Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 91949 |
| ensemblid | ENSG00000168434.13 |
| hgncid | 18622 |
| symbol | COG7 |
| name | component of oligomeric golgi complex 7 |
| refseq_nuc | NM_153603.4 |
| refseq_prot | NP_705831.1 |
| ensembl_nuc | ENST00000307149.10 |
| ensembl_prot | ENSP00000305442.5 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 23388493 |
| end | 23453189 |
| strand | - |
| ver | v1.2 |
| region | chr16:23388493-23453189 |
| region5000 | chr16:23383493-23458189 |
| regionname0 | COG7_chr16_23388493_23453189 |
| regionname5000 | COG7_chr16_23383493_23458189 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 770 | 227 | 59 | 37 | 88 | 10 | 31 | 70 | COG7_chr16_23383493_23458189 | COG7 | MDFSK others(765): Show |
chr16 | 23383493 | 23458189 |
| a0002 | 0/0 | 770 | 39 | 16 | 14 | 4 | 0 | 5 | 2 | COG7_chr16_23383493_23458189 | COG7 | MDFSK others(765): Show |
chr16 | 23383493 | 23458189 |
| a0003 | 0/0 | 770 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | MDFSK others(765): Show |
chr16 | 23383493 | 23458189 |
| a0004 | 0/0 | 770 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | MDFSK others(765): Show |
chr16 | 23383493 | 23458189 |
| a0005 | 0/0 | 770 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | MDFSK others(765): Show |
chr16 | 23383493 | 23458189 |
| a0006 | 0/0 | 770 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | MDFSK others(765): Show |
chr16 | 23383493 | 23458189 |
| a0007 | 0/0 | 770 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | MDFSK others(765): Show |
chr16 | 23383493 | 23458189 |
| a0008 | 0/0 | 770 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | MDFSK others(765): Show |
chr16 | 23383493 | 23458189 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2310 | 220 | 52 | 37 | 88 | 10 | 31 | COG7_chr16_23383493_23458189 | COG7 | ATGGA others(2305): Show |
chr16 | 23383493 | 23458189 | ||
| a0001c0003 | 0/0 | 2310 | 4 | 4 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | ATGGA others(2305): Show |
chr16 | 23383493 | 23458189 | ||
| a0001c0008 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | ATGGA others(2305): Show |
chr16 | 23383493 | 23458189 | ||
| a0001c0009 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | ATGGA others(2305): Show |
chr16 | 23383493 | 23458189 | ||
| a0001c0012 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | ATGGA others(2305): Show |
chr16 | 23383493 | 23458189 | ||
| a0002c0002 | 0/0 | 2310 | 39 | 16 | 14 | 4 | 0 | 5 | COG7_chr16_23383493_23458189 | COG7 | ATGGA others(2305): Show |
chr16 | 23383493 | 23458189 | ||
| a0003c0007 | 0/0 | 2310 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | ATGGA others(2305): Show |
chr16 | 23383493 | 23458189 | ||
| a0004c0010 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | ATGGA others(2305): Show |
chr16 | 23383493 | 23458189 | ||
| a0005c0005 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | ATGGA others(2305): Show |
chr16 | 23383493 | 23458189 | ||
| a0006c0011 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | ATGGA others(2305): Show |
chr16 | 23383493 | 23458189 | ||
| a0007c0004 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | ATGGA others(2305): Show |
chr16 | 23383493 | 23458189 | ||
| a0008c0006 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | ATGGA others(2305): Show |
chr16 | 23383493 | 23458189 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2935 | 115 | 20 | 27 | 44 | 4 | 18 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2930): Show |
chr16 | 23383493 | 23458189 |
| a0001c0001t0002 | 0/0 | 2934 | 88 | 26 | 10 | 37 | 5 | 10 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2929): Show |
chr16 | 23383493 | 23458189 |
| a0001c0001t0004 | 0/0 | 2936 | 9 | 1 | 0 | 5 | 1 | 2 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2931): Show |
chr16 | 23383493 | 23458189 |
| a0001c0001t0005 | 0/0 | 2935 | 4 | 2 | 0 | 2 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2930): Show |
chr16 | 23383493 | 23458189 |
| a0001c0001t0006 | 0/0 | 2935 | 3 | 3 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2930): Show |
chr16 | 23383493 | 23458189 |
| a0001c0001t0008 | 0/0 | 2934 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2929): Show |
chr16 | 23383493 | 23458189 |
| a0001c0003t0003 | 0/0 | 2934 | 3 | 3 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2929): Show |
chr16 | 23383493 | 23458189 |
| a0001c0003t0007 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2930): Show |
chr16 | 23383493 | 23458189 |
| a0001c0008t0001 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2930): Show |
chr16 | 23383493 | 23458189 |
| a0001c0009t0002 | 0/0 | 2934 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2929): Show |
chr16 | 23383493 | 23458189 |
| a0001c0012t0002 | 0/0 | 2934 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2929): Show |
chr16 | 23383493 | 23458189 |
| a0002c0002t0003 | 0/0 | 2934 | 38 | 16 | 13 | 4 | 0 | 5 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2929): Show |
chr16 | 23383493 | 23458189 |
| a0002c0002t0007 | 0/0 | 2935 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2930): Show |
chr16 | 23383493 | 23458189 |
| a0003c0007t0001 | 0/0 | 2935 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2930): Show |
chr16 | 23383493 | 23458189 |
| a0004c0010t0003 | 0/0 | 2934 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2929): Show |
chr16 | 23383493 | 23458189 |
| a0005c0005t0003 | 0/0 | 2934 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2929): Show |
chr16 | 23383493 | 23458189 |
| a0006c0011t0007 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2930): Show |
chr16 | 23383493 | 23458189 |
| a0007c0004t0002 | 0/0 | 2934 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2929): Show |
chr16 | 23383493 | 23458189 |
| a0008c0006t0001 | 0/0 | 2935 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | GAGGG others(2930): Show |
chr16 | 23383493 | 23458189 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 1 | 4 | 1 | 2 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0002 | 0/0 | 5 | 1 | 2 | 1 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0207 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0001t0008g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0003t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0003t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0003t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0003t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0008t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0009t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0001c0012t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0002c0002t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0003c0007t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0004c0010t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0005c0005t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0006c0011t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0007c0004t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| a0008c0006t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | GBR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0032 | EUR | GBR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0195 | EUR | GBR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | GBR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | CHS | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00423 | hp2 | a0002 | c0002 | t0003 | g0117 | EAS | CHS | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | CHS | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00639 | hp2 | a0002 | c0002 | t0003 | g0098 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00741 | hp1 | a0003 | c0007 | t0001 | g0237 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG00741 | hp2 | a0002 | c0002 | t0003 | g0118 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01070 | hp1 | a0002 | c0002 | t0003 | g0123 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01070 | hp2 | a0002 | c0002 | t0003 | g0129 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01071 | hp1 | a0002 | c0002 | t0003 | g0122 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01099 | hp2 | a0002 | c0002 | t0003 | g0119 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01109 | hp2 | a0002 | c0002 | t0003 | g0120 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0078 | EUR | IBS | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01934 | hp1 | a0002 | c0002 | t0003 | g0105 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01952 | hp2 | a0002 | c0002 | t0003 | g0128 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01981 | hp1 | a0002 | c0002 | t0003 | g0130 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG01993 | hp2 | a0002 | c0002 | t0003 | g0113 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02145 | hp1 | a0001 | c0012 | t0002 | g0013 | AFR | ACB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02145 | hp2 | a0004 | c0010 | t0003 | g0095 | AFR | ACB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02148 | hp1 | a0002 | c0002 | t0003 | g0126 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CDX | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | CDX | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0040 | AFR | ACB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02257 | hp2 | a0002 | c0002 | t0003 | g0110 | AFR | ACB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02258 | hp2 | a0002 | c0002 | t0003 | g0103 | AFR | ACB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ACB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02293 | hp2 | a0002 | c0002 | t0003 | g0111 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02300 | hp2 | a0002 | c0002 | t0007 | g0114 | AMR | PEL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02622 | hp2 | a0002 | c0002 | t0003 | g0006 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02630 | hp2 | a0005 | c0005 | t0003 | g0133 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0214 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02683 | hp1 | a0002 | c0002 | t0003 | g0010 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02717 | hp2 | a0001 | c0008 | t0001 | g0222 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0245 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02809 | hp1 | a0001 | c0003 | t0007 | g0248 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02895 | hp1 | a0002 | c0002 | t0003 | g0097 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0093 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0094 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02922 | hp1 | a0001 | c0003 | t0003 | g0135 | AFR | ESN | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02922 | hp2 | a0002 | c0002 | t0003 | g0096 | AFR | ESN | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02970 | hp1 | a0002 | c0002 | t0003 | g0106 | AFR | ESN | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03017 | hp2 | a0002 | c0002 | t0003 | g0121 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03098 | hp2 | a0002 | c0002 | t0003 | g0100 | AFR | MSL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03130 | hp2 | a0002 | c0002 | t0003 | g0109 | AFR | ESN | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ESN | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03195 | hp1 | a0002 | c0002 | t0003 | g0003 | AFR | ESN | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0092 | AFR | ESN | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03209 | hp2 | a0002 | c0002 | t0003 | g0101 | AFR | MSL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03225 | hp1 | a0001 | c0009 | t0002 | g0068 | AFR | MSL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | MSL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03579 | hp1 | a0002 | c0002 | t0003 | g0099 | AFR | MSL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03669 | hp1 | a0001 | c0001 | t0008 | g0154 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | STU | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03834 | hp2 | a0002 | c0002 | t0003 | g0115 | SAS | BEB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0244 | SAS | BEB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | BEB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03942 | hp2 | a0002 | c0002 | t0003 | g0112 | SAS | BEB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | STU | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | STU | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG04184 | hp2 | a0002 | c0002 | t0003 | g0124 | SAS | BEB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | STU | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | STU | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18522 | hp1 | a0006 | c0011 | t0007 | g0015 | AFR | YRI | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18747 | hp2 | a0002 | c0002 | t0003 | g0116 | EAS | CHB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | YRI | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18983 | hp1 | a0007 | c0004 | t0002 | g0009 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18990 | hp2 | a0002 | c0002 | t0003 | g0127 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18992 | hp2 | a0002 | c0002 | t0003 | g0125 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19003 | hp1 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19007 | hp2 | a0008 | c0006 | t0001 | g0209 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | LWK | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19030 | hp2 | a0002 | c0002 | t0003 | g0026 | AFR | LWK | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | LWK | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | LWK | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0003 | AFR | ASW | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ASW | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0077 | EUR | TSI | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0215 | EUR | TSI | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | TSI | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0076 | EUR | TSI | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02109 | hp2 | a0001 | c0003 | t0003 | g0131 | AFR | ACB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02486 | hp1 | a0001 | c0003 | t0003 | g0132 | AFR | ACB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG02559 | hp2 | a0002 | c0002 | t0003 | g0006 | AFR | ACB | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG03471 | hp2 | a0002 | c0002 | t0003 | g0102 | AFR | MSL | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG06807 | hp1 | a0002 | c0002 | t0003 | g0003 | AFR | USA | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | USA | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | USA | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | USA | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | LWK | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | LWK | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0207 | REF | REF | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0221 | REF | REF | COG7_chr16_23383493_23458189 | COG7 | chr16 | 23383493 | 23458189 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:23398119 | G | A | 2 | a0002 a0004 |
40 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(37): Show |
missense_variant | MODERATE | c.1814C>T | p.Thr605Met | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/17 | 2009/2935 | 1814/2313 | 605/770 | chr16 | 23398119 | |||
| chr16:23406239 | T | C | 1 | a0003 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1499A>G | p.Tyr500Cys | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 12/17 | 1694/2935 | 1499/2313 | 500/770 | chr16 | 23406239 | |||
| chr16:23424820 | C | T | 1 | a0008 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.938G>A | p.Arg313Lys | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/17 | 1133/2935 | 938/2313 | 313/770 | chr16 | 23424820 | |||
| chr16:23424908 | T | A | 1 | a0004 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.850A>T | p.Ile284Phe | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/17 | 1045/2935 | 850/2313 | 284/770 | chr16 | 23424908 | |||
| chr16:23442558 | C | A | 1 | a0006 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.523G>T | p.Val175Leu | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/17 | 718/2935 | 523/2313 | 175/770 | chr16 | 23442558 | |||
| chr16:23445164 | C | T | 1 | a0005 | 1 | HG02630.hp2 | missense_variant&splice_region_variant | MODERATE | c.319G>A | p.Val107Met | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/17 | 514/2935 | 319/2313 | 107/770 | chr16 | 23445164 | |||
| chr16:23452829 | C | G | 1 | a0007 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.166G>C | p.Glu56Gln | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/17 | 361/2935 | 166/2313 | 56/770 | chr16 | 23452829 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:23392423 | A | G | 4 | a0001c0003 a0002c0002 a0004c0010 others(1): Show |
45 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(42): Show |
synonymous_variant | LOW | c.2103T>C | p.Pro701Pro | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/17 | 2298/2935 | 2103/2313 | 701/770 | chr16 | 23392423 | |||
| chr16:23410315 | G | A | 1 | a0001c0008 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.1455C>T | p.Phe485Phe | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/17 | 1650/2935 | 1455/2313 | 485/770 | chr16 | 23410315 | |||
| chr16:23418724 | G | A | 1 | a0001c0009 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.1113C>T | p.Leu371Leu | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 8/17 | 1308/2935 | 1113/2313 | 371/770 | chr16 | 23418724 | |||
| chr16:23424858 | G | A | 1 | a0006c0011 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.900C>T | p.Asn300Asn | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/17 | 1095/2935 | 900/2313 | 300/770 | chr16 | 23424858 | |||
| chr16:23445117 | G | A | 1 | a0001c0012 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.366C>T | p.Ala122Ala | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/17 | 561/2935 | 366/2313 | 122/770 | chr16 | 23445117 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:23388624 | C | CT | 1 | a0001c0001t0004 | 9 | HG02155.hp2 HG02647.hp1 HG02738.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*295dupA | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 17/17 | 295 | chr16 | 23388624 | ||||||
| chr16:23388624 | CT | C | 9 | a0001c0001t0002 a0001c0001t0008 a0001c0003t0003 others(6): Show |
135 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*295delA | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 17/17 | 295 | chr16 | 23388624 | ||||||
| chr16:23388733 | T | C | 13 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(10): Show |
144 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*187A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 17/17 | 187 | chr16 | 23388733 | ||||||
| chr16:23388873 | G | A | 5 | a0001c0001t0002 a0001c0001t0005 a0001c0009t0002 others(2): Show |
95 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*47C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 17/17 | 47 | chr16 | 23388873 | ||||||
| chr16:23388911 | G | T | 1 | a0001c0001t0006 | 3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9C>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 17/17 | 9 | chr16 | 23388911 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:23389182 | G | C | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2147-96C>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23389182 | |||||||
| chr16:23389411 | GCACA | G | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0199 others(4): Show |
7 | HG02155.hp2 NA18959.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.2147-329_2147-326d others(6): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23389411 | |||||||
| chr16:23389657 | C | T | 4 | a0001c0001t0004g0168 a0001c0001t0004g0169 a0001c0001t0004g0196 others(1): Show |
4 | HG02155.hp2 NA18959.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.2147-571G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23389657 | |||||||
| chr16:23389755 | C | T | 87 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(84): Show |
88 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.2147-669G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23389755 | |||||||
| chr16:23389791 | T | C | 43 | a0001c0001t0001g0225 a0001c0003t0003g0131 a0001c0003t0003g0132 others(40): Show |
46 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.2147-705A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23389791 | |||||||
| chr16:23389840 | G | A | 1 | a0001c0003t0007g0248 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2147-754C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23389840 | |||||||
| chr16:23389867 | A | G | 42 | a0001c0001t0001g0225 a0001c0003t0003g0131 a0001c0003t0003g0132 others(39): Show |
45 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.2147-781T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23389867 | |||||||
| chr16:23390174 | G | A | 7 | a0001c0001t0001g0208 a0001c0001t0001g0210 a0001c0001t0001g0213 others(4): Show |
7 | HG01258.hp2 HG01261.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.2147-1088C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23390174 | |||||||
| chr16:23390190 | G | GT | 16 | a0001c0001t0001g0007 a0001c0001t0001g0173 a0001c0001t0001g0206 others(13): Show |
17 | HG00438.hp2 HG01175.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.2147-1105dupA | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23390190 | |||||||
| chr16:23390192 | T | G | 1 | a0001c0001t0001g0235 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2147-1106A>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23390192 | |||||||
| chr16:23390504 | C | A | 3 | a0001c0001t0002g0053 a0001c0001t0002g0072 a0001c0001t0002g0084 |
3 | HG00609.hp2 HG02300.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2147-1418G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23390504 | |||||||
| chr16:23390588 | T | C | 1 | a0002c0002t0003g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2147-1502A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23390588 | |||||||
| chr16:23390679 | G | A | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2147-1593C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23390679 | |||||||
| chr16:23390796 | T | C | 1 | a0001c0001t0002g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2146+1584A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23390796 | |||||||
| chr16:23390902 | G | A | 1 | a0001c0001t0004g0215 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2146+1478C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23390902 | |||||||
| chr16:23391100 | C | T | 1 | a0006c0011t0007g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2146+1280G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23391100 | |||||||
| chr16:23391130 | C | T | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2146+1250G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23391130 | |||||||
| chr16:23391607 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2146+773G>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23391607 | |||||||
| chr16:23391659 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0236 |
2 | HG01175.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.2146+721C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23391659 | |||||||
| chr16:23391688 | A | G | 1 | a0001c0001t0002g0050 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2146+692T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23391688 | |||||||
| chr16:23391710 | T | A | 148 | a0001c0001t0001g0139 a0001c0001t0001g0142 a0001c0001t0001g0174 others(145): Show |
154 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.2146+670A>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23391710 | |||||||
| chr16:23391788 | G | C | 3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2146+592C>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23391788 | |||||||
| chr16:23391854 | G | A | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2146+526C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23391854 | |||||||
| chr16:23391926 | G | A | 40 | a0001c0003t0003g0131 a0001c0003t0003g0132 a0002c0002t0003g0003 others(37): Show |
43 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.2146+454C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23391926 | |||||||
| chr16:23391930 | C | T | 4 | a0002c0002t0003g0116 a0002c0002t0003g0117 a0002c0002t0003g0125 others(1): Show |
4 | HG00423.hp2 NA18747.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.2146+450G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23391930 | |||||||
| chr16:23392189 | G | A | 138 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(135): Show |
144 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.2146+191C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 16/16 | chr16 | 23392189 | |||||||
| chr16:23392587 | G | A | 1 | a0001c0001t0002g0028 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2003-64C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 15/16 | chr16 | 23392587 | |||||||
| chr16:23392668 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2003-145C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 15/16 | chr16 | 23392668 | |||||||
| chr16:23392802 | G | A | 41 | a0001c0001t0002g0012 a0001c0001t0002g0032 a0001c0001t0002g0035 others(38): Show |
41 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.2003-279C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 15/16 | chr16 | 23392802 | |||||||
| chr16:23392837 | A | T | 1 | a0001c0001t0001g0232 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2003-314T>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 15/16 | chr16 | 23392837 | |||||||
| chr16:23392914 | C | G | 3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2002+319G>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 15/16 | chr16 | 23392914 | |||||||
| chr16:23392945 | T | C | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2002+288A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 15/16 | chr16 | 23392945 | |||||||
| chr16:23393364 | C | T | 1 | a0006c0011t0007g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1888-17G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23393364 | |||||||
| chr16:23393698 | C | A | 1 | a0001c0001t0002g0056 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1888-351G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23393698 | |||||||
| chr16:23393722 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1888-375C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23393722 | |||||||
| chr16:23393813 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1888-466C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23393813 | |||||||
| chr16:23393859 | T | G | 1 | a0001c0001t0004g0214 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1888-512A>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23393859 | |||||||
| chr16:23393898 | G | A | 5 | a0001c0001t0002g0004 a0001c0001t0002g0143 a0001c0001t0002g0191 others(2): Show |
7 | HG02559.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1888-551C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23393898 | |||||||
| chr16:23393965 | C | T | 1 | a0001c0001t0002g0020 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1888-618G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23393965 | |||||||
| chr16:23394057 | G | GA | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0151 others(3): Show |
6 | HG00438.hp2 HG00735.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1888-711dupT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23394057 | |||||||
| chr16:23394057 | GA | G | 80 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(77): Show |
81 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1888-711delT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23394057 | |||||||
| chr16:23394162 | A | G | 9 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(6): Show |
10 | HG01099.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1888-815T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23394162 | |||||||
| chr16:23394251 | G | T | 4 | a0001c0001t0001g0140 a0001c0001t0001g0158 a0001c0001t0001g0185 others(1): Show |
4 | HG02056.hp1 NA18951.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1888-904C>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23394251 | |||||||
| chr16:23394327 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1888-980C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23394327 | |||||||
| chr16:23394360 | G | A | 1 | a0001c0003t0007g0248 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1888-1013C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23394360 | |||||||
| chr16:23394686 | T | C | 3 | a0001c0001t0002g0017 a0001c0001t0002g0028 a0001c0001t0002g0029 |
3 | HG02647.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1888-1339A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23394686 | |||||||
| chr16:23394696 | A | C | 6 | a0002c0002t0003g0098 a0002c0002t0003g0099 a0002c0002t0003g0100 others(3): Show |
6 | HG00639.hp2 HG02258.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1888-1349T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23394696 | |||||||
| chr16:23394728 | C | G | 40 | a0001c0003t0003g0131 a0001c0003t0003g0132 a0002c0002t0003g0003 others(37): Show |
43 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1888-1381G>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23394728 | |||||||
| chr16:23394810 | CT | C | 40 | a0001c0003t0003g0131 a0001c0003t0003g0132 a0002c0002t0003g0003 others(37): Show |
43 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1888-1464delA | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23394810 | |||||||
| chr16:23394875 | G | A | 1 | a0001c0001t0004g0215 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1888-1528C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23394875 | |||||||
| chr16:23395149 | T | C | 3 | a0001c0001t0002g0057 a0001c0001t0002g0091 a0001c0001t0005g0040 |
3 | HG02257.hp1 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1888-1802A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23395149 | |||||||
| chr16:23395374 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1888-2027C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23395374 | |||||||
| chr16:23395383 | C | A | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1888-2036G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23395383 | |||||||
| chr16:23395974 | G | C | 4 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1887+2072C>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23395974 | |||||||
| chr16:23396233 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1887+1813C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23396233 | |||||||
| chr16:23396572 | G | A | 4 | a0002c0002t0003g0100 a0002c0002t0003g0101 a0002c0002t0003g0102 others(1): Show |
4 | HG02258.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1887+1474C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23396572 | |||||||
| chr16:23396634 | G | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0199 |
3 | NA18975.hp1 NA18980.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1887+1412C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23396634 | |||||||
| chr16:23396821 | C | A | 1 | a0006c0011t0007g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1887+1225G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23396821 | |||||||
| chr16:23396860 | G | A | 4 | a0001c0001t0002g0019 a0001c0001t0002g0041 a0001c0001t0002g0060 others(1): Show |
4 | HG04204.hp2 NA18973.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1887+1186C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23396860 | |||||||
| chr16:23396915 | CT | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0134 others(50): Show |
61 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1887+1130delA | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23396915 | |||||||
| chr16:23396975 | T | A | 1 | a0001c0003t0007g0248 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1887+1071A>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23396975 | |||||||
| chr16:23396976 | C | A | 1 | a0001c0001t0001g0211 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1887+1070G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23396976 | |||||||
| chr16:23396977 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1887+1069T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23396977 | |||||||
| chr16:23396995 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1887+1051C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23396995 | |||||||
| chr16:23397106 | C | G | 92 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(89): Show |
95 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.1887+940G>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23397106 | |||||||
| chr16:23397270 | A | G | 92 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(89): Show |
95 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.1887+776T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23397270 | |||||||
| chr16:23397271 | T | C | 37 | a0002c0002t0003g0003 a0002c0002t0003g0006 a0002c0002t0003g0010 others(34): Show |
40 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1887+775A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23397271 | |||||||
| chr16:23397339 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1887+707A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23397339 | |||||||
| chr16:23397371 | C | T | 7 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0150 others(4): Show |
7 | HG02683.hp2 HG03491.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.1887+675G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23397371 | |||||||
| chr16:23397624 | A | G | 1 | a0001c0001t0002g0050 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1887+422T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23397624 | |||||||
| chr16:23397662 | C | A | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1887+384G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23397662 | |||||||
| chr16:23397791 | C | T | 4 | a0002c0002t0003g0116 a0002c0002t0003g0117 a0002c0002t0003g0125 others(1): Show |
4 | HG00423.hp2 NA18747.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1887+255G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23397791 | |||||||
| chr16:23397865 | G | A | 1 | a0001c0001t0002g0030 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1887+181C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 14/16 | chr16 | 23397865 | |||||||
| chr16:23398163 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1804-34A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23398163 | |||||||
| chr16:23398732 | T | C | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1804-603A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23398732 | |||||||
| chr16:23398826 | C | A | 1 | a0001c0001t0001g0226 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1804-697G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23398826 | |||||||
| chr16:23398969 | A | G | 2 | a0001c0003t0003g0135 a0001c0003t0007g0248 |
2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1804-840T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23398969 | |||||||
| chr16:23399012 | GC | G | 137 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(134): Show |
143 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1804-884delG | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23399012 | |||||||
| chr16:23399047 | G | A | 6 | a0001c0001t0001g0137 a0001c0001t0001g0201 a0001c0001t0001g0234 others(3): Show |
6 | HG02523.hp2 NA18948.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1804-918C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23399047 | |||||||
| chr16:23399059 | G | A | 7 | a0002c0002t0003g0111 a0002c0002t0003g0118 a0002c0002t0003g0126 others(4): Show |
7 | HG00741.hp2 HG01070.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1804-930C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23399059 | |||||||
| chr16:23399076 | T | G | 1 | a0001c0001t0001g0183 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1804-947A>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23399076 | |||||||
| chr16:23399077 | G | A | 92 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(89): Show |
95 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.1804-948C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23399077 | |||||||
| chr16:23399098 | T | C | 137 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(134): Show |
143 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1804-969A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23399098 | |||||||
| chr16:23399211 | G | A | 40 | a0001c0003t0003g0131 a0001c0003t0003g0132 a0002c0002t0003g0003 others(37): Show |
43 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1804-1082C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23399211 | |||||||
| chr16:23399391 | C | T | 3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1804-1262G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23399391 | |||||||
| chr16:23399483 | C | T | 1 | a0003c0007t0001g0237 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1804-1354G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23399483 | |||||||
| chr16:23399586 | C | G | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1804-1457G>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23399586 | |||||||
| chr16:23400020 | A | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0239 |
2 | HG01261.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1804-1891T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23400020 | |||||||
| chr16:23400238 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1804-2109A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23400238 | |||||||
| chr16:23400262 | G | C | 1 | a0005c0005t0003g0133 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1804-2133C>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23400262 | |||||||
| chr16:23400516 | G | A | 135 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(132): Show |
141 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.1804-2387C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23400516 | |||||||
| chr16:23400571 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1804-2442G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23400571 | |||||||
| chr16:23400665 | A | T | 1 | a0001c0001t0002g0249 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1804-2536T>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23400665 | |||||||
| chr16:23400783 | T | A | 136 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(133): Show |
142 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.1804-2654A>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23400783 | |||||||
| chr16:23400817 | A | C | 1 | a0001c0001t0002g0058 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1804-2688T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23400817 | |||||||
| chr16:23400819 | A | C | 2 | a0001c0001t0002g0048 a0007c0004t0002g0009 |
2 | NA18983.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1804-2690T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23400819 | |||||||
| chr16:23400957 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1803+2737C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23400957 | |||||||
| chr16:23400982 | G | T | 5 | a0001c0001t0002g0004 a0001c0001t0002g0143 a0001c0001t0002g0191 others(2): Show |
7 | HG02559.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1803+2712C>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23400982 | |||||||
| chr16:23400989 | G | A | 131 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(128): Show |
137 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1803+2705C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23400989 | |||||||
| chr16:23400990 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1803+2704T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23400990 | |||||||
| chr16:23401362 | G | A | 37 | a0002c0002t0003g0003 a0002c0002t0003g0006 a0002c0002t0003g0010 others(34): Show |
40 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1803+2332C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23401362 | |||||||
| chr16:23401482 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1803+2212A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23401482 | |||||||
| chr16:23401576 | G | A | 93 | a0001c0001t0001g0155 a0001c0001t0002g0005 a0001c0001t0002g0012 others(90): Show |
94 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1803+2118C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23401576 | |||||||
| chr16:23401609 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1803+2085G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23401609 | |||||||
| chr16:23401618 | A | G | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1803+2076T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23401618 | |||||||
| chr16:23401780 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1803+1914C>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23401780 | |||||||
| chr16:23401890 | T | C | 3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1803+1804A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23401890 | |||||||
| chr16:23401950 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1803+1744C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23401950 | |||||||
| chr16:23402345 | AT | A | 126 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(123): Show |
130 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1803+1348delA | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23402345 | |||||||
| chr16:23402453 | T | C | 127 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(124): Show |
131 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1803+1241A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23402453 | |||||||
| chr16:23402643 | G | A | 1 | a0001c0003t0007g0248 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1803+1051C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23402643 | |||||||
| chr16:23402720 | C | T | 1 | a0002c0002t0003g0109 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1803+974G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23402720 | |||||||
| chr16:23402791 | G | A | 7 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0024 others(4): Show |
8 | HG01099.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1803+903C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23402791 | |||||||
| chr16:23402990 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1803+704G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23402990 | |||||||
| chr16:23402996 | A | T | 1 | a0001c0001t0002g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1803+698T>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23402996 | |||||||
| chr16:23403039 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1803+655G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23403039 | |||||||
| chr16:23403118 | T | C | 1 | a0001c0001t0004g0169 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1803+576A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23403118 | |||||||
| chr16:23403148 | G | A | 5 | a0001c0001t0002g0004 a0001c0001t0002g0143 a0001c0001t0002g0191 others(2): Show |
7 | HG02559.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1803+546C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23403148 | |||||||
| chr16:23403498 | C | T | 9 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(6): Show |
10 | HG01099.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1803+196G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23403498 | |||||||
| chr16:23403538 | A | G | 1 | a0002c0002t0003g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1803+156T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 13/16 | chr16 | 23403538 | |||||||
| chr16:23403986 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1663-152G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 12/16 | chr16 | 23403986 | |||||||
| chr16:23404010 | C | T | 4 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-176G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 12/16 | chr16 | 23404010 | |||||||
| chr16:23404031 | T | A | 6 | a0002c0002t0003g0098 a0002c0002t0003g0099 a0002c0002t0003g0100 others(3): Show |
6 | HG00639.hp2 HG02258.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663-197A>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 12/16 | chr16 | 23404031 | |||||||
| chr16:23404152 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0186 |
2 | NA18979.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1663-318C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 12/16 | chr16 | 23404152 | |||||||
| chr16:23404187 | G | T | 1 | a0001c0008t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1663-353C>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 12/16 | chr16 | 23404187 | |||||||
| chr16:23404197 | A | G | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1663-363T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 12/16 | chr16 | 23404197 | |||||||
| chr16:23404249 | G | A | 3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1663-415C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 12/16 | chr16 | 23404249 | |||||||
| chr16:23404350 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1663-516A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 12/16 | chr16 | 23404350 | |||||||
| chr16:23404577 | C | T | 131 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(128): Show |
135 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1663-743G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 12/16 | chr16 | 23404577 | |||||||
| chr16:23404741 | G | A | 1 | a0001c0001t0002g0084 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1663-907C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 12/16 | chr16 | 23404741 | |||||||
| chr16:23405421 | T | G | 1 | a0001c0001t0001g0172 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1662+655A>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 12/16 | chr16 | 23405421 | |||||||
| chr16:23405517 | C | CT | 6 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0001g0242 others(3): Show |
6 | HG02896.hp2 HG02897.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1662+558dupA | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 12/16 | chr16 | 23405517 | |||||||
| chr16:23405594 | G | A | 7 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0024 others(4): Show |
8 | HG01099.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1662+482C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 12/16 | chr16 | 23405594 | |||||||
| chr16:23405979 | G | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0025 |
2 | HG01099.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1662+97C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 12/16 | chr16 | 23405979 | |||||||
| chr16:23406285 | T | C | 4 | a0001c0001t0002g0045 a0001c0001t0002g0049 a0001c0001t0002g0052 others(1): Show |
4 | HG02015.hp2 NA18975.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1476-23A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23406285 | |||||||
| chr16:23406524 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1476-262G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23406524 | |||||||
| chr16:23406632 | G | A | 1 | a0001c0003t0007g0248 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1476-370C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23406632 | |||||||
| chr16:23406683 | T | C | 2 | a0001c0001t0002g0074 a0001c0001t0002g0083 |
2 | NA18948.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1476-421A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23406683 | |||||||
| chr16:23406960 | C | G | 6 | a0002c0002t0003g0098 a0002c0002t0003g0099 a0002c0002t0003g0100 others(3): Show |
6 | HG00639.hp2 HG02258.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1476-698G>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23406960 | |||||||
| chr16:23407085 | A | G | 40 | a0001c0003t0003g0131 a0001c0003t0003g0132 a0002c0002t0003g0003 others(37): Show |
43 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1476-823T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23407085 | |||||||
| chr16:23407097 | A | G | 37 | a0002c0002t0003g0003 a0002c0002t0003g0006 a0002c0002t0003g0010 others(34): Show |
40 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1476-835T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23407097 | |||||||
| chr16:23407462 | G | C | 3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1476-1200C>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23407462 | |||||||
| chr16:23407496 | T | C | 1 | a0002c0002t0003g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1476-1234A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23407496 | |||||||
| chr16:23407539 | C | G | 1 | a0002c0002t0003g0109 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1476-1277G>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23407539 | |||||||
| chr16:23407658 | G | A | 10 | a0002c0002t0003g0006 a0002c0002t0003g0026 a0002c0002t0003g0098 others(7): Show |
11 | HG00639.hp2 HG01934.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1476-1396C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23407658 | |||||||
| chr16:23407783 | C | A | 9 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(6): Show |
10 | HG01099.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1476-1521G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23407783 | |||||||
| chr16:23407827 | T | C | 4 | a0002c0002t0003g0116 a0002c0002t0003g0117 a0002c0002t0003g0125 others(1): Show |
4 | HG00423.hp2 NA18747.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1476-1565A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23407827 | |||||||
| chr16:23408080 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1476-1818C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408080 | |||||||
| chr16:23408121 | A | AGGGGCGA others(16): Show |
34 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0014 others(31): Show |
41 | HG00639.hp1 HG01106.hp2 HG01346.hp2 others(38): Show |
intron_variant | MODIFIER | c.1476-1882_1476-186 others(27): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408121 | |||||||
| chr16:23408132 | G | GGGCGGGA others(85): Show |
3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1476-1871_1476-187 others(96): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408132 | |||||||
| chr16:23408132 | G | GGGCGGGA others(39): Show |
2 | a0001c0001t0001g0175 a0001c0001t0001g0190 |
2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1476-1871_1476-187 others(50): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408132 | |||||||
| chr16:23408132 | GGGCGGGA others(16): Show |
G | 3 | a0001c0001t0001g0202 a0001c0001t0001g0228 a0001c0001t0001g0231 |
3 | HG01081.hp1 NA18954.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1476-1893_1476-187 others(27): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408132 | |||||||
| chr16:23408135 | C | T | 1 | a0002c0002t0003g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1476-1873G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408135 | |||||||
| chr16:23408149 | C | CGAGTGGG others(62): Show |
1 | a0001c0003t0007g0248 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1476-1888_1476-188 others(73): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408149 | |||||||
| chr16:23408149 | C | CGAGTGGG others(62): Show |
1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1476-1888_1476-188 others(73): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408149 | |||||||
| chr16:23408155 | T | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0134 others(193): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1476-1893A>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408155 | |||||||
| chr16:23408178 | T | G | 2 | a0001c0001t0001g0228 a0001c0001t0001g0232 |
2 | NA18973.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1476-1916A>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408178 | |||||||
| chr16:23408195 | C | CGAGTGTG others(16): Show |
11 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(8): Show |
12 | HG01099.hp1 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1476-1934_1476-193 others(27): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408195 | |||||||
| chr16:23408214 | G | T | 117 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(114): Show |
120 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1476-1952C>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408214 | |||||||
| chr16:23408218 | C | A | 117 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(114): Show |
120 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1476-1956G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408218 | |||||||
| chr16:23408247 | T | TGGCGGGA others(16): Show |
1 | a0001c0003t0007g0248 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1476-2008_1476-198 others(27): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408247 | |||||||
| chr16:23408270 | G | T | 118 | a0001c0001t0001g0223 a0001c0001t0002g0012 a0001c0001t0002g0016 others(115): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.1476-2008C>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408270 | |||||||
| chr16:23408280 | C | T | 1 | a0006c0011t0007g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1475+2015G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408280 | |||||||
| chr16:23408293 | G | T | 40 | a0001c0003t0003g0131 a0001c0003t0003g0132 a0002c0002t0003g0003 others(37): Show |
43 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1475+2002C>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408293 | |||||||
| chr16:23408303 | T | C | 121 | a0001c0001t0001g0223 a0001c0001t0002g0012 a0001c0001t0002g0016 others(118): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.1475+1992A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408303 | |||||||
| chr16:23408305 | G | GGGGGCGA others(15): Show |
1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1475+1968_1475+198 others(26): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408305 | |||||||
| chr16:23408305 | G | GGGGGCGA others(38): Show |
9 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(6): Show |
10 | HG01099.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1475+1989_1475+199 others(49): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408305 | |||||||
| chr16:23408305 | GGGGGCGA others(15): Show |
G | 1 | a0001c0001t0001g0223 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1475+1968_1475+198 others(26): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408305 | |||||||
| chr16:23408316 | G | T | 118 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(115): Show |
121 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.1475+1979C>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408316 | |||||||
| chr16:23408326 | T | C | 118 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(115): Show |
121 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.1475+1969A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408326 | |||||||
| chr16:23408327 | A | AG | 118 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(115): Show |
121 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.1475+1967dupC | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408327 | |||||||
| chr16:23408331 | G | GCGAGTGG others(38): Show |
3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1475+1963_1475+196 others(49): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408331 | |||||||
| chr16:23408354 | A | G | 118 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(115): Show |
121 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.1475+1941T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408354 | |||||||
| chr16:23408373 | GGGGACGA others(15): Show |
G | 3 | a0001c0001t0002g0053 a0001c0001t0002g0072 a0001c0001t0002g0084 |
3 | HG00609.hp2 HG02300.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1475+1900_1475+192 others(26): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408373 | |||||||
| chr16:23408377 | A | G | 115 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(112): Show |
118 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1475+1918T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408377 | |||||||
| chr16:23408378 | C | A | 2 | a0001c0001t0002g0045 a0001c0001t0002g0073 |
2 | NA18983.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1475+1917G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408378 | |||||||
| chr16:23408400 | T | C | 118 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(115): Show |
121 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.1475+1895A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408400 | |||||||
| chr16:23408540 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(242): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1475+1755G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408540 | |||||||
| chr16:23408685 | G | C | 87 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(84): Show |
88 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1475+1610C>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408685 | |||||||
| chr16:23408841 | G | A | 1 | a0001c0001t0004g0196 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1475+1454C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23408841 | |||||||
| chr16:23409064 | C | CGT | 6 | a0001c0001t0001g0137 a0001c0001t0001g0146 a0001c0001t0001g0156 others(3): Show |
6 | HG01928.hp1 HG02523.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1475+1229_1475+123 others(6): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409064 | |||||||
| chr16:23409086 | T | C | 1 | a0001c0001t0002g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1475+1209A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409086 | |||||||
| chr16:23409088 | T | C | 1 | a0001c0001t0002g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1475+1207A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGCGC | 6 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0024 others(3): Show |
7 | HG01099.hp1 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1475+1206_1475+120 others(10): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGTGC | 3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1475+1206_1475+120 others(10): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGTGCG others(5): Show |
3 | a0001c0003t0003g0131 a0001c0003t0003g0132 a0005c0005t0003g0133 |
3 | HG02109.hp2 HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1475+1206_1475+120 others(16): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGTGTG others(5): Show |
6 | a0001c0001t0002g0016 a0001c0001t0002g0060 a0001c0001t0002g0070 others(3): Show |
6 | HG00423.hp1 HG00621.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1475+1206_1475+120 others(16): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0002g0022 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1475+1206_1475+120 others(18): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGTGTG others(7): Show |
3 | a0001c0001t0002g0058 a0001c0001t0002g0079 a0001c0012t0002g0013 |
3 | HG02145.hp1 HG03927.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1475+1206_1475+120 others(18): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGTGTG others(9): Show |
3 | a0001c0001t0002g0067 a0002c0002t0003g0096 a0004c0010t0003g0095 |
3 | HG01928.hp2 HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1475+1206_1475+120 others(20): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGTGTG others(11): Show |
3 | a0002c0002t0003g0003 a0002c0002t0003g0113 a0002c0002t0003g0120 |
5 | HG01109.hp2 HG01993.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1475+1206_1475+120 others(22): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGTGTG others(9): Show |
49 | a0001c0001t0002g0012 a0001c0001t0002g0018 a0001c0001t0002g0019 others(46): Show |
49 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1475+1206_1475+120 others(20): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGTGTG others(11): Show |
16 | a0001c0001t0002g0066 a0002c0002t0003g0006 a0002c0002t0003g0010 others(13): Show |
17 | HG00741.hp2 HG01070.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1475+1206_1475+120 others(22): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGTGTG others(13): Show |
2 | a0002c0002t0003g0112 a0002c0002t0003g0119 |
2 | HG01099.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1475+1206_1475+120 others(24): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGTGTG others(9): Show |
1 | a0006c0011t0007g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1475+1206_1475+120 others(20): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGTGTG others(11): Show |
16 | a0001c0001t0002g0021 a0001c0001t0002g0031 a0001c0001t0002g0034 others(13): Show |
16 | HG00609.hp2 HG01109.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.1475+1206_1475+120 others(22): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGTGTG others(13): Show |
4 | a0002c0002t0003g0109 a0002c0002t0003g0117 a0002c0002t0003g0125 others(1): Show |
4 | HG00423.hp2 HG03130.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1475+1206_1475+120 others(24): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGTGTG others(13): Show |
2 | a0001c0001t0002g0020 a0001c0001t0002g0033 |
2 | HG00735.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1475+1206_1475+120 others(24): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGTGTG others(15): Show |
6 | a0002c0002t0003g0098 a0002c0002t0003g0099 a0002c0002t0003g0100 others(3): Show |
6 | HG00639.hp2 HG03098.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1475+1206_1475+120 others(26): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGTGTG others(15): Show |
1 | a0001c0001t0002g0054 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1475+1206_1475+120 others(26): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409088 | T | TGTGTGTG others(17): Show |
3 | a0002c0002t0003g0103 a0002c0002t0003g0116 a0002c0002t0003g0121 |
3 | HG02258.hp2 HG03017.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1475+1206_1475+120 others(28): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409088 | |||||||
| chr16:23409089 | G | A | 8 | a0001c0001t0001g0139 a0001c0001t0001g0142 a0001c0001t0001g0174 others(5): Show |
8 | HG02451.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1475+1206C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409089 | |||||||
| chr16:23409090 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1475+1205G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409090 | |||||||
| chr16:23409094 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1475+1201G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409094 | |||||||
| chr16:23409095 | A | ATG | 85 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(82): Show |
86 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.1475+1198_1475+119 others(6): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409095 | |||||||
| chr16:23409095 | A | G | 5 | a0001c0001t0002g0233 a0001c0001t0006g0092 a0001c0001t0006g0093 others(2): Show |
5 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1475+1200T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409095 | |||||||
| chr16:23409095 | ATGTG | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0224 |
3 | HG00140.hp2 HG06807.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1475+1196_1475+119 others(8): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409095 | |||||||
| chr16:23409097 | G | GTGTGTGT others(11): Show |
1 | a0001c0001t0002g0233 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1475+1197_1475+119 others(22): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409097 | |||||||
| chr16:23409117 | A | G | 1 | a0002c0002t0003g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1475+1178T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409117 | |||||||
| chr16:23409622 | A | G | 132 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(129): Show |
136 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1475+673T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23409622 | |||||||
| chr16:23410226 | G | A | 1 | a0002c0002t0003g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1475+69C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 11/16 | chr16 | 23410226 | |||||||
| chr16:23410592 | C | T | 1 | a0001c0001t0002g0042 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1410-232G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23410592 | |||||||
| chr16:23410873 | T | G | 87 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(84): Show |
88 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1410-513A>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23410873 | |||||||
| chr16:23410926 | C | T | 1 | a0002c0002t0003g0003 | 3 | HG03195.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1410-566G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23410926 | |||||||
| chr16:23411337 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1410-977C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23411337 | |||||||
| chr16:23411337 | G | C | 131 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(128): Show |
135 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1410-977C>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23411337 | |||||||
| chr16:23411351 | C | G | 131 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(128): Show |
135 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1410-991G>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23411351 | |||||||
| chr16:23411511 | A | T | 1 | a0001c0001t0005g0061 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1410-1151T>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23411511 | |||||||
| chr16:23411559 | T | C | 3 | a0001c0003t0003g0131 a0001c0003t0003g0132 a0005c0005t0003g0133 |
3 | HG02109.hp2 HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1410-1199A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23411559 | |||||||
| chr16:23411615 | T | A | 1 | a0006c0011t0007g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1410-1255A>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23411615 | |||||||
| chr16:23411874 | C | T | 9 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(6): Show |
10 | HG01099.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1410-1514G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23411874 | |||||||
| chr16:23411882 | C | CT | 9 | a0001c0001t0001g0144 a0001c0001t0001g0151 a0001c0001t0001g0155 others(6): Show |
9 | HG00735.hp2 HG00741.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1410-1523dupA | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23411882 | |||||||
| chr16:23412152 | A | T | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1409+1296T>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23412152 | |||||||
| chr16:23412396 | C | G | 1 | a0001c0001t0008g0154 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1409+1052G>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23412396 | |||||||
| chr16:23412446 | T | TAAAAACT others(2554): Show |
1 | a0001c0001t0002g0054 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1409+1001_1409+100 others(2565): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23412446 | |||||||
| chr16:23412505 | A | C | 4 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1409+943T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23412505 | |||||||
| chr16:23412587 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1409+861C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23412587 | |||||||
| chr16:23412766 | A | G | 78 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(75): Show |
78 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.1409+682T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23412766 | |||||||
| chr16:23412874 | C | T | 4 | a0002c0002t0003g0096 a0002c0002t0003g0097 a0002c0002t0003g0106 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1409+574G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23412874 | |||||||
| chr16:23413041 | A | G | 3 | a0001c0001t0001g0174 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG02451.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1409+407T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23413041 | |||||||
| chr16:23413246 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1409+202C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 10/16 | chr16 | 23413246 | |||||||
| chr16:23413595 | G | C | 1 | a0001c0001t0001g0183 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1293-31C>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23413595 | |||||||
| chr16:23413878 | G | A | 40 | a0001c0003t0003g0131 a0001c0003t0003g0132 a0002c0002t0003g0003 others(37): Show |
43 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1293-314C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23413878 | |||||||
| chr16:23413977 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1293-413T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23413977 | |||||||
| chr16:23414264 | A | G | 133 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(130): Show |
137 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1293-700T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23414264 | |||||||
| chr16:23414336 | A | G | 4 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1293-772T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23414336 | |||||||
| chr16:23414787 | T | A | 5 | a0001c0001t0002g0075 a0001c0001t0002g0077 a0001c0001t0002g0078 others(2): Show |
5 | HG01175.hp1 HG01516.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1293-1223A>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23414787 | |||||||
| chr16:23414827 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1293-1263T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23414827 | |||||||
| chr16:23415081 | G | A | 3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1293-1517C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23415081 | |||||||
| chr16:23415158 | C | T | 4 | a0001c0001t0004g0167 a0001c0001t0004g0168 a0001c0001t0004g0169 others(1): Show |
4 | HG02155.hp2 NA18959.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.1293-1594G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23415158 | |||||||
| chr16:23415385 | T | A | 1 | a0001c0001t0001g0224 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1292+1582A>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23415385 | |||||||
| chr16:23415736 | C | A | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1292+1231G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23415736 | |||||||
| chr16:23415789 | G | A | 130 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(127): Show |
134 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1292+1178C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23415789 | |||||||
| chr16:23416406 | C | T | 2 | a0001c0001t0002g0012 a0001c0001t0005g0011 |
2 | HG02451.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1292+561G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23416406 | |||||||
| chr16:23416612 | C | T | 2 | a0001c0001t0002g0024 a0001c0001t0002g0025 |
2 | HG01099.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1292+355G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23416612 | |||||||
| chr16:23416669 | A | G | 3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1292+298T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23416669 | |||||||
| chr16:23416737 | T | C | 78 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(75): Show |
78 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.1292+230A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23416737 | |||||||
| chr16:23416822 | T | C | 1 | a0001c0009t0002g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1292+145A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23416822 | |||||||
| chr16:23416830 | T | A | 1 | a0001c0001t0002g0053 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1292+137A>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23416830 | |||||||
| chr16:23416872 | A | G | 21 | a0002c0002t0003g0010 a0002c0002t0003g0111 a0002c0002t0003g0112 others(18): Show |
21 | HG00423.hp2 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.1292+95T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23416872 | |||||||
| chr16:23416939 | C | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0206 a0001c0001t0001g0231 |
3 | HG01081.hp1 HG01192.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1292+28G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 9/16 | chr16 | 23416939 | |||||||
| chr16:23417437 | C | T | 1 | a0002c0002t0003g0109 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1138-316G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 8/16 | chr16 | 23417437 | |||||||
| chr16:23417756 | T | C | 5 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0027 others(2): Show |
6 | HG02572.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1138-635A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 8/16 | chr16 | 23417756 | |||||||
| chr16:23417816 | C | T | 1 | a0002c0002t0003g0115 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1138-695G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 8/16 | chr16 | 23417816 | |||||||
| chr16:23417960 | A | G | 3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1137+740T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 8/16 | chr16 | 23417960 | |||||||
| chr16:23417967 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1137+733A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 8/16 | chr16 | 23417967 | |||||||
| chr16:23418033 | C | A | 1 | a0001c0001t0001g0160 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1137+667G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 8/16 | chr16 | 23418033 | |||||||
| chr16:23418056 | A | G | 3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1137+644T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 8/16 | chr16 | 23418056 | |||||||
| chr16:23418283 | T | G | 2 | a0002c0002t0003g0122 a0002c0002t0003g0123 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1137+417A>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 8/16 | chr16 | 23418283 | |||||||
| chr16:23418366 | A | G | 132 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(129): Show |
136 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1137+334T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 8/16 | chr16 | 23418366 | |||||||
| chr16:23418376 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0190 |
2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1137+324T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 8/16 | chr16 | 23418376 | |||||||
| chr16:23418464 | G | A | 3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1137+236C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 8/16 | chr16 | 23418464 | |||||||
| chr16:23418466 | A | G | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1137+234T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 8/16 | chr16 | 23418466 | |||||||
| chr16:23418478 | C | T | 4 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137+222G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 8/16 | chr16 | 23418478 | |||||||
| chr16:23418488 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1137+212C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 8/16 | chr16 | 23418488 | |||||||
| chr16:23418911 | A | C | 1 | a0006c0011t0007g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1010-84T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23418911 | |||||||
| chr16:23419013 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1010-186C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23419013 | |||||||
| chr16:23419148 | G | A | 3 | a0001c0001t0001g0174 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG02451.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1010-321C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23419148 | |||||||
| chr16:23419180 | C | A | 1 | a0001c0001t0001g0212 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1010-353G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23419180 | |||||||
| chr16:23419411 | C | CA | 125 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(122): Show |
129 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1010-585dupT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23419411 | |||||||
| chr16:23419562 | A | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | NA18980.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1010-735T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23419562 | |||||||
| chr16:23419748 | C | CA | 36 | a0001c0001t0001g0193 a0002c0002t0003g0003 a0002c0002t0003g0006 others(33): Show |
39 | HG00423.hp2 HG00639.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1010-922dupT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23419748 | |||||||
| chr16:23419748 | C | CAA | 13 | a0001c0001t0002g0023 a0001c0001t0002g0025 a0001c0001t0002g0030 others(10): Show |
13 | HG01099.hp1 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1010-923_1010-922d others(4): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23419748 | |||||||
| chr16:23419748 | C | CAAA | 81 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1010-924_1010-922d others(5): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23419748 | |||||||
| chr16:23420107 | C | T | 1 | a0001c0001t0002g0050 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1010-1280G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23420107 | |||||||
| chr16:23420124 | T | A | 1 | a0006c0011t0007g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1010-1297A>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23420124 | |||||||
| chr16:23420221 | G | C | 1 | a0002c0002t0003g0109 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1010-1394C>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23420221 | |||||||
| chr16:23420518 | A | G | 1 | a0001c0001t0002g0069 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1010-1691T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23420518 | |||||||
| chr16:23420681 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1010-1854G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23420681 | |||||||
| chr16:23420684 | A | C | 1 | a0001c0001t0005g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1010-1857T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23420684 | |||||||
| chr16:23420761 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1010-1934G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23420761 | |||||||
| chr16:23420910 | A | AT | 12 | a0001c0001t0001g0149 a0001c0001t0001g0152 a0001c0001t0001g0153 others(9): Show |
12 | HG00738.hp1 HG02630.hp1 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1010-2084dupA | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23420910 | |||||||
| chr16:23420910 | AT | A | 41 | a0001c0001t0001g0225 a0001c0001t0002g0022 a0001c0001t0002g0023 others(38): Show |
44 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.1010-2084delA | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23420910 | |||||||
| chr16:23420910 | ATTTTTTT others(3): Show |
A | 77 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(74): Show |
77 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1010-2093_1010-208 others(14): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23420910 | |||||||
| chr16:23420934 | T | G | 22 | a0002c0002t0003g0010 a0002c0002t0003g0109 a0002c0002t0003g0111 others(19): Show |
22 | HG00423.hp2 HG00741.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1010-2107A>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23420934 | |||||||
| chr16:23421149 | A | T | 1 | a0001c0001t0001g0210 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1010-2322T>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23421149 | |||||||
| chr16:23421203 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1010-2376A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23421203 | |||||||
| chr16:23421284 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | NA18971.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1010-2457C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23421284 | |||||||
| chr16:23421311 | A | G | 1 | a0001c0001t0001g0232 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1010-2484T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23421311 | |||||||
| chr16:23421539 | A | T | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1010-2712T>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23421539 | |||||||
| chr16:23421850 | C | CA | 7 | a0001c0001t0001g0182 a0001c0001t0001g0236 a0001c0001t0002g0039 others(4): Show |
7 | HG01175.hp2 HG02630.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1009+2898dupT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23421850 | |||||||
| chr16:23421988 | T | C | 1 | a0006c0011t0007g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1009+2761A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23421988 | |||||||
| chr16:23422005 | G | A | 21 | a0002c0002t0003g0010 a0002c0002t0003g0111 a0002c0002t0003g0112 others(18): Show |
21 | HG00423.hp2 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.1009+2744C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23422005 | |||||||
| chr16:23422590 | T | C | 1 | a0001c0001t0005g0040 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1009+2159A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23422590 | |||||||
| chr16:23422750 | T | C | 1 | a0001c0001t0002g0071 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1009+1999A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23422750 | |||||||
| chr16:23422778 | T | C | 1 | a0006c0011t0007g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1009+1971A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23422778 | |||||||
| chr16:23422843 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1009+1906C>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23422843 | |||||||
| chr16:23422977 | A | G | 133 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(130): Show |
137 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1009+1772T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23422977 | |||||||
| chr16:23422993 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1009+1756G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23422993 | |||||||
| chr16:23423044 | C | CA | 75 | a0001c0001t0001g0198 a0001c0001t0001g0226 a0001c0001t0002g0012 others(72): Show |
75 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1009+1704dupT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23423044 | |||||||
| chr16:23423044 | C | CAA | 7 | a0001c0001t0002g0016 a0001c0001t0002g0039 a0001c0001t0002g0047 others(4): Show |
7 | HG00609.hp2 HG00621.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1009+1703_1009+170 others(6): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23423044 | |||||||
| chr16:23423174 | T | A | 2 | a0001c0003t0003g0131 a0001c0003t0003g0132 |
2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1009+1575A>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23423174 | |||||||
| chr16:23423191 | C | A | 130 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(127): Show |
134 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1009+1558G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23423191 | |||||||
| chr16:23423326 | C | T | 1 | a0002c0002t0003g0109 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1009+1423G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23423326 | |||||||
| chr16:23423514 | C | G | 1 | a0002c0002t0003g0109 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1009+1235G>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23423514 | |||||||
| chr16:23423858 | A | G | 40 | a0001c0003t0003g0131 a0001c0003t0003g0132 a0002c0002t0003g0003 others(37): Show |
43 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1009+891T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23423858 | |||||||
| chr16:23423918 | G | A | 22 | a0002c0002t0003g0010 a0002c0002t0003g0109 a0002c0002t0003g0111 others(19): Show |
22 | HG00423.hp2 HG00741.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1009+831C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23423918 | |||||||
| chr16:23423992 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0227 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1009+757G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23423992 | |||||||
| chr16:23424073 | G | A | 1 | a0001c0001t0002g0030 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1009+676C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23424073 | |||||||
| chr16:23424157 | C | T | 5 | a0001c0001t0001g0139 a0001c0001t0001g0142 a0001c0001t0001g0174 others(2): Show |
5 | HG02451.hp2 HG02486.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1009+592G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23424157 | |||||||
| chr16:23424231 | A | AGGTTGTG | 2 | a0001c0001t0002g0004 a0001c0001t0002g0143 |
4 | HG02559.hp1 HG03225.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1009+511_1009+517d others(9): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23424231 | |||||||
| chr16:23424297 | C | CA | 82 | a0001c0001t0001g0146 a0001c0001t0001g0162 a0001c0001t0001g0174 others(79): Show |
82 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1009+451dupT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23424297 | |||||||
| chr16:23424379 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1009+370C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 7/16 | chr16 | 23424379 | |||||||
| chr16:23425037 | C | T | 131 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(128): Show |
135 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.811-90G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23425037 | |||||||
| chr16:23425081 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.811-134T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23425081 | |||||||
| chr16:23425203 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.811-256C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23425203 | |||||||
| chr16:23426012 | G | A | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.811-1065C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23426012 | |||||||
| chr16:23426819 | A | C | 87 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(84): Show |
88 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.811-1872T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23426819 | |||||||
| chr16:23426834 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.811-1887T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23426834 | |||||||
| chr16:23426834 | AAAAG | A | 76 | a0001c0001t0001g0228 a0001c0001t0002g0012 a0001c0001t0002g0016 others(73): Show |
76 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.811-1891_811-1888d others(6): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23426834 | |||||||
| chr16:23426835 | AAAG | A | 13 | a0001c0001t0002g0005 a0001c0001t0002g0022 a0001c0001t0002g0023 others(10): Show |
14 | HG01516.hp1 HG02257.hp1 HG02965.hp2 others(11): Show |
intron_variant | MODIFIER | c.811-1891_811-1889d others(5): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23426835 | |||||||
| chr16:23426842 | G | A | 86 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(83): Show |
87 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.811-1895C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23426842 | |||||||
| chr16:23427274 | A | C | 1 | a0001c0001t0001g0206 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.811-2327T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23427274 | |||||||
| chr16:23427478 | G | GA | 40 | a0001c0003t0003g0131 a0001c0003t0003g0132 a0002c0002t0003g0003 others(37): Show |
43 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.811-2532dupT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23427478 | |||||||
| chr16:23428014 | A | G | 40 | a0001c0003t0003g0131 a0001c0003t0003g0132 a0002c0002t0003g0003 others(37): Show |
43 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.811-3067T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23428014 | |||||||
| chr16:23428290 | A | C | 2 | a0001c0001t0001g0175 a0001c0001t0001g0190 |
2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.811-3343T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23428290 | |||||||
| chr16:23428340 | C | T | 9 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(6): Show |
10 | HG01099.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.811-3393G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23428340 | |||||||
| chr16:23428393 | T | A | 1 | a0001c0001t0001g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.811-3446A>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23428393 | |||||||
| chr16:23428427 | G | T | 2 | a0002c0002t0003g0098 a0002c0002t0003g0099 |
2 | HG00639.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.811-3480C>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23428427 | |||||||
| chr16:23428485 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.811-3538G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23428485 | |||||||
| chr16:23428676 | T | C | 132 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(129): Show |
136 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.811-3729A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23428676 | |||||||
| chr16:23428692 | C | CT | 8 | a0001c0001t0001g0150 a0001c0001t0001g0175 a0001c0001t0001g0185 others(5): Show |
8 | HG01109.hp1 HG02056.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.811-3746dupA | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23428692 | |||||||
| chr16:23428708 | T | C | 3 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0036 |
3 | HG00735.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.811-3761A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23428708 | |||||||
| chr16:23428726 | C | T | 1 | a0001c0001t0002g0018 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.811-3779G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23428726 | |||||||
| chr16:23428936 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.811-3989C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23428936 | |||||||
| chr16:23428945 | G | A | 1 | a0001c0012t0002g0013 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.811-3998C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23428945 | |||||||
| chr16:23429058 | T | G | 1 | a0006c0011t0007g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.811-4111A>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23429058 | |||||||
| chr16:23429290 | C | G | 132 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(129): Show |
136 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.810+4255G>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23429290 | |||||||
| chr16:23429383 | CA | C | 130 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(127): Show |
134 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.810+4161delT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23429383 | |||||||
| chr16:23429398 | C | A | 2 | a0002c0002t0003g0098 a0002c0002t0003g0099 |
2 | HG00639.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.810+4147G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23429398 | |||||||
| chr16:23429591 | C | T | 1 | a0001c0001t0004g0244 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.810+3954G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23429591 | |||||||
| chr16:23429640 | C | T | 133 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(130): Show |
137 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.810+3905G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23429640 | |||||||
| chr16:23429872 | C | T | 4 | a0002c0002t0003g0006 a0002c0002t0003g0026 a0002c0002t0003g0105 others(1): Show |
5 | HG01934.hp1 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.810+3673G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23429872 | |||||||
| chr16:23430144 | G | C | 87 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(84): Show |
88 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.810+3401C>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23430144 | |||||||
| chr16:23430368 | G | C | 1 | a0001c0001t0002g0249 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.810+3177C>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23430368 | |||||||
| chr16:23430829 | C | T | 4 | a0002c0002t0003g0096 a0002c0002t0003g0097 a0002c0002t0003g0106 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.810+2716G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23430829 | |||||||
| chr16:23431116 | T | C | 1 | a0002c0002t0003g0109 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.810+2429A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23431116 | |||||||
| chr16:23431275 | G | A | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.810+2270C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23431275 | |||||||
| chr16:23431563 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.810+1982T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23431563 | |||||||
| chr16:23431785 | G | C | 21 | a0002c0002t0003g0010 a0002c0002t0003g0111 a0002c0002t0003g0112 others(18): Show |
21 | HG00423.hp2 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.810+1760C>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23431785 | |||||||
| chr16:23431928 | G | A | 8 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0039 others(5): Show |
8 | HG02738.hp1 NA18948.hp1 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.810+1617C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23431928 | |||||||
| chr16:23431939 | A | G | 132 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(129): Show |
136 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.810+1606T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23431939 | |||||||
| chr16:23431988 | T | A | 4 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.810+1557A>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23431988 | |||||||
| chr16:23432255 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.810+1290C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23432255 | |||||||
| chr16:23432361 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG01346.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.810+1184C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23432361 | |||||||
| chr16:23432386 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.810+1159G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23432386 | |||||||
| chr16:23432494 | GT | G | 3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.810+1050delA | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23432494 | |||||||
| chr16:23432637 | C | A | 4 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.810+908G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23432637 | |||||||
| chr16:23432667 | C | T | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.810+878G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23432667 | |||||||
| chr16:23432732 | C | A | 3 | a0001c0003t0003g0131 a0001c0003t0003g0132 a0005c0005t0003g0133 |
3 | HG02109.hp2 HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.810+813G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23432732 | |||||||
| chr16:23432888 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.810+657C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23432888 | |||||||
| chr16:23432947 | T | C | 78 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(75): Show |
78 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.810+598A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23432947 | |||||||
| chr16:23433079 | C | T | 1 | a0002c0002t0007g0114 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.810+466G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23433079 | |||||||
| chr16:23433387 | G | A | 9 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(6): Show |
10 | HG01099.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.810+158C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23433387 | |||||||
| chr16:23433399 | T | A | 1 | a0001c0001t0001g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.810+146A>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23433399 | |||||||
| chr16:23433431 | C | T | 1 | a0001c0001t0002g0055 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.810+114G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 6/16 | chr16 | 23433431 | |||||||
| chr16:23433819 | G | GA | 122 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(119): Show |
125 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.688-153dupT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 5/16 | chr16 | 23433819 | |||||||
| chr16:23433819 | G | GAA | 9 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(6): Show |
10 | HG01099.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.688-154_688-153dup others(2): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 5/16 | chr16 | 23433819 | |||||||
| chr16:23434300 | G | A | 4 | a0002c0002t0003g0096 a0002c0002t0003g0097 a0002c0002t0003g0106 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+336C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 5/16 | chr16 | 23434300 | |||||||
| chr16:23434377 | T | A | 2 | a0001c0001t0002g0045 a0001c0001t0002g0073 |
2 | NA18983.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.687+259A>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 5/16 | chr16 | 23434377 | |||||||
| chr16:23434764 | G | A | 1 | a0001c0001t0002g0047 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.605-46C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23434764 | |||||||
| chr16:23434815 | T | C | 2 | a0001c0001t0002g0048 a0007c0004t0002g0009 |
2 | NA18983.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.605-97A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23434815 | |||||||
| chr16:23434937 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0190 |
2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.605-219T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23434937 | |||||||
| chr16:23435075 | T | C | 78 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(75): Show |
78 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.605-357A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23435075 | |||||||
| chr16:23435442 | G | A | 1 | a0001c0003t0007g0248 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.605-724C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23435442 | |||||||
| chr16:23435656 | TTAGAAC | T | 49 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(46): Show |
53 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.605-944_605-939del others(6): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23435656 | |||||||
| chr16:23435729 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.605-1011A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23435729 | |||||||
| chr16:23435870 | G | A | 9 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(6): Show |
10 | HG01099.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.605-1152C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23435870 | |||||||
| chr16:23435931 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.605-1213A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23435931 | |||||||
| chr16:23436141 | G | A | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.605-1423C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23436141 | |||||||
| chr16:23436256 | T | C | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.605-1538A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23436256 | |||||||
| chr16:23436456 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.605-1738C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23436456 | |||||||
| chr16:23436602 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.605-1884C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23436602 | |||||||
| chr16:23436604 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.605-1886C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23436604 | |||||||
| chr16:23436621 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.605-1903C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23436621 | |||||||
| chr16:23436641 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.605-1923C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23436641 | |||||||
| chr16:23436727 | A | T | 5 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0027 others(2): Show |
6 | HG02572.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.605-2009T>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23436727 | |||||||
| chr16:23436820 | G | A | 1 | a0006c0011t0007g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.605-2102C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23436820 | |||||||
| chr16:23436931 | C | A | 1 | a0001c0001t0001g0008 | 2 | NA19012.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.605-2213G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23436931 | |||||||
| chr16:23437059 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.605-2341C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23437059 | |||||||
| chr16:23437364 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.605-2646G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23437364 | |||||||
| chr16:23437606 | A | C | 1 | a0001c0001t0002g0054 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.605-2888T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23437606 | |||||||
| chr16:23437635 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.605-2917C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23437635 | |||||||
| chr16:23437673 | A | AT | 79 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(76): Show |
79 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.605-2956dupA | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23437673 | |||||||
| chr16:23437848 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.605-3130T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23437848 | |||||||
| chr16:23438010 | G | A | 131 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(128): Show |
135 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.605-3292C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23438010 | |||||||
| chr16:23438083 | CA | C | 133 | a0001c0001t0001g0140 a0001c0001t0001g0204 a0001c0001t0001g0205 others(130): Show |
137 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.605-3366delT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23438083 | |||||||
| chr16:23438730 | C | CA | 132 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(129): Show |
136 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.604+3746dupT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23438730 | |||||||
| chr16:23439003 | C | A | 1 | a0001c0001t0001g0232 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.604+3474G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23439003 | |||||||
| chr16:23439072 | C | T | 1 | a0002c0002t0003g0010 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.604+3405G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23439072 | |||||||
| chr16:23439107 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.604+3370C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23439107 | |||||||
| chr16:23439129 | G | C | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.604+3348C>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23439129 | |||||||
| chr16:23439135 | ACAACAGA others(139): Show |
A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0143 a0001c0001t0002g0194 |
5 | HG02559.hp1 HG02818.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.604+3196_604+3341d others(2): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23439135 | |||||||
| chr16:23439158 | C | CA | 129 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0139 others(126): Show |
135 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.604+3318dupT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23439158 | |||||||
| chr16:23439158 | C | CAA | 6 | a0001c0001t0002g0037 a0001c0001t0006g0092 a0001c0001t0006g0093 others(3): Show |
6 | HG02056.hp2 HG02145.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.604+3317_604+3318d others(4): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23439158 | |||||||
| chr16:23439303 | C | T | 1 | a0002c0002t0003g0109 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.604+3174G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23439303 | |||||||
| chr16:23439304 | CA | C | 49 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0149 others(46): Show |
52 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.604+3172delT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23439304 | |||||||
| chr16:23439304 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0201 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.604+3163_604+3172d others(12): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23439304 | |||||||
| chr16:23439307 | A | C | 1 | a0002c0002t0003g0129 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.604+3170T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23439307 | |||||||
| chr16:23439335 | A | G | 87 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(84): Show |
88 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.604+3142T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23439335 | |||||||
| chr16:23439613 | G | A | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0199 others(4): Show |
7 | HG02155.hp2 NA18959.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.604+2864C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23439613 | |||||||
| chr16:23439694 | T | G | 3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.604+2783A>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23439694 | |||||||
| chr16:23439828 | A | C | 1 | a0001c0001t0002g0051 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.604+2649T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23439828 | |||||||
| chr16:23439838 | A | G | 1 | a0001c0001t0002g0138 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.604+2639T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23439838 | |||||||
| chr16:23440085 | CA | C | 126 | a0001c0001t0001g0147 a0001c0001t0002g0005 a0001c0001t0002g0012 others(123): Show |
130 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.604+2391delT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23440085 | |||||||
| chr16:23440261 | A | G | 1 | a0001c0001t0001g0243 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.604+2216T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23440261 | |||||||
| chr16:23440510 | A | AT | 81 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.604+1966dupA | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23440510 | |||||||
| chr16:23440603 | G | A | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.604+1874C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23440603 | |||||||
| chr16:23440607 | G | A | 40 | a0001c0003t0003g0131 a0001c0003t0003g0132 a0002c0002t0003g0003 others(37): Show |
43 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.604+1870C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23440607 | |||||||
| chr16:23440729 | T | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0200 |
3 | HG00738.hp2 HG01256.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.604+1748A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23440729 | |||||||
| chr16:23440809 | T | G | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.604+1668A>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23440809 | |||||||
| chr16:23441076 | A | T | 1 | a0001c0001t0001g0252 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.604+1401T>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23441076 | |||||||
| chr16:23441172 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.604+1305A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23441172 | |||||||
| chr16:23441285 | T | G | 1 | a0001c0001t0001g0236 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.604+1192A>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23441285 | |||||||
| chr16:23441312 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0134 others(48): Show |
59 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.604+1165G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23441312 | |||||||
| chr16:23441388 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.604+1089C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23441388 | |||||||
| chr16:23441503 | G | A | 132 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(129): Show |
136 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.604+974C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23441503 | |||||||
| chr16:23441647 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.604+830C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23441647 | |||||||
| chr16:23441727 | A | C | 2 | a0002c0002t0003g0098 a0002c0002t0003g0099 |
2 | HG00639.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.604+750T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23441727 | |||||||
| chr16:23441769 | CA | C | 131 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(128): Show |
135 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.604+707delT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23441769 | |||||||
| chr16:23441840 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.604+637C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23441840 | |||||||
| chr16:23441900 | T | G | 37 | a0002c0002t0003g0003 a0002c0002t0003g0006 a0002c0002t0003g0010 others(34): Show |
40 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.604+577A>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23441900 | |||||||
| chr16:23441942 | T | C | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.604+535A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23441942 | |||||||
| chr16:23442100 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0186 |
2 | NA18979.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.604+377C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23442100 | |||||||
| chr16:23442291 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.604+186C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23442291 | |||||||
| chr16:23442299 | A | T | 3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.604+178T>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23442299 | |||||||
| chr16:23442333 | CA | C | 85 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0002g0005 others(82): Show |
86 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.604+143delT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23442333 | |||||||
| chr16:23442333 | CAA | C | 46 | a0001c0001t0002g0029 a0001c0001t0002g0048 a0001c0001t0002g0051 others(43): Show |
49 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.604+142_604+143del others(2): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 4/16 | chr16 | 23442333 | |||||||
| chr16:23442687 | C | G | 3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.436-42G>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/16 | chr16 | 23442687 | |||||||
| chr16:23442710 | A | G | 1 | a0001c0001t0002g0050 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.436-65T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/16 | chr16 | 23442710 | |||||||
| chr16:23442761 | C | A | 1 | a0001c0001t0001g0184 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.436-116G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/16 | chr16 | 23442761 | |||||||
| chr16:23442800 | T | C | 78 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(75): Show |
78 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.436-155A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/16 | chr16 | 23442800 | |||||||
| chr16:23442949 | A | C | 1 | a0001c0001t0005g0040 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.436-304T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/16 | chr16 | 23442949 | |||||||
| chr16:23443025 | C | G | 3 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 |
3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.436-380G>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/16 | chr16 | 23443025 | |||||||
| chr16:23443029 | G | A | 2 | a0001c0001t0002g0038 a0001c0001t0002g0086 |
2 | NA19012.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.436-384C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/16 | chr16 | 23443029 | |||||||
| chr16:23443033 | C | CA | 130 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(127): Show |
134 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.436-389dupT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/16 | chr16 | 23443033 | |||||||
| chr16:23443198 | T | G | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.436-553A>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/16 | chr16 | 23443198 | |||||||
| chr16:23443746 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.436-1101T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/16 | chr16 | 23443746 | |||||||
| chr16:23443840 | G | C | 1 | a0002c0002t0003g0129 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.436-1195C>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/16 | chr16 | 23443840 | |||||||
| chr16:23444108 | A | G | 3 | a0001c0001t0002g0039 a0001c0001t0002g0048 a0007c0004t0002g0009 |
3 | HG02738.hp1 NA18983.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.435+940T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/16 | chr16 | 23444108 | |||||||
| chr16:23444188 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.435+860A>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/16 | chr16 | 23444188 | |||||||
| chr16:23444358 | A | C | 1 | a0001c0001t0002g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.435+690T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/16 | chr16 | 23444358 | |||||||
| chr16:23444432 | C | T | 1 | a0006c0011t0007g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.435+616G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/16 | chr16 | 23444432 | |||||||
| chr16:23444453 | C | T | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.435+595G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/16 | chr16 | 23444453 | |||||||
| chr16:23444511 | C | CT | 125 | a0001c0001t0001g0139 a0001c0001t0001g0188 a0001c0001t0002g0005 others(122): Show |
129 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.435+536dupA | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 3/16 | chr16 | 23444511 | |||||||
| chr16:23445227 | G | C | 40 | a0001c0003t0003g0131 a0001c0003t0003g0132 a0002c0002t0003g0003 others(37): Show |
43 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.319-63C>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 2/16 | chr16 | 23445227 | |||||||
| chr16:23445257 | T | C | 132 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(129): Show |
136 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.319-93A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 2/16 | chr16 | 23445257 | |||||||
| chr16:23445283 | C | A | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.319-119G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 2/16 | chr16 | 23445283 | |||||||
| chr16:23445969 | TA | T | 89 | a0001c0001t0001g0014 a0001c0001t0002g0005 a0001c0001t0002g0012 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.170-9delT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23445969 | |||||||
| chr16:23445984 | A | C | 1 | a0001c0001t0001g0144 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.170-23T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23445984 | |||||||
| chr16:23445986 | AC | A | 4 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-26delG | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23445986 | |||||||
| chr16:23446262 | C | T | 133 | a0001c0001t0001g0014 a0001c0001t0002g0005 a0001c0001t0002g0012 others(130): Show |
137 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.170-301G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23446262 | |||||||
| chr16:23446318 | G | A | 1 | a0002c0002t0003g0127 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.170-357C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23446318 | |||||||
| chr16:23446445 | C | CT | 21 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(18): Show |
23 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.170-485dupA | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23446445 | |||||||
| chr16:23446445 | CT | C | 84 | a0001c0001t0001g0014 a0001c0001t0001g0136 a0001c0001t0001g0185 others(81): Show |
85 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.170-485delA | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23446445 | |||||||
| chr16:23446537 | T | C | 2 | a0001c0001t0001g0234 a0001c0001t0001g0247 |
2 | NA18952.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.170-576A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23446537 | |||||||
| chr16:23446565 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.170-604G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23446565 | |||||||
| chr16:23446597 | G | A | 2 | a0001c0001t0002g0080 a0001c0001t0002g0081 |
2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.170-636C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23446597 | |||||||
| chr16:23446747 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.170-786G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23446747 | |||||||
| chr16:23446940 | C | CAG | 130 | a0001c0001t0001g0014 a0001c0001t0002g0005 a0001c0001t0002g0012 others(127): Show |
134 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.170-981_170-980dup others(2): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23446940 | |||||||
| chr16:23446951 | T | C | 30 | a0001c0001t0002g0032 a0001c0001t0002g0075 a0001c0001t0002g0076 others(27): Show |
30 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.170-990A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23446951 | |||||||
| chr16:23447164 | T | C | 129 | a0001c0001t0001g0014 a0001c0001t0002g0005 a0001c0001t0002g0012 others(126): Show |
133 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.170-1203A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23447164 | |||||||
| chr16:23447479 | G | A | 1 | a0002c0002t0003g0109 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.170-1518C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23447479 | |||||||
| chr16:23447488 | G | A | 2 | a0001c0001t0006g0093 a0001c0001t0006g0094 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.170-1527C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23447488 | |||||||
| chr16:23447803 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.170-1842C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23447803 | |||||||
| chr16:23447832 | G | A | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.170-1871C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23447832 | |||||||
| chr16:23447983 | G | A | 1 | a0002c0002t0003g0010 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.170-2022C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23447983 | |||||||
| chr16:23448257 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.170-2296G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23448257 | |||||||
| chr16:23448258 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.170-2297C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23448258 | |||||||
| chr16:23448640 | T | C | 4 | a0002c0002t0003g0100 a0002c0002t0003g0101 a0002c0002t0003g0102 others(1): Show |
4 | HG02258.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-2679A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23448640 | |||||||
| chr16:23448831 | C | T | 72 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(69): Show |
72 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.170-2870G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23448831 | |||||||
| chr16:23448894 | G | A | 1 | a0002c0002t0003g0129 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.170-2933C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23448894 | |||||||
| chr16:23449160 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.170-3199C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23449160 | |||||||
| chr16:23449232 | G | A | 1 | a0001c0003t0003g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.170-3271C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23449232 | |||||||
| chr16:23449236 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.170-3275C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23449236 | |||||||
| chr16:23449380 | T | A | 1 | a0001c0001t0002g0086 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.170-3419A>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23449380 | |||||||
| chr16:23449380 | T | TTAAAA | 24 | a0001c0001t0001g0014 a0001c0001t0001g0236 a0001c0001t0001g0238 others(21): Show |
24 | HG00438.hp2 HG00639.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.170-3424_170-3420d others(7): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23449380 | |||||||
| chr16:23449380 | T | TTAAAATA others(3): Show |
9 | a0001c0001t0001g0243 a0001c0001t0002g0104 a0001c0001t0002g0107 others(6): Show |
9 | HG01109.hp1 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.170-3429_170-3420d others(12): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23449380 | |||||||
| chr16:23449380 | T | TTAAAATA others(8): Show |
2 | a0002c0002t0003g0006 a0002c0002t0003g0109 |
3 | HG02559.hp2 HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.169+3431_170-3420d others(17): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23449380 | |||||||
| chr16:23449380 | T | TTAAAATA others(13): Show |
1 | a0001c0001t0002g0024 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.169+3426_170-3420d others(22): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23449380 | |||||||
| chr16:23449380 | T | TTAAAATA others(18): Show |
1 | a0001c0001t0002g0025 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.169+3421_170-3420d others(27): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23449380 | |||||||
| chr16:23449380 | TTAAAA | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0134 others(63): Show |
75 | HG00140.hp2 HG00423.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.170-3424_170-3420d others(7): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23449380 | |||||||
| chr16:23449380 | TTAAAATA others(3): Show |
T | 29 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0002g0030 others(26): Show |
31 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.170-3429_170-3420d others(12): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23449380 | |||||||
| chr16:23449380 | TTAAAATA others(8): Show |
T | 3 | a0001c0001t0002g0249 a0001c0003t0007g0248 a0002c0002t0003g0130 |
3 | HG01981.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.169+3431_170-3420d others(17): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23449380 | |||||||
| chr16:23449380 | TTAAAATA others(13): Show |
T | 1 | a0001c0001t0001g0250 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.169+3426_170-3420d others(22): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23449380 | |||||||
| chr16:23449486 | G | A | 2 | a0001c0001t0002g0017 a0001c0001t0002g0029 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.169+3340C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23449486 | |||||||
| chr16:23449751 | C | CA | 8 | a0001c0001t0002g0016 a0001c0001t0002g0087 a0001c0001t0002g0088 others(5): Show |
8 | HG00621.hp1 HG01981.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+3074dupT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23449751 | |||||||
| chr16:23449884 | C | A | 4 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(1): Show |
6 | HG02896.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+2942G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23449884 | |||||||
| chr16:23450416 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.169+2410A>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23450416 | |||||||
| chr16:23450433 | A | C | 131 | a0001c0001t0001g0014 a0001c0001t0002g0005 a0001c0001t0002g0012 others(128): Show |
135 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.169+2393T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23450433 | |||||||
| chr16:23450554 | G | A | 1 | a0001c0001t0004g0246 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.169+2272C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23450554 | |||||||
| chr16:23450734 | G | A | 130 | a0001c0001t0001g0014 a0001c0001t0002g0005 a0001c0001t0002g0012 others(127): Show |
134 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.169+2092C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23450734 | |||||||
| chr16:23450773 | G | A | 21 | a0002c0002t0003g0010 a0002c0002t0003g0111 a0002c0002t0003g0112 others(18): Show |
21 | HG00423.hp2 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.169+2053C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23450773 | |||||||
| chr16:23450950 | T | G | 1 | a0002c0002t0003g0003 | 3 | HG03195.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.169+1876A>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23450950 | |||||||
| chr16:23450963 | G | A | 1 | a0001c0003t0007g0248 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.169+1863C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23450963 | |||||||
| chr16:23451180 | G | A | 72 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0018 others(69): Show |
72 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.169+1646C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23451180 | |||||||
| chr16:23451309 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.169+1517C>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23451309 | |||||||
| chr16:23451318 | C | A | 78 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(75): Show |
79 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.169+1508G>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23451318 | |||||||
| chr16:23451338 | C | CTGTGAAT others(2): Show |
3 | a0001c0003t0003g0131 a0001c0003t0003g0132 a0005c0005t0003g0133 |
3 | HG02109.hp2 HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.169+1487_169+1488i others(11): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23451338 | |||||||
| chr16:23451569 | A | G | 4 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(1): Show |
6 | HG02896.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+1257T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23451569 | |||||||
| chr16:23451668 | A | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | NA18980.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.169+1158T>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23451668 | |||||||
| chr16:23451725 | CA | C | 81 | a0001c0001t0001g0014 a0001c0001t0001g0134 a0001c0001t0002g0005 others(78): Show |
82 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.169+1100delT | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23451725 | |||||||
| chr16:23451725 | CAA | C | 48 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(45): Show |
51 | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.169+1099_169+1100d others(4): Show |
COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23451725 | |||||||
| chr16:23451856 | T | A | 1 | a0001c0003t0007g0248 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.169+970A>T | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23451856 | |||||||
| chr16:23451883 | A | G | 1 | a0001c0001t0002g0016 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.169+943T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23451883 | |||||||
| chr16:23451984 | C | G | 82 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0016 others(79): Show |
83 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.169+842G>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23451984 | |||||||
| chr16:23452270 | G | C | 1 | a0001c0001t0002g0249 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.169+556C>G | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23452270 | |||||||
| chr16:23452312 | A | G | 2 | a0001c0001t0001g0014 a0006c0011t0007g0015 |
2 | HG02258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.169+514T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23452312 | |||||||
| chr16:23452418 | A | G | 3 | a0001c0001t0002g0012 a0001c0001t0005g0011 a0001c0012t0002g0013 |
3 | HG02145.hp1 HG02451.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.169+408T>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23452418 | |||||||
| chr16:23452699 | C | T | 1 | a0002c0002t0003g0010 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.169+127G>A | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23452699 | |||||||
| chr16:23452766 | T | G | 1 | a0001c0001t0001g0250 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.169+60A>C | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23452766 | |||||||
| chr16:23452807 | AG | A | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG00609.hp1 HG00621.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.169+18delC | COG7 | ENSG00000168434.13 | transcript | ENST00000307149.10 | protein_coding | 1/16 | chr16 | 23452807 |