806 | |||||||
| chr7:77549817 | G | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+12172G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77549817 | |||||||
| chr7:77549871 | T | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+12226T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77549871 | |||||||
| chr7:77550203 | T | G | 5 | a0001c0001t0001g0110 a0001c0001t0001g0162 a0001c0001t0001g0163 others(2): Show |
5 | HG00280.hp1 HG00323.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+12558T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77550203 | |||||||
| chr7:77550398 | C | T | 256 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(253): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.99+12753C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77550398 | |||||||
| chr7:77550598 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | NA19056.hp1 NA19079.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.99+12953C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77550598 | |||||||
| chr7:77550683 | A | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+13038A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77550683 | |||||||
| chr7:77550718 | G | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+13073G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77550718 | |||||||
| chr7:77550808 | T | A | 8 | a0003c0003t0001g0185 a0003c0003t0001g0186 a0003c0003t0001g0187 others(5): Show |
8 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+13163T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77550808 | |||||||
| chr7:77550935 | G | GTC | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+13290_99+13291i others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77550935 | |||||||
| chr7:77551105 | G | T | 3 | a0002c0002t0001g0090 a0002c0002t0001g0091 a0002c0002t0001g0092 |
3 | HG02922.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.99+13460G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551105 | |||||||
| chr7:77551221 | C | A | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.99+13576C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551221 | |||||||
| chr7:77551289 | T | G | 246 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(243): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.99+13644T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551289 | |||||||
| chr7:77551308 | G | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(72): Show |
75 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.99+13663G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551308 | |||||||
| chr7:77551328 | T | A | 1 | a0002c0002t0001g0111 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.99+13683T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551328 | |||||||
| chr7:77551373 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+13728C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551373 | |||||||
| chr7:77551415 | C | T | 245 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(242): Show |
245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.99+13770C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551415 | |||||||
| chr7:77551551 | A | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+13906A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551551 | |||||||
| chr7:77551601 | A | C | 1 | a0002c0002t0001g0089 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.99+13956A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551601 | |||||||
| chr7:77551835 | T | C | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+14190T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77551835 | |||||||
| chr7:77552009 | T | C | 112 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(109): Show |
112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.99+14364T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77552009 | |||||||
| chr7:77552037 | C | T | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.99+14392C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77552037 | |||||||
| chr7:77552074 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.99+14429A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77552074 | |||||||
| chr7:77552210 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.99+14565G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77552210 | |||||||
| chr7:77552280 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.99+14635G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77552280 | |||||||
| chr7:77552300 | GT | G | 101 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(98): Show |
101 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.99+14668delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77552300 | ||||||
| chr7:77552355 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.99+14710C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77552355 | |||||||
| chr7:77552878 | T | A | 1 | a0001c0001t0001g0243 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.99+15233T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77552878 | |||||||
| chr7:77552972 | G | A | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+15327G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77552972 | |||||||
| chr7:77553266 | G | A | 5 | a0001c0001t0001g0110 a0001c0001t0001g0162 a0001c0001t0001g0163 others(2): Show |
5 | HG00280.hp1 HG00323.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+15621G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77553266 | |||||||
| chr7:77553289 | G | T | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+15644G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77553289 | |||||||
| chr7:77553480 | A | T | 1 | a0002c0002t0001g0103 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.99+15835A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77553480 | |||||||
| chr7:77553534 | A | C | 1 | a0001c0001t0004g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.99+15889A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77553534 | |||||||
| chr7:77553534 | A | T | 160 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(157): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.99+15889A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77553534 | |||||||
| chr7:77553763 | C | G | 1 | a0001c0001t0001g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.99+16118C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77553763 | |||||||
| chr7:77553807 | A | C | 1 | a0001c0001t0001g0139 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.99+16162A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77553807 | |||||||
| chr7:77553851 | A | AT | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(121): Show |
124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.99+16217dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77553851 | ||||||
| chr7:77553851 | A | ATT | 112 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(109): Show |
112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.99+16216_99+16217d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77553851 | ||||||
| chr7:77553908 | CAT | C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(70): Show |
73 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.99+16266_99+16267d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77553908 | ||||||
| chr7:77553945 | CT | C | 246 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(243): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.99+16311delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77553945 | ||||||
| chr7:77554085 | C | T | 161 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(158): Show |
161 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.99+16440C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77554085 | |||||||
| chr7:77554250 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+16605C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77554250 | |||||||
| chr7:77554326 | C | G | 1 | a0002c0002t0001g0306 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.99+16681C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77554326 | |||||||
| chr7:77554691 | T | C | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-16387T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77554691 | |||||||
| chr7:77554699 | A | G | 160 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(157): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.100-16379A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77554699 | |||||||
| chr7:77554713 | T | G | 1 | a0002c0002t0001g0220 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.100-16365T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77554713 | |||||||
| chr7:77554848 | T | G | 1 | a0002c0002t0001g0089 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.100-16230T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77554848 | |||||||
| chr7:77555083 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-15995C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77555083 | |||||||
| chr7:77555193 | C | T | 111 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(108): Show |
111 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.100-15885C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77555193 | |||||||
| chr7:77555206 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-15872C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77555206 | |||||||
| chr7:77555218 | CT | C | 11 | a0001c0001t0001g0110 a0001c0001t0001g0290 a0001c0001t0001g0305 others(8): Show |
11 | HG01109.hp2 HG01243.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-15846delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77555218 | ||||||
| chr7:77555434 | C | A | 1 | a0002c0002t0001g0089 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.100-15644C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77555434 | |||||||
| chr7:77555452 | C | T | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-15626C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77555452 | |||||||
| chr7:77555598 | T | C | 1 | a0001c0001t0004g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100-15480T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77555598 | |||||||
| chr7:77555609 | T | A | 2 | a0002c0002t0001g0032 a0002c0002t0001g0033 |
2 | HG00609.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.100-15469T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77555609 | |||||||
| chr7:77555832 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.100-15246G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77555832 | |||||||
| chr7:77556048 | GGTGTTTG others(5): Show |
G | 1 | a0001c0001t0001g0277 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.100-15029_100-1501 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77556048 | |||||||
| chr7:77556049 | G | GTGTT | 5 | a0003c0003t0001g0020 a0003c0003t0001g0286 a0003c0003t0001g0301 others(2): Show |
5 | HG00140.hp2 HG01256.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-15005_100-1500 others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77556049 | ||||||
| chr7:77556049 | GTGTTTGT others(5): Show |
G | 240 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(237): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.100-15013_100-1500 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77556049 | ||||||
| chr7:77556146 | C | T | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-14932C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77556146 | |||||||
| chr7:77556338 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-14740C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77556338 | |||||||
| chr7:77556602 | C | T | 1 | a0003c0003t0001g0208 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.100-14476C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77556602 | |||||||
| chr7:77556634 | G | A | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-14444G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77556634 | |||||||
| chr7:77556952 | TTTTG | T | 160 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(157): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.100-14110_100-1410 others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77556952 | ||||||
| chr7:77556978 | GT | G | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(69): Show |
72 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.100-14090delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77556978 | ||||||
| chr7:77557000 | G | A | 1 | a0001c0007t0001g0227 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.100-14078G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557000 | |||||||
| chr7:77557213 | C | T | 2 | a0002c0002t0001g0006 a0002c0002t0001g0013 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.100-13865C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557213 | |||||||
| chr7:77557266 | C | G | 1 | a0001c0001t0001g0274 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.100-13812C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557266 | |||||||
| chr7:77557392 | C | T | 1 | a0002c0002t0001g0085 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.100-13686C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557392 | |||||||
| chr7:77557563 | T | G | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.100-13515T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557563 | |||||||
| chr7:77557626 | A | C | 1 | a0002c0002t0001g0031 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.100-13452A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557626 | |||||||
| chr7:77557675 | C | G | 1 | a0001c0001t0001g0126 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.100-13403C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557675 | |||||||
| chr7:77557797 | CA | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0004g0132 |
3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-13280delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557797 | |||||||
| chr7:77557945 | T | C | 7 | a0002c0002t0001g0018 a0002c0002t0001g0086 a0002c0002t0001g0087 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-13133T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557945 | |||||||
| chr7:77557990 | C | T | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-13088C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77557990 | |||||||
| chr7:77558210 | CA | C | 125 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(122): Show |
125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.100-12851delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77558210 | ||||||
| chr7:77558210 | CAA | C | 12 | a0001c0001t0001g0125 a0001c0001t0001g0136 a0001c0001t0001g0273 others(9): Show |
12 | HG01243.hp1 HG02055.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.100-12852_100-1285 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77558210 | ||||||
| chr7:77558283 | C | A | 2 | a0002c0002t0001g0034 a0002c0002t0001g0035 |
2 | HG01169.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.100-12795C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77558283 | |||||||
| chr7:77558535 | A | C | 9 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0229 others(6): Show |
9 | HG02818.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-12543A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77558535 | |||||||
| chr7:77558574 | C | T | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-12504C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77558574 | |||||||
| chr7:77558741 | A | G | 256 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(253): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.100-12337A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77558741 | |||||||
| chr7:77558847 | A | C | 1 | a0002c0002t0001g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.100-12231A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77558847 | |||||||
| chr7:77559003 | GA | G | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-12074delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77559003 | |||||||
| chr7:77559004 | A | ACT | 5 | a0002c0002t0001g0006 a0002c0002t0001g0011 a0002c0002t0001g0012 others(2): Show |
5 | HG02257.hp2 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-12065_100-1206 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77559004 | ||||||
| chr7:77559040 | G | C | 1 | a0002c0002t0001g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.100-12038G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77559040 | |||||||
| chr7:77559155 | C | T | 2 | a0002c0002t0001g0084 a0002c0002t0001g0097 |
2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.100-11923C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77559155 | |||||||
| chr7:77559216 | G | A | 3 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0023 |
3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.100-11862G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77559216 | |||||||
| chr7:77559321 | T | C | 247 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(244): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.100-11757T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77559321 | |||||||
| chr7:77559581 | CT | C | 36 | a0001c0001t0001g0114 a0001c0001t0001g0135 a0001c0001t0001g0139 others(33): Show |
36 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.100-11495delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77559581 | ||||||
| chr7:77559584 | C | T | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(70): Show |
73 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.100-11494C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77559584 | |||||||
| chr7:77559604 | A | G | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.100-11474A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77559604 | |||||||
| chr7:77559766 | A | AT | 112 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(109): Show |
112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.100-11310dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77559766 | ||||||
| chr7:77559830 | G | A | 1 | a0002c0002t0001g0099 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.100-11248G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77559830 | |||||||
| chr7:77560077 | A | G | 2 | a0001c0001t0001g0287 a0001c0001t0001g0294 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.100-11001A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560077 | |||||||
| chr7:77560098 | A | G | 1 | a0002c0002t0001g0306 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.100-10980A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560098 | |||||||
| chr7:77560279 | C | T | 1 | a0002c0002t0001g0014 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.100-10799C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560279 | |||||||
| chr7:77560284 | G | A | 161 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(158): Show |
161 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.100-10794G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560284 | |||||||
| chr7:77560478 | A | G | 4 | a0002c0002t0001g0006 a0002c0002t0001g0011 a0002c0002t0001g0012 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-10600A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560478 | |||||||
| chr7:77560527 | AACC | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-10547_100-1054 others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77560527 | ||||||
| chr7:77560592 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-10486C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560592 | |||||||
| chr7:77560623 | G | A | 1 | a0003c0003t0001g0210 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.100-10455G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560623 | |||||||
| chr7:77560753 | T | C | 79 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(76): Show |
79 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.100-10325T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560753 | |||||||
| chr7:77560834 | A | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-10244A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560834 | |||||||
| chr7:77560971 | C | T | 1 | a0002c0002t0001g0220 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.100-10107C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77560971 | |||||||
| chr7:77561057 | T | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.100-10021T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561057 | |||||||
| chr7:77561128 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.100-9950C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561128 | |||||||
| chr7:77561232 | G | T | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100-9846G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561232 | |||||||
| chr7:77561549 | C | T | 256 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(253): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.100-9529C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561549 | |||||||
| chr7:77561602 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.100-9476A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561602 | |||||||
| chr7:77561614 | G | A | 2 | a0002c0002t0001g0002 a0002c0002t0001g0037 |
2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.100-9464G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561614 | |||||||
| chr7:77561681 | G | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-9397G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561681 | |||||||
| chr7:77561759 | TTTAA | T | 253 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(250): Show |
253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.100-9296_100-9293d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77561759 | ||||||
| chr7:77561768 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-9310T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561768 | |||||||
| chr7:77561782 | A | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-9296A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561782 | |||||||
| chr7:77561783 | A | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-9295A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561783 | |||||||
| chr7:77561784 | T | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-9294T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561784 | |||||||
| chr7:77561855 | G | A | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-9223G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561855 | |||||||
| chr7:77561860 | C | G | 3 | a0002c0002t0001g0018 a0002c0002t0001g0107 a0002c0002t0001g0108 |
3 | HG01070.hp2 HG01071.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.100-9218C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561860 | |||||||
| chr7:77561946 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0276 |
2 | NA18998.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.100-9132C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561946 | |||||||
| chr7:77561994 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-9084G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77561994 | |||||||
| chr7:77562065 | A | G | 9 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0229 others(6): Show |
9 | HG02818.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-9013A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77562065 | |||||||
| chr7:77562217 | C | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-8861C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77562217 | |||||||
| chr7:77562656 | G | T | 1 | a0002c0002t0001g0083 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.100-8422G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77562656 | |||||||
| chr7:77562688 | G | T | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-8390G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77562688 | |||||||
| chr7:77562797 | A | G | 5 | a0002c0002t0001g0018 a0002c0002t0001g0107 a0002c0002t0001g0108 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-8281A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77562797 | |||||||
| chr7:77562854 | T | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-8224T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77562854 | |||||||
| chr7:77562885 | A | G | 1 | a0002c0002t0001g0279 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.100-8193A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77562885 | |||||||
| chr7:77562949 | T | C | 2 | a0003c0003t0001g0112 a0003c0003t0001g0116 |
2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.100-8129T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77562949 | |||||||
| chr7:77562958 | C | CA | 7 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0003c0003t0001g0020 others(4): Show |
7 | HG00140.hp2 HG01256.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-8107dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77562958 | ||||||
| chr7:77562958 | C | CAA | 56 | a0001c0001t0001g0114 a0001c0001t0001g0129 a0001c0001t0001g0130 others(53): Show |
56 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.100-8108_100-8107d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77562958 | ||||||
| chr7:77562958 | C | CAAA | 112 | a0001c0001t0001g0110 a0001c0001t0001g0165 a0002c0002t0001g0002 others(109): Show |
112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.100-8109_100-8107d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77562958 | ||||||
| chr7:77562958 | C | CAAAA | 80 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(77): Show |
80 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.100-8110_100-8107d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77562958 | ||||||
| chr7:77563103 | T | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-7975T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77563103 | |||||||
| chr7:77563481 | G | T | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-7597G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77563481 | |||||||
| chr7:77563538 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.100-7540G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77563538 | |||||||
| chr7:77564149 | G | A | 1 | a0003c0003t0001g0113 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.100-6929G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564149 | |||||||
| chr7:77564176 | G | A | 2 | a0002c0002t0001g0029 a0002c0002t0001g0030 |
2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100-6902G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564176 | |||||||
| chr7:77564215 | T | A | 1 | a0001c0001t0001g0166 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.100-6863T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564215 | |||||||
| chr7:77564249 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.100-6829G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564249 | |||||||
| chr7:77564656 | T | G | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-6422T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564656 | |||||||
| chr7:77564746 | G | GT | 14 | a0001c0001t0004g0132 a0003c0003t0001g0112 a0003c0003t0001g0133 others(11): Show |
14 | HG01167.hp1 HG01261.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-6302dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTGTTTTT others(2): Show |
6 | a0002c0002t0001g0025 a0002c0002t0001g0038 a0002c0002t0001g0039 others(3): Show |
6 | NA18939.hp1 NA18946.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-6331_100-6330i others(11): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTGTTTTT others(3): Show |
1 | a0002c0002t0001g0041 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.100-6331_100-6330i others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTT | 10 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0003c0003t0001g0113 others(7): Show |
10 | HG00735.hp2 HG00738.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-6303_100-6302d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTGTTT others(3): Show |
1 | a0002c0002t0001g0042 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.100-6329_100-6328i others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTT | 20 | a0001c0001t0001g0019 a0001c0001t0001g0117 a0001c0001t0001g0119 others(17): Show |
20 | HG00438.hp2 HG02015.hp1 HG02523.hp1 others(17): Show |
intron_variant | MODIFIER | c.100-6305_100-6302d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTTT | 13 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(10): Show |
13 | HG01243.hp1 HG02132.hp1 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-6306_100-6302d others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTTTT | 20 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0027 others(17): Show |
20 | HG00673.hp1 HG01074.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-6307_100-6302d others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTTTTT | 31 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0234 others(28): Show |
31 | HG00423.hp1 HG00738.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.100-6308_100-6302d others(9): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTTTTT others(1): Show |
33 | a0001c0001t0001g0135 a0001c0001t0001g0237 a0001c0001t0001g0238 others(30): Show |
33 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.100-6309_100-6302d others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTTTTT others(2): Show |
17 | a0001c0001t0001g0233 a0002c0002t0001g0010 a0002c0002t0001g0013 others(14): Show |
17 | HG00140.hp1 HG00733.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-6310_100-6302d others(11): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTTTTT others(3): Show |
17 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0001g0162 others(14): Show |
17 | HG00673.hp2 HG01243.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-6311_100-6302d others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTTTTT others(4): Show |
7 | a0001c0001t0001g0137 a0001c0001t0001g0239 a0002c0002t0001g0022 others(4): Show |
7 | HG02109.hp2 HG03486.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-6312_100-6302d others(13): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTTTTT others(5): Show |
2 | a0001c0001t0001g0138 a0002c0002t0001g0088 |
2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.100-6313_100-6302d others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTTTTT others(6): Show |
2 | a0001c0001t0001g0280 a0004c0004t0001g0270 |
2 | HG00099.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.100-6314_100-6302d others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTTTTT others(7): Show |
1 | a0001c0001t0001g0225 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.100-6315_100-6302d others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTTTTT others(8): Show |
5 | a0002c0002t0001g0033 a0002c0002t0001g0081 a0002c0002t0001g0084 others(2): Show |
5 | HG00408.hp2 HG00609.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-6316_100-6302d others(17): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTTTTT others(9): Show |
4 | a0001c0001t0001g0110 a0002c0002t0001g0018 a0002c0002t0001g0082 others(1): Show |
4 | HG01070.hp2 HG02135.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-6317_100-6302d others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTTTTT others(10): Show |
1 | a0002c0002t0001g0107 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.100-6318_100-6302d others(19): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTTTTT others(11): Show |
1 | a0002c0002t0001g0212 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.100-6319_100-6302d others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTTTTT others(14): Show |
3 | a0002c0002t0001g0092 a0002c0002t0001g0097 a0002c0002t0001g0108 |
3 | HG02293.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.100-6322_100-6302d others(23): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | G | GTTTTTTT others(15): Show |
1 | a0002c0002t0001g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.100-6323_100-6302d others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | GTTTTTTT others(3): Show |
G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-6311_100-6302d others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | GTTTTTTT others(6): Show |
G | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.100-6314_100-6302d others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564746 | GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0001g0245 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.100-6315_100-6302d others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564746 | ||||||
| chr7:77564748 | T | TTTTTTG | 11 | a0001c0001t0001g0114 a0001c0001t0001g0146 a0001c0001t0001g0148 others(8): Show |
11 | HG00609.hp1 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-6325_100-6324i others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564748 | ||||||
| chr7:77564749 | T | TTTTTG | 22 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(19): Show |
22 | HG00280.hp2 HG00735.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.100-6325_100-6324i others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564749 | ||||||
| chr7:77564761 | T | G | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-6317T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564761 | |||||||
| chr7:77564762 | T | G | 1 | a0001c0001t0001g0290 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-6316T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564762 | |||||||
| chr7:77564795 | T | G | 248 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(245): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.100-6283T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564795 | |||||||
| chr7:77564796 | G | T | 248 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(245): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.100-6282G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564796 | |||||||
| chr7:77564820 | C | T | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-6258C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564820 | |||||||
| chr7:77564886 | T | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-6192T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564886 | |||||||
| chr7:77564960 | G | T | 2 | a0002c0002t0001g0072 a0002c0002t0001g0073 |
2 | HG01099.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.100-6118G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77564960 | |||||||
| chr7:77564979 | A | ATCTCCTG others(86): Show |
4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-6097_100-6005d others(95): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77564979 | ||||||
| chr7:77565182 | G | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-5896G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77565182 | |||||||
| chr7:77565462 | T | G | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-5616T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77565462 | |||||||
| chr7:77565477 | G | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-5601G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77565477 | |||||||
| chr7:77565494 | C | G | 1 | a0002c0002t0001g0080 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.100-5584C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77565494 | |||||||
| chr7:77565544 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.100-5534T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77565544 | |||||||
| chr7:77566082 | A | G | 1 | a0004c0004t0001g0269 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.100-4996A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566082 | |||||||
| chr7:77566113 | A | G | 248 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(245): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.100-4965A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566113 | |||||||
| chr7:77566138 | G | A | 46 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(43): Show |
46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.100-4940G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566138 | |||||||
| chr7:77566178 | A | G | 255 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(252): Show |
255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.100-4900A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566178 | |||||||
| chr7:77566222 | A | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-4856A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566222 | |||||||
| chr7:77566361 | T | C | 1 | a0003c0003t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.100-4717T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566361 | |||||||
| chr7:77566596 | A | G | 1 | a0002c0002t0001g0058 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.100-4482A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566596 | |||||||
| chr7:77566599 | G | A | 1 | a0001c0001t0004g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100-4479G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566599 | |||||||
| chr7:77566705 | CAG | C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(70): Show |
73 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.100-4370_100-4369d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77566705 | ||||||
| chr7:77566823 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.100-4255G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566823 | |||||||
| chr7:77566886 | A | G | 3 | a0002c0002t0001g0104 a0002c0002t0001g0105 a0002c0002t0001g0106 |
3 | HG01256.hp2 HG01258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.100-4192A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77566886 | |||||||
| chr7:77567115 | A | G | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-3963A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567115 | |||||||
| chr7:77567195 | T | TA | 45 | a0001c0001t0001g0122 a0001c0001t0001g0243 a0001c0001t0001g0297 others(42): Show |
45 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.100-3868dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77567195 | ||||||
| chr7:77567195 | TA | T | 7 | a0001c0001t0001g0295 a0002c0002t0001g0048 a0002c0002t0001g0055 others(4): Show |
7 | HG01081.hp1 HG01358.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-3868delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77567195 | ||||||
| chr7:77567214 | G | A | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0004g0132 |
3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-3864G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567214 | |||||||
| chr7:77567253 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.100-3825G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567253 | |||||||
| chr7:77567269 | T | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0004g0132 |
3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-3809T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567269 | |||||||
| chr7:77567456 | G | A | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100-3622G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567456 | |||||||
| chr7:77567573 | A | G | 5 | a0002c0002t0001g0098 a0002c0002t0001g0100 a0002c0002t0001g0101 others(2): Show |
5 | HG01952.hp1 HG01975.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-3505A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567573 | |||||||
| chr7:77567614 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-3464C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567614 | |||||||
| chr7:77567632 | A | ATG | 4 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(1): Show |
4 | HG00280.hp2 HG01358.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3443_100-3442d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 77567632 | ||||||
| chr7:77567900 | G | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-3178G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567900 | |||||||
| chr7:77567986 | T | C | 277 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.100-3092T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77567986 | |||||||
| chr7:77568236 | G | T | 1 | a0003c0003t0001g0181 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.100-2842G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568236 | |||||||
| chr7:77568250 | C | T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.100-2828C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568250 | |||||||
| chr7:77568315 | T | C | 246 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(243): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.100-2763T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568315 | |||||||
| chr7:77568316 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-2762G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568316 | |||||||
| chr7:77568373 | C | T | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-2705C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568373 | |||||||
| chr7:77568392 | T | C | 1 | a0002c0002t0001g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.100-2686T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568392 | |||||||
| chr7:77568455 | A | G | 6 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-2623A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568455 | |||||||
| chr7:77568638 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.100-2440G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568638 | |||||||
| chr7:77568847 | A | AT | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-2231_100-2230i others(3): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568847 | |||||||
| chr7:77568850 | A | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-2228A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568850 | |||||||
| chr7:77568899 | C | G | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-2179C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77568899 | |||||||
| chr7:77569396 | A | T | 5 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(2): Show |
5 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-1682A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77569396 | |||||||
| chr7:77569433 | T | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.100-1645T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77569433 | |||||||
| chr7:77569671 | T | C | 1 | a0002c0002t0001g0084 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.100-1407T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77569671 | |||||||
| chr7:77569678 | C | T | 1 | a0002c0002t0001g0045 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.100-1400C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77569678 | |||||||
| chr7:77569718 | C | T | 2 | a0003c0003t0001g0299 a0003c0003t0001g0300 |
2 | HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.100-1360C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77569718 | |||||||
| chr7:77569725 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.100-1353C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77569725 | |||||||
| chr7:77570012 | A | G | 1 | a0002c0002t0001g0057 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.100-1066A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77570012 | |||||||
| chr7:77570162 | C | G | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-916C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77570162 | |||||||
| chr7:77570349 | T | C | 256 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(253): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.100-729T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77570349 | |||||||
| chr7:77570351 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.100-727A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77570351 | |||||||
| chr7:77570647 | T | C | 6 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(3): Show |
6 | NA18946.hp1 NA18981.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-431T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77570647 | |||||||
| chr7:77570828 | A | G | 1 | a0002c0002t0001g0082 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.100-250A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77570828 | |||||||
| chr7:77571035 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.100-43C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77571035 | |||||||
| chr7:77571043 | C | G | 4 | a0003c0003t0001g0003 a0003c0003t0001g0178 a0003c0003t0001g0179 others(1): Show |
4 | HG00408.hp1 NA18964.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-35C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77571043 | |||||||
| chr7:77571075 | A | T | 80 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(77): Show |
80 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(77): Show |
splice_region_variant&intron_variant | LOW | c.100-3A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 1/17 | chr7 | 77571075 | |||||||
| chr7:77571320 | A | T | 8 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(5): Show |
8 | HG02080.hp2 HG02132.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.208+134A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571320 | |||||||
| chr7:77571508 | C | G | 1 | a0002c0002t0001g0100 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.208+322C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571508 | |||||||
| chr7:77571572 | A | G | 112 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(109): Show |
112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.208+386A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571572 | |||||||
| chr7:77571608 | A | G | 1 | a0002c0002t0005g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.208+422A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571608 | |||||||
| chr7:77571628 | T | G | 1 | a0001c0001t0001g0249 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.208+442T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571628 | |||||||
| chr7:77571695 | TTTTA | T | 171 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(168): Show |
171 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.208+533_208+536del others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77571695 | ||||||
| chr7:77571695 | TTTTATTT others(1): Show |
T | 79 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(76): Show |
79 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.208+529_208+536del others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77571695 | ||||||
| chr7:77571695 | TTTTATTT others(5): Show |
T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+525_208+536del others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77571695 | ||||||
| chr7:77571719 | A | ATTTG | 3 | a0003c0003t0001g0195 a0003c0003t0001g0202 a0003c0003t0001g0214 |
3 | HG02257.hp1 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.208+549_208+552dup others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77571719 | ||||||
| chr7:77571719 | A | G | 9 | a0002c0002t0001g0007 a0002c0002t0001g0008 a0002c0002t0001g0014 others(6): Show |
9 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.208+533A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571719 | |||||||
| chr7:77571795 | C | T | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.208+609C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571795 | |||||||
| chr7:77571952 | G | A | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.208+766G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571952 | |||||||
| chr7:77571993 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208+807C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77571993 | |||||||
| chr7:77572098 | CT | C | 11 | a0001c0001t0001g0155 a0001c0001t0001g0307 a0001c0001t0001g0308 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.208+928delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77572098 | ||||||
| chr7:77572098 | CTT | C | 245 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(242): Show |
245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.208+927_208+928del others(2): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77572098 | ||||||
| chr7:77572342 | G | C | 8 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(5): Show |
8 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+1156G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77572342 | |||||||
| chr7:77572541 | TTTG | T | 79 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(76): Show |
79 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.208+1361_208+1363d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77572541 | ||||||
| chr7:77572678 | A | G | 5 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0292 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+1492A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77572678 | |||||||
| chr7:77572851 | G | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+1665G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77572851 | |||||||
| chr7:77572919 | T | C | 248 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(245): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.208+1733T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77572919 | |||||||
| chr7:77572968 | A | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+1782A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77572968 | |||||||
| chr7:77573032 | G | A | 108 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(105): Show |
108 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.208+1846G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573032 | |||||||
| chr7:77573039 | C | T | 111 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(108): Show |
111 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.208+1853C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573039 | |||||||
| chr7:77573082 | C | CAAAAAAA others(5): Show |
1 | a0002c0002t0001g0049 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.208+1899_208+1910d others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573082 | ||||||
| chr7:77573082 | C | CAAAAAAA others(6): Show |
2 | a0002c0002t0001g0002 a0002c0002t0001g0037 |
2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.208+1898_208+1910d others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573082 | ||||||
| chr7:77573082 | C | CAAAAAAA others(9): Show |
1 | a0002c0002t0001g0059 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.208+1910_208+1911i others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573082 | ||||||
| chr7:77573082 | C | CAAAAAAA others(14): Show |
1 | a0002c0002t0001g0024 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.208+1910_208+1911i others(23): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573082 | ||||||
| chr7:77573082 | C | CAAAAAAA others(36): Show |
1 | a0002c0002t0001g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.208+1910_208+1911i others(45): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573082 | ||||||
| chr7:77573090 | AAAAAAAC others(8): Show |
A | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0004g0132 others(1): Show |
4 | HG02572.hp2 HG02965.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+1911_208+1925d others(17): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573090 | ||||||
| chr7:77573091 | AAAAAAC | A | 12 | a0001c0001t0001g0110 a0001c0001t0001g0129 a0001c0001t0001g0134 others(9): Show |
12 | HG00280.hp1 HG02109.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.208+1911_208+1916d others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573091 | ||||||
| chr7:77573092 | AAAAAC | A | 6 | a0001c0001t0001g0155 a0001c0001t0001g0252 a0001c0001t0001g0255 others(3): Show |
6 | HG01884.hp2 HG01993.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+1911_208+1915d others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573092 | ||||||
| chr7:77573093 | AAAAC | A | 87 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0019 others(84): Show |
87 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.208+1911_208+1914d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573093 | ||||||
| chr7:77573094 | AAAC | A | 27 | a0001c0001t0001g0005 a0001c0001t0001g0122 a0001c0001t0001g0139 others(24): Show |
27 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.208+1911_208+1913d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573094 | ||||||
| chr7:77573096 | AC | A | 6 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0116 others(3): Show |
6 | HG01243.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+1911delC | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573096 | |||||||
| chr7:77573097 | C | A | 106 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0002c0002t0001g0002 others(103): Show |
106 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.208+1911C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573097 | |||||||
| chr7:77573100 | A | AAAAAAAA others(7): Show |
4 | a0002c0002t0001g0060 a0002c0002t0001g0091 a0002c0002t0001g0106 others(1): Show |
4 | HG01258.hp1 HG02683.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+1918_208+1919i others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573100 | ||||||
| chr7:77573100 | A | AAAAAAAA others(6): Show |
34 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0010 others(31): Show |
34 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.208+1918_208+1919i others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573100 | ||||||
| chr7:77573100 | A | AAAAAAAA others(5): Show |
47 | a0002c0002t0001g0007 a0002c0002t0001g0009 a0002c0002t0001g0011 others(44): Show |
47 | HG00639.hp2 HG00673.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.208+1918_208+1919i others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573100 | ||||||
| chr7:77573100 | A | AAAAAAAA others(4): Show |
5 | a0002c0002t0001g0021 a0002c0002t0001g0023 a0002c0002t0001g0047 others(2): Show |
5 | HG01074.hp1 HG01243.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+1918_208+1919i others(13): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573100 | ||||||
| chr7:77573100 | A | AAACAAAA others(5): Show |
1 | a0002c0002t0001g0067 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.208+1916_208+1917i others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573100 | ||||||
| chr7:77573100 | A | AACAAAAA others(4): Show |
1 | a0002c0002t0001g0084 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.208+1915_208+1916i others(13): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573100 | ||||||
| chr7:77573101 | A | AAAAAAAA others(5): Show |
1 | a0002c0002t0001g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.208+1918_208+1919i others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77573101 | ||||||
| chr7:77573105 | C | A | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(238): Show |
241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.208+1919C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573105 | |||||||
| chr7:77573112 | A | C | 1 | a0002c0002t0001g0108 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.208+1926A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573112 | |||||||
| chr7:77573130 | A | G | 4 | a0003c0003t0001g0003 a0003c0003t0001g0178 a0003c0003t0001g0179 others(1): Show |
4 | HG00408.hp1 NA18964.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+1944A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573130 | |||||||
| chr7:77573202 | T | C | 2 | a0002c0002t0001g0084 a0002c0002t0001g0097 |
2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.208+2016T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573202 | |||||||
| chr7:77573377 | G | C | 35 | a0001c0001t0001g0114 a0001c0001t0001g0139 a0001c0001t0001g0140 others(32): Show |
35 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.208+2191G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573377 | |||||||
| chr7:77573415 | G | A | 27 | a0001c0001t0001g0027 a0001c0001t0001g0234 a0001c0001t0001g0235 others(24): Show |
27 | HG00423.hp1 HG00438.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.208+2229G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573415 | |||||||
| chr7:77573475 | G | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+2289G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573475 | |||||||
| chr7:77573498 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG02132.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.208+2312A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573498 | |||||||
| chr7:77573755 | T | C | 1 | a0002c0002t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208+2569T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573755 | |||||||
| chr7:77573802 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+2616C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573802 | |||||||
| chr7:77573830 | C | T | 1 | a0003c0003t0001g0303 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.208+2644C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77573830 | |||||||
| chr7:77574003 | C | T | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.208+2817C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574003 | |||||||
| chr7:77574037 | CT | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+2853delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77574037 | ||||||
| chr7:77574196 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+3010C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574196 | |||||||
| chr7:77574213 | G | C | 1 | a0002c0002t0001g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.208+3027G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574213 | |||||||
| chr7:77574241 | C | T | 2 | a0002c0002t0001g0084 a0002c0002t0001g0097 |
2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.208+3055C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574241 | |||||||
| chr7:77574390 | G | A | 1 | a0002c0002t0001g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.208+3204G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574390 | |||||||
| chr7:77574555 | C | A | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.208+3369C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574555 | |||||||
| chr7:77574566 | T | C | 256 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(253): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.208+3380T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574566 | |||||||
| chr7:77574768 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+3582C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574768 | |||||||
| chr7:77574848 | T | G | 1 | a0001c0001t0004g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.208+3662T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574848 | |||||||
| chr7:77574942 | G | T | 2 | a0002c0002t0001g0084 a0002c0002t0001g0097 |
2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.208+3756G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574942 | |||||||
| chr7:77574980 | T | C | 256 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(253): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.208+3794T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77574980 | |||||||
| chr7:77575019 | A | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+3833A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77575019 | |||||||
| chr7:77575026 | G | A | 1 | a0002c0002t0001g0306 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.208+3840G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77575026 | |||||||
| chr7:77575038 | C | T | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(238): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.208+3852C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77575038 | |||||||
| chr7:77575325 | ACACG | A | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(70): Show |
73 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.208+4155_208+4158d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77575325 | ||||||
| chr7:77575434 | G | A | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0004g0132 |
3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.208+4248G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77575434 | |||||||
| chr7:77575849 | C | G | 3 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0116 |
3 | HG02559.hp1 HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.208+4663C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77575849 | |||||||
| chr7:77575859 | A | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+4673A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77575859 | |||||||
| chr7:77576019 | T | C | 2 | a0003c0003t0001g0112 a0003c0003t0001g0116 |
2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.208+4833T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576019 | |||||||
| chr7:77576182 | C | G | 1 | a0001c0001t0001g0027 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.208+4996C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576182 | |||||||
| chr7:77576197 | A | G | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(71): Show |
74 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.208+5011A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576197 | |||||||
| chr7:77576278 | A | G | 2 | a0002c0002t0001g0062 a0002c0002t0001g0079 |
2 | HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.208+5092A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576278 | |||||||
| chr7:77576342 | C | T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.209-5085C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576342 | |||||||
| chr7:77576604 | C | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-4823C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576604 | |||||||
| chr7:77576605 | G | A | 2 | a0002c0002t0001g0062 a0002c0002t0001g0079 |
2 | HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.209-4822G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576605 | |||||||
| chr7:77576665 | C | G | 1 | a0001c0001t0004g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.209-4762C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576665 | |||||||
| chr7:77576731 | C | T | 1 | a0003c0003t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.209-4696C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77576731 | |||||||
| chr7:77577160 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.209-4267G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77577160 | |||||||
| chr7:77577204 | A | G | 1 | a0002c0002t0001g0064 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.209-4223A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77577204 | |||||||
| chr7:77577285 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.209-4142G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77577285 | |||||||
| chr7:77577328 | A | G | 1 | a0003c0003t0001g0199 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.209-4099A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77577328 | |||||||
| chr7:77577432 | A | G | 112 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(109): Show |
112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.209-3995A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77577432 | |||||||
| chr7:77577691 | G | A | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.209-3736G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77577691 | |||||||
| chr7:77578273 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.209-3154C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77578273 | |||||||
| chr7:77578356 | C | T | 2 | a0002c0002t0001g0072 a0002c0002t0001g0073 |
2 | HG01099.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.209-3071C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77578356 | |||||||
| chr7:77578466 | T | C | 1 | a0001c0001t0001g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.209-2961T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77578466 | |||||||
| chr7:77578530 | A | C | 1 | a0002c0002t0001g0087 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.209-2897A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77578530 | |||||||
| chr7:77578850 | G | A | 1 | a0003c0003t0001g0183 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.209-2577G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77578850 | |||||||
| chr7:77578868 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.209-2559A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77578868 | |||||||
| chr7:77579207 | C | T | 1 | a0002c0002t0001g0080 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.209-2220C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77579207 | |||||||
| chr7:77579360 | T | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-2067T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77579360 | |||||||
| chr7:77579591 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.209-1836A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77579591 | |||||||
| chr7:77579645 | T | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-1782T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77579645 | |||||||
| chr7:77579656 | A | T | 1 | a0002c0002t0001g0279 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.209-1771A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77579656 | |||||||
| chr7:77579972 | T | C | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.209-1455T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77579972 | |||||||
| chr7:77580184 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.209-1243G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77580184 | |||||||
| chr7:77580249 | T | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-1178T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77580249 | |||||||
| chr7:77580465 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.209-962A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77580465 | |||||||
| chr7:77580707 | T | C | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.209-720T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77580707 | |||||||
| chr7:77580815 | A | G | 2 | a0002c0002t0001g0070 a0002c0002t0001g0071 |
2 | HG00733.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.209-612A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77580815 | |||||||
| chr7:77581038 | T | TTTTTG | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG00609.hp1 NA19003.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.209-364_209-360dup others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77581038 | ||||||
| chr7:77581038 | TTTTTG | T | 4 | a0003c0003t0001g0195 a0003c0003t0001g0202 a0003c0003t0001g0214 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-364_209-360del others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77581038 | ||||||
| chr7:77581038 | TTTTTGTT others(8): Show |
T | 112 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(109): Show |
112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.209-374_209-360del others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 77581038 | ||||||
| chr7:77581075 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.209-352T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77581075 | |||||||
| chr7:77581172 | T | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-255T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77581172 | |||||||
| chr7:77581399 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-28A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 2/17 | chr7 | 77581399 | |||||||
| chr7:77581816 | A | G | 1 | a0003c0003t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.285+313A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77581816 | |||||||
| chr7:77581954 | C | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+451C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77581954 | |||||||
| chr7:77582084 | C | CT | 15 | a0001c0001t0001g0017 a0001c0001t0001g0131 a0001c0001t0001g0217 others(12): Show |
15 | HG00140.hp2 HG01175.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.285+609dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | ||||||
| chr7:77582084 | C | CTTTTTT | 9 | a0001c0001t0001g0019 a0001c0001t0001g0219 a0001c0001t0001g0234 others(6): Show |
9 | HG01952.hp2 HG02015.hp1 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.285+604_285+609dup others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | ||||||
| chr7:77582084 | C | CTTTTTTT | 9 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0253 others(6): Show |
9 | HG02004.hp2 HG02922.hp2 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.285+603_285+609dup others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | ||||||
| chr7:77582084 | C | CTTTTTTT others(1): Show |
10 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0240 others(7): Show |
10 | HG00423.hp1 HG01981.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+602_285+609dup others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | ||||||
| chr7:77582084 | C | CTTTTTTT others(2): Show |
25 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0120 others(22): Show |
25 | HG00099.hp2 HG00438.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.285+601_285+609dup others(9): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | ||||||
| chr7:77582084 | C | CTTTTTTT others(3): Show |
11 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0122 others(8): Show |
11 | HG00741.hp1 HG01258.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.285+600_285+609dup others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | ||||||
| chr7:77582084 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0242 a0001c0001t0001g0252 a0001c0001t0001g0258 others(1): Show |
4 | HG00639.hp1 HG00673.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+599_285+609dup others(11): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | ||||||
| chr7:77582084 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0114 a0001c0001t0001g0125 a0001c0001t0001g0262 |
3 | HG02523.hp1 HG06807.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.285+598_285+609dup others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | ||||||
| chr7:77582084 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0124 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.285+597_285+609dup others(13): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | ||||||
| chr7:77582084 | C | CTTTTTTT others(10): Show |
1 | a0004c0004t0001g0267 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.285+593_285+609dup others(17): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | ||||||
| chr7:77582084 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.285+588_285+609dup others(22): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | ||||||
| chr7:77582084 | C | CTTTTTTT others(21): Show |
1 | a0001c0001t0001g0126 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.285+582_285+609dup others(28): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | ||||||
| chr7:77582084 | CT | C | 74 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0142 others(71): Show |
74 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.285+609delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | ||||||
| chr7:77582084 | CTT | C | 116 | a0001c0001t0001g0110 a0001c0001t0001g0129 a0001c0001t0001g0134 others(113): Show |
116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.285+608_285+609del others(2): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | ||||||
| chr7:77582084 | CTTTTTTT others(8): Show |
C | 1 | a0002c0002t0001g0103 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.285+595_285+609del others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582084 | ||||||
| chr7:77582126 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.285+623G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582126 | |||||||
| chr7:77582193 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+690C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582193 | |||||||
| chr7:77582196 | G | A | 1 | a0002c0002t0001g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.285+693G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582196 | |||||||
| chr7:77582312 | G | T | 304 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(301): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.285+809G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582312 | |||||||
| chr7:77582381 | C | G | 5 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
5 | HG02280.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+878C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582381 | |||||||
| chr7:77582386 | A | T | 245 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(242): Show |
245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.285+883A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582386 | |||||||
| chr7:77582506 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.285+1003G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582506 | |||||||
| chr7:77582526 | G | A | 2 | a0002c0002t0001g0070 a0002c0002t0001g0071 |
2 | HG00733.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.285+1023G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582526 | |||||||
| chr7:77582745 | A | G | 1 | a0002c0002t0001g0087 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.286-810A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582745 | |||||||
| chr7:77582748 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.286-807C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582748 | |||||||
| chr7:77582762 | T | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.286-793T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582762 | |||||||
| chr7:77582783 | C | CA | 99 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(96): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.286-756dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 77582783 | ||||||
| chr7:77582947 | A | G | 2 | a0002c0002t0001g0088 a0002c0002t0001g0220 |
2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.286-608A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77582947 | |||||||
| chr7:77583119 | T | C | 1 | a0002c0002t0001g0078 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.286-436T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77583119 | |||||||
| chr7:77583133 | G | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-422G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77583133 | |||||||
| chr7:77583265 | T | C | 1 | a0003c0003t0001g0182 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.286-290T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77583265 | |||||||
| chr7:77583275 | T | C | 112 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(109): Show |
112 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.286-280T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77583275 | |||||||
| chr7:77583324 | C | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-231C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77583324 | |||||||
| chr7:77583429 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.286-126A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 3/17 | chr7 | 77583429 | |||||||
| chr7:77583740 | A | T | 1 | a0001c0001t0001g0288 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.381+90A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77583740 | |||||||
| chr7:77583928 | G | T | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.381+278G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77583928 | |||||||
| chr7:77583992 | TCTC | T | 3 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0002g0161 |
3 | HG01243.hp1 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.381+343_381+345del others(3): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77583992 | |||||||
| chr7:77584023 | T | A | 1 | a0001c0001t0001g0293 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.381+373T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584023 | |||||||
| chr7:77584046 | A | G | 256 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(253): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.381+396A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584046 | |||||||
| chr7:77584142 | A | ATTAG | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+493_381+496dup others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 77584142 | ||||||
| chr7:77584155 | G | A | 97 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(94): Show |
97 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.381+505G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584155 | |||||||
| chr7:77584249 | A | T | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.381+599A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584249 | |||||||
| chr7:77584311 | G | C | 256 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(253): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.381+661G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584311 | |||||||
| chr7:77584601 | C | T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.382-942C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584601 | |||||||
| chr7:77584669 | A | T | 1 | a0001c0001t0001g0251 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.382-874A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584669 | |||||||
| chr7:77584674 | G | A | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(238): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.382-869G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584674 | |||||||
| chr7:77584731 | G | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-812G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584731 | |||||||
| chr7:77584745 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-798C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584745 | |||||||
| chr7:77584766 | A | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0305 |
3 | HG01109.hp2 HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.382-777A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584766 | |||||||
| chr7:77584794 | G | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0280 |
2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.382-749G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584794 | |||||||
| chr7:77584834 | G | A | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-709G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77584834 | |||||||
| chr7:77584876 | C | CA | 23 | a0001c0001t0001g0114 a0001c0001t0001g0130 a0001c0001t0001g0131 others(20): Show |
23 | HG00438.hp1 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.382-650dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 77584876 | ||||||
| chr7:77584876 | C | CAA | 6 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0003c0003t0001g0020 others(3): Show |
6 | HG00140.hp2 HG01256.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-651_382-650dup others(2): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 77584876 | ||||||
| chr7:77585165 | G | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-378G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77585165 | |||||||
| chr7:77585257 | T | C | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.382-286T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77585257 | |||||||
| chr7:77585266 | T | C | 1 | a0002c0002t0001g0072 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.382-277T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77585266 | |||||||
| chr7:77585307 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-236C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77585307 | |||||||
| chr7:77585315 | A | G | 1 | a0003c0003t0001g0184 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.382-228A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 4/17 | chr7 | 77585315 | |||||||
| chr7:77585642 | A | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.420+61A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77585642 | |||||||
| chr7:77585680 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.420+99T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77585680 | |||||||
| chr7:77585726 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.420+145A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77585726 | |||||||
| chr7:77585838 | C | T | 3 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 |
3 | HG00639.hp1 HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.420+257C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77585838 | |||||||
| chr7:77586123 | T | C | 1 | a0003c0003t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.420+542T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77586123 | |||||||
| chr7:77586126 | G | A | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(238): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.420+545G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77586126 | |||||||
| chr7:77586164 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.420+583G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77586164 | |||||||
| chr7:77586294 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.420+713G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77586294 | |||||||
| chr7:77586439 | ACCAGGAA others(20): Show |
A | 1 | a0005c0005t0001g0050 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.420+863_420+889del others(27): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 77586439 | ||||||
| chr7:77586481 | G | A | 46 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(43): Show |
46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.420+900G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77586481 | |||||||
| chr7:77586524 | C | T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.420+943C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77586524 | |||||||
| chr7:77586657 | A | G | 2 | a0001c0001t0001g0253 a0001c0001t0001g0259 |
2 | HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.420+1076A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77586657 | |||||||
| chr7:77587098 | C | T | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(70): Show |
73 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.420+1517C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587098 | |||||||
| chr7:77587163 | T | G | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.420+1582T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587163 | |||||||
| chr7:77587245 | A | T | 1 | a0002c0002t0001g0038 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.420+1664A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587245 | |||||||
| chr7:77587385 | A | AT | 80 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(77): Show |
80 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.420+1813dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 77587385 | ||||||
| chr7:77587468 | T | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.420+1887T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587468 | |||||||
| chr7:77587479 | A | G | 1 | a0003c0003t0001g0199 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.420+1898A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587479 | |||||||
| chr7:77587557 | A | G | 1 | a0002c0002t0001g0058 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.420+1976A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587557 | |||||||
| chr7:77587686 | C | A | 61 | a0002c0002t0001g0007 a0002c0002t0001g0008 a0002c0002t0001g0009 others(58): Show |
61 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.420+2105C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587686 | |||||||
| chr7:77587686 | C | G | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(71): Show |
74 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.420+2105C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587686 | |||||||
| chr7:77587722 | C | T | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.420+2141C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587722 | |||||||
| chr7:77587787 | T | C | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.420+2206T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587787 | |||||||
| chr7:77587829 | A | C | 256 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(253): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.420+2248A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587829 | |||||||
| chr7:77587851 | T | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.420+2270T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587851 | |||||||
| chr7:77587961 | G | T | 1 | a0003c0003t0001g0170 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.420+2380G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77587961 | |||||||
| chr7:77588157 | T | A | 35 | a0001c0001t0001g0114 a0001c0001t0001g0139 a0001c0001t0001g0140 others(32): Show |
35 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.420+2576T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588157 | |||||||
| chr7:77588167 | G | T | 61 | a0002c0002t0001g0007 a0002c0002t0001g0008 a0002c0002t0001g0009 others(58): Show |
61 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.420+2586G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588167 | |||||||
| chr7:77588184 | A | G | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.420+2603A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588184 | |||||||
| chr7:77588202 | C | G | 11 | a0001c0001t0001g0110 a0001c0001t0001g0129 a0001c0001t0001g0134 others(8): Show |
11 | HG00280.hp1 HG00323.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.420+2621C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588202 | |||||||
| chr7:77588328 | C | T | 1 | a0002c0002t0001g0064 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.420+2747C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588328 | |||||||
| chr7:77588507 | T | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.420+2926T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588507 | |||||||
| chr7:77588625 | A | G | 114 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(111): Show |
114 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.420+3044A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588625 | |||||||
| chr7:77588698 | A | G | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.420+3117A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588698 | |||||||
| chr7:77588725 | A | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.420+3144A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588725 | |||||||
| chr7:77588737 | C | G | 1 | a0002c0002t0001g0081 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.420+3156C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588737 | |||||||
| chr7:77588944 | C | T | 1 | a0002c0002t0001g0211 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.421-3241C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77588944 | |||||||
| chr7:77589017 | C | T | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(69): Show |
72 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.421-3168C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77589017 | |||||||
| chr7:77589203 | CTGTT | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-2977_421-2974d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 77589203 | ||||||
| chr7:77589221 | G | C | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421-2964G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77589221 | |||||||
| chr7:77589360 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.421-2825G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77589360 | |||||||
| chr7:77589462 | C | A | 3 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0023 |
3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.421-2723C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77589462 | |||||||
| chr7:77589643 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.421-2542A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77589643 | |||||||
| chr7:77589922 | T | G | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(75): Show |
78 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.421-2263T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77589922 | |||||||
| chr7:77590030 | T | C | 1 | a0002c0002t0001g0039 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.421-2155T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590030 | |||||||
| chr7:77590180 | T | G | 1 | a0001c0001t0001g0308 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.421-2005T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590180 | |||||||
| chr7:77590243 | T | C | 1 | a0001c0001t0001g0290 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.421-1942T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590243 | |||||||
| chr7:77590299 | A | G | 1 | a0003c0003t0001g0198 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.421-1886A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590299 | |||||||
| chr7:77590346 | A | C | 1 | a0001c0001t0001g0134 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.421-1839A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590346 | |||||||
| chr7:77590559 | C | CT | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(71): Show |
74 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.421-1612dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 77590559 | ||||||
| chr7:77590559 | C | CTT | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.421-1613_421-1612d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 77590559 | ||||||
| chr7:77590562 | T | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.421-1623T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590562 | |||||||
| chr7:77590618 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.421-1567T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590618 | |||||||
| chr7:77590843 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.421-1342C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590843 | |||||||
| chr7:77590873 | T | TA | 6 | a0002c0002t0001g0068 a0003c0003t0001g0020 a0003c0003t0001g0286 others(3): Show |
6 | HG00140.hp2 HG01256.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-1298dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 77590873 | ||||||
| chr7:77590985 | C | T | 157 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(154): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.421-1200C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77590985 | |||||||
| chr7:77591051 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.421-1134A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591051 | |||||||
| chr7:77591077 | A | G | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.421-1108A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591077 | |||||||
| chr7:77591178 | C | T | 1 | a0003c0003t0001g0184 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.421-1007C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591178 | |||||||
| chr7:77591189 | A | G | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.421-996A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591189 | |||||||
| chr7:77591231 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.421-954G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591231 | |||||||
| chr7:77591403 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-782C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591403 | |||||||
| chr7:77591468 | T | G | 1 | a0001c0001t0001g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.421-717T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591468 | |||||||
| chr7:77591585 | C | G | 256 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(253): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.421-600C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591585 | |||||||
| chr7:77591717 | C | T | 3 | a0002c0002t0001g0090 a0002c0002t0001g0091 a0002c0002t0001g0092 |
3 | HG02922.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.421-468C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | chr7 | 77591717 | |||||||
| chr7:77592164 | A | AT | 46 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(43): Show |
46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.421-10dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 77592164 | ||||||
| chr7:77592348 | T | A | 2 | a0002c0002t0001g0084 a0002c0002t0001g0097 |
2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.492+92T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77592348 | |||||||
| chr7:77592393 | T | C | 1 | a0001c0001t0001g0276 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.492+137T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77592393 | |||||||
| chr7:77592855 | A | G | 5 | a0002c0002t0001g0002 a0002c0002t0001g0029 a0002c0002t0001g0030 others(2): Show |
5 | HG01175.hp2 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.492+599A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77592855 | |||||||
| chr7:77592914 | A | T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.492+658A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77592914 | |||||||
| chr7:77592979 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.492+723A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77592979 | |||||||
| chr7:77593039 | C | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.492+783C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593039 | |||||||
| chr7:77593254 | G | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.492+998G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593254 | |||||||
| chr7:77593269 | CA | C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(82): Show |
85 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.492+1029delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 77593269 | ||||||
| chr7:77593269 | CAA | C | 161 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(158): Show |
161 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.492+1028_492+1029d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 77593269 | ||||||
| chr7:77593482 | T | G | 1 | a0002c0002t0001g0108 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.492+1226T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593482 | |||||||
| chr7:77593536 | T | A | 1 | a0002c0002t0001g0045 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.492+1280T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593536 | |||||||
| chr7:77593551 | G | A | 1 | a0001c0001t0004g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.492+1295G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593551 | |||||||
| chr7:77593568 | C | T | 1 | a0002c0002t0001g0083 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.492+1312C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593568 | |||||||
| chr7:77593569 | A | G | 167 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(164): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.492+1313A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593569 | |||||||
| chr7:77593583 | A | C | 1 | a0002c0002t0001g0094 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.492+1327A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593583 | |||||||
| chr7:77593621 | C | A | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(75): Show |
78 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.492+1365C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593621 | |||||||
| chr7:77593831 | C | G | 113 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(110): Show |
113 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.492+1575C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593831 | |||||||
| chr7:77593894 | G | A | 3 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 |
3 | HG00639.hp1 HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.492+1638G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593894 | |||||||
| chr7:77593948 | T | C | 113 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(110): Show |
113 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.492+1692T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77593948 | |||||||
| chr7:77594027 | T | A | 246 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(243): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.492+1771T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77594027 | |||||||
| chr7:77594118 | G | T | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.492+1862G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77594118 | |||||||
| chr7:77594141 | T | A | 1 | a0002c0002t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.492+1885T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77594141 | |||||||
| chr7:77594303 | A | AAAAACGT others(24): Show |
1 | a0002c0002t0001g0111 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.492+2048_492+2078d others(33): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 77594303 | ||||||
| chr7:77594304 | A | G | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(69): Show |
72 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.492+2048A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77594304 | |||||||
| chr7:77594377 | T | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.492+2121T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77594377 | |||||||
| chr7:77594431 | T | C | 1 | a0001c0001t0001g0277 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.492+2175T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77594431 | |||||||
| chr7:77595162 | G | A | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.493-2680G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77595162 | |||||||
| chr7:77595555 | G | A | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0305 |
3 | HG01109.hp2 HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.493-2287G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77595555 | |||||||
| chr7:77595682 | A | C | 1 | a0004c0004t0001g0270 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.493-2160A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77595682 | |||||||
| chr7:77595736 | T | A | 1 | a0002c0002t0001g0097 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.493-2106T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77595736 | |||||||
| chr7:77595805 | T | A | 1 | a0003c0003t0001g0176 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.493-2037T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77595805 | |||||||
| chr7:77595811 | T | A | 1 | a0001c0001t0001g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.493-2031T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77595811 | |||||||
| chr7:77596122 | G | A | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.493-1720G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77596122 | |||||||
| chr7:77596213 | CA | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.493-1626delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 77596213 | ||||||
| chr7:77596282 | A | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.493-1560A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77596282 | |||||||
| chr7:77596392 | A | T | 1 | a0002c0002t0001g0039 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.493-1450A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77596392 | |||||||
| chr7:77596527 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.493-1315C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77596527 | |||||||
| chr7:77596548 | G | C | 279 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(276): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.493-1294G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77596548 | |||||||
| chr7:77596752 | A | T | 1 | a0002c0002t0001g0085 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.493-1090A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77596752 | |||||||
| chr7:77596896 | C | T | 2 | a0002c0002t0001g0047 a0002c0002t0001g0048 |
2 | HG01074.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.493-946C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77596896 | |||||||
| chr7:77596983 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.493-859A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77596983 | |||||||
| chr7:77596988 | G | GAATAGTG others(9): Show |
119 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0002c0002t0001g0002 others(116): Show |
119 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.493-846_493-845ins others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 77596988 | ||||||
| chr7:77597147 | G | A | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(52): Show |
55 | HG00099.hp2 HG00438.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.493-695G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77597147 | |||||||
| chr7:77597162 | C | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.493-680C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77597162 | |||||||
| chr7:77597342 | C | T | 1 | a0003c0003t0001g0199 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.493-500C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77597342 | |||||||
| chr7:77597416 | C | T | 1 | a0002c0002t0001g0024 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.493-426C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77597416 | |||||||
| chr7:77597432 | T | C | 1 | a0002c0002t0001g0070 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.493-410T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 6/17 | chr7 | 77597432 | |||||||
| chr7:77597924 | C | T | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(75): Show |
78 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.552+23C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77597924 | |||||||
| chr7:77598265 | C | G | 113 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(110): Show |
113 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.552+364C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598265 | |||||||
| chr7:77598433 | A | G | 3 | a0002c0002t0001g0118 a0002c0002t0001g0284 a0002c0002t0001g0285 |
3 | HG00423.hp1 HG00673.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.552+532A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598433 | |||||||
| chr7:77598502 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+601C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598502 | |||||||
| chr7:77598572 | A | G | 1 | a0002c0002t0001g0094 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.552+671A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598572 | |||||||
| chr7:77598678 | G | C | 4 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
4 | HG02615.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+777G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598678 | |||||||
| chr7:77598790 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.552+889T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598790 | |||||||
| chr7:77598935 | T | A | 1 | a0002c0002t0001g0220 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.552+1034T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598935 | |||||||
| chr7:77598993 | T | G | 1 | a0001c0001t0001g0146 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.552+1092T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598993 | |||||||
| chr7:77598997 | A | G | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(69): Show |
72 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.552+1096A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77598997 | |||||||
| chr7:77599143 | C | G | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+1242C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77599143 | |||||||
| chr7:77599158 | A | G | 1 | a0002c0002t0001g0014 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.552+1257A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77599158 | |||||||
| chr7:77599253 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.552+1352A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77599253 | |||||||
| chr7:77599279 | T | C | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.552+1378T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77599279 | |||||||
| chr7:77599317 | C | CT | 13 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0275 others(10): Show |
13 | HG00140.hp2 HG00438.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.553-1329dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 77599317 | ||||||
| chr7:77599317 | C | CTT | 180 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.553-1330_553-1329d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 77599317 | ||||||
| chr7:77599317 | C | CTTT | 10 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(7): Show |
10 | HG00423.hp1 HG00673.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.553-1331_553-1329d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 77599317 | ||||||
| chr7:77599320 | T | A | 2 | a0003c0003t0001g0299 a0003c0003t0001g0300 |
2 | HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.553-1344T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77599320 | |||||||
| chr7:77599408 | A | G | 1 | a0002c0002t0001g0045 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.553-1256A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77599408 | |||||||
| chr7:77599617 | G | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-1047G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77599617 | |||||||
| chr7:77599932 | G | A | 256 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(253): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.553-732G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77599932 | |||||||
| chr7:77600036 | A | G | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(238): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.553-628A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77600036 | |||||||
| chr7:77600092 | T | A | 2 | a0003c0003t0001g0112 a0003c0003t0001g0116 |
2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.553-572T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77600092 | |||||||
| chr7:77600318 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.553-346T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77600318 | |||||||
| chr7:77600324 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-340C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77600324 | |||||||
| chr7:77600468 | T | A | 6 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0116 others(3): Show |
6 | HG01243.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.553-196T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77600468 | |||||||
| chr7:77600544 | T | C | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.553-120T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77600544 | |||||||
| chr7:77600660 | G | A | 1 | a0002c0002t0001g0105 | 1 | NA20129.hp1 | splice_region_variant&intron_variant | LOW | c.553-4G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 7/17 | chr7 | 77600660 | |||||||
| chr7:77600927 | G | A | 1 | a0002c0002t0001g0306 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.695+121G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77600927 | |||||||
| chr7:77601011 | A | G | 1 | a0001c0001t0004g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.695+205A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601011 | |||||||
| chr7:77601022 | G | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | NA19056.hp1 NA19079.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.695+216G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601022 | |||||||
| chr7:77601253 | C | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0004g0132 |
3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.695+447C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601253 | |||||||
| chr7:77601378 | T | A | 8 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(5): Show |
8 | HG00140.hp2 HG01256.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.695+572T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601378 | |||||||
| chr7:77601680 | T | C | 1 | a0002c0002t0001g0009 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.695+874T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601680 | |||||||
| chr7:77601728 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.695+922A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601728 | |||||||
| chr7:77601827 | A | G | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.695+1021A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601827 | |||||||
| chr7:77601949 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.695+1143A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601949 | |||||||
| chr7:77601993 | A | C | 5 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0292 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.695+1187A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77601993 | |||||||
| chr7:77602066 | T | A | 4 | a0001c0001t0001g0117 a0001c0001t0001g0240 a0001c0001t0001g0241 others(1): Show |
4 | HG00639.hp1 HG02486.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.695+1260T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77602066 | |||||||
| chr7:77602168 | A | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+1362A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77602168 | |||||||
| chr7:77602193 | G | A | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.695+1387G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77602193 | |||||||
| chr7:77602212 | T | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+1406T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77602212 | |||||||
| chr7:77602257 | A | G | 1 | a0002c0002t0005g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.695+1451A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77602257 | |||||||
| chr7:77602488 | A | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+1682A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77602488 | |||||||
| chr7:77602605 | G | A | 1 | a0002c0002t0001g0220 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.695+1799G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77602605 | |||||||
| chr7:77602620 | T | TA | 10 | a0002c0002t0001g0128 a0003c0003t0001g0020 a0003c0003t0001g0113 others(7): Show |
10 | HG00140.hp2 HG00639.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.695+1827dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77602620 | ||||||
| chr7:77602621 | A | T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.695+1815A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77602621 | |||||||
| chr7:77603192 | A | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+2386A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77603192 | |||||||
| chr7:77603313 | T | A | 2 | a0003c0003t0001g0112 a0003c0003t0001g0116 |
2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.695+2507T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77603313 | |||||||
| chr7:77603375 | A | G | 1 | a0003c0003t0001g0210 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.695+2569A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77603375 | |||||||
| chr7:77603379 | A | G | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.695+2573A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77603379 | |||||||
| chr7:77603507 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.695+2701C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77603507 | |||||||
| chr7:77603883 | C | CT | 57 | a0001c0001t0001g0017 a0001c0001t0001g0126 a0001c0001t0001g0165 others(54): Show |
57 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.695+3100dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77603883 | ||||||
| chr7:77603883 | C | CTT | 45 | a0001c0001t0001g0114 a0001c0001t0001g0129 a0001c0001t0001g0134 others(42): Show |
45 | HG00280.hp1 HG00280.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.695+3099_695+3100d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77603883 | ||||||
| chr7:77603883 | CT | C | 8 | a0001c0001t0001g0253 a0001c0001t0001g0259 a0001c0001t0001g0307 others(5): Show |
8 | HG01167.hp1 HG01891.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.695+3100delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77603883 | ||||||
| chr7:77604209 | C | CATTTTT | 3 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0303 |
3 | HG01256.hp1 HG03239.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.696-3026_696-3025i others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604209 | |||||||
| chr7:77604209 | C | CT | 111 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0027 others(108): Show |
111 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.696-3002dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77604209 | ||||||
| chr7:77604209 | C | CTT | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0114 others(98): Show |
101 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.696-3003_696-3002d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77604209 | ||||||
| chr7:77604209 | C | CTTT | 25 | a0001c0001t0001g0110 a0001c0001t0001g0129 a0001c0001t0001g0134 others(22): Show |
25 | HG00140.hp1 HG00639.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.696-3004_696-3002d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77604209 | ||||||
| chr7:77604209 | C | CTTTT | 9 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(6): Show |
9 | HG00423.hp1 HG00735.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.696-3005_696-3002d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77604209 | ||||||
| chr7:77604209 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.696-3014_696-3002d others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77604209 | ||||||
| chr7:77604209 | CT | C | 6 | a0003c0003t0001g0113 a0003c0003t0001g0115 a0003c0003t0001g0168 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-3002delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77604209 | ||||||
| chr7:77604209 | CTTTTTTT others(5): Show |
C | 17 | a0003c0003t0001g0003 a0003c0003t0001g0127 a0003c0003t0001g0169 others(14): Show |
17 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(14): Show |
intron_variant | MODIFIER | c.696-3013_696-3002d others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77604209 | ||||||
| chr7:77604239 | G | A | 1 | a0002c0002t0001g0097 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.696-2996G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604239 | |||||||
| chr7:77604272 | A | G | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.696-2963A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604272 | |||||||
| chr7:77604475 | A | G | 1 | a0003c0003t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.696-2760A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604475 | |||||||
| chr7:77604501 | A | G | 1 | a0003c0003t0001g0174 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.696-2734A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604501 | |||||||
| chr7:77604510 | A | G | 246 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(243): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.696-2725A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604510 | |||||||
| chr7:77604807 | A | T | 2 | a0003c0003t0001g0112 a0003c0003t0001g0116 |
2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.696-2428A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604807 | |||||||
| chr7:77604809 | T | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.696-2426T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604809 | |||||||
| chr7:77604836 | A | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0004g0132 |
3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.696-2399A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77604836 | |||||||
| chr7:77605058 | C | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-2177C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605058 | |||||||
| chr7:77605206 | G | C | 1 | a0002c0002t0001g0039 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.696-2029G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605206 | |||||||
| chr7:77605282 | T | G | 49 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(46): Show |
49 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.696-1953T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605282 | |||||||
| chr7:77605323 | T | C | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(75): Show |
78 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.696-1912T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605323 | |||||||
| chr7:77605409 | G | GGTTT | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG02717.hp2 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-1826_696-1825i others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | |||||||
| chr7:77605409 | G | GGTTTTTT | 4 | a0001c0001t0001g0019 a0001c0001t0001g0230 a0001c0001t0001g0259 others(1): Show |
4 | HG02015.hp1 HG02897.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.696-1826_696-1825i others(9): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | |||||||
| chr7:77605409 | G | GGTTTTTT others(1): Show |
11 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0131 others(8): Show |
11 | HG00673.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.696-1826_696-1825i others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | |||||||
| chr7:77605409 | G | GGTTTTTT others(2): Show |
24 | a0001c0001t0001g0027 a0001c0001t0001g0117 a0001c0001t0001g0126 others(21): Show |
24 | HG00438.hp2 HG00642.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.696-1826_696-1825i others(11): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | |||||||
| chr7:77605409 | G | GGTTTTTT others(3): Show |
19 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0125 others(16): Show |
19 | HG00639.hp1 HG01952.hp2 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.696-1826_696-1825i others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | |||||||
| chr7:77605409 | G | GGTTTTTT others(4): Show |
7 | a0001c0001t0001g0124 a0001c0001t0001g0236 a0001c0001t0001g0257 others(4): Show |
7 | HG00741.hp1 HG01884.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.696-1826_696-1825i others(13): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | |||||||
| chr7:77605409 | G | GGTTTTTT others(5): Show |
3 | a0001c0001t0001g0122 a0001c0001t0001g0282 a0004c0004t0001g0270 |
3 | HG00099.hp2 HG02080.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.696-1826_696-1825i others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | |||||||
| chr7:77605409 | G | GGTTTTTT others(6): Show |
2 | a0001c0001t0001g0119 a0001c0001t0001g0247 |
2 | NA18949.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.696-1826_696-1825i others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | |||||||
| chr7:77605409 | G | GGTTTTTT others(8): Show |
1 | a0001c0001t0001g0123 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.696-1826_696-1825i others(17): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605409 | |||||||
| chr7:77605409 | G | GT | 11 | a0003c0003t0001g0174 a0003c0003t0001g0181 a0003c0003t0001g0192 others(8): Show |
11 | HG00733.hp2 HG00735.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.696-1798dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | ||||||
| chr7:77605409 | G | GTTTGTTT others(7): Show |
1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.696-1823_696-1822i others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | ||||||
| chr7:77605409 | G | GTTTTTTT others(3): Show |
3 | a0003c0003t0001g0168 a0003c0003t0001g0286 a0003c0003t0002g0160 |
3 | HG02055.hp1 HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.696-1807_696-1798d others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | ||||||
| chr7:77605409 | G | GTTTTTTT others(4): Show |
2 | a0003c0003t0001g0113 a0003c0003t0002g0161 |
2 | HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.696-1808_696-1798d others(13): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | ||||||
| chr7:77605409 | G | GTTTTTTT others(5): Show |
1 | a0003c0003t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.696-1809_696-1798d others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | ||||||
| chr7:77605409 | G | GTTTTTTT others(8): Show |
2 | a0003c0003t0001g0116 a0003c0003t0002g0159 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.696-1812_696-1798d others(17): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | ||||||
| chr7:77605409 | GT | G | 18 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0001g0135 others(15): Show |
18 | HG00280.hp2 HG00323.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.696-1798delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | ||||||
| chr7:77605409 | GTT | G | 38 | a0001c0001t0001g0114 a0001c0001t0001g0141 a0001c0001t0001g0143 others(35): Show |
38 | HG00609.hp1 HG00735.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.696-1799_696-1798d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | ||||||
| chr7:77605409 | GTTT | G | 89 | a0001c0001t0001g0287 a0001c0007t0001g0227 a0002c0002t0001g0002 others(86): Show |
89 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.696-1800_696-1798d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | ||||||
| chr7:77605409 | GTTTT | G | 13 | a0002c0002t0001g0010 a0002c0002t0001g0021 a0002c0002t0001g0022 others(10): Show |
13 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.696-1801_696-1798d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | ||||||
| chr7:77605409 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.696-1807_696-1798d others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605409 | ||||||
| chr7:77605410 | T | G | 6 | a0001c0001t0001g0110 a0001c0001t0001g0136 a0001c0001t0001g0162 others(3): Show |
6 | HG00280.hp1 HG00323.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-1825T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605410 | |||||||
| chr7:77605411 | T | G | 15 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0001g0135 others(12): Show |
15 | HG00280.hp2 HG01358.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.696-1824T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605411 | |||||||
| chr7:77605412 | T | G | 38 | a0001c0001t0001g0114 a0001c0001t0001g0141 a0001c0001t0001g0143 others(35): Show |
38 | HG00609.hp1 HG00735.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.696-1823T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605412 | |||||||
| chr7:77605413 | T | G | 89 | a0001c0001t0001g0287 a0001c0007t0001g0227 a0002c0002t0001g0002 others(86): Show |
89 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.696-1822T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605413 | |||||||
| chr7:77605414 | T | G | 13 | a0002c0002t0001g0010 a0002c0002t0001g0021 a0002c0002t0001g0022 others(10): Show |
13 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.696-1821T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605414 | |||||||
| chr7:77605416 | T | G | 1 | a0001c0001t0001g0276 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.696-1819T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605416 | |||||||
| chr7:77605418 | T | G | 1 | a0001c0001t0001g0281 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.696-1817T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605418 | |||||||
| chr7:77605420 | T | G | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.696-1815T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605420 | |||||||
| chr7:77605442 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-1793C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605442 | |||||||
| chr7:77605580 | C | T | 1 | a0002c0002t0001g0080 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.696-1655C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605580 | |||||||
| chr7:77605586 | AT | A | 256 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(253): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.696-1637delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605586 | ||||||
| chr7:77605725 | A | G | 1 | a0003c0003t0001g0001 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.696-1510A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605725 | |||||||
| chr7:77605744 | C | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-1491C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605744 | |||||||
| chr7:77605872 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-1363C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605872 | |||||||
| chr7:77605888 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.696-1347C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605888 | |||||||
| chr7:77605945 | C | CT | 63 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(60): Show |
63 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.696-1264dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605945 | ||||||
| chr7:77605945 | C | CTT | 27 | a0001c0001t0001g0017 a0001c0001t0001g0110 a0001c0001t0001g0135 others(24): Show |
27 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.696-1265_696-1264d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605945 | ||||||
| chr7:77605945 | C | CTTT | 22 | a0001c0001t0001g0134 a0001c0001t0001g0138 a0001c0001t0001g0145 others(19): Show |
22 | HG00642.hp2 HG01109.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.696-1266_696-1264d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605945 | ||||||
| chr7:77605945 | C | CTTTT | 9 | a0001c0001t0001g0114 a0001c0001t0001g0129 a0001c0001t0001g0143 others(6): Show |
9 | HG00735.hp1 HG02486.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.696-1267_696-1264d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605945 | ||||||
| chr7:77605945 | CT | C | 120 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0002c0002t0001g0002 others(117): Show |
120 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.696-1264delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605945 | ||||||
| chr7:77605945 | CTT | C | 11 | a0002c0002t0001g0098 a0002c0002t0001g0100 a0002c0002t0001g0101 others(8): Show |
11 | HG00323.hp1 HG01952.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.696-1265_696-1264d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77605945 | ||||||
| chr7:77605948 | T | C | 5 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.696-1287T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605948 | |||||||
| chr7:77605949 | T | C | 3 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0002g0161 |
3 | HG01243.hp1 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.696-1286T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605949 | |||||||
| chr7:77605989 | T | C | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(238): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.696-1246T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77605989 | |||||||
| chr7:77606108 | G | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-1127G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77606108 | |||||||
| chr7:77606200 | G | T | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.696-1035G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77606200 | |||||||
| chr7:77606470 | T | G | 1 | a0002c0002t0001g0103 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.696-765T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77606470 | |||||||
| chr7:77606565 | TAA | T | 256 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(253): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.696-666_696-665del others(2): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 77606565 | ||||||
| chr7:77606831 | T | C | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(238): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.696-404T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77606831 | |||||||
| chr7:77606880 | C | T | 1 | a0002c0002t0001g0066 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.696-355C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77606880 | |||||||
| chr7:77607169 | A | T | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.696-66A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77607169 | |||||||
| chr7:77607186 | A | C | 3 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0116 |
3 | HG02559.hp1 HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.696-49A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 8/17 | chr7 | 77607186 | |||||||
| chr7:77607659 | G | C | 279 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(276): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.762+358G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77607659 | |||||||
| chr7:77607664 | A | G | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.762+363A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77607664 | |||||||
| chr7:77607695 | G | A | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.762+394G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77607695 | |||||||
| chr7:77607746 | C | CT | 7 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0001g0135 others(4): Show |
7 | HG02109.hp2 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.762+458dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 77607746 | ||||||
| chr7:77607858 | A | G | 2 | a0002c0002t0001g0087 a0003c0003t0001g0115 |
2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.762+557A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77607858 | |||||||
| chr7:77607934 | T | C | 5 | a0001c0001t0001g0259 a0003c0003t0001g0020 a0003c0003t0001g0301 others(2): Show |
5 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.762+633T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77607934 | |||||||
| chr7:77607936 | G | T | 5 | a0001c0001t0001g0259 a0003c0003t0001g0020 a0003c0003t0001g0301 others(2): Show |
5 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.762+635G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77607936 | |||||||
| chr7:77607945 | G | A | 5 | a0001c0001t0001g0248 a0001c0001t0001g0250 a0001c0001t0001g0251 others(2): Show |
5 | HG00438.hp2 HG00673.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.762+644G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77607945 | |||||||
| chr7:77607975 | G | A | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.762+674G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77607975 | |||||||
| chr7:77608073 | C | T | 143 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(140): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.762+772C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608073 | |||||||
| chr7:77608424 | C | A | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.762+1123C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608424 | |||||||
| chr7:77608592 | T | C | 1 | a0002c0002t0001g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.762+1291T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608592 | |||||||
| chr7:77608740 | C | G | 9 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0229 others(6): Show |
9 | HG02818.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.762+1439C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608740 | |||||||
| chr7:77608763 | C | T | 1 | a0002c0002t0005g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.762+1462C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608763 | |||||||
| chr7:77608827 | C | T | 107 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(104): Show |
107 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.762+1526C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608827 | |||||||
| chr7:77608867 | A | G | 84 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(81): Show |
84 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.762+1566A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608867 | |||||||
| chr7:77608883 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.762+1582A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608883 | |||||||
| chr7:77608912 | T | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.762+1611T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608912 | |||||||
| chr7:77608978 | T | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.762+1677T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77608978 | |||||||
| chr7:77609033 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.762+1732A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609033 | |||||||
| chr7:77609214 | C | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.763-1551C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609214 | |||||||
| chr7:77609215 | G | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | NA19056.hp1 NA19079.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.763-1550G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609215 | |||||||
| chr7:77609261 | T | TTC | 3 | a0001c0001t0001g0232 a0001c0001t0001g0240 a0001c0001t0001g0273 |
3 | HG02723.hp2 HG02895.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.763-1492_763-1491d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 77609261 | ||||||
| chr7:77609273 | C | CT | 163 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(160): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.763-1476dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 77609273 | ||||||
| chr7:77609273 | C | CTCT | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(67): Show |
70 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.763-1491_763-1490i others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 77609273 | ||||||
| chr7:77609273 | C | CTCTT | 6 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0237 others(3): Show |
6 | HG03471.hp2 NA18946.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.763-1491_763-1490i others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 77609273 | ||||||
| chr7:77609273 | C | CTT | 10 | a0001c0001t0001g0164 a0002c0002t0001g0009 a0003c0003t0001g0112 others(7): Show |
10 | HG01243.hp1 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.763-1477_763-1476d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 77609273 | ||||||
| chr7:77609274 | T | TC | 3 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0023 |
3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.763-1491_763-1490i others(3): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609274 | |||||||
| chr7:77609275 | T | C | 1 | a0003c0003t0001g0185 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.763-1490T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609275 | |||||||
| chr7:77609325 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.763-1440G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609325 | |||||||
| chr7:77609361 | T | A | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(71): Show |
74 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.763-1404T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609361 | |||||||
| chr7:77609651 | C | T | 1 | a0002c0002t0001g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.763-1114C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609651 | |||||||
| chr7:77609724 | T | TA | 46 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(43): Show |
46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.763-1033dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 77609724 | ||||||
| chr7:77609888 | A | C | 4 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0002c0002t0001g0080 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.763-877A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609888 | |||||||
| chr7:77609894 | C | CA | 106 | a0001c0001t0001g0131 a0001c0001t0001g0307 a0001c0001t0001g0308 others(103): Show |
106 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.763-861dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 77609894 | ||||||
| chr7:77609896 | A | AC | 3 | a0002c0002t0001g0016 a0002c0002t0001g0042 a0002c0002t0001g0093 |
3 | HG03669.hp2 NA19043.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.763-869_763-868ins others(1): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609896 | |||||||
| chr7:77609905 | C | A | 250 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(247): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.763-860C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77609905 | |||||||
| chr7:77610037 | C | T | 7 | a0002c0002t0001g0018 a0002c0002t0001g0086 a0002c0002t0001g0087 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.763-728C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610037 | |||||||
| chr7:77610139 | T | G | 35 | a0001c0001t0001g0114 a0001c0001t0001g0139 a0001c0001t0001g0140 others(32): Show |
35 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.763-626T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610139 | |||||||
| chr7:77610148 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.763-617A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610148 | |||||||
| chr7:77610149 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.763-616C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610149 | |||||||
| chr7:77610163 | A | G | 1 | a0003c0003t0001g0188 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.763-602A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610163 | |||||||
| chr7:77610353 | C | T | 3 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0023 |
3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.763-412C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610353 | |||||||
| chr7:77610418 | T | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0245 others(9): Show |
12 | HG00099.hp2 HG00642.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.763-347T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610418 | |||||||
| chr7:77610584 | A | G | 1 | a0002c0002t0001g0093 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.763-181A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610584 | |||||||
| chr7:77610638 | T | G | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.763-127T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610638 | |||||||
| chr7:77610752 | T | C | 62 | a0002c0002t0001g0007 a0002c0002t0001g0008 a0002c0002t0001g0009 others(59): Show |
62 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.763-13T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 9/17 | chr7 | 77610752 | |||||||
| chr7:77611123 | G | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+77G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611123 | |||||||
| chr7:77611295 | T | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+249T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611295 | |||||||
| chr7:77611427 | T | C | 243 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(240): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.939+381T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611427 | |||||||
| chr7:77611435 | A | G | 1 | a0003c0003t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.939+389A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611435 | |||||||
| chr7:77611458 | T | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+412T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611458 | |||||||
| chr7:77611495 | A | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(74): Show |
77 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.939+449A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611495 | |||||||
| chr7:77611576 | C | A | 3 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 |
3 | HG00639.hp1 HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.939+530C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611576 | |||||||
| chr7:77611691 | C | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG00280.hp2 HG01358.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.939+645C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611691 | |||||||
| chr7:77611969 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.939+923G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77611969 | |||||||
| chr7:77611981 | A | AT | 109 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0138 others(106): Show |
109 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+951dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77611981 | ||||||
| chr7:77612117 | G | C | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.939+1071G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612117 | |||||||
| chr7:77612236 | A | T | 3 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0002g0161 |
3 | HG01243.hp1 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.939+1190A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612236 | |||||||
| chr7:77612243 | C | T | 1 | a0002c0002t0001g0015 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.939+1197C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612243 | |||||||
| chr7:77612244 | A | C | 1 | a0002c0002t0001g0062 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.939+1198A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612244 | |||||||
| chr7:77612472 | A | G | 1 | a0002c0002t0001g0038 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.939+1426A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612472 | |||||||
| chr7:77612524 | C | T | 1 | a0002c0002t0001g0067 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.939+1478C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612524 | |||||||
| chr7:77612542 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.939+1496G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612542 | |||||||
| chr7:77612665 | C | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0167 |
2 | NA19003.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.939+1619C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612665 | |||||||
| chr7:77612727 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.939+1681G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612727 | |||||||
| chr7:77612757 | T | C | 117 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0004g0132 others(114): Show |
117 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.939+1711T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612757 | |||||||
| chr7:77612770 | G | GT | 8 | a0003c0003t0001g0185 a0003c0003t0001g0186 a0003c0003t0001g0187 others(5): Show |
8 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.939+1732dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77612770 | ||||||
| chr7:77612770 | G | T | 3 | a0001c0001t0001g0243 a0001c0001t0001g0254 a0001c0001t0001g0305 |
3 | HG01109.hp2 HG03704.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.939+1724G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612770 | |||||||
| chr7:77612790 | T | G | 166 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(163): Show |
166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.939+1744T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612790 | |||||||
| chr7:77612794 | G | GT | 7 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0002c0002t0001g0034 others(4): Show |
7 | HG01169.hp1 HG01175.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.939+1758dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77612794 | ||||||
| chr7:77612821 | T | C | 243 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(240): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.939+1775T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612821 | |||||||
| chr7:77612864 | C | T | 1 | a0002c0002t0001g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.939+1818C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612864 | |||||||
| chr7:77612874 | C | T | 1 | a0002c0002t0001g0058 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.939+1828C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77612874 | |||||||
| chr7:77613023 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.939+1977A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613023 | |||||||
| chr7:77613167 | G | GT | 12 | a0001c0001t0001g0137 a0001c0001t0001g0162 a0002c0002t0001g0062 others(9): Show |
12 | HG00642.hp1 HG01109.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.939+2146dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77613167 | ||||||
| chr7:77613167 | GT | G | 108 | a0001c0001t0001g0156 a0001c0001t0001g0167 a0001c0001t0001g0215 others(105): Show |
108 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.939+2146delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77613167 | ||||||
| chr7:77613167 | GTT | G | 107 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(104): Show |
107 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.939+2145_939+2146d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77613167 | ||||||
| chr7:77613167 | GTTT | G | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(3): Show |
6 | HG01109.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.939+2144_939+2146d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77613167 | ||||||
| chr7:77613173 | T | G | 4 | a0001c0001t0001g0264 a0001c0001t0001g0271 a0001c0001t0001g0298 others(1): Show |
4 | HG01981.hp2 HG02683.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.939+2127T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613173 | |||||||
| chr7:77613174 | T | G | 66 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(63): Show |
66 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.939+2128T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613174 | |||||||
| chr7:77613175 | T | G | 1 | a0001c0001t0001g0234 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.939+2129T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613175 | |||||||
| chr7:77613180 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.939+2134T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613180 | |||||||
| chr7:77613189 | T | A | 1 | a0002c0002t0001g0211 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.939+2143T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613189 | |||||||
| chr7:77613222 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.939+2176T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613222 | |||||||
| chr7:77613272 | T | C | 119 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0307 others(116): Show |
119 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.939+2226T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613272 | |||||||
| chr7:77613340 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.939+2294A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613340 | |||||||
| chr7:77613468 | C | T | 12 | a0001c0001t0001g0027 a0001c0001t0001g0234 a0001c0001t0001g0235 others(9): Show |
12 | HG01952.hp2 HG01975.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.939+2422C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613468 | |||||||
| chr7:77613620 | G | A | 1 | a0002c0002t0001g0008 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.939+2574G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613620 | |||||||
| chr7:77613728 | G | A | 46 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(43): Show |
46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.939+2682G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613728 | |||||||
| chr7:77613778 | G | A | 256 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(253): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.939+2732G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613778 | |||||||
| chr7:77613783 | G | T | 1 | a0002c0002t0001g0039 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.939+2737G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613783 | |||||||
| chr7:77613807 | G | C | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.939+2761G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613807 | |||||||
| chr7:77613853 | T | C | 1 | a0002c0002t0001g0060 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.939+2807T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613853 | |||||||
| chr7:77613859 | A | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+2813A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613859 | |||||||
| chr7:77613879 | T | G | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.939+2833T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613879 | |||||||
| chr7:77613956 | A | G | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.939+2910A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613956 | |||||||
| chr7:77613984 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.939+2938C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77613984 | |||||||
| chr7:77614028 | A | C | 1 | a0005c0005t0001g0053 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.939+2982A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77614028 | |||||||
| chr7:77614068 | A | T | 75 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(72): Show |
75 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.939+3022A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77614068 | |||||||
| chr7:77614075 | T | TTTGTAGA others(4): Show |
250 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(247): Show |
250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.939+3033_939+3043d others(13): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77614075 | ||||||
| chr7:77614075 | T | TTTTGTAG others(5): Show |
2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.939+3031_939+3032i others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77614075 | ||||||
| chr7:77614087 | T | TTGTCTCA others(5): Show |
4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+3043_939+3044i others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77614087 | ||||||
| chr7:77614094 | G | C | 3 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG02486.hp1 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.939+3048G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77614094 | |||||||
| chr7:77614274 | A | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+3228A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77614274 | |||||||
| chr7:77614405 | G | A | 1 | a0002c0002t0001g0094 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.939+3359G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77614405 | |||||||
| chr7:77614611 | C | G | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.939+3565C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77614611 | |||||||
| chr7:77614696 | G | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | HG02135.hp1 NA18990.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.939+3650G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77614696 | |||||||
| chr7:77614746 | A | G | 1 | a0002c0002t0001g0111 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.939+3700A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77614746 | |||||||
| chr7:77615014 | C | G | 46 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(43): Show |
46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.940-3466C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77615014 | |||||||
| chr7:77615158 | G | A | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.940-3322G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77615158 | |||||||
| chr7:77615448 | CAA | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-3031_940-3030d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77615448 | |||||||
| chr7:77615673 | C | T | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.940-2807C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77615673 | |||||||
| chr7:77615780 | A | G | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.940-2700A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77615780 | |||||||
| chr7:77615837 | G | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-2643G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77615837 | |||||||
| chr7:77616316 | G | A | 5 | a0002c0002t0001g0018 a0002c0002t0001g0107 a0002c0002t0001g0108 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-2164G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77616316 | |||||||
| chr7:77616336 | G | A | 3 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0116 |
3 | HG02559.hp1 HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.940-2144G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77616336 | |||||||
| chr7:77616657 | G | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(68): Show |
71 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.940-1823G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77616657 | |||||||
| chr7:77616806 | G | A | 52 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(49): Show |
52 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.940-1674G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77616806 | |||||||
| chr7:77616874 | T | C | 256 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(253): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.940-1606T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77616874 | |||||||
| chr7:77616939 | C | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(74): Show |
77 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.940-1541C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77616939 | |||||||
| chr7:77617088 | G | A | 12 | a0001c0001t0001g0027 a0001c0001t0001g0234 a0001c0001t0001g0235 others(9): Show |
12 | HG01952.hp2 HG01975.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.940-1392G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77617088 | |||||||
| chr7:77617099 | G | A | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.940-1381G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77617099 | |||||||
| chr7:77617517 | G | A | 1 | a0003c0003t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.940-963G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77617517 | |||||||
| chr7:77617784 | A | AGTCCTAA others(7): Show |
4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-693_940-680dup others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 77617784 | ||||||
| chr7:77617796 | A | T | 1 | a0002c0002t0001g0087 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.940-684A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77617796 | |||||||
| chr7:77618126 | A | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-354A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77618126 | |||||||
| chr7:77618266 | T | C | 3 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0002g0161 |
3 | HG01243.hp1 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.940-214T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77618266 | |||||||
| chr7:77618278 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.940-202G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 11/17 | chr7 | 77618278 | |||||||
| chr7:77618606 | G | T | 1 | a0002c0002t0001g0099 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1025+41G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77618606 | |||||||
| chr7:77618666 | CT | C | 8 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
8 | HG02818.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1025+105delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77618666 | ||||||
| chr7:77619247 | T | C | 2 | a0002c0002t0001g0084 a0002c0002t0001g0097 |
2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1025+682T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77619247 | |||||||
| chr7:77619267 | G | A | 3 | a0002c0002t0001g0090 a0002c0002t0001g0091 a0002c0002t0001g0092 |
3 | HG02922.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1025+702G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77619267 | |||||||
| chr7:77619302 | A | G | 12 | a0001c0001t0001g0027 a0001c0001t0001g0234 a0001c0001t0001g0235 others(9): Show |
12 | HG01952.hp2 HG01975.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.1025+737A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77619302 | |||||||
| chr7:77619399 | A | T | 4 | a0001c0001t0001g0252 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+834A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77619399 | |||||||
| chr7:77619551 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1025+986G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77619551 | |||||||
| chr7:77619740 | T | A | 3 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 |
3 | HG00639.hp1 HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1025+1175T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77619740 | |||||||
| chr7:77620034 | A | T | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+1469A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77620034 | |||||||
| chr7:77620135 | A | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+1570A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77620135 | |||||||
| chr7:77620212 | CTCT | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0004g0132 |
3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1025+1652_1025+165 others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77620212 | ||||||
| chr7:77620374 | T | C | 1 | a0003c0003t0001g0180 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1025+1809T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77620374 | |||||||
| chr7:77620385 | A | T | 1 | a0001c0001t0001g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1025+1820A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77620385 | |||||||
| chr7:77620602 | A | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0004g0132 |
3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1025+2037A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77620602 | |||||||
| chr7:77620619 | A | T | 2 | a0003c0003t0001g0196 a0003c0003t0001g0197 |
2 | NA18971.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1025+2054A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77620619 | |||||||
| chr7:77620773 | C | T | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+2208C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77620773 | |||||||
| chr7:77620961 | C | G | 44 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(41): Show |
44 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1025+2396C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77620961 | |||||||
| chr7:77621046 | G | A | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+2481G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621046 | |||||||
| chr7:77621051 | C | CAT | 4 | a0001c0001t0001g0019 a0001c0001t0001g0255 a0001c0001t0001g0307 others(1): Show |
4 | HG01891.hp1 HG02015.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+2504_1025+250 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77621051 | ||||||
| chr7:77621051 | CAT | C | 90 | a0001c0001t0001g0017 a0001c0001t0001g0114 a0001c0001t0001g0139 others(87): Show |
90 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.1025+2504_1025+250 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77621051 | ||||||
| chr7:77621069 | T | A | 1 | a0002c0002t0001g0033 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1025+2504T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621069 | |||||||
| chr7:77621071 | A | T | 1 | a0002c0002t0001g0082 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1025+2506A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621071 | |||||||
| chr7:77621098 | T | TTTTA | 7 | a0001c0001t0001g0305 a0003c0003t0001g0112 a0003c0003t0001g0113 others(4): Show |
7 | HG01109.hp2 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1025+2554_1025+255 others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77621098 | ||||||
| chr7:77621098 | T | TTTTATTT others(1): Show |
4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+2550_1025+255 others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77621098 | ||||||
| chr7:77621098 | TTTTA | T | 8 | a0002c0002t0001g0025 a0002c0002t0001g0038 a0002c0002t0001g0040 others(5): Show |
8 | NA18946.hp2 NA18949.hp1 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.1025+2554_1025+255 others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77621098 | ||||||
| chr7:77621242 | C | CAG | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+2677_1025+267 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621242 | |||||||
| chr7:77621439 | T | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+2874T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621439 | |||||||
| chr7:77621573 | G | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | HG02135.hp1 NA18990.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1025+3008G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621573 | |||||||
| chr7:77621616 | C | T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1025+3051C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621616 | |||||||
| chr7:77621670 | C | CA | 52 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(49): Show |
52 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1025+3115dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77621670 | ||||||
| chr7:77621763 | A | G | 40 | a0001c0001t0001g0114 a0001c0001t0001g0139 a0001c0001t0001g0140 others(37): Show |
40 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1025+3198A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621763 | |||||||
| chr7:77621773 | G | A | 9 | a0003c0003t0001g0193 a0003c0003t0001g0194 a0003c0003t0001g0201 others(6): Show |
9 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1025+3208G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621773 | |||||||
| chr7:77621906 | A | G | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1025+3341A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621906 | |||||||
| chr7:77621909 | G | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+3344G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77621909 | |||||||
| chr7:77622047 | C | T | 1 | a0002c0002t0001g0010 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1025+3482C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77622047 | |||||||
| chr7:77622095 | T | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+3530T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77622095 | |||||||
| chr7:77622206 | T | C | 5 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1025+3641T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77622206 | |||||||
| chr7:77622654 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-4051C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77622654 | |||||||
| chr7:77622671 | T | TACTCAG | 114 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0002c0002t0001g0002 others(111): Show |
114 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1026-4034_1026-403 others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77622671 | |||||||
| chr7:77622849 | T | TTTCCAAT others(33): Show |
4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-3844_1026-384 others(44): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77622849 | ||||||
| chr7:77623012 | C | CA | 48 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(45): Show |
48 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.1026-3681dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77623012 | ||||||
| chr7:77623137 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1026-3568T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77623137 | |||||||
| chr7:77623267 | G | A | 1 | a0002c0002t0001g0039 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1026-3438G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77623267 | |||||||
| chr7:77623389 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1026-3316G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77623389 | |||||||
| chr7:77623713 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1026-2992C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77623713 | |||||||
| chr7:77623934 | G | A | 8 | a0003c0003t0001g0185 a0003c0003t0001g0186 a0003c0003t0001g0187 others(5): Show |
8 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-2771G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77623934 | |||||||
| chr7:77624156 | G | A | 279 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(276): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1026-2549G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77624156 | |||||||
| chr7:77624773 | C | T | 1 | a0002c0002t0001g0057 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1026-1932C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77624773 | |||||||
| chr7:77624901 | G | A | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1026-1804G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77624901 | |||||||
| chr7:77625067 | A | G | 5 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026-1638A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625067 | |||||||
| chr7:77625230 | A | G | 23 | a0003c0003t0001g0133 a0003c0003t0001g0184 a0003c0003t0001g0185 others(20): Show |
23 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1026-1475A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625230 | |||||||
| chr7:77625253 | G | GT | 15 | a0001c0001t0001g0126 a0001c0001t0001g0150 a0001c0001t0001g0152 others(12): Show |
15 | HG00140.hp2 HG00438.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1026-1437dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625253 | ||||||
| chr7:77625413 | A | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1292A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625413 | |||||||
| chr7:77625453 | C | T | 279 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(276): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1026-1252C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625453 | |||||||
| chr7:77625468 | G | GCGCCCTC others(11): Show |
1 | a0001c0001t0001g0149 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1026-1236_1026-123 others(22): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | ||||||
| chr7:77625468 | G | GCGCCCTC others(13): Show |
1 | a0001c0001t0001g0148 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1026-1236_1026-123 others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | ||||||
| chr7:77625468 | G | GCGCCTCT others(12): Show |
1 | a0001c0001t0001g0150 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1026-1236_1026-123 others(23): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | ||||||
| chr7:77625468 | G | GCGCGCGC others(25): Show |
1 | a0001c0001t0001g0167 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1026-1236_1026-123 others(36): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | ||||||
| chr7:77625468 | G | GCGCTCTC others(9): Show |
2 | a0001c0001t0001g0140 a0001c0001t0001g0142 |
2 | HG00280.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1026-1236_1026-123 others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | ||||||
| chr7:77625468 | G | GCGCTCTC others(15): Show |
1 | a0001c0001t0001g0114 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1026-1236_1026-123 others(26): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | ||||||
| chr7:77625468 | G | GCTCTCTC others(11): Show |
2 | a0001c0001t0001g0288 a0001c0001t0001g0296 |
2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1026-1234_1026-123 others(22): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | ||||||
| chr7:77625468 | G | GCTCTCTC others(13): Show |
3 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0001g0294 |
3 | HG02486.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1026-1234_1026-123 others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | ||||||
| chr7:77625468 | G | GCTCTCTC others(21): Show |
2 | a0001c0001t0001g0291 a0001c0001t0001g0293 |
2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1026-1234_1026-123 others(32): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | ||||||
| chr7:77625468 | G | GCTCTCTC others(25): Show |
1 | a0001c0001t0001g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1026-1234_1026-123 others(36): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | ||||||
| chr7:77625468 | G | GCTCTCTC others(37): Show |
1 | a0001c0001t0001g0295 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1026-1234_1026-123 others(48): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | ||||||
| chr7:77625468 | GCTCGCTC others(7): Show |
G | 1 | a0001c0001t0001g0290 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1026-1233_1026-122 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625468 | ||||||
| chr7:77625470 | T | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG00609.hp1 HG01358.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1026-1235T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625470 | |||||||
| chr7:77625470 | T | TCGCTCG | 6 | a0002c0002t0001g0033 a0002c0002t0001g0049 a0002c0002t0001g0062 others(3): Show |
6 | HG00609.hp2 HG00738.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625470 | ||||||
| chr7:77625470 | T | TCGCTCGC others(3): Show |
6 | a0001c0001t0001g0239 a0001c0001t0001g0247 a0001c0001t0001g0250 others(3): Show |
6 | HG00438.hp2 HG01255.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625470 | ||||||
| chr7:77625470 | TCG | T | 3 | a0001c0001t0001g0164 a0003c0003t0001g0205 a0003c0003t0001g0214 |
3 | HG02280.hp1 HG02698.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1026-1233_1026-123 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625470 | ||||||
| chr7:77625472 | G | GCT | 6 | a0003c0003t0001g0178 a0003c0003t0001g0180 a0003c0003t0001g0183 others(3): Show |
6 | HG00733.hp2 HG01516.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-1183_1026-118 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(7): Show |
1 | a0002c0002t0001g0013 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(9): Show |
1 | a0004c0004t0001g0270 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(19): Show |
1 | a0001c0001t0001g0281 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(30): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(5): Show |
6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0246 others(3): Show |
6 | HG00741.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(7): Show |
7 | a0001c0001t0001g0027 a0001c0001t0001g0226 a0001c0001t0001g0256 others(4): Show |
7 | HG01952.hp2 HG01975.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(9): Show |
3 | a0001c0001t0001g0232 a0001c0001t0001g0240 a0001c0001t0001g0276 |
3 | HG02723.hp2 HG02895.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(11): Show |
3 | a0001c0001t0001g0219 a0001c0001t0001g0230 a0001c0001t0001g0244 |
3 | HG02897.hp2 NA19030.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(22): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(13): Show |
8 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0223 others(5): Show |
8 | HG01884.hp2 HG02165.hp1 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(15): Show |
1 | a0001c0001t0001g0215 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(26): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(17): Show |
4 | a0001c0001t0001g0119 a0001c0001t0001g0126 a0001c0001t0001g0218 others(1): Show |
4 | HG02486.hp2 HG03209.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(28): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(19): Show |
4 | a0001c0001t0001g0117 a0001c0001t0001g0123 a0001c0001t0001g0216 others(1): Show |
4 | HG02647.hp1 HG02818.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(30): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(21): Show |
4 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG02080.hp2 HG02132.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(32): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(23): Show |
1 | a0001c0001t0001g0017 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(34): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(3): Show |
2 | a0002c0002t0001g0097 a0002c0002t0001g0128 |
2 | HG00639.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(5): Show |
2 | a0001c0001t0001g0130 a0002c0002t0001g0077 |
2 | HG02572.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(9): Show |
2 | a0002c0002t0001g0022 a0002c0002t0001g0093 |
2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(11): Show |
1 | a0002c0002t0001g0084 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(22): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(13): Show |
3 | a0001c0001t0001g0131 a0002c0002t0001g0010 a0002c0002t0001g0105 |
3 | HG02165.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(15): Show |
1 | a0002c0002t0001g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(26): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(17): Show |
1 | a0002c0002t0001g0051 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(28): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(19): Show |
1 | a0002c0002t0001g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(30): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(23): Show |
2 | a0002c0002t0001g0090 a0002c0002t0001g0091 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(34): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(25): Show |
4 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(36): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(27): Show |
1 | a0001c0001t0001g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(38): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(31): Show |
1 | a0001c0001t0001g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(42): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(37): Show |
1 | a0001c0001t0001g0136 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(48): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(1): Show |
6 | a0002c0002t0001g0015 a0002c0002t0001g0026 a0002c0002t0001g0055 others(3): Show |
6 | HG01516.hp2 HG01517.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(3): Show |
8 | a0002c0002t0001g0009 a0002c0002t0001g0029 a0002c0002t0001g0032 others(5): Show |
8 | HG02698.hp1 HG03195.hp1 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(5): Show |
9 | a0001c0001t0001g0225 a0001c0001t0001g0280 a0002c0002t0001g0028 others(6): Show |
9 | HG00280.hp1 HG00323.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(7): Show |
11 | a0002c0002t0001g0016 a0002c0002t0001g0024 a0002c0002t0001g0025 others(8): Show |
11 | HG00140.hp1 HG00673.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(9): Show |
6 | a0002c0002t0001g0018 a0002c0002t0001g0031 a0002c0002t0001g0075 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(11): Show |
8 | a0002c0002t0001g0038 a0002c0002t0001g0042 a0002c0002t0001g0044 others(5): Show |
8 | HG00408.hp2 HG00733.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(22): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(13): Show |
7 | a0002c0002t0001g0058 a0002c0002t0001g0059 a0002c0002t0001g0074 others(4): Show |
7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(15): Show |
3 | a0002c0002t0001g0099 a0002c0002t0001g0111 a0002c0002t0005g0054 |
3 | HG03710.hp2 NA18964.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(26): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(17): Show |
2 | a0002c0002t0001g0064 a0002c0002t0001g0088 |
2 | HG01891.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(28): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(19): Show |
1 | a0002c0002t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(30): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(21): Show |
1 | a0002c0002t0001g0002 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(32): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCGC others(23): Show |
1 | a0002c0002t0001g0037 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(34): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCTC others(13): Show |
1 | a0001c0001t0001g0153 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCGCTC others(19): Show |
1 | a0003c0006t0001g0190 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1026-1230_1026-122 others(30): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCT | 5 | a0003c0003t0001g0169 a0003c0003t0001g0172 a0003c0003t0001g0181 others(2): Show |
5 | HG02015.hp2 NA18993.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026-1185_1026-118 others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCTCT | 4 | a0003c0003t0001g0003 a0003c0003t0001g0182 a0003c0003t0001g0186 others(1): Show |
4 | HG00408.hp1 HG03704.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-1187_1026-118 others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCTCTC others(1): Show |
4 | a0003c0003t0001g0171 a0003c0003t0001g0173 a0003c0003t0001g0176 others(1): Show |
4 | HG00438.hp1 HG01255.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1189_1026-118 others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCTCTC others(3): Show |
3 | a0001c0001t0001g0156 a0003c0003t0001g0179 a0003c0003t0001g0191 |
3 | HG01261.hp1 NA19060.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1026-1191_1026-118 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCTCTC others(7): Show |
1 | a0003c0003t0001g0187 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1026-1195_1026-118 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCTCTC others(11): Show |
3 | a0001c0001t0001g0158 a0003c0003t0001g0185 a0003c0003t0001g0189 |
3 | HG00323.hp1 HG01109.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1026-1199_1026-118 others(22): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCTCTC others(13): Show |
1 | a0003c0003t0001g0127 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1026-1201_1026-118 others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCTCTC others(15): Show |
1 | a0003c0003t0001g0188 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1026-1203_1026-118 others(26): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCTCTC others(19): Show |
1 | a0003c0003t0001g0194 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1026-1207_1026-118 others(30): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCTCTC others(27): Show |
2 | a0001c0001t0001g0151 a0001c0001t0001g0154 |
2 | HG00735.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1026-1215_1026-118 others(38): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCTCTC others(29): Show |
2 | a0001c0001t0001g0152 a0001c0001t0001g0155 |
2 | HG01169.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1026-1217_1026-118 others(40): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTCTCTC others(31): Show |
1 | a0003c0003t0001g0192 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1026-1219_1026-118 others(42): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTTGCGC others(3): Show |
1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1026-1231_1026-123 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTTGCGC others(5): Show |
2 | a0003c0003t0001g0112 a0003c0003t0001g0116 |
2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1026-1231_1026-123 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTTGCGC others(7): Show |
1 | a0003c0003t0001g0113 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1026-1231_1026-123 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | GCTTGCGC others(13): Show |
1 | a0003c0003t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1026-1231_1026-123 others(24): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | G | T | 23 | a0001c0001t0001g0114 a0001c0001t0001g0139 a0001c0001t0001g0140 others(20): Show |
23 | HG00280.hp2 HG01243.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.1026-1233G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625472 | |||||||
| chr7:77625472 | GCT | G | 8 | a0001c0001t0001g0110 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG02135.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-1183_1026-118 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | GCTCTCT | G | 4 | a0003c0003t0001g0001 a0003c0003t0001g0184 a0003c0003t0001g0210 others(1): Show |
4 | HG01070.hp1 HG01074.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-1187_1026-118 others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | GCTCTCTC others(3): Show |
G | 2 | a0003c0003t0001g0133 a0003c0003t0001g0299 |
2 | HG01071.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1026-1191_1026-118 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | GCTCTCTC others(5): Show |
G | 1 | a0003c0003t0001g0283 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1026-1193_1026-118 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625472 | GCTCTCTC others(7): Show |
G | 1 | a0003c0003t0001g0208 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1026-1195_1026-118 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625472 | ||||||
| chr7:77625474 | T | TCG | 4 | a0002c0002t0001g0068 a0002c0002t0001g0085 a0002c0002t0001g0087 others(1): Show |
4 | HG01975.hp2 HG03225.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625474 | ||||||
| chr7:77625474 | T | TCGCG | 14 | a0001c0001t0001g0231 a0001c0001t0001g0233 a0001c0001t0001g0242 others(11): Show |
14 | HG00639.hp1 HG01099.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625474 | ||||||
| chr7:77625474 | T | TCGCGCG | 6 | a0001c0001t0001g0228 a0001c0001t0001g0235 a0001c0001t0001g0238 others(3): Show |
6 | HG03130.hp2 HG03139.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625474 | ||||||
| chr7:77625474 | T | TCGCGCGC others(1): Show |
17 | a0001c0001t0001g0019 a0001c0001t0001g0234 a0001c0001t0001g0236 others(14): Show |
17 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.1026-1230_1026-122 others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625474 | ||||||
| chr7:77625476 | T | G | 46 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0231 others(43): Show |
46 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.1026-1229T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625476 | |||||||
| chr7:77625478 | T | A | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1026-1227T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625478 | |||||||
| chr7:77625478 | T | G | 41 | a0001c0001t0001g0110 a0001c0001t0001g0162 a0001c0001t0001g0163 others(38): Show |
41 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1026-1227T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625478 | |||||||
| chr7:77625480 | T | G | 14 | a0001c0001t0001g0110 a0001c0001t0001g0162 a0001c0001t0001g0163 others(11): Show |
14 | HG00140.hp2 HG01256.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1026-1225T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625480 | |||||||
| chr7:77625481 | C | CTCTCTCT others(9): Show |
1 | a0001c0001t0001g0157 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1026-1209_1026-120 others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625481 | ||||||
| chr7:77625482 | T | G | 6 | a0001c0001t0001g0229 a0001c0001t0001g0257 a0003c0003t0001g0020 others(3): Show |
6 | HG00140.hp2 HG01256.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026-1223T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625482 | |||||||
| chr7:77625504 | T | A | 6 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-1201T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625504 | |||||||
| chr7:77625504 | TCTCTCTC others(19): Show |
T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1026-1195_1026-117 others(30): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625504 | ||||||
| chr7:77625506 | TCTCTCTC others(17): Show |
T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1193_1026-117 others(28): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625506 | ||||||
| chr7:77625508 | TCTCTCTC others(9): Show |
T | 2 | a0002c0002t0001g0034 a0002c0002t0001g0035 |
2 | HG01169.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1026-1191_1026-117 others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625508 | ||||||
| chr7:77625510 | T | A | 10 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0001g0135 others(7): Show |
10 | HG00280.hp1 HG00323.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1026-1195T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625510 | |||||||
| chr7:77625510 | TCTCTCTC others(7): Show |
T | 1 | a0002c0002t0001g0045 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1026-1189_1026-117 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625510 | ||||||
| chr7:77625511 | C | G | 1 | a0002c0002t0001g0309 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1026-1194C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625511 | |||||||
| chr7:77625512 | TCTCTCTC others(5): Show |
T | 4 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0002c0002t0001g0007 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1187_1026-117 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625512 | ||||||
| chr7:77625516 | TCTCTCTC others(7): Show |
T | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1026-1183_1026-117 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625516 | ||||||
| chr7:77625518 | T | A | 1 | a0003c0003t0001g0184 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1026-1187T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625518 | |||||||
| chr7:77625518 | TCTCTCA | T | 3 | a0002c0002t0001g0061 a0002c0002t0001g0065 a0002c0002t0001g0109 |
3 | NA18987.hp1 NA18992.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1026-1171_1026-116 others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625518 | ||||||
| chr7:77625520 | T | A | 9 | a0001c0001t0001g0114 a0001c0001t0001g0139 a0001c0001t0001g0140 others(6): Show |
9 | HG00280.hp2 HG01358.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026-1185T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625520 | |||||||
| chr7:77625520 | T | TCTCTCTC others(9): Show |
2 | a0001c0001t0001g0166 a0003c0003t0002g0161 |
2 | HG00609.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1026-1182_1026-118 others(20): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625520 | ||||||
| chr7:77625520 | T | TCTCTCTC others(11): Show |
2 | a0001c0001t0001g0146 a0003c0003t0002g0160 |
2 | HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1026-1182_1026-118 others(22): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625520 | ||||||
| chr7:77625520 | T | TCTCTCTC others(15): Show |
2 | a0001c0001t0001g0145 a0001c0001t0001g0147 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1026-1182_1026-118 others(26): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625520 | ||||||
| chr7:77625520 | T | TCTCTCTC others(17): Show |
1 | a0003c0003t0002g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1026-1182_1026-118 others(28): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625520 | ||||||
| chr7:77625520 | T | TCTCTCTC others(21): Show |
1 | a0001c0001t0001g0165 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1026-1182_1026-118 others(32): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625520 | ||||||
| chr7:77625522 | T | A | 21 | a0001c0001t0001g0019 a0001c0001t0001g0228 a0001c0001t0001g0231 others(18): Show |
21 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1026-1183T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625522 | |||||||
| chr7:77625522 | TCA | T | 3 | a0001c0001t0004g0132 a0002c0002t0001g0036 a0002c0002t0001g0066 |
3 | HG02293.hp2 HG03471.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1026-1181_1026-118 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625522 | ||||||
| chr7:77625524 | A | ACT | 52 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0027 others(49): Show |
52 | HG00099.hp2 HG00438.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.1026-1177_1026-117 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625524 | ||||||
| chr7:77625524 | A | T | 135 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0130 others(132): Show |
135 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1026-1181A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625524 | |||||||
| chr7:77625526 | T | A | 1 | a0002c0002t0001g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1026-1179T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625526 | |||||||
| chr7:77625530 | A | G | 36 | a0001c0001t0001g0114 a0001c0001t0001g0139 a0001c0001t0001g0140 others(33): Show |
36 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1026-1175A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625530 | |||||||
| chr7:77625530 | A | T | 7 | a0001c0001t0001g0157 a0002c0002t0001g0010 a0002c0002t0001g0055 others(4): Show |
7 | HG01081.hp1 HG01516.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.1026-1175A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625530 | |||||||
| chr7:77625532 | T | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1026-1173T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625532 | |||||||
| chr7:77625536 | A | G | 5 | a0001c0001t0001g0305 a0003c0003t0001g0020 a0003c0003t0001g0301 others(2): Show |
5 | HG00140.hp2 HG01109.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026-1169A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625536 | |||||||
| chr7:77625540 | G | T | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1026-1165G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625540 | |||||||
| chr7:77625542 | G | A | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1026-1163G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625542 | |||||||
| chr7:77625548 | T | A | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1026-1157T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625548 | |||||||
| chr7:77625550 | T | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1155T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625550 | |||||||
| chr7:77625552 | T | G | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1026-1153T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625552 | |||||||
| chr7:77625554 | G | A | 36 | a0001c0001t0001g0114 a0001c0001t0001g0139 a0001c0001t0001g0140 others(33): Show |
36 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1026-1151G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625554 | |||||||
| chr7:77625554 | G | T | 1 | a0001c0001t0001g0281 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1026-1151G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625554 | |||||||
| chr7:77625554 | GCT | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1140_1026-113 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625554 | ||||||
| chr7:77625556 | T | G | 1 | a0001c0001t0001g0281 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1026-1149T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625556 | |||||||
| chr7:77625558 | T | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1147T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625558 | |||||||
| chr7:77625563 | C | CT | 50 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0117 others(47): Show |
50 | HG00438.hp2 HG00639.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1026-1141dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | ||||||
| chr7:77625563 | C | CTT | 88 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0121 others(85): Show |
88 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1026-1141_1026-114 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | ||||||
| chr7:77625563 | C | CTTT | 36 | a0001c0001t0001g0005 a0001c0001t0001g0151 a0001c0001t0001g0153 others(33): Show |
36 | HG00609.hp2 HG00673.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1026-1141_1026-114 others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | ||||||
| chr7:77625563 | C | CTTTT | 4 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0002c0002t0001g0031 others(1): Show |
4 | HG01175.hp1 HG02055.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1141_1026-114 others(8): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | ||||||
| chr7:77625563 | C | CTTTTT | 8 | a0001c0001t0001g0131 a0001c0001t0001g0152 a0001c0001t0001g0290 others(5): Show |
8 | HG01169.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-1141_1026-114 others(9): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | ||||||
| chr7:77625563 | C | CTTTTTT | 3 | a0001c0001t0001g0130 a0001c0001t0001g0147 a0001c0001t0001g0155 |
3 | HG02451.hp1 HG02572.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1026-1141_1026-114 others(10): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | ||||||
| chr7:77625563 | C | CTTTTTTT | 4 | a0001c0001t0001g0164 a0001c0001t0001g0287 a0001c0001t0001g0288 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-1141_1026-114 others(11): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | ||||||
| chr7:77625563 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0142 a0001c0001t0001g0165 |
2 | HG01517.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1026-1141_1026-114 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | ||||||
| chr7:77625563 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0139 a0001c0001t0001g0167 |
2 | HG01358.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1026-1141_1026-114 others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | ||||||
| chr7:77625563 | C | T | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0003c0003t0001g0168 |
3 | HG00280.hp2 HG02055.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1026-1142C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625563 | |||||||
| chr7:77625563 | CTCTTTTT | C | 10 | a0001c0001t0001g0110 a0001c0001t0001g0134 a0001c0001t0001g0135 others(7): Show |
10 | HG00280.hp1 HG00323.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1026-1140_1026-113 others(11): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | ||||||
| chr7:77625563 | CTCTTTTT others(3): Show |
C | 1 | a0002c0002t0001g0042 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1026-1140_1026-113 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | ||||||
| chr7:77625563 | CTCTTTTT others(4): Show |
C | 2 | a0002c0002t0001g0073 a0002c0002t0001g0080 |
2 | HG02004.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1026-1140_1026-113 others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | ||||||
| chr7:77625563 | CTCTTTTT others(5): Show |
C | 5 | a0001c0001t0001g0114 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
5 | HG02258.hp2 NA18970.hp2 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026-1140_1026-112 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | ||||||
| chr7:77625563 | CTCTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1026-1140_1026-112 others(18): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625563 | ||||||
| chr7:77625565 | C | CT | 10 | a0001c0001t0001g0256 a0003c0003t0001g0001 a0003c0003t0001g0174 others(7): Show |
10 | HG00735.hp2 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1026-1117dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625565 | ||||||
| chr7:77625565 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0166 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1026-1126_1026-111 others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625565 | ||||||
| chr7:77625565 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0146 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1026-1127_1026-111 others(15): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625565 | ||||||
| chr7:77625565 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1026-1128_1026-111 others(16): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 77625565 | ||||||
| chr7:77625565 | C | T | 215 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(212): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1026-1140C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625565 | |||||||
| chr7:77625594 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1026-1111C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625594 | |||||||
| chr7:77625640 | A | G | 5 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0292 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026-1065A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77625640 | |||||||
| chr7:77626060 | G | A | 2 | a0002c0002t0001g0062 a0002c0002t0001g0079 |
2 | HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1026-645G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626060 | |||||||
| chr7:77626228 | A | G | 5 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026-477A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626228 | |||||||
| chr7:77626238 | A | T | 98 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(95): Show |
98 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1026-467A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626238 | |||||||
| chr7:77626313 | T | C | 1 | a0002c0002t0001g0087 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1026-392T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626313 | |||||||
| chr7:77626362 | G | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0232 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1026-343G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626362 | |||||||
| chr7:77626489 | G | A | 1 | a0002c0002t0001g0038 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1026-216G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626489 | |||||||
| chr7:77626505 | C | A | 254 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(251): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1026-200C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626505 | |||||||
| chr7:77626547 | C | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(68): Show |
71 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1026-158C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626547 | |||||||
| chr7:77626624 | T | C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(70): Show |
73 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1026-81T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 12/17 | chr7 | 77626624 | |||||||
| chr7:77627859 | A | G | 1 | a0002c0002t0001g0031 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1996+184A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77627859 | |||||||
| chr7:77627923 | TTTTTCTT others(5): Show |
T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1996+251_1996+262d others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 77627923 | ||||||
| chr7:77627975 | C | G | 4 | a0002c0002t0001g0006 a0002c0002t0001g0011 a0002c0002t0001g0012 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1996+300C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77627975 | |||||||
| chr7:77627977 | G | T | 1 | a0001c0001t0001g0121 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1996+302G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77627977 | |||||||
| chr7:77627994 | TAA | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1996+320_1996+321d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77627994 | |||||||
| chr7:77627998 | T | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1996+323T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77627998 | |||||||
| chr7:77628338 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1996+663A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77628338 | |||||||
| chr7:77628560 | A | AT | 117 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0271 others(114): Show |
117 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1996+900dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 77628560 | ||||||
| chr7:77628560 | A | ATT | 6 | a0002c0002t0001g0007 a0002c0002t0001g0008 a0002c0002t0001g0014 others(3): Show |
6 | HG02004.hp1 NA18953.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1996+899_1996+900d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 77628560 | ||||||
| chr7:77628582 | T | C | 1 | a0003c0003t0001g0198 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1996+907T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77628582 | |||||||
| chr7:77628650 | G | A | 1 | a0001c0001t0004g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1996+975G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77628650 | |||||||
| chr7:77628682 | C | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(74): Show |
77 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.1996+1007C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77628682 | |||||||
| chr7:77628798 | A | G | 1 | a0002c0002t0001g0095 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1996+1123A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77628798 | |||||||
| chr7:77629011 | G | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1996+1336G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629011 | |||||||
| chr7:77629030 | A | C | 5 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1996+1355A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629030 | |||||||
| chr7:77629240 | C | T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1996+1565C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629240 | |||||||
| chr7:77629243 | C | G | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1996+1568C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629243 | |||||||
| chr7:77629500 | T | C | 1 | a0002c0002t0001g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1996+1825T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629500 | |||||||
| chr7:77629564 | T | A | 12 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0229 others(9): Show |
12 | HG02818.hp1 HG02895.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.1996+1889T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629564 | |||||||
| chr7:77629696 | T | C | 254 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(251): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1996+2021T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629696 | |||||||
| chr7:77629714 | G | A | 6 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1996+2039G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629714 | |||||||
| chr7:77629758 | A | T | 1 | a0002c0002t0001g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1996+2083A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629758 | |||||||
| chr7:77629798 | G | A | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1996+2123G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629798 | |||||||
| chr7:77629939 | C | CA | 81 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0019 others(78): Show |
81 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1996+2283dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 77629939 | ||||||
| chr7:77629939 | CA | C | 22 | a0002c0002t0001g0025 a0002c0002t0001g0038 a0002c0002t0001g0040 others(19): Show |
22 | HG00140.hp2 HG01099.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.1996+2283delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 77629939 | ||||||
| chr7:77629966 | A | C | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(238): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1996+2291A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77629966 | |||||||
| chr7:77630202 | C | T | 2 | a0002c0002t0001g0088 a0002c0002t0001g0220 |
2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1997-2146C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77630202 | |||||||
| chr7:77630252 | A | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1997-2096A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77630252 | |||||||
| chr7:77630518 | C | G | 247 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(244): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1997-1830C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77630518 | |||||||
| chr7:77631101 | A | G | 5 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1997-1247A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631101 | |||||||
| chr7:77631152 | A | G | 5 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1997-1196A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631152 | |||||||
| chr7:77631285 | A | G | 2 | a0002c0002t0001g0212 a0002c0002t0001g0213 |
2 | HG03831.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1997-1063A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631285 | |||||||
| chr7:77631331 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1997-1017A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631331 | |||||||
| chr7:77631584 | A | G | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1997-764A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631584 | |||||||
| chr7:77631639 | C | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1997-709C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631639 | |||||||
| chr7:77631767 | T | A | 4 | a0002c0002t0001g0006 a0002c0002t0001g0011 a0002c0002t0001g0012 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1997-581T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631767 | |||||||
| chr7:77631824 | A | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1997-524A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631824 | |||||||
| chr7:77631825 | T | C | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1997-523T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631825 | |||||||
| chr7:77631980 | T | A | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1997-368T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77631980 | |||||||
| chr7:77632033 | T | A | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1997-315T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77632033 | |||||||
| chr7:77632082 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1997-266G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77632082 | |||||||
| chr7:77632282 | A | G | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1997-66A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77632282 | |||||||
| chr7:77632301 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1997-47T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77632301 | |||||||
| chr7:77632331 | T | G | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1997-17T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 13/17 | chr7 | 77632331 | |||||||
| chr7:77632503 | T | G | 117 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0004g0132 others(114): Show |
117 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.2074+78T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77632503 | |||||||
| chr7:77632745 | T | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(68): Show |
71 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.2074+320T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77632745 | |||||||
| chr7:77632746 | C | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(68): Show |
71 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.2074+321C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77632746 | |||||||
| chr7:77632762 | G | A | 3 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0023 |
3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2074+337G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77632762 | |||||||
| chr7:77632913 | C | T | 3 | a0001c0001t0001g0244 a0001c0001t0001g0272 a0001c0001t0001g0276 |
3 | NA18998.hp1 NA19066.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2074+488C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77632913 | |||||||
| chr7:77632936 | G | A | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2074+511G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77632936 | |||||||
| chr7:77632951 | G | A | 1 | a0002c0002t0001g0025 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2074+526G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77632951 | |||||||
| chr7:77632965 | A | G | 35 | a0001c0001t0001g0114 a0001c0001t0001g0139 a0001c0001t0001g0140 others(32): Show |
35 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2074+540A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77632965 | |||||||
| chr7:77633100 | G | A | 1 | a0003c0003t0001g0286 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2074+675G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633100 | |||||||
| chr7:77633192 | C | T | 2 | a0002c0002t0001g0031 a0002c0002t0001g0058 |
2 | HG02135.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2074+767C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633192 | |||||||
| chr7:77633270 | T | TA | 163 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0129 others(160): Show |
163 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.2074+855dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 77633270 | ||||||
| chr7:77633363 | A | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2074+938A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633363 | |||||||
| chr7:77633375 | C | G | 6 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2074+950C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633375 | |||||||
| chr7:77633534 | C | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2074+1109C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633534 | |||||||
| chr7:77633658 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2074+1233T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633658 | |||||||
| chr7:77633793 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2074+1368C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633793 | |||||||
| chr7:77633820 | T | A | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(238): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.2074+1395T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633820 | |||||||
| chr7:77633876 | G | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2074+1451G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633876 | |||||||
| chr7:77633979 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2074+1554C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77633979 | |||||||
| chr7:77634180 | C | CAG | 254 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(251): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.2075-1601_2075-160 others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 77634180 | ||||||
| chr7:77634205 | A | G | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2075-1577A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634205 | |||||||
| chr7:77634249 | T | C | 4 | a0002c0002t0001g0006 a0002c0002t0001g0011 a0002c0002t0001g0012 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2075-1533T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634249 | |||||||
| chr7:77634369 | T | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2075-1413T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634369 | |||||||
| chr7:77634409 | T | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2075-1373T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634409 | |||||||
| chr7:77634457 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2075-1325T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634457 | |||||||
| chr7:77634472 | T | C | 254 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(251): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.2075-1310T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634472 | |||||||
| chr7:77634499 | G | A | 1 | a0002c0002t0001g0087 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2075-1283G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634499 | |||||||
| chr7:77634542 | C | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(68): Show |
71 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.2075-1240C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634542 | |||||||
| chr7:77634636 | G | A | 33 | a0001c0001t0001g0114 a0001c0001t0001g0139 a0001c0001t0001g0140 others(30): Show |
33 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.2075-1146G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634636 | |||||||
| chr7:77634772 | G | T | 1 | a0001c0001t0001g0223 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2075-1010G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634772 | |||||||
| chr7:77634855 | G | A | 1 | a0003c0003t0001g0184 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2075-927G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634855 | |||||||
| chr7:77634976 | G | C | 1 | a0002c0002t0001g0012 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2075-806G>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77634976 | |||||||
| chr7:77635188 | A | T | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2075-594A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77635188 | |||||||
| chr7:77635189 | C | T | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2075-593C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77635189 | |||||||
| chr7:77635341 | A | G | 2 | a0002c0002t0001g0029 a0002c0002t0001g0030 |
2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2075-441A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77635341 | |||||||
| chr7:77635394 | A | C | 1 | a0002c0002t0001g0066 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2075-388A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77635394 | |||||||
| chr7:77635536 | T | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2075-246T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77635536 | |||||||
| chr7:77635585 | CAG | C | 3 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0116 |
3 | HG02559.hp1 HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2075-195_2075-194d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 77635585 | ||||||
| chr7:77635615 | AT | A | 15 | a0001c0001t0001g0110 a0001c0001t0001g0129 a0001c0001t0001g0134 others(12): Show |
15 | HG00280.hp1 HG00323.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.2075-155delT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 77635615 | ||||||
| chr7:77635660 | A | G | 1 | a0002c0002t0001g0028 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2075-122A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 14/17 | chr7 | 77635660 | |||||||
| chr7:77635889 | T | A | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2142+40T>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77635889 | |||||||
| chr7:77636164 | A | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0023 |
3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2142+315A>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636164 | |||||||
| chr7:77636202 | A | G | 2 | a0002c0002t0001g0084 a0002c0002t0001g0097 |
2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2142+353A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636202 | |||||||
| chr7:77636270 | G | A | 8 | a0003c0003t0001g0185 a0003c0003t0001g0186 a0003c0003t0001g0187 others(5): Show |
8 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.2142+421G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636270 | |||||||
| chr7:77636341 | G | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2142+492G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636341 | |||||||
| chr7:77636355 | A | G | 8 | a0003c0003t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0115 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2142+506A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636355 | |||||||
| chr7:77636390 | T | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2142+541T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636390 | |||||||
| chr7:77636391 | G | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2142+542G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636391 | |||||||
| chr7:77636408 | C | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0004g0132 |
3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2142+559C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636408 | |||||||
| chr7:77636436 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2143-582G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636436 | |||||||
| chr7:77636441 | G | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2143-577G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636441 | |||||||
| chr7:77636507 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2143-511C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636507 | |||||||
| chr7:77636636 | T | C | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2143-382T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636636 | |||||||
| chr7:77636680 | A | G | 1 | a0001c0001t0001g0275 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2143-338A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636680 | |||||||
| chr7:77636761 | GCAAAA | G | 3 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0023 |
3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2143-254_2143-250d others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 77636761 | ||||||
| chr7:77636816 | C | A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2143-202C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636816 | |||||||
| chr7:77636870 | A | G | 1 | a0003c0003t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2143-148A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636870 | |||||||
| chr7:77636907 | A | G | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2143-111A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636907 | |||||||
| chr7:77636996 | G | T | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2143-22G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 15/17 | chr7 | 77636996 | |||||||
| chr7:77637252 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0215 a0001c0001t0001g0216 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2173+204A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637252 | |||||||
| chr7:77637310 | T | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2173+262T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637310 | |||||||
| chr7:77637422 | AG | A | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2173+375delG | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637422 | |||||||
| chr7:77637541 | T | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2173+493T>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637541 | |||||||
| chr7:77637571 | A | G | 4 | a0003c0003t0001g0020 a0003c0003t0001g0301 a0003c0003t0001g0302 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2173+523A>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637571 | |||||||
| chr7:77637814 | G | A | 3 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0002g0161 |
3 | HG01243.hp1 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2173+766G>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637814 | |||||||
| chr7:77637852 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2174-772C>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637852 | |||||||
| chr7:77637857 | C | CA | 30 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0143 others(27): Show |
30 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.2174-748dupA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 77637857 | ||||||
| chr7:77637857 | C | CAA | 17 | a0001c0001t0001g0110 a0001c0001t0001g0129 a0001c0001t0001g0135 others(14): Show |
17 | HG00280.hp1 HG00323.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.2174-749_2174-748d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 77637857 | ||||||
| chr7:77637857 | C | CAAA | 103 | a0001c0001t0001g0114 a0001c0001t0001g0134 a0001c0001t0001g0137 others(100): Show |
103 | HG00140.hp1 HG00280.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.2174-750_2174-748d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 77637857 | ||||||
| chr7:77637857 | C | CAAAA | 36 | a0001c0001t0001g0147 a0001c0001t0001g0150 a0001c0001t0001g0151 others(33): Show |
36 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.2174-751_2174-748d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 77637857 | ||||||
| chr7:77637941 | TA | T | 18 | a0001c0001t0001g0017 a0001c0001t0001g0129 a0001c0001t0001g0131 others(15): Show |
18 | HG00280.hp1 HG00323.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.2174-679delA | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 77637941 | ||||||
| chr7:77637943 | A | ATTT | 4 | a0002c0002t0001g0018 a0002c0002t0001g0107 a0002c0002t0001g0108 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2174-681_2174-680i others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637943 | |||||||
| chr7:77637944 | A | AT | 51 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0154 others(48): Show |
51 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.2174-680_2174-679i others(3): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | |||||||
| chr7:77637944 | A | ATT | 46 | a0001c0001t0001g0139 a0001c0001t0001g0142 a0001c0001t0001g0151 others(43): Show |
46 | HG00408.hp2 HG00609.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.2174-680_2174-679i others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | |||||||
| chr7:77637944 | A | ATTT | 28 | a0001c0001t0001g0114 a0001c0001t0001g0149 a0001c0001t0001g0150 others(25): Show |
28 | HG00423.hp1 HG00609.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.2174-680_2174-679i others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | |||||||
| chr7:77637944 | A | ATTTTT | 3 | a0002c0002t0001g0078 a0002c0002t0001g0097 a0003c0003t0001g0115 |
3 | HG02976.hp2 HG03579.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.2174-680_2174-679i others(7): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | |||||||
| chr7:77637944 | A | T | 5 | a0002c0002t0001g0018 a0002c0002t0001g0107 a0002c0002t0001g0108 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.2174-680A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | |||||||
| chr7:77637944 | AAT | A | 19 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(16): Show |
19 | HG00140.hp2 HG00438.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.2174-679_2174-678d others(4): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | |||||||
| chr7:77637944 | AATT | A | 50 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0027 others(47): Show |
50 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.2174-679_2174-677d others(5): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | |||||||
| chr7:77637944 | AATTT | A | 3 | a0001c0001t0001g0234 a0003c0003t0001g0286 a0004c0004t0001g0267 |
3 | HG01993.hp2 HG02451.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.2174-679_2174-676d others(6): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | |||||||
| chr7:77637944 | AATTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0164 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2174-679_2174-670d others(12): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | |||||||
| chr7:77637944 | AATTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2174-679_2174-668d others(14): Show |
PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637944 | |||||||
| chr7:77637945 | A | AT | 27 | a0001c0001t0001g0144 a0003c0003t0001g0003 a0003c0003t0001g0171 others(24): Show |
27 | HG00408.hp1 HG00642.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.2174-650dupT | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 77637945 | ||||||
| chr7:77637945 | A | T | 162 | a0001c0001t0001g0019 a0001c0001t0001g0110 a0001c0001t0001g0114 others(159): Show |
162 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.2174-679A>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77637945 | |||||||
| chr7:77638139 | T | C | 1 | a0002c0002t0001g0080 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2174-485T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77638139 | |||||||
| chr7:77638196 | G | T | 1 | a0001c0001t0001g0281 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2174-428G>T | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 16/17 | chr7 | 77638196 | |||||||
| chr7:77638815 | C | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0260 |
3 | HG01255.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2281+84C>G | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 17/17 | chr7 | 77638815 | |||||||
| chr7:77638885 | C | A | 67 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0008 others(64): Show |
67 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.2281+154C>A | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 17/17 | chr7 | 77638885 | |||||||
| chr7:77639121 | T | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG02132.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.2282-98T>C | PTPN12 | ENSG00000127947.16 | transcript | ENST00000248594.11 | protein_coding | 17/17 | chr7 | 77639121 |