Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26958 |
| ensemblid | ENSG00000158623.14 |
| hgncid | 2237 |
| symbol | COPG2 |
| name | COPI coat complex subunit gamma 2 |
| refseq_nuc | NM_012133.6 |
| refseq_prot | NP_036265.3 |
| ensembl_nuc | ENST00000425248.5 |
| ensembl_prot | ENSP00000402346.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 130506238 |
| end | 130668748 |
| strand | - |
| ver | v1.2 |
| region | chr7:130506238-130668748 |
| region5000 | chr7:130501238-130673748 |
| regionname0 | COPG2_chr7_130506238_130668748 |
| regionname5000 | COPG2_chr7_130501238_130673748 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 871 | 313 | 87 | 59 | 108 | 13 | 44 | 80 | COPG2_chr7_130501238_130673748 | COPG2 | MIKKF others(866): Show |
chr7 | 130501238 | 130673748 |
| a0002 | 0/0 | 871 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | MIKKF others(866): Show |
chr7 | 130501238 | 130673748 |
| a0003 | 0/0 | 871 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | COPG2_chr7_130501238_130673748 | COPG2 | MIKKF others(866): Show |
chr7 | 130501238 | 130673748 |
| a0004 | 0/0 | 871 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | MIKKF others(866): Show |
chr7 | 130501238 | 130673748 |
| a0005 | 0/0 | 871 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | MIKKF others(866): Show |
chr7 | 130501238 | 130673748 |
| a0006 | 0/0 | 871 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | MIKKF others(866): Show |
chr7 | 130501238 | 130673748 |
| a0007 | 0/0 | 871 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | MIKKF others(866): Show |
chr7 | 130501238 | 130673748 |
| a0008 | 0/0 | 871 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | MIKKF others(866): Show |
chr7 | 130501238 | 130673748 |
| a0009 | 0/0 | 871 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | MIKKF others(866): Show |
chr7 | 130501238 | 130673748 |
| a0010 | 0/0 | 871 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | MIKKF others(866): Show |
chr7 | 130501238 | 130673748 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2613 | 203 | 63 | 39 | 62 | 11 | 26 | COPG2_chr7_130501238_130673748 | COPG2 | ATGAT others(2608): Show |
chr7 | 130501238 | 130673748 | ||
| a0001c0002 | 0/0 | 2613 | 105 | 21 | 20 | 44 | 2 | 18 | COPG2_chr7_130501238_130673748 | COPG2 | ATGAT others(2608): Show |
chr7 | 130501238 | 130673748 | ||
| a0001c0005 | 0/0 | 2613 | 2 | 2 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | ATGAT others(2608): Show |
chr7 | 130501238 | 130673748 | ||
| a0001c0006 | 0/0 | 2613 | 2 | 0 | 0 | 2 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | ATGAT others(2608): Show |
chr7 | 130501238 | 130673748 | ||
| a0001c0012 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | ATGAT others(2608): Show |
chr7 | 130501238 | 130673748 | ||
| a0002c0003 | 0/0 | 2613 | 3 | 2 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | ATGAT others(2608): Show |
chr7 | 130501238 | 130673748 | ||
| a0003c0004 | 0/0 | 2613 | 2 | 0 | 0 | 2 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | ATGAT others(2608): Show |
chr7 | 130501238 | 130673748 | ||
| a0003c0008 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | ATGAT others(2608): Show |
chr7 | 130501238 | 130673748 | ||
| a0004c0011 | 0/0 | 2613 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | ATGAT others(2608): Show |
chr7 | 130501238 | 130673748 | ||
| a0005c0015 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | ATGAT others(2608): Show |
chr7 | 130501238 | 130673748 | ||
| a0006c0007 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | ATGAT others(2608): Show |
chr7 | 130501238 | 130673748 | ||
| a0007c0010 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | ATGAT others(2608): Show |
chr7 | 130501238 | 130673748 | ||
| a0008c0013 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | ATGAT others(2608): Show |
chr7 | 130501238 | 130673748 | ||
| a0009c0014 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | ATGAT others(2608): Show |
chr7 | 130501238 | 130673748 | ||
| a0010c0009 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | ATGAT others(2608): Show |
chr7 | 130501238 | 130673748 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3134 | 96 | 43 | 16 | 21 | 8 | 7 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3129): Show |
chr7 | 130501238 | 130673748 |
| a0001c0001t0002 | 0/1 | 3133 | 78 | 5 | 17 | 36 | 3 | 16 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3128): Show |
chr7 | 130501238 | 130673748 |
| a0001c0001t0004 | 0/0 | 3135 | 8 | 2 | 4 | 0 | 0 | 2 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3130): Show |
chr7 | 130501238 | 130673748 |
| a0001c0001t0005 | 0/0 | 3134 | 6 | 6 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3129): Show |
chr7 | 130501238 | 130673748 |
| a0001c0001t0006 | 0/0 | 3134 | 8 | 2 | 2 | 3 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3129): Show |
chr7 | 130501238 | 130673748 |
| a0001c0001t0008 | 0/0 | 3133 | 3 | 3 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3128): Show |
chr7 | 130501238 | 130673748 |
| a0001c0001t0009 | 0/0 | 3135 | 2 | 2 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3130): Show |
chr7 | 130501238 | 130673748 |
| a0001c0001t0010 | 0/0 | 3134 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3129): Show |
chr7 | 130501238 | 130673748 |
| a0001c0001t0012 | 0/0 | 3133 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3128): Show |
chr7 | 130501238 | 130673748 |
| a0001c0002t0001 | 0/0 | 3134 | 71 | 17 | 8 | 33 | 1 | 12 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3129): Show |
chr7 | 130501238 | 130673748 |
| a0001c0002t0002 | 0/0 | 3133 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3128): Show |
chr7 | 130501238 | 130673748 |
| a0001c0002t0003 | 0/0 | 3127 | 20 | 0 | 6 | 9 | 1 | 4 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3122): Show |
chr7 | 130501238 | 130673748 |
| a0001c0002t0004 | 0/0 | 3135 | 4 | 0 | 0 | 2 | 0 | 2 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3130): Show |
chr7 | 130501238 | 130673748 |
| a0001c0002t0005 | 0/0 | 3134 | 3 | 0 | 3 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3129): Show |
chr7 | 130501238 | 130673748 |
| a0001c0002t0007 | 0/0 | 3134 | 5 | 3 | 2 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3129): Show |
chr7 | 130501238 | 130673748 |
| a0001c0002t0011 | 0/0 | 3135 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3130): Show |
chr7 | 130501238 | 130673748 |
| a0001c0005t0002 | 0/0 | 3133 | 2 | 2 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3128): Show |
chr7 | 130501238 | 130673748 |
| a0001c0006t0002 | 0/0 | 3133 | 2 | 0 | 0 | 2 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3128): Show |
chr7 | 130501238 | 130673748 |
| a0001c0012t0002 | 0/0 | 3133 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3128): Show |
chr7 | 130501238 | 130673748 |
| a0002c0003t0001 | 0/0 | 3134 | 3 | 2 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3129): Show |
chr7 | 130501238 | 130673748 |
| a0003c0004t0001 | 0/0 | 3134 | 2 | 0 | 0 | 2 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3129): Show |
chr7 | 130501238 | 130673748 |
| a0003c0008t0001 | 0/0 | 3134 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3129): Show |
chr7 | 130501238 | 130673748 |
| a0004c0011t0001 | 0/0 | 3134 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3129): Show |
chr7 | 130501238 | 130673748 |
| a0005c0015t0001 | 0/0 | 3134 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3129): Show |
chr7 | 130501238 | 130673748 |
| a0006c0007t0001 | 0/0 | 3134 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3129): Show |
chr7 | 130501238 | 130673748 |
| a0007c0010t0001 | 0/0 | 3134 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3129): Show |
chr7 | 130501238 | 130673748 |
| a0008c0013t0001 | 0/0 | 3134 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3129): Show |
chr7 | 130501238 | 130673748 |
| a0009c0014t0001 | 0/0 | 3134 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3129): Show |
chr7 | 130501238 | 130673748 |
| a0010c0009t0002 | 0/0 | 3133 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | CTTCC others(3128): Show |
chr7 | 130501238 | 130673748 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0050 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0029 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0004g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0008g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0008g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0008g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0009g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0009g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0010g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0012g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0005g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0007g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0007g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0007g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0007g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0007g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0011g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0005t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0005t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0006t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0006t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0012t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0002c0003t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0002c0003t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0002c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0003c0004t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0003c0004t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0003c0008t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0004c0011t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0005c0015t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0006c0007t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0007c0010t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0008c0013t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0009c0014t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0010c0009t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0038 | EUR | GBR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00099 | hp2 | a0004 | c0011 | t0001 | g0276 | EUR | GBR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0271 | EUR | GBR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0195 | EUR | GBR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0110 | EUR | FIN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0323 | EUR | FIN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00544 | hp1 | a0001 | c0002 | t0003 | g0107 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0245 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01192 | hp2 | a0001 | c0002 | t0007 | g0239 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0089 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01256 | hp1 | a0001 | c0002 | t0005 | g0079 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0322 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01258 | hp1 | a0001 | c0002 | t0005 | g0078 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0215 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0088 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0072 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01433 | hp2 | a0002 | c0003 | t0001 | g0243 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0286 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0221 | EUR | IBS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0285 | EUR | IBS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0311 | EUR | IBS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0197 | EUR | IBS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0104 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0320 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0122 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0112 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0267 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0081 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0178 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01993 | hp1 | a0001 | c0002 | t0007 | g0237 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01993 | hp2 | a0001 | c0002 | t0005 | g0080 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02015 | hp1 | a0001 | c0002 | t0003 | g0108 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0256 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02056 | hp2 | a0001 | c0002 | t0003 | g0106 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0149 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02148 | hp1 | a0001 | c0002 | t0003 | g0111 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | CDX | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | CDX | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CDX | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | CDX | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0113 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02451 | hp2 | a0001 | c0005 | t0002 | g0012 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0109 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02622 | hp1 | a0005 | c0015 | t0001 | g0259 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0251 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0258 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0312 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0255 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0130 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0066 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0202 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0097 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0242 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02818 | hp1 | a0001 | c0002 | t0007 | g0238 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0128 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0316 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02976 | hp1 | a0001 | c0002 | t0007 | g0236 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0248 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0048 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0319 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0252 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03490 | hp2 | a0001 | c0002 | t0003 | g0124 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0041 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0034 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0226 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0065 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0067 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0059 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03831 | hp1 | a0001 | c0002 | t0003 | g0070 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0127 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0247 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03927 | hp2 | a0001 | c0002 | t0004 | g0103 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03942 | hp2 | a0001 | c0002 | t0003 | g0125 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04115 | hp1 | a0001 | c0002 | t0004 | g0053 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0196 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04184 | hp1 | a0001 | c0002 | t0003 | g0123 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0306 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0030 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0105 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | YRI | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18522 | hp2 | a0001 | c0005 | t0002 | g0011 | AFR | YRI | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | YRI | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0241 | AFR | YRI | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18941 | hp2 | a0001 | c0006 | t0002 | g0153 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18945 | hp1 | a0001 | c0006 | t0002 | g0154 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18947 | hp2 | a0001 | c0001 | t0006 | g0170 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18960 | hp2 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18962 | hp2 | a0006 | c0007 | t0001 | g0098 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18965 | hp1 | a0003 | c0004 | t0001 | g0292 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18966 | hp2 | a0001 | c0002 | t0004 | g0082 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18967 | hp1 | a0001 | c0001 | t0012 | g0201 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0164 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19010 | hp1 | a0001 | c0002 | t0003 | g0115 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19010 | hp2 | a0003 | c0004 | t0001 | g0290 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19030 | hp1 | a0007 | c0010 | t0001 | g0147 | AFR | LWK | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19030 | hp2 | a0001 | c0002 | t0007 | g0235 | AFR | LWK | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19043 | hp1 | a0001 | c0012 | t0002 | g0161 | AFR | LWK | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19054 | hp1 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19054 | hp2 | a0001 | c0002 | t0003 | g0261 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19066 | hp1 | a0001 | c0002 | t0003 | g0116 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19070 | hp1 | a0001 | c0002 | t0003 | g0114 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19078 | hp2 | a0001 | c0002 | t0003 | g0120 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19079 | hp2 | a0008 | c0013 | t0001 | g0069 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19081 | hp1 | a0009 | c0014 | t0001 | g0090 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19082 | hp2 | a0010 | c0009 | t0002 | g0217 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0250 | AFR | ASW | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ASW | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | TSI | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0268 | EUR | TSI | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02486 | hp1 | a0001 | c0002 | t0011 | g0240 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0062 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG06807 | hp1 | a0003 | c0008 | t0001 | g0117 | AFR | USA | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | USA | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18955 | hp1 | a0001 | c0002 | t0004 | g0084 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | USA | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0244 | AFR | USA | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | LWK | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0029 | REF | REF | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0050 | REF | REF | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130506741 | T | C | 1 | a0007 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.2551A>G | p.Met851Val | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 2631/3134 | 2551/2616 | 851/871 | chr7 | 130506741 | |||
| chr7:130506746 | A | C | 1 | a0006 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.2546T>G | p.Val849Gly | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 2626/3134 | 2546/2616 | 849/871 | chr7 | 130506746 | |||
| chr7:130506747 | C | A | 1 | a0006 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.2545G>T | p.Val849Leu | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 2625/3134 | 2545/2616 | 849/871 | chr7 | 130506747 | |||
| chr7:130507288 | G | A | 1 | a0003 | 3 | HG06807.hp1 NA18965.hp1 NA19010.hp2 |
missense_variant | MODERATE | c.2471C>T | p.Ser824Leu | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 23/24 | 2551/3134 | 2471/2616 | 824/871 | chr7 | 130507288 | |||
| chr7:130547718 | A | G | 1 | a0010 | 1 | NA19082.hp2 | missense_variant | MODERATE | c.2105T>C | p.Ile702Thr | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/24 | 2185/3134 | 2105/2616 | 702/871 | chr7 | 130547718 | |||
| chr7:130547741 | G | C | 1 | a0004 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.2082C>G | p.Ser694Arg | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/24 | 2162/3134 | 2082/2616 | 694/871 | chr7 | 130547741 | |||
| chr7:130611083 | G | C | 1 | a0008 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.607C>G | p.Leu203Val | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/24 | 687/3134 | 607/2616 | 203/871 | chr7 | 130611083 | |||
| chr7:130612195 | T | C | 1 | a0009 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.536A>G | p.Asn179Ser | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/24 | 616/3134 | 536/2616 | 179/871 | chr7 | 130612195 | |||
| chr7:130612222 | C | T | 1 | a0002 | 3 | HG01433.hp2 HG02809.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.509G>A | p.Ser170Asn | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/24 | 589/3134 | 509/2616 | 170/871 | chr7 | 130612222 | |||
| chr7:130667522 | T | C | 1 | a0005 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.50A>G | p.Asn17Ser | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 2/24 | 130/3134 | 50/2616 | 17/871 | chr7 | 130667522 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130547783 | T | C | 1 | a0001c0012 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.2040A>G | p.Pro680Pro | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/24 | 2120/3134 | 2040/2616 | 680/871 | chr7 | 130547783 | |||
| chr7:130549333 | G | A | 1 | a0001c0005 | 2 | HG02451.hp2 NA18522.hp2 |
synonymous_variant | LOW | c.1818C>T | p.Ser606Ser | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/24 | 1898/3134 | 1818/2616 | 606/871 | chr7 | 130549333 | |||
| chr7:130550642 | C | T | 7 | a0001c0002 a0002c0003 a0003c0008 others(4): Show |
113 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
synonymous_variant | LOW | c.1656G>A | p.Thr552Thr | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/24 | 1736/3134 | 1656/2616 | 552/871 | chr7 | 130550642 | |||
| chr7:130563323 | G | A | 1 | a0001c0006 | 2 | NA18941.hp2 NA18945.hp1 |
synonymous_variant | LOW | c.885C>T | p.Phe295Phe | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 11/24 | 965/3134 | 885/2616 | 295/871 | chr7 | 130563323 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130506318 | T | TC | 5 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0009 others(2): Show |
23 | HG01099.hp2 HG01256.hp2 HG01261.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*357dupG | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 357 | chr7 | 130506318 | ||||||
| chr7:130506318 | TCCCCCCC | T | 1 | a0001c0002t0003 | 20 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*351_*357delGGGGGG others(1): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 351 | chr7 | 130506318 | ||||||
| chr7:130506325 | C | T | 1 | a0001c0001t0008 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*351G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 351 | chr7 | 130506325 | ||||||
| chr7:130506473 | G | A | 2 | a0001c0002t0007 a0001c0002t0011 |
6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*203C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 203 | chr7 | 130506473 | ||||||
| chr7:130506485 | GA | G | 9 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(6): Show |
96 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*190delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 190 | chr7 | 130506485 | ||||||
| chr7:130506501 | C | A | 3 | a0001c0001t0005 a0001c0001t0009 a0001c0002t0005 |
11 | HG01256.hp1 HG01258.hp1 HG01993.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*175G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 175 | chr7 | 130506501 | ||||||
| chr7:130506644 | T | C | 1 | a0001c0001t0012 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 32 | chr7 | 130506644 | ||||||
| chr7:130668694 | C | G | 1 | a0001c0001t0010 | 1 | NA18960.hp2 | 5_prime_UTR_variant | MODIFIER | c.-26G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/24 | 26 | chr7 | 130668694 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130506825 | G | A | 1 | a0006c0007t0001g0098 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2486-19C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 23/23 | chr7 | 130506825 | |||||||
| chr7:130506826 | A | G | 1 | a0006c0007t0001g0098 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2486-20T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 23/23 | chr7 | 130506826 | |||||||
| chr7:130506866 | A | C | 1 | a0001c0001t0001g0323 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2486-60T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 23/23 | chr7 | 130506866 | |||||||
| chr7:130507178 | G | C | 10 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0002t0001g0093 others(7): Show |
10 | NA18939.hp1 NA18941.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.2485+96C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 23/23 | chr7 | 130507178 | |||||||
| chr7:130507217 | A | C | 1 | a0006c0007t0001g0098 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2485+57T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 23/23 | chr7 | 130507217 | |||||||
| chr7:130507466 | T | G | 100 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0208 others(97): Show |
100 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2387-94A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 22/23 | chr7 | 130507466 | |||||||
| chr7:130507868 | T | C | 1 | a0001c0001t0002g0188 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2248-45A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 21/23 | chr7 | 130507868 | |||||||
| chr7:130507938 | T | A | 1 | a0006c0007t0001g0098 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2248-115A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 21/23 | chr7 | 130507938 | |||||||
| chr7:130507966 | A | C | 1 | a0001c0002t0001g0068 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2248-143T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 21/23 | chr7 | 130507966 | |||||||
| chr7:130508135 | T | G | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2248-312A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 21/23 | chr7 | 130508135 | |||||||
| chr7:130508248 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2247+314G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 21/23 | chr7 | 130508248 | |||||||
| chr7:130508508 | G | T | 1 | a0001c0002t0001g0118 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2247+54C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 21/23 | chr7 | 130508508 | |||||||
| chr7:130508666 | G | A | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
splice_region_variant&intron_variant | LOW | c.2150-7C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130508666 | |||||||
| chr7:130508718 | C | A | 1 | a0001c0001t0002g0185 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2150-59G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130508718 | |||||||
| chr7:130508731 | C | A | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-72G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130508731 | |||||||
| chr7:130508789 | T | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-130A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130508789 | |||||||
| chr7:130508855 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2150-196T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130508855 | |||||||
| chr7:130508976 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(84): Show |
89 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.2150-317C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130508976 | |||||||
| chr7:130509028 | C | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-369G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509028 | |||||||
| chr7:130509040 | C | CA | 12 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 others(9): Show |
12 | HG00099.hp1 HG00639.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2150-382dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509040 | |||||||
| chr7:130509062 | A | G | 105 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0001g0246 others(102): Show |
105 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.2150-403T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509062 | |||||||
| chr7:130509143 | T | G | 1 | a0001c0001t0001g0284 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2150-484A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509143 | |||||||
| chr7:130509220 | G | C | 105 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0001g0246 others(102): Show |
105 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.2150-561C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509220 | |||||||
| chr7:130509406 | AAAG | A | 4 | a0001c0001t0002g0159 a0001c0001t0002g0169 a0001c0001t0002g0183 others(1): Show |
4 | HG00544.hp2 HG00558.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-750_2150-748d others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509406 | |||||||
| chr7:130509430 | G | A | 6 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(3): Show |
6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2150-771C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509430 | |||||||
| chr7:130509435 | G | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-776C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509435 | |||||||
| chr7:130509485 | G | A | 99 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(96): Show |
99 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.2150-826C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509485 | |||||||
| chr7:130509486 | T | G | 1 | a0001c0001t0002g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2150-827A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509486 | |||||||
| chr7:130509519 | A | G | 1 | a0001c0001t0004g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2150-860T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509519 | |||||||
| chr7:130509733 | TAAATA | T | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-1079_2150-107 others(9): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509733 | |||||||
| chr7:130509833 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0015 others(4): Show |
7 | HG01243.hp1 HG02258.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150-1174G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509833 | |||||||
| chr7:130509852 | G | C | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2150-1193C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509852 | |||||||
| chr7:130510178 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0001t0001g0132 others(5): Show |
9 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.2150-1519C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510178 | |||||||
| chr7:130510271 | C | G | 6 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(3): Show |
6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2150-1612G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510271 | |||||||
| chr7:130510286 | A | C | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-1627T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510286 | |||||||
| chr7:130510711 | CTGAAACC others(4): Show |
C | 107 | a0001c0001t0001g0032 a0001c0001t0001g0073 a0001c0001t0001g0074 others(104): Show |
107 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.2150-2063_2150-205 others(15): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510711 | |||||||
| chr7:130510713 | G | A | 1 | a0001c0002t0001g0121 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2150-2054C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510713 | |||||||
| chr7:130510804 | G | A | 1 | a0001c0001t0002g0175 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2150-2145C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510804 | |||||||
| chr7:130510824 | C | T | 1 | a0001c0001t0001g0324 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2150-2165G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510824 | |||||||
| chr7:130510825 | G | A | 1 | a0001c0001t0004g0130 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2150-2166C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510825 | |||||||
| chr7:130510864 | G | A | 93 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(90): Show |
93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.2150-2205C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510864 | |||||||
| chr7:130510884 | A | C | 2 | a0002c0003t0001g0243 a0002c0003t0001g0244 |
2 | HG01433.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2150-2225T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510884 | |||||||
| chr7:130511091 | G | C | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-2432C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130511091 | |||||||
| chr7:130511242 | A | G | 99 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(96): Show |
99 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.2150-2583T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130511242 | |||||||
| chr7:130511391 | G | A | 12 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0001g0135 others(9): Show |
12 | HG01891.hp1 HG01943.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2150-2732C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130511391 | |||||||
| chr7:130511600 | T | C | 2 | a0001c0002t0005g0078 a0001c0002t0005g0079 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2150-2941A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130511600 | |||||||
| chr7:130511642 | A | G | 2 | a0001c0001t0001g0032 a0001c0002t0004g0082 |
2 | HG02818.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.2150-2983T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130511642 | |||||||
| chr7:130511692 | T | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-3033A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130511692 | |||||||
| chr7:130511853 | T | G | 64 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(61): Show |
64 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.2150-3194A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130511853 | |||||||
| chr7:130512052 | T | TA | 35 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0018 others(32): Show |
35 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.2150-3394dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512052 | |||||||
| chr7:130512052 | T | TAA | 20 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0073 others(17): Show |
20 | HG00639.hp2 HG01261.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.2150-3395_2150-339 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512052 | |||||||
| chr7:130512052 | TA | T | 7 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0323 others(4): Show |
7 | HG00323.hp2 HG01070.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.2150-3394delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512052 | |||||||
| chr7:130512052 | TAAA | T | 85 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(82): Show |
85 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.2150-3396_2150-339 others(7): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512052 | |||||||
| chr7:130512091 | G | A | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG01934.hp1 HG02165.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.2150-3432C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512091 | |||||||
| chr7:130512182 | C | T | 1 | a0001c0002t0001g0055 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2150-3523G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512182 | |||||||
| chr7:130512345 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2150-3686A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512345 | |||||||
| chr7:130512473 | A | G | 1 | a0001c0002t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2150-3814T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512473 | |||||||
| chr7:130512616 | C | A | 4 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 others(1): Show |
4 | HG01099.hp1 HG02257.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-3957G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512616 | |||||||
| chr7:130512739 | C | T | 3 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0006g0215 |
3 | HG00639.hp1 HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2150-4080G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512739 | |||||||
| chr7:130512934 | G | T | 1 | a0001c0001t0002g0199 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2150-4275C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512934 | |||||||
| chr7:130513044 | A | G | 111 | a0001c0001t0001g0032 a0001c0001t0001g0073 a0001c0001t0001g0074 others(108): Show |
111 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.2150-4385T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513044 | |||||||
| chr7:130513210 | C | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-4551G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513210 | |||||||
| chr7:130513290 | T | TA | 9 | a0001c0001t0002g0156 a0001c0001t0002g0159 a0001c0001t0002g0163 others(6): Show |
9 | HG01433.hp2 HG02004.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.2150-4632dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513290 | |||||||
| chr7:130513302 | AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0001g0014 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2150-4663_2150-464 others(24): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513302 | |||||||
| chr7:130513304 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0253 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2150-4646_2150-464 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513304 | |||||||
| chr7:130513304 | A | T | 7 | a0001c0002t0001g0023 a0001c0002t0001g0060 a0001c0002t0001g0061 others(4): Show |
7 | HG01099.hp1 HG01358.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2150-4645T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513304 | |||||||
| chr7:130513304 | AAAAAATA others(3): Show |
A | 1 | a0001c0001t0001g0254 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2150-4655_2150-464 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513304 | |||||||
| chr7:130513304 | AAAAAATA others(5): Show |
A | 2 | a0001c0001t0009g0252 a0001c0001t0009g0256 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2150-4657_2150-464 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513304 | |||||||
| chr7:130513304 | AAAAAATA others(7): Show |
A | 4 | a0001c0001t0005g0250 a0001c0001t0005g0251 a0001c0001t0005g0255 others(1): Show |
4 | HG02630.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-4659_2150-464 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513304 | |||||||
| chr7:130513304 | AAAAAATA others(13): Show |
A | 1 | a0001c0001t0001g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2150-4665_2150-464 others(24): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513304 | |||||||
| chr7:130513304 | AAAAAATA others(15): Show |
A | 1 | a0001c0001t0001g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2150-4667_2150-464 others(26): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513304 | |||||||
| chr7:130513306 | A | ATATATAT others(4): Show |
1 | a0001c0001t0004g0286 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2150-4648_2150-464 others(15): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513306 | |||||||
| chr7:130513306 | A | T | 62 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(59): Show |
62 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.2150-4647T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513306 | |||||||
| chr7:130513308 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0138 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2150-4650_2150-464 others(22): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | |||||||
| chr7:130513308 | A | AAAAAATA others(5): Show |
1 | a0001c0001t0001g0139 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2150-4650_2150-464 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | |||||||
| chr7:130513308 | A | AAAAAATA others(7): Show |
1 | a0001c0001t0001g0137 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2150-4650_2150-464 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | |||||||
| chr7:130513308 | A | AAT | 6 | a0001c0001t0001g0269 a0001c0001t0001g0279 a0001c0001t0001g0303 others(3): Show |
6 | HG01168.hp2 HG01256.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.2150-4651_2150-465 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | |||||||
| chr7:130513308 | A | AATAT | 13 | a0001c0001t0001g0270 a0001c0001t0001g0275 a0001c0001t0001g0282 others(10): Show |
13 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2150-4653_2150-465 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | |||||||
| chr7:130513308 | A | AATATATA others(5): Show |
1 | a0001c0001t0001g0300 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2150-4661_2150-465 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | |||||||
| chr7:130513308 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0294 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2150-4663_2150-465 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | |||||||
| chr7:130513308 | A | AT | 4 | a0001c0001t0001g0032 a0001c0001t0001g0296 a0002c0003t0001g0244 others(1): Show |
4 | HG02818.hp2 HG06807.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-4650_2150-464 others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | |||||||
| chr7:130513308 | A | T | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(133): Show |
136 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.2150-4649T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | |||||||
| chr7:130513308 | AATATATA others(3): Show |
A | 1 | a0001c0001t0004g0267 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2150-4659_2150-465 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | |||||||
| chr7:130513310 | T | A | 88 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(85): Show |
88 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.2150-4651A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513310 | |||||||
| chr7:130513312 | T | A | 86 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(83): Show |
86 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.2150-4653A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513312 | |||||||
| chr7:130513314 | T | A | 73 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0150 others(70): Show |
73 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.2150-4655A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513314 | |||||||
| chr7:130513315 | ATATATAT others(37): Show |
A | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-4700_2150-465 others(48): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513315 | |||||||
| chr7:130513316 | T | A | 7 | a0001c0001t0002g0171 a0001c0001t0002g0193 a0001c0001t0002g0204 others(4): Show |
7 | HG00597.hp2 HG02083.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150-4657A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513316 | |||||||
| chr7:130513321 | A | ATATGTGT others(9): Show |
1 | a0006c0007t0001g0098 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2150-4663_2150-466 others(20): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513321 | |||||||
| chr7:130513321 | A | ATATGTGT others(13): Show |
2 | a0001c0002t0001g0093 a0001c0002t0001g0118 |
2 | NA18961.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2150-4663_2150-466 others(24): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513321 | |||||||
| chr7:130513321 | A | ATGTGTGT others(5): Show |
1 | a0001c0002t0001g0030 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2150-4663_2150-466 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513321 | |||||||
| chr7:130513321 | ATATATAT others(31): Show |
A | 1 | a0001c0002t0007g0237 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2150-4700_2150-466 others(42): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513321 | |||||||
| chr7:130513323 | A | ATATGTGT others(11): Show |
1 | a0001c0002t0003g0112 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2150-4665_2150-466 others(22): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513323 | |||||||
| chr7:130513323 | A | ATGTGTGT others(5): Show |
2 | a0001c0002t0001g0039 a0001c0002t0001g0061 |
2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2150-4665_2150-466 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513323 | |||||||
| chr7:130513323 | A | ATGTGTGT others(7): Show |
33 | a0001c0002t0001g0021 a0001c0002t0001g0034 a0001c0002t0001g0035 others(30): Show |
33 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.2150-4665_2150-466 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513323 | |||||||
| chr7:130513323 | A | ATGTGTGT others(9): Show |
53 | a0001c0001t0005g0048 a0001c0002t0001g0004 a0001c0002t0001g0007 others(50): Show |
53 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.2150-4665_2150-466 others(20): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513323 | |||||||
| chr7:130513323 | A | ATGTGTGT others(11): Show |
11 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0002t0001g0077 others(8): Show |
11 | HG03927.hp2 NA18939.hp1 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.2150-4665_2150-466 others(22): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513323 | |||||||
| chr7:130513323 | A | G | 1 | a0001c0002t0001g0030 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2150-4664T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513323 | |||||||
| chr7:130513325 | A | ATGTGTGT others(9): Show |
1 | a0001c0002t0001g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2150-4667_2150-466 others(20): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513325 | |||||||
| chr7:130513325 | A | G | 41 | a0001c0001t0005g0048 a0001c0002t0001g0021 a0001c0002t0001g0022 others(38): Show |
41 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.2150-4666T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513325 | |||||||
| chr7:130513327 | A | G | 35 | a0001c0002t0001g0021 a0001c0002t0001g0030 a0001c0002t0001g0034 others(32): Show |
35 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.2150-4668T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513327 | |||||||
| chr7:130513329 | A | G | 4 | a0001c0002t0001g0039 a0001c0002t0001g0047 a0001c0002t0001g0049 others(1): Show |
4 | HG02615.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-4670T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513329 | |||||||
| chr7:130513331 | ATATATAT others(21): Show |
A | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2150-4700_2150-467 others(32): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513331 | |||||||
| chr7:130513337 | A | G | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | HG02572.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2150-4678T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513337 | |||||||
| chr7:130513339 | A | G | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-4680T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513339 | |||||||
| chr7:130513341 | A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0001 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2150-4683_2150-468 others(34): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | A | ATATATAT others(15): Show |
5 | a0001c0001t0001g0140 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
5 | HG01346.hp1 HG01891.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150-4683_2150-468 others(26): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | A | ATATATAT others(19): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0144 |
2 | HG01069.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2150-4683_2150-468 others(30): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | A | ATATATAT others(13): Show |
4 | a0001c0001t0001g0273 a0001c0001t0001g0312 a0001c0001t0001g0323 others(1): Show |
4 | HG00323.hp2 HG02683.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-4683_2150-468 others(24): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | A | ATATATAT others(9): Show |
4 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0001g0257 others(1): Show |
4 | HG02280.hp2 HG02698.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-4683_2150-468 others(20): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0141 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2150-4683_2150-468 others(22): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0145 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2150-4683_2150-468 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0129 a0001c0001t0001g0285 a0001c0001t0001g0311 |
3 | HG01516.hp1 HG01517.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2150-4683_2150-468 others(20): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0284 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2150-4683_2150-468 others(22): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | A | ATATATAT others(7): Show |
2 | a0001c0001t0004g0133 a0001c0001t0004g0247 |
2 | HG02572.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2150-4683_2150-468 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0146 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2150-4683_2150-468 others(20): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0006 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2150-4683_2150-468 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | A | ATATATAT others(5): Show |
2 | a0001c0001t0001g0131 a0001c0001t0001g0293 |
2 | HG03239.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2150-4683_2150-468 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0135 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2150-4683_2150-468 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | A | ATATATAT others(5): Show |
1 | a0007c0010t0001g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2150-4683_2150-468 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | A | ATATG | 4 | a0001c0001t0001g0005 a0001c0001t0001g0271 a0001c0001t0001g0287 others(1): Show |
4 | HG00140.hp1 HG02155.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-4683_2150-468 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0020 others(17): Show |
20 | HG00558.hp2 HG02055.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.2150-4682T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | ATGTGTGT others(9): Show |
A | 2 | a0001c0001t0002g0026 a0001c0001t0012g0201 |
2 | HG01978.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.2150-4698_2150-468 others(20): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513341 | ATGTGTGT others(11): Show |
A | 1 | a0001c0012t0002g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2150-4700_2150-468 others(22): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | |||||||
| chr7:130513343 | G | A | 95 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0001g0283 others(92): Show |
95 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.2150-4684C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513343 | |||||||
| chr7:130513343 | GTGTGTGT others(25): Show |
G | 1 | a0001c0002t0007g0239 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2150-4716_2150-468 others(36): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513343 | |||||||
| chr7:130513345 | G | A | 19 | a0001c0001t0002g0148 a0001c0001t0002g0158 a0001c0001t0002g0169 others(16): Show |
19 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.2150-4686C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513345 | |||||||
| chr7:130513345 | GTGTGTGT others(23): Show |
G | 6 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0002t0007g0236 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2150-4716_2150-468 others(34): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513345 | |||||||
| chr7:130513347 | G | A | 4 | a0001c0001t0002g0175 a0001c0001t0002g0180 a0001c0001t0002g0182 others(1): Show |
4 | HG00639.hp1 HG03710.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-4688C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513347 | |||||||
| chr7:130513347 | GTGTGTGT others(21): Show |
G | 2 | a0001c0001t0002g0188 a0001c0002t0007g0238 |
2 | HG00558.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2150-4716_2150-468 others(32): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513347 | |||||||
| chr7:130513349 | GTGTGTGT others(19): Show |
G | 23 | a0001c0001t0002g0150 a0001c0001t0002g0156 a0001c0001t0002g0157 others(20): Show |
23 | HG00140.hp2 HG01167.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.2150-4716_2150-469 others(30): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513349 | |||||||
| chr7:130513351 | GTGTGTGT others(17): Show |
G | 47 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0027 others(44): Show |
47 | HG00597.hp2 HG01168.hp1 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.2150-4716_2150-469 others(28): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513351 | |||||||
| chr7:130513353 | GTGTGTGT others(15): Show |
G | 15 | a0001c0001t0002g0148 a0001c0001t0002g0158 a0001c0001t0002g0168 others(12): Show |
15 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.2150-4716_2150-469 others(26): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513353 | |||||||
| chr7:130513355 | GTGTGTAT others(13): Show |
G | 4 | a0001c0001t0002g0175 a0001c0001t0002g0180 a0001c0001t0002g0182 others(1): Show |
4 | HG00639.hp1 HG03710.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-4716_2150-469 others(24): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513355 | |||||||
| chr7:130513357 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2150-4698C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513357 | |||||||
| chr7:130513359 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0020 others(64): Show |
68 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.2150-4700C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513359 | |||||||
| chr7:130513359 | G | GTA | 5 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0019 others(2): Show |
5 | HG01167.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150-4702_2150-470 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513359 | |||||||
| chr7:130513359 | G | GTGTA | 3 | a0001c0001t0001g0031 a0001c0001t0001g0132 a0001c0001t0001g0139 |
3 | HG03654.hp1 HG06807.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2150-4701_2150-470 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513359 | |||||||
| chr7:130513361 | A | G | 6 | a0001c0001t0001g0283 a0001c0001t0001g0300 a0001c0001t0004g0247 others(3): Show |
6 | HG01496.hp1 HG02717.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2150-4702T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513361 | |||||||
| chr7:130513363 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2150-4704T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513363 | |||||||
| chr7:130513369 | A | G | 2 | a0001c0001t0002g0026 a0001c0001t0012g0201 |
2 | HG01978.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.2150-4710T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513369 | |||||||
| chr7:130513371 | A | G | 3 | a0001c0001t0002g0026 a0001c0001t0012g0201 a0001c0012t0002g0161 |
3 | HG01978.hp2 NA18967.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2150-4712T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513371 | |||||||
| chr7:130513373 | A | G | 4 | a0001c0001t0002g0026 a0001c0001t0012g0201 a0001c0002t0007g0237 others(1): Show |
4 | HG01978.hp2 HG01993.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-4714T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513373 | |||||||
| chr7:130513375 | A | ATG | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0302 others(2): Show |
5 | HG01070.hp1 HG01243.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.2150-4718_2150-471 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513375 | |||||||
| chr7:130513375 | A | G | 72 | a0001c0001t0001g0025 a0001c0001t0001g0269 a0001c0001t0002g0026 others(69): Show |
72 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.2150-4716T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513375 | |||||||
| chr7:130513377 | G | A | 3 | a0001c0001t0001g0262 a0001c0002t0001g0059 a0001c0002t0001g0065 |
3 | HG02922.hp1 HG03654.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2150-4718C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513377 | |||||||
| chr7:130513387 | G | GTA | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | HG02572.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2150-4729_2150-472 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513387 | |||||||
| chr7:130513389 | G | A | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | HG02572.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2150-4730C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513389 | |||||||
| chr7:130513390 | T | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0129 others(28): Show |
32 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.2150-4731A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513390 | |||||||
| chr7:130513391 | A | G | 4 | a0001c0001t0002g0186 a0001c0001t0008g0316 a0001c0001t0008g0319 others(1): Show |
4 | HG01891.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-4732T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513391 | |||||||
| chr7:130513393 | A | G | 1 | a0001c0001t0002g0186 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2150-4734T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513393 | |||||||
| chr7:130513471 | G | C | 1 | a0001c0001t0002g0152 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2150-4812C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513471 | |||||||
| chr7:130513602 | T | C | 1 | a0001c0001t0002g0225 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2150-4943A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513602 | |||||||
| chr7:130513656 | A | C | 1 | a0001c0012t0002g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2150-4997T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513656 | |||||||
| chr7:130513695 | G | A | 1 | a0001c0002t0001g0071 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2150-5036C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513695 | |||||||
| chr7:130513758 | C | T | 1 | a0001c0002t0001g0023 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2150-5099G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513758 | |||||||
| chr7:130513856 | T | C | 3 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0009 |
3 | HG00438.hp1 NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2150-5197A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513856 | |||||||
| chr7:130513937 | A | G | 3 | a0001c0002t0001g0052 a0001c0002t0001g0054 a0001c0002t0001g0056 |
3 | HG00597.hp1 HG00621.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.2150-5278T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513937 | |||||||
| chr7:130514040 | T | C | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-5381A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514040 | |||||||
| chr7:130514132 | T | C | 13 | a0001c0002t0001g0040 a0001c0002t0001g0051 a0001c0002t0001g0052 others(10): Show |
13 | HG00597.hp1 HG00621.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2150-5473A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514132 | |||||||
| chr7:130514356 | T | G | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0001g0277 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.2150-5697A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514356 | |||||||
| chr7:130514564 | T | A | 1 | a0001c0002t0007g0237 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2150-5905A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514564 | |||||||
| chr7:130514618 | G | A | 1 | a0001c0001t0002g0192 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2150-5959C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514618 | |||||||
| chr7:130514644 | C | T | 10 | a0001c0001t0002g0168 a0001c0001t0002g0179 a0001c0001t0002g0180 others(7): Show |
10 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.2150-5985G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514644 | |||||||
| chr7:130514662 | G | A | 97 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(94): Show |
97 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.2150-6003C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514662 | |||||||
| chr7:130514687 | A | G | 1 | a0001c0002t0001g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2150-6028T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514687 | |||||||
| chr7:130514753 | C | A | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.2150-6094G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514753 | |||||||
| chr7:130514845 | T | C | 1 | a0001c0002t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2150-6186A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514845 | |||||||
| chr7:130515053 | T | C | 2 | a0001c0001t0001g0266 a0001c0001t0004g0267 |
2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2150-6394A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130515053 | |||||||
| chr7:130515058 | T | C | 6 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(3): Show |
6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2150-6399A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130515058 | |||||||
| chr7:130515226 | G | A | 1 | a0001c0002t0003g0123 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2150-6567C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130515226 | |||||||
| chr7:130515342 | A | AGT | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-6684_2150-668 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130515342 | |||||||
| chr7:130515346 | AC | A | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-6688delG | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130515346 | |||||||
| chr7:130515494 | G | T | 1 | a0001c0001t0001g0254 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2150-6835C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130515494 | |||||||
| chr7:130515890 | A | T | 1 | a0001c0012t0002g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2150-7231T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130515890 | |||||||
| chr7:130516079 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2150-7420C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130516079 | |||||||
| chr7:130516200 | A | G | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-7541T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130516200 | |||||||
| chr7:130516571 | T | C | 1 | a0001c0002t0001g0099 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2150-7912A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130516571 | |||||||
| chr7:130516699 | A | G | 5 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(2): Show |
5 | HG00140.hp2 HG00639.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150-8040T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130516699 | |||||||
| chr7:130516738 | T | C | 1 | a0001c0002t0001g0065 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2150-8079A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130516738 | |||||||
| chr7:130516842 | G | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-8183C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130516842 | |||||||
| chr7:130516916 | G | A | 1 | a0001c0002t0001g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2150-8257C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130516916 | |||||||
| chr7:130517065 | G | C | 1 | a0001c0002t0001g0024 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2150-8406C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130517065 | |||||||
| chr7:130517334 | G | C | 1 | a0001c0001t0005g0248 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2150-8675C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130517334 | |||||||
| chr7:130517392 | G | A | 1 | a0001c0001t0002g0222 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2150-8733C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130517392 | |||||||
| chr7:130517753 | A | G | 1 | a0001c0001t0002g0206 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2150-9094T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130517753 | |||||||
| chr7:130517909 | A | G | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-9250T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130517909 | |||||||
| chr7:130517933 | G | GA | 107 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0208 others(104): Show |
107 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.2150-9275dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130517933 | |||||||
| chr7:130518274 | G | C | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2150-9615C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518274 | |||||||
| chr7:130518284 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2150-9625T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518284 | |||||||
| chr7:130518347 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2150-9688C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518347 | |||||||
| chr7:130518496 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2150-9837A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518496 | |||||||
| chr7:130518514 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2150-9855C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518514 | |||||||
| chr7:130518536 | T | C | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-9877A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518536 | |||||||
| chr7:130518660 | A | G | 1 | a0001c0002t0002g0089 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2150-10001T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518660 | |||||||
| chr7:130518837 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2150-10178G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518837 | |||||||
| chr7:130518894 | T | G | 3 | a0001c0002t0001g0241 a0002c0003t0001g0243 a0002c0003t0001g0244 |
3 | HG01433.hp2 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2150-10235A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518894 | |||||||
| chr7:130518909 | G | C | 3 | a0001c0001t0001g0271 a0001c0001t0001g0303 a0001c0001t0001g0305 |
3 | HG00140.hp1 HG01175.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.2150-10250C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518909 | |||||||
| chr7:130518931 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2150-10272G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518931 | |||||||
| chr7:130518955 | G | A | 3 | a0001c0001t0002g0166 a0001c0001t0002g0224 a0001c0001t0002g0225 |
3 | HG01258.hp2 HG01346.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.2150-10296C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518955 | |||||||
| chr7:130518988 | A | G | 1 | a0001c0001t0002g0026 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2150-10329T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518988 | |||||||
| chr7:130519005 | C | CA | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(203): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.2150-10347dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519005 | |||||||
| chr7:130519005 | CA | C | 12 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0002g0165 others(9): Show |
12 | HG00140.hp2 HG01346.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.2150-10347delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519005 | |||||||
| chr7:130519005 | CAA | C | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(89): Show |
92 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.2150-10348_2150-10 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519005 | |||||||
| chr7:130519229 | T | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2150-10570A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519229 | |||||||
| chr7:130519240 | G | C | 2 | a0001c0001t0002g0227 a0001c0001t0006g0226 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2150-10581C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519240 | |||||||
| chr7:130519324 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2150-10665C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519324 | |||||||
| chr7:130519339 | T | C | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2150-10680A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519339 | |||||||
| chr7:130519364 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2150-10705C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519364 | |||||||
| chr7:130519807 | C | G | 2 | a0001c0002t0001g0036 a0001c0002t0001g0037 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2150-11148G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519807 | |||||||
| chr7:130519844 | T | C | 103 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(100): Show |
103 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.2150-11185A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519844 | |||||||
| chr7:130519856 | T | C | 107 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0208 others(104): Show |
107 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.2150-11197A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519856 | |||||||
| chr7:130520011 | T | C | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-11352A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520011 | |||||||
| chr7:130520038 | T | C | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-11379A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520038 | |||||||
| chr7:130520062 | T | C | 2 | a0001c0005t0002g0011 a0001c0005t0002g0012 |
2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2150-11403A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520062 | |||||||
| chr7:130520083 | T | C | 109 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0208 others(106): Show |
109 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.2150-11424A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520083 | |||||||
| chr7:130520234 | A | T | 1 | a0001c0001t0002g0152 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2150-11575T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520234 | |||||||
| chr7:130520375 | T | C | 1 | a0001c0002t0007g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2150-11716A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520375 | |||||||
| chr7:130520576 | A | G | 2 | a0001c0001t0001g0262 a0001c0001t0001g0264 |
2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2150-11917T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520576 | |||||||
| chr7:130520602 | A | C | 3 | a0001c0002t0001g0241 a0002c0003t0001g0243 a0002c0003t0001g0244 |
3 | HG01433.hp2 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2150-11943T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520602 | |||||||
| chr7:130520611 | A | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(209): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.2150-11952T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520611 | |||||||
| chr7:130520988 | A | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(7): Show |
10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2150-12329T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520988 | |||||||
| chr7:130521103 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(208): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.2150-12444G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521103 | |||||||
| chr7:130521106 | C | T | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.2150-12447G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521106 | |||||||
| chr7:130521242 | A | G | 1 | a0001c0002t0001g0127 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2150-12583T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521242 | |||||||
| chr7:130521296 | G | C | 1 | a0001c0002t0001g0121 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2150-12637C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521296 | |||||||
| chr7:130521438 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(208): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.2150-12779T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521438 | |||||||
| chr7:130521441 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(208): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.2150-12782T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521441 | |||||||
| chr7:130521496 | C | T | 2 | a0001c0001t0002g0165 a0001c0001t0006g0178 |
2 | HG01981.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2150-12837G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521496 | |||||||
| chr7:130521741 | G | A | 1 | a0001c0002t0001g0009 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2150-13082C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521741 | |||||||
| chr7:130521845 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(208): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.2150-13186A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521845 | |||||||
| chr7:130521849 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2150-13190T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521849 | |||||||
| chr7:130521939 | G | A | 1 | a0001c0001t0006g0149 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2150-13280C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521939 | |||||||
| chr7:130521950 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2150-13291G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521950 | |||||||
| chr7:130522000 | G | C | 1 | a0001c0002t0001g0121 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2150-13341C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130522000 | |||||||
| chr7:130522511 | C | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2150-13852G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130522511 | |||||||
| chr7:130522570 | A | C | 1 | a0001c0001t0002g0196 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2150-13911T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130522570 | |||||||
| chr7:130522742 | A | C | 11 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0262 others(8): Show |
11 | HG01891.hp2 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2150-14083T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130522742 | |||||||
| chr7:130522773 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2150-14114A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130522773 | |||||||
| chr7:130522804 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2150-14145A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130522804 | |||||||
| chr7:130522838 | T | G | 1 | a0001c0001t0001g0302 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2150-14179A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130522838 | |||||||
| chr7:130523048 | G | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-14389C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523048 | |||||||
| chr7:130523048 | G | C | 1 | a0001c0001t0006g0178 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2150-14389C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523048 | |||||||
| chr7:130523079 | C | A | 1 | a0001c0002t0001g0126 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2150-14420G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523079 | |||||||
| chr7:130523106 | G | T | 10 | a0001c0001t0002g0162 a0001c0001t0002g0171 a0001c0001t0002g0172 others(7): Show |
10 | HG02083.hp1 HG04184.hp2 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.2150-14447C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523106 | |||||||
| chr7:130523119 | C | CAAAAAAA others(1): Show |
12 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0008g0316 others(9): Show |
12 | HG01258.hp1 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2150-14468_2150-14 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523119 | |||||||
| chr7:130523119 | C | CAAAAAAA others(2): Show |
93 | a0001c0001t0001g0269 a0001c0001t0001g0283 a0001c0001t0001g0301 others(90): Show |
93 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.2150-14469_2150-14 others(15): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523119 | |||||||
| chr7:130523119 | C | CAAAAAAA others(4): Show |
24 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0129 others(21): Show |
24 | HG00639.hp2 HG01361.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2150-14471_2150-14 others(17): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523119 | |||||||
| chr7:130523119 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0002g0231 a0001c0002t0001g0077 a0001c0002t0011g0240 |
3 | HG02486.hp1 NA19082.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2150-14472_2150-14 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523119 | |||||||
| chr7:130523119 | C | CAAAAAAA others(7): Show |
5 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150-14474_2150-14 others(20): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523119 | |||||||
| chr7:130523157 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2150-14498C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523157 | |||||||
| chr7:130523161 | C | G | 1 | a0001c0002t0001g0121 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2150-14502G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523161 | |||||||
| chr7:130523230 | A | G | 1 | a0007c0010t0001g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2150-14571T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523230 | |||||||
| chr7:130523237 | G | C | 1 | a0001c0001t0002g0193 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2150-14578C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523237 | |||||||
| chr7:130523458 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(101): Show |
106 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.2150-14799A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523458 | |||||||
| chr7:130523487 | G | A | 1 | a0001c0001t0002g0165 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2150-14828C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523487 | |||||||
| chr7:130523506 | C | T | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-14847G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523506 | |||||||
| chr7:130523570 | C | G | 1 | a0001c0001t0006g0184 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2150-14911G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523570 | |||||||
| chr7:130523577 | G | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0144 |
3 | HG01069.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2150-14918C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523577 | |||||||
| chr7:130523609 | T | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-14950A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523609 | |||||||
| chr7:130523617 | A | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-14958T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523617 | |||||||
| chr7:130523774 | CG | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(87): Show |
92 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.2150-15116delC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523774 | |||||||
| chr7:130523965 | G | A | 7 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0008g0316 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150-15306C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523965 | |||||||
| chr7:130523986 | G | A | 3 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 |
3 | HG01099.hp1 HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2150-15327C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523986 | |||||||
| chr7:130524006 | C | T | 1 | a0001c0002t0001g0058 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2150-15347G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524006 | |||||||
| chr7:130524007 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2150-15348C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524007 | |||||||
| chr7:130524099 | GGA | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-15442_2150-15 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524099 | |||||||
| chr7:130524301 | T | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-15642A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524301 | |||||||
| chr7:130524308 | C | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0129 others(18): Show |
22 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.2150-15649G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524308 | |||||||
| chr7:130524348 | G | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(101): Show |
106 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.2150-15689C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524348 | |||||||
| chr7:130524406 | A | G | 1 | a0001c0002t0003g0261 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2150-15747T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524406 | |||||||
| chr7:130524602 | C | T | 28 | a0001c0002t0001g0021 a0001c0002t0001g0030 a0001c0002t0001g0036 others(25): Show |
28 | HG00597.hp1 HG00621.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.2150-15943G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524602 | |||||||
| chr7:130524749 | G | A | 93 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(90): Show |
93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.2150-16090C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524749 | |||||||
| chr7:130524830 | G | T | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-16171C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524830 | |||||||
| chr7:130524910 | C | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-16251G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524910 | |||||||
| chr7:130525052 | G | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-16393C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525052 | |||||||
| chr7:130525261 | T | A | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2150-16602A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525261 | |||||||
| chr7:130525285 | T | G | 1 | a0001c0001t0001g0010 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2150-16626A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525285 | |||||||
| chr7:130525437 | T | C | 1 | a0001c0002t0001g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2150-16778A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525437 | |||||||
| chr7:130525468 | C | T | 1 | a0001c0002t0003g0107 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2150-16809G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525468 | |||||||
| chr7:130525724 | A | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150-17065T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525724 | |||||||
| chr7:130525914 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2150-17255C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525914 | |||||||
| chr7:130525950 | G | GAAATGAG others(15): Show |
108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(105): Show |
110 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.2150-17313_2150-17 others(28): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525950 | |||||||
| chr7:130525960 | A | ACCTGGAC others(16): Show |
1 | a0003c0004t0001g0292 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2150-17302_2150-17 others(29): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525960 | |||||||
| chr7:130526087 | C | A | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-17428G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130526087 | |||||||
| chr7:130526564 | G | A | 1 | a0001c0002t0001g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2150-17905C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130526564 | |||||||
| chr7:130526580 | GGGCAGGA others(8): Show |
G | 1 | a0001c0002t0001g0072 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2150-17936_2150-17 others(21): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130526580 | |||||||
| chr7:130526773 | A | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(106): Show |
111 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.2150-18114T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130526773 | |||||||
| chr7:130526821 | G | C | 1 | a0001c0002t0001g0099 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2150-18162C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130526821 | |||||||
| chr7:130526845 | G | A | 2 | a0001c0005t0002g0011 a0001c0005t0002g0012 |
2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2150-18186C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130526845 | |||||||
| chr7:130527013 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2150-18354C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527013 | |||||||
| chr7:130527138 | TG | T | 95 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(92): Show |
95 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.2150-18480delC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527138 | |||||||
| chr7:130527322 | T | C | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2150-18663A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527322 | |||||||
| chr7:130527331 | G | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150-18672C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527331 | |||||||
| chr7:130527422 | C | G | 1 | a0001c0001t0002g0152 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2150-18763G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527422 | |||||||
| chr7:130527561 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0137 others(3): Show |
7 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150-18902C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527561 | |||||||
| chr7:130527564 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0137 others(3): Show |
7 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150-18905C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527564 | |||||||
| chr7:130527665 | G | A | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2150-19006C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527665 | |||||||
| chr7:130527680 | T | TGGACACG others(5): Show |
1 | a0003c0004t0001g0292 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2150-19033_2150-19 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527680 | |||||||
| chr7:130527710 | T | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(277): Show |
282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.2150-19051A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527710 | |||||||
| chr7:130527712 | C | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(277): Show |
282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.2150-19053G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527712 | |||||||
| chr7:130527721 | C | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(277): Show |
282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.2150-19062G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527721 | |||||||
| chr7:130527823 | G | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(110): Show |
115 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2150-19164C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527823 | |||||||
| chr7:130527957 | G | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-19298C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527957 | |||||||
| chr7:130528013 | G | A | 14 | a0001c0002t0001g0040 a0001c0002t0001g0051 a0001c0002t0001g0052 others(11): Show |
14 | HG00597.hp1 HG00621.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.2150-19354C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528013 | |||||||
| chr7:130528046 | C | A | 1 | a0001c0002t0003g0123 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2150-19387G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528046 | |||||||
| chr7:130528134 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2150-19475A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528134 | |||||||
| chr7:130528284 | C | T | 3 | a0001c0001t0001g0246 a0001c0001t0004g0245 a0001c0001t0004g0247 |
3 | HG01099.hp2 HG02886.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2149+19390G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528284 | |||||||
| chr7:130528298 | A | G | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149+19376T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528298 | |||||||
| chr7:130528452 | G | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+19222C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528452 | |||||||
| chr7:130528458 | T | C | 4 | a0001c0001t0001g0271 a0001c0001t0001g0303 a0001c0001t0001g0305 others(1): Show |
4 | HG00140.hp1 HG01175.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149+19216A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528458 | |||||||
| chr7:130528632 | G | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(207): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.2149+19042C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528632 | |||||||
| chr7:130528786 | T | C | 2 | a0001c0001t0004g0245 a0001c0001t0004g0247 |
2 | HG01099.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2149+18888A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528786 | |||||||
| chr7:130528807 | C | T | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2149+18867G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528807 | |||||||
| chr7:130528815 | T | G | 3 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0009 |
3 | HG00438.hp1 NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2149+18859A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528815 | |||||||
| chr7:130528850 | C | T | 1 | a0001c0001t0002g0152 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2149+18824G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528850 | |||||||
| chr7:130528851 | G | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0129 others(18): Show |
22 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.2149+18823C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528851 | |||||||
| chr7:130529019 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0144 |
3 | HG01069.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2149+18655G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130529019 | |||||||
| chr7:130529062 | G | C | 1 | a0001c0001t0001g0143 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2149+18612C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130529062 | |||||||
| chr7:130529241 | G | A | 1 | a0001c0001t0002g0260 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2149+18433C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130529241 | |||||||
| chr7:130529328 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(101): Show |
106 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.2149+18346C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130529328 | |||||||
| chr7:130529349 | C | A | 94 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(91): Show |
94 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.2149+18325G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130529349 | |||||||
| chr7:130529455 | T | C | 1 | a0001c0002t0007g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2149+18219A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130529455 | |||||||
| chr7:130529459 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2149+18215C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130529459 | |||||||
| chr7:130529473 | A | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2149+18201T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130529473 | |||||||
| chr7:130530029 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2149+17645T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530029 | |||||||
| chr7:130530051 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(110): Show |
115 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2149+17623G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530051 | |||||||
| chr7:130530059 | G | A | 1 | a0001c0001t0002g0260 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2149+17615C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530059 | |||||||
| chr7:130530061 | G | C | 1 | a0001c0001t0005g0258 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2149+17613C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530061 | |||||||
| chr7:130530313 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+17361A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530313 | |||||||
| chr7:130530336 | G | A | 60 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(57): Show |
60 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.2149+17338C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530336 | |||||||
| chr7:130530415 | G | A | 3 | a0001c0001t0001g0262 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | HG02922.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2149+17259C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530415 | |||||||
| chr7:130530442 | C | T | 1 | a0001c0002t0001g0071 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2149+17232G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530442 | |||||||
| chr7:130530810 | A | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(105): Show |
110 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.2149+16864T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530810 | |||||||
| chr7:130530812 | T | C | 3 | a0001c0002t0001g0060 a0001c0002t0001g0063 a0001c0002t0001g0064 |
3 | HG02280.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2149+16862A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530812 | |||||||
| chr7:130530890 | T | C | 1 | a0001c0002t0001g0039 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2149+16784A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530890 | |||||||
| chr7:130530950 | G | C | 3 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0038 |
3 | HG00099.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2149+16724C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530950 | |||||||
| chr7:130530978 | G | A | 3 | a0001c0001t0001g0283 a0001c0001t0001g0300 a0001c0001t0004g0286 |
3 | HG01496.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2149+16696C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530978 | |||||||
| chr7:130531038 | G | A | 1 | a0001c0001t0002g0185 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2149+16636C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531038 | |||||||
| chr7:130531047 | G | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(7): Show |
10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2149+16627C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531047 | |||||||
| chr7:130531198 | T | G | 1 | a0001c0001t0001g0282 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2149+16476A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531198 | |||||||
| chr7:130531199 | G | T | 1 | a0001c0001t0001g0282 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2149+16475C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531199 | |||||||
| chr7:130531468 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+16206A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531468 | |||||||
| chr7:130531634 | G | C | 1 | a0001c0001t0001g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2149+16040C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531634 | |||||||
| chr7:130531716 | A | G | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2149+15958T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531716 | |||||||
| chr7:130531722 | T | C | 1 | a0001c0001t0005g0248 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2149+15952A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531722 | |||||||
| chr7:130531756 | ACTGGAGA others(4): Show |
A | 1 | a0001c0002t0001g0102 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2149+15907_2149+15 others(17): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531756 | |||||||
| chr7:130531759 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2149+15915C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531759 | |||||||
| chr7:130531797 | G | A | 1 | a0001c0001t0004g0306 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2149+15877C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531797 | |||||||
| chr7:130531810 | C | T | 2 | a0001c0001t0004g0306 a0001c0002t0001g0119 |
2 | HG02155.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2149+15864G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531810 | |||||||
| chr7:130531831 | T | A | 1 | a0001c0001t0002g0159 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2149+15843A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531831 | |||||||
| chr7:130531837 | A | G | 1 | a0001c0002t0001g0119 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2149+15837T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531837 | |||||||
| chr7:130531846 | T | G | 1 | a0001c0002t0001g0102 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2149+15828A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531846 | |||||||
| chr7:130531968 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+15706C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531968 | |||||||
| chr7:130532110 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2149+15564C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532110 | |||||||
| chr7:130532160 | G | T | 2 | a0001c0001t0002g0192 a0001c0002t0003g0120 |
2 | NA18983.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2149+15514C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532160 | |||||||
| chr7:130532161 | G | A | 2 | a0001c0001t0002g0192 a0001c0002t0003g0120 |
2 | NA18983.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2149+15513C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532161 | |||||||
| chr7:130532167 | T | C | 2 | a0001c0001t0002g0192 a0001c0002t0003g0120 |
2 | NA18983.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2149+15507A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532167 | |||||||
| chr7:130532239 | T | A | 1 | a0001c0001t0001g0282 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2149+15435A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532239 | |||||||
| chr7:130532281 | G | A | 1 | a0001c0002t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2149+15393C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532281 | |||||||
| chr7:130532338 | T | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(170): Show |
175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.2149+15336A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532338 | |||||||
| chr7:130532342 | C | T | 1 | a0001c0002t0007g0239 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2149+15332G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532342 | |||||||
| chr7:130532344 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2149+15330C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532344 | |||||||
| chr7:130532376 | T | C | 1 | a0001c0002t0003g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2149+15298A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532376 | |||||||
| chr7:130532506 | C | T | 2 | a0001c0001t0002g0227 a0001c0001t0006g0226 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2149+15168G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532506 | |||||||
| chr7:130532551 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+15123A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532551 | |||||||
| chr7:130532552 | T | G | 90 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(87): Show |
90 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.2149+15122A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532552 | |||||||
| chr7:130532667 | C | T | 320 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(317): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.2149+15007G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532667 | |||||||
| chr7:130532673 | G | T | 1 | a0001c0001t0001g0282 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2149+15001C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532673 | |||||||
| chr7:130532703 | G | A | 1 | a0001c0002t0003g0110 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2149+14971C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532703 | |||||||
| chr7:130532800 | G | A | 2 | a0001c0001t0001g0270 a0001c0001t0001g0304 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2149+14874C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532800 | |||||||
| chr7:130532840 | G | A | 1 | a0001c0001t0002g0175 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2149+14834C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532840 | |||||||
| chr7:130532884 | A | C | 1 | a0001c0001t0002g0209 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2149+14790T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532884 | |||||||
| chr7:130532888 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2149+14786A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532888 | |||||||
| chr7:130532918 | G | A | 3 | a0001c0002t0003g0123 a0001c0002t0003g0124 a0001c0002t0003g0125 |
3 | HG03490.hp2 HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2149+14756C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532918 | |||||||
| chr7:130532959 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+14715A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532959 | |||||||
| chr7:130533048 | C | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0310 |
4 | NA18945.hp2 NA18963.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+14626G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533048 | |||||||
| chr7:130533120 | C | T | 93 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(90): Show |
93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.2149+14554G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533120 | |||||||
| chr7:130533121 | G | A | 1 | a0001c0002t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2149+14553C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533121 | |||||||
| chr7:130533275 | C | G | 1 | a0001c0002t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2149+14399G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533275 | |||||||
| chr7:130533516 | G | A | 1 | a0001c0002t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2149+14158C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533516 | |||||||
| chr7:130533639 | G | C | 1 | a0006c0007t0001g0098 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2149+14035C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533639 | |||||||
| chr7:130533986 | T | G | 1 | a0001c0002t0001g0004 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2149+13688A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533986 | |||||||
| chr7:130533986 | T | TG | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(276): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.2149+13687dupC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533986 | |||||||
| chr7:130533986 | T | TGG | 36 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(33): Show |
36 | HG01255.hp1 HG01361.hp1 HG01952.hp2 others(33): Show |
intron_variant | MODIFIER | c.2149+13686_2149+13 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533986 | |||||||
| chr7:130534037 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+13637G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534037 | |||||||
| chr7:130534058 | T | C | 2 | a0001c0001t0001g0299 a0001c0001t0001g0314 |
2 | HG00639.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2149+13616A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534058 | |||||||
| chr7:130534085 | A | T | 1 | a0001c0002t0001g0039 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2149+13589T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534085 | |||||||
| chr7:130534143 | C | A | 1 | a0001c0001t0002g0182 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2149+13531G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534143 | |||||||
| chr7:130534348 | C | T | 1 | a0001c0002t0001g0066 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2149+13326G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534348 | |||||||
| chr7:130534350 | T | A | 1 | a0001c0001t0004g0306 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2149+13324A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534350 | |||||||
| chr7:130534508 | G | C | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+13166C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534508 | |||||||
| chr7:130534584 | A | G | 1 | a0001c0002t0001g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2149+13090T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534584 | |||||||
| chr7:130534641 | G | T | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2149+13033C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534641 | |||||||
| chr7:130534670 | GA | G | 5 | a0001c0001t0001g0246 a0001c0001t0001g0253 a0001c0001t0001g0257 others(2): Show |
5 | HG01099.hp2 HG02886.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2149+13003delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534670 | |||||||
| chr7:130534902 | A | G | 216 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0208 others(213): Show |
216 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.2149+12772T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534902 | |||||||
| chr7:130535147 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2149+12527C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535147 | |||||||
| chr7:130535276 | T | C | 2 | a0003c0004t0001g0290 a0003c0004t0001g0292 |
2 | NA18965.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2149+12398A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535276 | |||||||
| chr7:130535324 | A | G | 1 | a0001c0002t0001g0126 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2149+12350T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535324 | |||||||
| chr7:130535374 | G | A | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.2149+12300C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535374 | |||||||
| chr7:130535461 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2149+12213T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535461 | |||||||
| chr7:130535597 | GGGCCA | G | 4 | a0001c0001t0001g0283 a0001c0001t0001g0300 a0001c0001t0004g0286 others(1): Show |
4 | HG01496.hp1 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+12072_2149+12 others(11): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535597 | |||||||
| chr7:130535699 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0131 others(6): Show |
10 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.2149+11975C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535699 | |||||||
| chr7:130535699 | G | C | 1 | a0001c0002t0001g0059 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2149+11975C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535699 | |||||||
| chr7:130535715 | C | T | 1 | a0001c0001t0006g0202 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2149+11959G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535715 | |||||||
| chr7:130535782 | C | T | 208 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0208 others(205): Show |
208 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2149+11892G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535782 | |||||||
| chr7:130535860 | G | A | 113 | a0001c0001t0001g0074 a0001c0002t0001g0004 a0001c0002t0001g0007 others(110): Show |
113 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2149+11814C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535860 | |||||||
| chr7:130535967 | T | C | 1 | a0001c0002t0001g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2149+11707A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535967 | |||||||
| chr7:130536037 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2149+11637G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536037 | |||||||
| chr7:130536371 | T | C | 1 | a0001c0001t0002g0177 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2149+11303A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536371 | |||||||
| chr7:130536387 | C | T | 1 | a0001c0002t0001g0095 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2149+11287G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536387 | |||||||
| chr7:130536508 | C | T | 260 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(257): Show |
261 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.2149+11166G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536508 | |||||||
| chr7:130536577 | G | A | 2 | a0001c0005t0002g0011 a0001c0005t0002g0012 |
2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2149+11097C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536577 | |||||||
| chr7:130536613 | G | C | 2 | a0001c0001t0001g0308 a0001c0001t0001g0318 |
2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2149+11061C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536613 | |||||||
| chr7:130536685 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
262 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.2149+10989G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536685 | |||||||
| chr7:130536694 | G | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
262 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.2149+10980C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536694 | |||||||
| chr7:130536826 | G | A | 1 | a0001c0002t0001g0008 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2149+10848C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536826 | |||||||
| chr7:130536830 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2149+10844C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536830 | |||||||
| chr7:130536874 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0246 others(13): Show |
16 | HG01099.hp2 HG02055.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.2149+10800G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536874 | |||||||
| chr7:130536908 | C | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+10766G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536908 | |||||||
| chr7:130536955 | C | T | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2149+10719G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536955 | |||||||
| chr7:130536956 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2149+10718C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536956 | |||||||
| chr7:130536976 | AAGG | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(53): Show |
57 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.2149+10695_2149+10 others(9): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536976 | |||||||
| chr7:130537207 | C | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(53): Show |
57 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.2149+10467G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537207 | |||||||
| chr7:130537348 | G | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.2149+10326C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537348 | |||||||
| chr7:130537361 | G | A | 1 | a0001c0002t0001g0091 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2149+10313C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537361 | |||||||
| chr7:130537448 | G | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
262 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.2149+10226C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537448 | |||||||
| chr7:130537556 | C | T | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2149+10118G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537556 | |||||||
| chr7:130537580 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2149+10094G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537580 | |||||||
| chr7:130537649 | T | A | 1 | a0001c0001t0002g0186 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2149+10025A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537649 | |||||||
| chr7:130537685 | A | T | 1 | a0010c0009t0002g0217 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2149+9989T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537685 | |||||||
| chr7:130537748 | G | A | 1 | a0001c0001t0002g0214 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2149+9926C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537748 | |||||||
| chr7:130537758 | C | G | 1 | a0001c0002t0003g0110 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2149+9916G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537758 | |||||||
| chr7:130537771 | AAAAGGGG others(4419): Show |
A | 1 | a0001c0001t0001g0315 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2149+5477_2149+990 others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537771 | |||||||
| chr7:130537780 | G | C | 4 | a0001c0002t0001g0105 a0001c0002t0005g0078 a0001c0002t0005g0079 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149+9894C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537780 | |||||||
| chr7:130537805 | G | A | 2 | a0001c0001t0002g0227 a0001c0001t0006g0226 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2149+9869C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537805 | |||||||
| chr7:130537830 | C | T | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2149+9844G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537830 | |||||||
| chr7:130537941 | A | G | 1 | a0001c0001t0002g0187 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2149+9733T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537941 | |||||||
| chr7:130538049 | C | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
262 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.2149+9625G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538049 | |||||||
| chr7:130538192 | A | T | 1 | a0001c0001t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2149+9482T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538192 | |||||||
| chr7:130538283 | A | T | 1 | a0001c0001t0002g0186 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2149+9391T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538283 | |||||||
| chr7:130538323 | G | T | 113 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(110): Show |
113 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2149+9351C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538323 | |||||||
| chr7:130538397 | C | T | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.2149+9277G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538397 | |||||||
| chr7:130538398 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2149+9276C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538398 | |||||||
| chr7:130538528 | A | G | 1 | a0001c0002t0001g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2149+9146T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538528 | |||||||
| chr7:130538540 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2149+9134A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538540 | |||||||
| chr7:130538688 | GA | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(254): Show |
258 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.2149+8985delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538688 | |||||||
| chr7:130538814 | G | T | 1 | a0001c0001t0001g0310 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2149+8860C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538814 | |||||||
| chr7:130538853 | A | T | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2149+8821T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538853 | |||||||
| chr7:130539413 | C | G | 2 | a0001c0001t0002g0227 a0001c0001t0006g0226 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2149+8261G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130539413 | |||||||
| chr7:130539531 | T | C | 1 | a0001c0002t0003g0123 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2149+8143A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130539531 | |||||||
| chr7:130539774 | A | G | 2 | a0001c0005t0002g0011 a0001c0005t0002g0012 |
2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2149+7900T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130539774 | |||||||
| chr7:130539804 | C | A | 27 | a0001c0002t0001g0021 a0001c0002t0001g0030 a0001c0002t0001g0036 others(24): Show |
27 | HG00597.hp1 HG00621.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.2149+7870G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130539804 | |||||||
| chr7:130539829 | G | A | 40 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(37): Show |
40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.2149+7845C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130539829 | |||||||
| chr7:130539832 | G | T | 4 | a0001c0001t0005g0250 a0001c0001t0005g0255 a0001c0001t0009g0252 others(1): Show |
4 | HG02055.hp2 HG02723.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+7842C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130539832 | |||||||
| chr7:130539973 | T | G | 1 | a0001c0001t0002g0185 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2149+7701A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130539973 | |||||||
| chr7:130540014 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2149+7660A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540014 | |||||||
| chr7:130540046 | GGGGATGG others(5): Show |
G | 2 | a0001c0002t0005g0078 a0001c0002t0005g0079 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2149+7616_2149+762 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540046 | |||||||
| chr7:130540073 | G | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(28): Show |
32 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.2149+7601C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540073 | |||||||
| chr7:130540076 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(111): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.2149+7598C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540076 | |||||||
| chr7:130540076 | G | C | 62 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(59): Show |
62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.2149+7598C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540076 | |||||||
| chr7:130540218 | A | C | 1 | a0001c0002t0001g0004 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2149+7456T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540218 | |||||||
| chr7:130540305 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): Show |
51 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.2149+7369G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540305 | |||||||
| chr7:130540356 | A | C | 1 | a0001c0001t0006g0184 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2149+7318T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540356 | |||||||
| chr7:130540506 | A | T | 1 | a0001c0002t0003g0122 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2149+7168T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540506 | |||||||
| chr7:130540521 | G | A | 1 | a0001c0001t0005g0248 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2149+7153C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540521 | |||||||
| chr7:130540753 | A | G | 1 | a0001c0002t0005g0080 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2149+6921T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540753 | |||||||
| chr7:130540908 | A | G | 1 | a0001c0002t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2149+6766T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540908 | |||||||
| chr7:130540937 | T | G | 1 | a0001c0012t0002g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2149+6737A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540937 | |||||||
| chr7:130540987 | C | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2149+6687G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540987 | |||||||
| chr7:130541008 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0002g0026 a0001c0001t0002g0027 others(1): Show |
4 | HG01168.hp1 HG01978.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149+6666G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541008 | |||||||
| chr7:130541027 | G | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2149+6647C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541027 | |||||||
| chr7:130541082 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2149+6592C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541082 | |||||||
| chr7:130541140 | C | A | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+6534G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541140 | |||||||
| chr7:130541173 | G | A | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(318): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.2149+6501C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541173 | |||||||
| chr7:130541304 | C | T | 1 | a0001c0005t0002g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2149+6370G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541304 | |||||||
| chr7:130541338 | C | T | 1 | a0001c0002t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2149+6336G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541338 | |||||||
| chr7:130541398 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2149+6276G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541398 | |||||||
| chr7:130541406 | A | AAGGAGGG others(3): Show |
1 | a0001c0002t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2149+6258_2149+626 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541406 | |||||||
| chr7:130541695 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2149+5979C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541695 | |||||||
| chr7:130541813 | C | A | 1 | a0001c0001t0001g0282 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2149+5861G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541813 | |||||||
| chr7:130541867 | C | G | 2 | a0001c0001t0001g0129 a0005c0015t0001g0259 |
2 | HG02622.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2149+5807G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541867 | |||||||
| chr7:130541874 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2149+5800C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541874 | |||||||
| chr7:130541914 | C | T | 20 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0131 others(17): Show |
21 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.2149+5760G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541914 | |||||||
| chr7:130542058 | A | G | 8 | a0001c0002t0001g0021 a0001c0002t0001g0030 a0001c0002t0001g0036 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.2149+5616T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542058 | |||||||
| chr7:130542095 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(111): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.2149+5579C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542095 | |||||||
| chr7:130542197 | C | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(111): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.2149+5477G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542197 | |||||||
| chr7:130542205 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+5469A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542205 | |||||||
| chr7:130542242 | G | A | 1 | a0001c0001t0002g0192 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2149+5432C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542242 | |||||||
| chr7:130542362 | C | T | 1 | a0001c0001t0002g0191 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2149+5312G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542362 | |||||||
| chr7:130542435 | G | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0073 a0001c0001t0001g0074 others(61): Show |
65 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.2149+5239C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542435 | |||||||
| chr7:130542520 | C | T | 1 | a0008c0013t0001g0069 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2149+5154G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542520 | |||||||
| chr7:130542548 | C | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(204): Show |
209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.2149+5126G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542548 | |||||||
| chr7:130542557 | G | C | 1 | a0001c0001t0001g0293 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2149+5117C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542557 | |||||||
| chr7:130542810 | G | T | 4 | a0001c0002t0007g0236 a0001c0002t0007g0237 a0001c0002t0007g0238 others(1): Show |
4 | HG01192.hp2 HG01993.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+4864C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542810 | |||||||
| chr7:130543133 | A | G | 1 | a0001c0001t0002g0171 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2149+4541T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543133 | |||||||
| chr7:130543202 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2149+4472C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543202 | |||||||
| chr7:130543256 | C | A | 1 | a0001c0002t0007g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2149+4418G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543256 | |||||||
| chr7:130543438 | G | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+4236C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543438 | |||||||
| chr7:130543610 | T | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0073 a0001c0001t0001g0074 others(61): Show |
65 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.2149+4064A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543610 | |||||||
| chr7:130543789 | T | C | 3 | a0001c0001t0001g0283 a0001c0001t0001g0300 a0001c0001t0004g0286 |
3 | HG01496.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2149+3885A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543789 | |||||||
| chr7:130543858 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2149+3816A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543858 | |||||||
| chr7:130543876 | T | C | 1 | a0001c0002t0001g0043 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2149+3798A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543876 | |||||||
| chr7:130543878 | G | A | 1 | a0001c0002t0001g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2149+3796C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543878 | |||||||
| chr7:130543955 | A | T | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2149+3719T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543955 | |||||||
| chr7:130543969 | C | T | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.2149+3705G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543969 | |||||||
| chr7:130544169 | A | C | 1 | a0001c0002t0001g0055 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2149+3505T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130544169 | |||||||
| chr7:130544379 | A | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+3295T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130544379 | |||||||
| chr7:130544407 | A | G | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.2149+3267T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130544407 | |||||||
| chr7:130544749 | G | A | 5 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0249 others(2): Show |
5 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2149+2925C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130544749 | |||||||
| chr7:130545170 | T | TATTTC | 62 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(59): Show |
62 | HG00438.hp1 HG00544.hp1 HG01106.hp1 others(59): Show |
intron_variant | MODIFIER | c.2149+2499_2149+250 others(9): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545170 | |||||||
| chr7:130545170 | T | TATTTCAT others(3): Show |
29 | a0001c0002t0001g0021 a0001c0002t0001g0030 a0001c0002t0001g0036 others(26): Show |
29 | HG00597.hp1 HG00621.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.2149+2494_2149+250 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545170 | |||||||
| chr7:130545170 | T | TATTTCAT others(8): Show |
3 | a0001c0002t0001g0038 a0001c0002t0001g0062 a0001c0002t0002g0089 |
3 | HG00099.hp1 HG01255.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2149+2489_2149+250 others(19): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545170 | |||||||
| chr7:130545170 | T | TATTTCAT others(18): Show |
2 | a0001c0002t0001g0034 a0001c0002t0001g0035 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2149+2479_2149+250 others(29): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545170 | |||||||
| chr7:130545170 | TATTTC | T | 153 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0212 others(150): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.2149+2499_2149+250 others(9): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545170 | |||||||
| chr7:130545170 | TATTTCAT others(3): Show |
T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+2494_2149+250 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545170 | |||||||
| chr7:130545170 | TATTTCAT others(8): Show |
T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
52 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.2149+2489_2149+250 others(19): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545170 | |||||||
| chr7:130545479 | A | G | 6 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0002t0001g0093 others(3): Show |
6 | NA18941.hp1 NA18944.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.2149+2195T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545479 | |||||||
| chr7:130545485 | G | T | 1 | a0001c0002t0003g0107 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2149+2189C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545485 | |||||||
| chr7:130545497 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2149+2177C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545497 | |||||||
| chr7:130545700 | T | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.2149+1974A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545700 | |||||||
| chr7:130545829 | C | A | 3 | a0001c0002t0001g0060 a0001c0002t0001g0063 a0001c0002t0001g0064 |
3 | HG02280.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2149+1845G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545829 | |||||||
| chr7:130546019 | G | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+1655C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130546019 | |||||||
| chr7:130546079 | T | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0073 a0001c0001t0001g0074 others(61): Show |
65 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.2149+1595A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130546079 | |||||||
| chr7:130546183 | T | A | 1 | a0001c0002t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2149+1491A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130546183 | |||||||
| chr7:130546326 | T | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2149+1348A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130546326 | |||||||
| chr7:130546550 | G | T | 113 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(110): Show |
113 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2149+1124C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130546550 | |||||||
| chr7:130546579 | G | A | 1 | a0005c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2149+1095C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130546579 | |||||||
| chr7:130546645 | G | A | 1 | a0001c0001t0004g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2149+1029C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130546645 | |||||||
| chr7:130546704 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(45): Show |
49 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.2149+970G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130546704 | |||||||
| chr7:130547430 | C | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+244G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130547430 | |||||||
| chr7:130547496 | A | G | 1 | a0001c0001t0002g0220 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2149+178T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130547496 | |||||||
| chr7:130547562 | CATT | C | 3 | a0001c0002t0005g0078 a0001c0002t0005g0079 a0001c0002t0005g0080 |
3 | HG01256.hp1 HG01258.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.2149+109_2149+111d others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130547562 | |||||||
| chr7:130548355 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.1977+48T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 19/23 | chr7 | 130548355 | |||||||
| chr7:130548782 | G | GT | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1838-241dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/23 | chr7 | 130548782 | |||||||
| chr7:130548811 | G | A | 1 | a0001c0001t0005g0248 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1838-269C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/23 | chr7 | 130548811 | |||||||
| chr7:130548871 | T | C | 1 | a0006c0007t0001g0098 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1838-329A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/23 | chr7 | 130548871 | |||||||
| chr7:130549043 | C | CA | 102 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(99): Show |
102 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1837+270dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/23 | chr7 | 130549043 | |||||||
| chr7:130549043 | CAA | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(44): Show |
48 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.1837+269_1837+270d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/23 | chr7 | 130549043 | |||||||
| chr7:130549043 | CAAA | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1837+268_1837+270d others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/23 | chr7 | 130549043 | |||||||
| chr7:130549290 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1837+24G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/23 | chr7 | 130549290 | |||||||
| chr7:130549291 | G | A | 1 | a0001c0002t0001g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1837+23C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/23 | chr7 | 130549291 | |||||||
| chr7:130549432 | C | G | 17 | a0001c0002t0003g0070 a0001c0002t0003g0081 a0001c0002t0003g0088 others(14): Show |
17 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.1775-56G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549432 | |||||||
| chr7:130549436 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0131 others(6): Show |
10 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1775-60C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549436 | |||||||
| chr7:130549597 | A | G | 1 | a0001c0001t0002g0189 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1775-221T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549597 | |||||||
| chr7:130549815 | AG | A | 113 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(110): Show |
113 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1775-440delC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549815 | |||||||
| chr7:130549816 | G | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1775-440C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549816 | |||||||
| chr7:130549817 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1775-441T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549817 | |||||||
| chr7:130549838 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1775-462A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549838 | |||||||
| chr7:130549852 | C | T | 3 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0009 |
3 | HG00438.hp1 NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1775-476G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549852 | |||||||
| chr7:130549853 | G | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(53): Show |
57 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.1775-477C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549853 | |||||||
| chr7:130549938 | C | T | 1 | a0001c0001t0004g0322 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1775-562G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549938 | |||||||
| chr7:130549989 | C | T | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1774+535G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549989 | |||||||
| chr7:130550074 | T | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.1774+450A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130550074 | |||||||
| chr7:130550105 | A | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1774+419T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130550105 | |||||||
| chr7:130550411 | C | CA | 230 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0212 others(227): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1774+112dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130550411 | |||||||
| chr7:130550411 | C | CAA | 21 | a0001c0001t0001g0294 a0001c0001t0001g0305 a0001c0001t0002g0166 others(18): Show |
21 | HG01175.hp1 HG01192.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.1774+111_1774+112d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130550411 | |||||||
| chr7:130550411 | C | CAAAAAA | 29 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0015 others(26): Show |
30 | HG01099.hp2 HG01167.hp1 HG01515.hp2 others(27): Show |
intron_variant | MODIFIER | c.1774+107_1774+112d others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130550411 | |||||||
| chr7:130550411 | C | CAAAAAAA | 17 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(14): Show |
17 | HG01243.hp1 HG02055.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.1774+106_1774+112d others(9): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130550411 | |||||||
| chr7:130550510 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
262 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.1774+14A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130550510 | |||||||
| chr7:130550665 | A | C | 1 | a0001c0001t0001g0016 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1649-16T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 16/23 | chr7 | 130550665 | |||||||
| chr7:130550871 | C | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(28): Show |
32 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1649-222G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 16/23 | chr7 | 130550871 | |||||||
| chr7:130550949 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1648+292C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 16/23 | chr7 | 130550949 | |||||||
| chr7:130551037 | A | G | 1 | a0001c0001t0002g0148 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1648+204T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 16/23 | chr7 | 130551037 | |||||||
| chr7:130551091 | TATAAACA others(1): Show |
T | 8 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 others(5): Show |
8 | HG01167.hp2 HG01168.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1648+142_1648+149d others(10): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 16/23 | chr7 | 130551091 | |||||||
| chr7:130551101 | G | A | 8 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 others(5): Show |
8 | HG01167.hp2 HG01168.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1648+140C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 16/23 | chr7 | 130551101 | |||||||
| chr7:130551102 | G | T | 8 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 others(5): Show |
8 | HG01167.hp2 HG01168.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1648+139C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 16/23 | chr7 | 130551102 | |||||||
| chr7:130551361 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1545-17C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 15/23 | chr7 | 130551361 | |||||||
| chr7:130551396 | T | C | 1 | a0004c0011t0001g0276 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1545-52A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 15/23 | chr7 | 130551396 | |||||||
| chr7:130551446 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1545-102A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 15/23 | chr7 | 130551446 | |||||||
| chr7:130551726 | T | C | 1 | a0001c0001t0002g0183 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1545-382A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 15/23 | chr7 | 130551726 | |||||||
| chr7:130551972 | T | C | 1 | a0001c0002t0001g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1544+383A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 15/23 | chr7 | 130551972 | |||||||
| chr7:130552179 | T | C | 20 | a0001c0002t0003g0070 a0001c0002t0003g0081 a0001c0002t0003g0088 others(17): Show |
20 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1544+176A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 15/23 | chr7 | 130552179 | |||||||
| chr7:130552247 | T | A | 1 | a0001c0002t0001g0008 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1544+108A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 15/23 | chr7 | 130552247 | |||||||
| chr7:130552274 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1544+81C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 15/23 | chr7 | 130552274 | |||||||
| chr7:130552614 | A | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469-184T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130552614 | |||||||
| chr7:130552962 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1469-532A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130552962 | |||||||
| chr7:130553002 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0310 |
4 | NA18945.hp2 NA18963.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469-572G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553002 | |||||||
| chr7:130553004 | G | A | 1 | a0001c0001t0002g0188 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1469-574C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553004 | |||||||
| chr7:130553133 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.1469-703G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553133 | |||||||
| chr7:130553330 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1469-900G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553330 | |||||||
| chr7:130553333 | C | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(28): Show |
32 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1469-903G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553333 | |||||||
| chr7:130553461 | T | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+1020A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553461 | |||||||
| chr7:130553671 | A | G | 1 | a0005c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1468+810T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553671 | |||||||
| chr7:130553772 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(261): Show |
265 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.1468+709C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553772 | |||||||
| chr7:130553905 | T | G | 2 | a0001c0001t0001g0270 a0001c0001t0001g0304 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1468+576A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553905 | |||||||
| chr7:130553951 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1468+530G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553951 | |||||||
| chr7:130553959 | T | C | 1 | a0001c0001t0012g0201 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1468+522A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553959 | |||||||
| chr7:130553966 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(28): Show |
32 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468+515C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553966 | |||||||
| chr7:130554032 | C | A | 1 | a0001c0001t0001g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1468+449G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130554032 | |||||||
| chr7:130554176 | G | A | 2 | a0001c0005t0002g0011 a0001c0005t0002g0012 |
2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1468+305C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130554176 | |||||||
| chr7:130554183 | A | AATAT | 40 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(37): Show |
40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.1468+294_1468+297d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130554183 | |||||||
| chr7:130554935 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1224+102G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 13/23 | chr7 | 130554935 | |||||||
| chr7:130555624 | C | T | 5 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(2): Show |
5 | HG01192.hp2 HG01993.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1129-492G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130555624 | |||||||
| chr7:130555664 | TA | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1129-533delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130555664 | |||||||
| chr7:130555717 | T | C | 14 | a0001c0002t0001g0040 a0001c0002t0001g0051 a0001c0002t0001g0052 others(11): Show |
14 | HG00597.hp1 HG00621.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.1129-585A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130555717 | |||||||
| chr7:130555977 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.1129-845G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130555977 | |||||||
| chr7:130556435 | G | C | 1 | a0001c0001t0001g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1129-1303C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130556435 | |||||||
| chr7:130556574 | T | C | 2 | a0001c0006t0002g0153 a0001c0006t0002g0154 |
2 | NA18941.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1129-1442A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130556574 | |||||||
| chr7:130556656 | T | C | 12 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0001g0135 others(9): Show |
12 | HG01891.hp1 HG01943.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1129-1524A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130556656 | |||||||
| chr7:130556704 | T | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1129-1572A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130556704 | |||||||
| chr7:130557241 | A | G | 1 | a0001c0002t0001g0071 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1129-2109T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557241 | |||||||
| chr7:130557310 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1129-2178A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557310 | |||||||
| chr7:130557408 | G | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1129-2276C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557408 | |||||||
| chr7:130557459 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1129-2327A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557459 | |||||||
| chr7:130557578 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1129-2446C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557578 | |||||||
| chr7:130557723 | G | A | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1129-2591C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557723 | |||||||
| chr7:130557817 | C | CAAAAA | 53 | a0001c0001t0001g0002 a0001c0001t0001g0268 a0001c0001t0001g0269 others(50): Show |
54 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1129-2690_1129-268 others(9): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557817 | |||||||
| chr7:130557817 | C | CAAAAAAA | 90 | a0001c0001t0001g0032 a0001c0001t0001g0073 a0001c0001t0001g0074 others(87): Show |
90 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.1129-2692_1129-268 others(11): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557817 | |||||||
| chr7:130557817 | C | CAAAAAAA others(1): Show |
47 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(44): Show |
48 | HG01069.hp1 HG01106.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.1129-2693_1129-268 others(12): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557817 | |||||||
| chr7:130557817 | C | CAAAAAAA others(2): Show |
19 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0131 others(16): Show |
19 | HG01099.hp2 HG02055.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.1129-2694_1129-268 others(13): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557817 | |||||||
| chr7:130557817 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0253 a0001c0001t0005g0248 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1129-2695_1129-268 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557817 | |||||||
| chr7:130557817 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1129-2696_1129-268 others(15): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557817 | |||||||
| chr7:130557817 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0006 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1129-2697_1129-268 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557817 | |||||||
| chr7:130557817 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1129-2698_1129-268 others(17): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557817 | |||||||
| chr7:130558003 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1129-2871G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130558003 | |||||||
| chr7:130558004 | G | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1129-2872C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130558004 | |||||||
| chr7:130558157 | T | C | 6 | a0001c0001t0002g0150 a0001c0001t0002g0197 a0001c0001t0002g0198 others(3): Show |
6 | HG01175.hp2 HG01515.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1128+2876A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130558157 | |||||||
| chr7:130558202 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1128+2831T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130558202 | |||||||
| chr7:130558580 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1128+2453T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130558580 | |||||||
| chr7:130558608 | C | A | 1 | a0001c0002t0001g0043 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1128+2425G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130558608 | |||||||
| chr7:130558706 | G | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1128+2327C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130558706 | |||||||
| chr7:130558926 | C | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1128+2107G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130558926 | |||||||
| chr7:130559069 | T | C | 3 | a0001c0001t0002g0148 a0001c0001t0002g0163 a0001c0001t0002g0175 |
3 | HG00621.hp1 NA18954.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1128+1964A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130559069 | |||||||
| chr7:130559079 | G | A | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+1954C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130559079 | |||||||
| chr7:130559197 | A | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0131 others(6): Show |
10 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1128+1836T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130559197 | |||||||
| chr7:130559203 | A | G | 6 | a0001c0001t0002g0150 a0001c0001t0002g0197 a0001c0001t0002g0198 others(3): Show |
6 | HG01175.hp2 HG01515.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1128+1830T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130559203 | |||||||
| chr7:130559647 | A | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0015 others(3): Show |
6 | HG01243.hp1 HG02258.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1128+1386T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130559647 | |||||||
| chr7:130559796 | A | G | 2 | a0001c0002t0001g0101 a0001c0002t0001g0102 |
2 | NA18980.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1128+1237T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130559796 | |||||||
| chr7:130559877 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1128+1156C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130559877 | |||||||
| chr7:130560196 | T | C | 1 | a0001c0001t0002g0193 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1128+837A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130560196 | |||||||
| chr7:130560308 | G | A | 1 | a0001c0001t0002g0223 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1128+725C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130560308 | |||||||
| chr7:130560549 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1128+484C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130560549 | |||||||
| chr7:130560586 | A | G | 1 | a0001c0002t0001g0071 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1128+447T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130560586 | |||||||
| chr7:130560810 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1128+223A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130560810 | |||||||
| chr7:130560905 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1128+128C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130560905 | |||||||
| chr7:130561839 | C | A | 6 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0002t0001g0093 others(3): Show |
6 | NA18941.hp1 NA18944.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-618G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 11/23 | chr7 | 130561839 | |||||||
| chr7:130561865 | C | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.940-644G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 11/23 | chr7 | 130561865 | |||||||
| chr7:130562215 | C | T | 5 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(2): Show |
5 | HG01192.hp2 HG01993.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-994G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 11/23 | chr7 | 130562215 | |||||||
| chr7:130562314 | G | A | 1 | a0001c0012t0002g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.939+955C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 11/23 | chr7 | 130562314 | |||||||
| chr7:130562454 | C | T | 2 | a0001c0001t0002g0227 a0001c0001t0006g0226 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.939+815G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 11/23 | chr7 | 130562454 | |||||||
| chr7:130562758 | T | C | 1 | a0001c0001t0009g0256 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.939+511A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 11/23 | chr7 | 130562758 | |||||||
| chr7:130563067 | A | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.939+202T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 11/23 | chr7 | 130563067 | |||||||
| chr7:130563345 | A | AAAT | 6 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0291 others(3): Show |
6 | HG02129.hp1 HG02155.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.872-12_872-10dupAT others(1): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563345 | |||||||
| chr7:130563345 | A | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(57): Show |
61 | HG01069.hp1 HG01099.hp2 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.872-9T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563345 | |||||||
| chr7:130563362 | T | C | 2 | a0001c0001t0005g0251 a0001c0001t0005g0258 |
2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.872-26A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563362 | |||||||
| chr7:130563394 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0131 others(6): Show |
10 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.872-58C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563394 | |||||||
| chr7:130563537 | A | C | 1 | a0001c0002t0001g0072 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.872-201T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563537 | |||||||
| chr7:130563666 | A | G | 1 | a0001c0002t0001g0096 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.872-330T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563666 | |||||||
| chr7:130563772 | A | G | 1 | a0001c0001t0002g0189 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.872-436T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563772 | |||||||
| chr7:130563773 | A | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0212 others(144): Show |
148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.872-437T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563773 | |||||||
| chr7:130563774 | G | A | 148 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0212 others(145): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.872-438C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563774 | |||||||
| chr7:130563774 | G | GA | 150 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(147): Show |
151 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.872-439dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563774 | |||||||
| chr7:130563895 | T | C | 1 | a0001c0001t0002g0189 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.871+365A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563895 | |||||||
| chr7:130563919 | C | T | 1 | a0001c0012t0002g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.871+341G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563919 | |||||||
| chr7:130563957 | A | C | 1 | a0001c0001t0002g0179 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.871+303T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563957 | |||||||
| chr7:130564021 | T | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.871+239A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130564021 | |||||||
| chr7:130564122 | T | A | 1 | a0001c0002t0001g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.871+138A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130564122 | |||||||
| chr7:130564194 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.871+66A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130564194 | |||||||
| chr7:130564438 | G | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(54): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.738-45C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130564438 | |||||||
| chr7:130564519 | C | A | 1 | a0001c0001t0001g0294 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.738-126G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130564519 | |||||||
| chr7:130564866 | G | A | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.738-473C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130564866 | |||||||
| chr7:130565135 | A | G | 1 | a0001c0002t0003g0123 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.738-742T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130565135 | |||||||
| chr7:130565145 | C | T | 1 | a0001c0002t0003g0123 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.738-752G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130565145 | |||||||
| chr7:130565230 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.738-837C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130565230 | |||||||
| chr7:130565765 | T | C | 1 | a0005c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.738-1372A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130565765 | |||||||
| chr7:130565827 | T | A | 1 | a0001c0002t0001g0030 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.738-1434A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130565827 | |||||||
| chr7:130565859 | G | C | 1 | a0001c0002t0001g0075 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.738-1466C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130565859 | |||||||
| chr7:130566058 | T | G | 1 | a0001c0001t0002g0160 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.738-1665A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130566058 | |||||||
| chr7:130566160 | T | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-1767A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130566160 | |||||||
| chr7:130566278 | T | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(44): Show |
48 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.738-1885A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130566278 | |||||||
| chr7:130566597 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.738-2204G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130566597 | |||||||
| chr7:130566599 | G | A | 1 | a0001c0002t0003g0124 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.738-2206C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130566599 | |||||||
| chr7:130566873 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.738-2480T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130566873 | |||||||
| chr7:130566879 | T | C | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.738-2486A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130566879 | |||||||
| chr7:130567221 | A | G | 1 | a0001c0002t0001g0119 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.738-2828T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130567221 | |||||||
| chr7:130568068 | G | A | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.738-3675C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568068 | |||||||
| chr7:130568135 | C | A | 1 | a0001c0002t0001g0102 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.738-3742G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568135 | |||||||
| chr7:130568211 | G | A | 1 | a0001c0002t0003g0107 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.738-3818C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568211 | |||||||
| chr7:130568314 | G | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-3921C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568314 | |||||||
| chr7:130568324 | T | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-3931A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568324 | |||||||
| chr7:130568413 | A | G | 1 | a0001c0001t0002g0189 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.738-4020T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568413 | |||||||
| chr7:130568745 | A | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-4352T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568745 | |||||||
| chr7:130568783 | A | G | 1 | a0001c0002t0001g0101 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.738-4390T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568783 | |||||||
| chr7:130568960 | T | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-4567A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568960 | |||||||
| chr7:130569014 | C | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-4621G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130569014 | |||||||
| chr7:130569096 | A | G | 3 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0038 |
3 | HG00099.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.738-4703T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130569096 | |||||||
| chr7:130569190 | G | C | 1 | a0001c0001t0001g0257 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.738-4797C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130569190 | |||||||
| chr7:130569302 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.738-4909G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130569302 | |||||||
| chr7:130569366 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-4973C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130569366 | |||||||
| chr7:130570182 | T | C | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-5789A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130570182 | |||||||
| chr7:130570248 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-5855T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130570248 | |||||||
| chr7:130570408 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(44): Show |
48 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.738-6015C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130570408 | |||||||
| chr7:130570586 | G | T | 1 | a0001c0002t0001g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.738-6193C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130570586 | |||||||
| chr7:130570587 | A | T | 1 | a0001c0002t0001g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.738-6194T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130570587 | |||||||
| chr7:130570654 | C | T | 5 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(2): Show |
5 | HG00140.hp2 HG00639.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-6261G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130570654 | |||||||
| chr7:130570941 | A | G | 1 | a0001c0002t0001g0101 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.738-6548T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130570941 | |||||||
| chr7:130570992 | G | C | 1 | a0001c0001t0002g0177 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.738-6599C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130570992 | |||||||
| chr7:130571020 | C | A | 1 | a0001c0001t0012g0201 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.738-6627G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571020 | |||||||
| chr7:130571228 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.738-6835G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571228 | |||||||
| chr7:130571229 | G | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-6836C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571229 | |||||||
| chr7:130571338 | C | T | 2 | a0001c0002t0001g0039 a0001c0002t0001g0062 |
2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.738-6945G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571338 | |||||||
| chr7:130571667 | A | G | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.738-7274T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571667 | |||||||
| chr7:130571834 | C | CCT | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(96): Show |
101 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.738-7443_738-7442d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571834 | |||||||
| chr7:130571845 | C | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG02486.hp2 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.738-7452G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571845 | |||||||
| chr7:130571845 | C | CTA | 12 | a0001c0001t0001g0031 a0001c0001t0001g0131 a0001c0001t0001g0132 others(9): Show |
12 | HG01099.hp2 HG01167.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.738-7454_738-7453d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571845 | |||||||
| chr7:130571847 | A | C | 271 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(268): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.738-7454T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571847 | |||||||
| chr7:130571849 | A | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0129 a0001c0001t0001g0136 others(136): Show |
140 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.738-7456T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571849 | |||||||
| chr7:130571873 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.738-7480C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571873 | |||||||
| chr7:130572005 | C | A | 4 | a0001c0002t0007g0236 a0001c0002t0007g0237 a0001c0002t0007g0238 others(1): Show |
4 | HG01192.hp2 HG01993.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-7612G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130572005 | |||||||
| chr7:130572072 | T | C | 1 | a0001c0002t0003g0108 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.738-7679A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130572072 | |||||||
| chr7:130572683 | A | G | 1 | a0001c0001t0002g0151 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.738-8290T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130572683 | |||||||
| chr7:130572831 | A | T | 1 | a0001c0001t0001g0031 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.738-8438T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130572831 | |||||||
| chr7:130572991 | C | T | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.738-8598G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130572991 | |||||||
| chr7:130573213 | C | CA | 96 | a0001c0001t0001g0131 a0001c0001t0001g0208 a0001c0001t0001g0212 others(93): Show |
96 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.738-8821dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130573213 | |||||||
| chr7:130573213 | CA | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(97): Show |
101 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.738-8821delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130573213 | |||||||
| chr7:130573285 | C | T | 1 | a0001c0002t0003g0261 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.738-8892G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130573285 | |||||||
| chr7:130573382 | A | G | 4 | a0001c0001t0005g0250 a0001c0001t0005g0255 a0001c0001t0009g0252 others(1): Show |
4 | HG02055.hp2 HG02723.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-8989T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130573382 | |||||||
| chr7:130573501 | T | C | 3 | a0001c0001t0001g0283 a0001c0001t0001g0300 a0001c0001t0004g0286 |
3 | HG01496.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.738-9108A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130573501 | |||||||
| chr7:130573610 | A | G | 4 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0047 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-9217T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130573610 | |||||||
| chr7:130573900 | G | A | 2 | a0001c0001t0002g0026 a0001c0001t0002g0028 |
2 | HG01978.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.738-9507C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130573900 | |||||||
| chr7:130573956 | A | G | 4 | a0001c0002t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0243 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-9563T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130573956 | |||||||
| chr7:130574125 | G | A | 4 | a0001c0002t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0243 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-9732C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574125 | |||||||
| chr7:130574177 | A | C | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.738-9784T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574177 | |||||||
| chr7:130574274 | G | T | 1 | a0001c0001t0002g0199 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.738-9881C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574274 | |||||||
| chr7:130574425 | C | T | 1 | a0001c0002t0001g0064 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.738-10032G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574425 | |||||||
| chr7:130574519 | C | T | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-10126G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574519 | |||||||
| chr7:130574529 | A | T | 1 | a0001c0001t0001g0309 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.738-10136T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574529 | |||||||
| chr7:130574654 | C | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(276): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.738-10261G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574654 | |||||||
| chr7:130574823 | A | G | 1 | a0001c0001t0004g0130 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.738-10430T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574823 | |||||||
| chr7:130574935 | G | C | 1 | a0001c0002t0001g0030 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.738-10542C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574935 | |||||||
| chr7:130575092 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.738-10699T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130575092 | |||||||
| chr7:130575174 | T | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-10781A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130575174 | |||||||
| chr7:130575197 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.738-10804G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130575197 | |||||||
| chr7:130575277 | G | A | 1 | a0001c0002t0003g0107 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.738-10884C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130575277 | |||||||
| chr7:130575285 | T | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(7): Show |
10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.738-10892A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130575285 | |||||||
| chr7:130575454 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.738-11061T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130575454 | |||||||
| chr7:130575455 | G | C | 1 | a0001c0002t0001g0091 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.738-11062C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130575455 | |||||||
| chr7:130575522 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.738-11129G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130575522 | |||||||
| chr7:130576401 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-12008G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130576401 | |||||||
| chr7:130576527 | G | A | 1 | a0001c0001t0002g0213 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.738-12134C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130576527 | |||||||
| chr7:130576611 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.738-12218A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130576611 | |||||||
| chr7:130576695 | T | C | 2 | a0001c0001t0001g0273 a0004c0011t0001g0276 |
2 | HG00099.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.738-12302A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130576695 | |||||||
| chr7:130576761 | G | C | 1 | a0001c0002t0001g0105 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.738-12368C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130576761 | |||||||
| chr7:130576781 | GAAAC | G | 6 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(3): Show |
6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.738-12392_738-1238 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130576781 | |||||||
| chr7:130576796 | A | T | 2 | a0001c0001t0002g0227 a0001c0001t0006g0226 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.738-12403T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130576796 | |||||||
| chr7:130576797 | C | A | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-12404G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130576797 | |||||||
| chr7:130577273 | T | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(28): Show |
32 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.738-12880A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577273 | |||||||
| chr7:130577304 | T | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-12911A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577304 | |||||||
| chr7:130577329 | G | A | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.738-12936C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577329 | |||||||
| chr7:130577345 | T | C | 1 | a0001c0002t0001g0024 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.738-12952A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577345 | |||||||
| chr7:130577363 | G | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.738-12970C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577363 | |||||||
| chr7:130577446 | T | C | 4 | a0001c0002t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0243 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-13053A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577446 | |||||||
| chr7:130577551 | G | C | 1 | a0001c0001t0001g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.738-13158C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577551 | |||||||
| chr7:130577683 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-13290G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577683 | |||||||
| chr7:130577755 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.738-13362C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577755 | |||||||
| chr7:130577767 | C | CA | 40 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(37): Show |
40 | HG00621.hp2 HG01167.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.738-13375dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577767 | |||||||
| chr7:130577767 | C | CAA | 6 | a0001c0002t0001g0086 a0001c0002t0001g0127 a0001c0002t0001g0241 others(3): Show |
6 | HG03834.hp2 HG04115.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.738-13376_738-1337 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577767 | |||||||
| chr7:130577767 | CA | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(48): Show |
52 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.738-13375delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577767 | |||||||
| chr7:130577775 | A | C | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.738-13382T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577775 | |||||||
| chr7:130577777 | A | C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0253 a0001c0001t0001g0257 |
3 | HG02630.hp1 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.738-13384T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577777 | |||||||
| chr7:130577781 | A | C | 8 | a0001c0001t0002g0176 a0001c0001t0002g0181 a0001c0001t0002g0196 others(5): Show |
8 | HG02451.hp1 HG02717.hp2 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.738-13388T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577781 | |||||||
| chr7:130577784 | A | AC | 4 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0264 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-13392_738-1339 others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577784 | |||||||
| chr7:130577785 | A | C | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.738-13392T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577785 | |||||||
| chr7:130577788 | A | C | 1 | a0001c0001t0004g0322 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.738-13395T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577788 | |||||||
| chr7:130577789 | C | A | 9 | a0001c0001t0001g0303 a0001c0001t0004g0322 a0001c0002t0001g0241 others(6): Show |
9 | HG01256.hp2 HG01361.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.738-13396G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577789 | |||||||
| chr7:130577793 | A | C | 8 | a0001c0001t0002g0151 a0001c0001t0002g0166 a0001c0001t0002g0169 others(5): Show |
8 | HG00544.hp2 HG01258.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.738-13400T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577793 | |||||||
| chr7:130577841 | G | T | 2 | a0001c0002t0001g0034 a0001c0002t0001g0035 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.738-13448C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577841 | |||||||
| chr7:130577858 | A | G | 5 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(2): Show |
5 | HG01192.hp2 HG01993.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-13465T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577858 | |||||||
| chr7:130577896 | T | C | 1 | a0003c0008t0001g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.738-13503A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577896 | |||||||
| chr7:130577904 | G | A | 1 | a0005c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.738-13511C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577904 | |||||||
| chr7:130578015 | C | A | 1 | a0001c0001t0001g0274 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.738-13622G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578015 | |||||||
| chr7:130578226 | C | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.738-13833G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578226 | |||||||
| chr7:130578322 | G | A | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.738-13929C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578322 | |||||||
| chr7:130578482 | A | G | 1 | a0001c0001t0002g0174 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.738-14089T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578482 | |||||||
| chr7:130578510 | C | T | 2 | a0001c0001t0001g0271 a0001c0001t0002g0206 |
2 | HG00140.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.738-14117G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578510 | |||||||
| chr7:130578715 | A | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-14322T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578715 | |||||||
| chr7:130578750 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-14357T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578750 | |||||||
| chr7:130578779 | G | A | 1 | a0001c0002t0001g0093 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.738-14386C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578779 | |||||||
| chr7:130578866 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.738-14473T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578866 | |||||||
| chr7:130578938 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.738-14545T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578938 | |||||||
| chr7:130579043 | T | C | 20 | a0001c0002t0003g0070 a0001c0002t0003g0081 a0001c0002t0003g0088 others(17): Show |
20 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.738-14650A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579043 | |||||||
| chr7:130579114 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.738-14721G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579114 | |||||||
| chr7:130579152 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0144 |
3 | HG01069.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.738-14759C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579152 | |||||||
| chr7:130579370 | A | G | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.738-14977T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579370 | |||||||
| chr7:130579415 | C | T | 1 | a0001c0002t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.738-15022G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579415 | |||||||
| chr7:130579477 | G | A | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.738-15084C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579477 | |||||||
| chr7:130579550 | T | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.738-15157A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579550 | |||||||
| chr7:130579572 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.738-15179G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579572 | |||||||
| chr7:130579737 | C | A | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-15344G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579737 | |||||||
| chr7:130580077 | T | C | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.738-15684A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580077 | |||||||
| chr7:130580269 | C | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(44): Show |
48 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.738-15876G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580269 | |||||||
| chr7:130580334 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.738-15941C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580334 | |||||||
| chr7:130580444 | G | C | 1 | a0001c0001t0002g0151 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.738-16051C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580444 | |||||||
| chr7:130580448 | G | C | 1 | a0001c0001t0002g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.738-16055C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580448 | |||||||
| chr7:130580461 | CA | C | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.738-16069delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580461 | |||||||
| chr7:130580467 | C | G | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.738-16074G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580467 | |||||||
| chr7:130580472 | A | G | 1 | a0001c0001t0002g0192 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.738-16079T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580472 | |||||||
| chr7:130580590 | G | A | 1 | a0005c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.738-16197C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580590 | |||||||
| chr7:130580594 | G | A | 1 | a0003c0008t0001g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.738-16201C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580594 | |||||||
| chr7:130580634 | A | G | 7 | a0001c0001t0005g0248 a0001c0001t0005g0250 a0001c0001t0005g0251 others(4): Show |
7 | HG02055.hp2 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.738-16241T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580634 | |||||||
| chr7:130580673 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.738-16280T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580673 | |||||||
| chr7:130580723 | C | T | 1 | a0001c0002t0002g0089 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.738-16330G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580723 | |||||||
| chr7:130580794 | AG | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(44): Show |
48 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.738-16402delC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580794 | |||||||
| chr7:130580903 | A | T | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-16510T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580903 | |||||||
| chr7:130581092 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(205): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.738-16699A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581092 | |||||||
| chr7:130581188 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.738-16795G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581188 | |||||||
| chr7:130581195 | C | G | 2 | a0001c0002t0001g0022 a0001c0002t0001g0023 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.738-16802G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581195 | |||||||
| chr7:130581195 | C | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-16802G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581195 | |||||||
| chr7:130581465 | C | T | 2 | a0001c0002t0001g0060 a0001c0002t0001g0064 |
2 | HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.738-17072G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581465 | |||||||
| chr7:130581723 | A | G | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.738-17330T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581723 | |||||||
| chr7:130581745 | C | T | 2 | a0001c0001t0002g0218 a0001c0001t0002g0230 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.738-17352G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581745 | |||||||
| chr7:130581857 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.738-17464G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581857 | |||||||
| chr7:130581956 | A | C | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.738-17563T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581956 | |||||||
| chr7:130581999 | T | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.738-17606A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581999 | |||||||
| chr7:130582188 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0142 |
2 | HG01891.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.738-17795G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582188 | |||||||
| chr7:130582248 | AGGATTCC others(5289): Show |
A | 1 | a0001c0002t0001g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.738-23151_738-1785 others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582248 | |||||||
| chr7:130582249 | G | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0230 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.738-17856C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582249 | |||||||
| chr7:130582333 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-17940A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582333 | |||||||
| chr7:130582344 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-17951T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582344 | |||||||
| chr7:130582370 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.738-17977C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582370 | |||||||
| chr7:130582432 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.738-18039G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582432 | |||||||
| chr7:130582488 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.738-18095A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582488 | |||||||
| chr7:130582580 | A | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.738-18187T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582580 | |||||||
| chr7:130582666 | C | A | 1 | a0001c0002t0004g0084 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.738-18273G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582666 | |||||||
| chr7:130582684 | G | A | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.738-18291C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582684 | |||||||
| chr7:130582700 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.738-18307G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582700 | |||||||
| chr7:130582760 | C | G | 1 | a0001c0001t0002g0185 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.738-18367G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582760 | |||||||
| chr7:130582814 | G | A | 1 | a0005c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.738-18421C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582814 | |||||||
| chr7:130582870 | A | G | 6 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0303 others(3): Show |
6 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.738-18477T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582870 | |||||||
| chr7:130583047 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.738-18654G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583047 | |||||||
| chr7:130583061 | A | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(44): Show |
48 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.738-18668T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583061 | |||||||
| chr7:130583061 | A | G | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-18668T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583061 | |||||||
| chr7:130583120 | G | A | 9 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 others(6): Show |
9 | HG00639.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.738-18727C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583120 | |||||||
| chr7:130583241 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.738-18848C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583241 | |||||||
| chr7:130583348 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.738-18955C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583348 | |||||||
| chr7:130583357 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.738-18964C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583357 | |||||||
| chr7:130583366 | G | A | 3 | a0001c0001t0001g0283 a0001c0001t0001g0300 a0001c0001t0004g0286 |
3 | HG01496.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.738-18973C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583366 | |||||||
| chr7:130583493 | T | TA | 38 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0141 others(35): Show |
38 | HG01099.hp2 HG01106.hp1 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.738-19101dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583493 | |||||||
| chr7:130583493 | T | TAA | 10 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(7): Show |
10 | HG02258.hp1 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.738-19102_738-1910 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583493 | |||||||
| chr7:130583493 | T | TAAA | 7 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.738-19103_738-1910 others(7): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583493 | |||||||
| chr7:130583493 | TA | T | 91 | a0001c0001t0001g0032 a0001c0001t0001g0073 a0001c0001t0001g0208 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.738-19101delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583493 | |||||||
| chr7:130583493 | TAA | T | 6 | a0001c0001t0001g0074 a0001c0001t0002g0155 a0001c0001t0002g0163 others(3): Show |
6 | HG02523.hp2 HG02717.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.738-19102_738-1910 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583493 | |||||||
| chr7:130583533 | G | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-19140C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583533 | |||||||
| chr7:130583544 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0131 |
2 | HG03239.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.738-19151G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583544 | |||||||
| chr7:130583794 | A | G | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.738-19401T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583794 | |||||||
| chr7:130583805 | C | CA | 75 | a0001c0001t0001g0005 a0001c0001t0001g0074 a0001c0001t0001g0208 others(72): Show |
75 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.738-19413dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583805 | |||||||
| chr7:130583805 | C | CAA | 11 | a0001c0001t0002g0193 a0001c0001t0002g0218 a0001c0001t0006g0164 others(8): Show |
11 | HG00597.hp2 HG02080.hp1 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.738-19414_738-1941 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583805 | |||||||
| chr7:130583805 | CA | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(46): Show |
50 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.738-19413delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583805 | |||||||
| chr7:130583805 | CAA | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0020 others(40): Show |
44 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.738-19414_738-1941 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583805 | |||||||
| chr7:130583928 | C | G | 1 | a0001c0001t0001g0257 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.738-19535G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583928 | |||||||
| chr7:130583950 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-19557C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583950 | |||||||
| chr7:130584240 | G | C | 5 | a0001c0002t0003g0081 a0001c0002t0003g0088 a0001c0002t0003g0111 others(2): Show |
5 | HG01261.hp2 HG01975.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-19847C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130584240 | |||||||
| chr7:130584244 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.738-19851A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130584244 | |||||||
| chr7:130584469 | G | T | 1 | a0001c0002t0003g0122 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.738-20076C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130584469 | |||||||
| chr7:130584676 | G | C | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-20283C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130584676 | |||||||
| chr7:130585010 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(205): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.738-20617T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585010 | |||||||
| chr7:130585046 | A | G | 1 | a0001c0001t0002g0189 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.738-20653T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585046 | |||||||
| chr7:130585281 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.738-20888A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585281 | |||||||
| chr7:130585301 | T | C | 1 | a0001c0002t0001g0105 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.738-20908A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585301 | |||||||
| chr7:130585392 | T | C | 1 | a0006c0007t0001g0098 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.738-20999A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585392 | |||||||
| chr7:130585588 | T | C | 1 | a0001c0002t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.738-21195A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585588 | |||||||
| chr7:130585701 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.738-21308C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585701 | |||||||
| chr7:130585738 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.738-21345C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585738 | |||||||
| chr7:130585761 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-21368T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585761 | |||||||
| chr7:130585783 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.738-21390G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585783 | |||||||
| chr7:130586170 | A | T | 9 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 others(6): Show |
9 | HG00639.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.738-21777T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586170 | |||||||
| chr7:130586285 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(205): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.738-21892T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586285 | |||||||
| chr7:130586361 | A | AGT | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-21970_738-2196 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586361 | |||||||
| chr7:130586367 | T | C | 1 | a0001c0001t0002g0232 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.738-21974A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586367 | |||||||
| chr7:130586500 | T | G | 4 | a0001c0002t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0243 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-22107A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586500 | |||||||
| chr7:130586611 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-22218G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586611 | |||||||
| chr7:130586623 | G | A | 6 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(3): Show |
6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.738-22230C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586623 | |||||||
| chr7:130586656 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(204): Show |
209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.738-22263T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586656 | |||||||
| chr7:130586819 | T | C | 3 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0038 |
3 | HG00099.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.738-22426A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586819 | |||||||
| chr7:130586844 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.738-22451G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586844 | |||||||
| chr7:130587033 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.738-22640C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587033 | |||||||
| chr7:130587060 | A | C | 1 | a0001c0002t0001g0042 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.738-22667T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587060 | |||||||
| chr7:130587081 | C | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(44): Show |
48 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.738-22688G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587081 | |||||||
| chr7:130587233 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0310 |
4 | NA18945.hp2 NA18963.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-22840C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587233 | |||||||
| chr7:130587246 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(109): Show |
114 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.738-22853T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587246 | |||||||
| chr7:130587256 | G | A | 1 | a0001c0002t0001g0004 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.738-22863C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587256 | |||||||
| chr7:130587773 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.737+23180T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587773 | |||||||
| chr7:130587778 | C | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(44): Show |
48 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.737+23175G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587778 | |||||||
| chr7:130587988 | T | C | 3 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0009 |
3 | HG00438.hp1 NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.737+22965A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587988 | |||||||
| chr7:130588025 | A | G | 2 | a0001c0002t0001g0099 a0008c0013t0001g0069 |
2 | HG01358.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.737+22928T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588025 | |||||||
| chr7:130588038 | T | C | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.737+22915A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588038 | |||||||
| chr7:130588102 | T | A | 1 | a0001c0001t0004g0306 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.737+22851A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588102 | |||||||
| chr7:130588108 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(205): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.737+22845T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588108 | |||||||
| chr7:130588109 | A | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(205): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.737+22844T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588109 | |||||||
| chr7:130588167 | GAGAAATA others(11): Show |
G | 1 | a0001c0001t0005g0248 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.737+22768_737+2278 others(22): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588167 | |||||||
| chr7:130588186 | A | G | 1 | a0001c0001t0005g0248 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.737+22767T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588186 | |||||||
| chr7:130588187 | C | T | 1 | a0001c0001t0005g0248 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.737+22766G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588187 | |||||||
| chr7:130588188 | A | G | 1 | a0001c0001t0005g0248 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.737+22765T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588188 | |||||||
| chr7:130588417 | C | G | 62 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(59): Show |
62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.737+22536G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588417 | |||||||
| chr7:130588418 | C | T | 1 | a0001c0001t0002g0231 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.737+22535G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588418 | |||||||
| chr7:130588452 | A | G | 1 | a0001c0002t0002g0089 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.737+22501T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588452 | |||||||
| chr7:130588651 | C | A | 1 | a0001c0012t0002g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.737+22302G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588651 | |||||||
| chr7:130588720 | A | G | 1 | a0001c0002t0001g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.737+22233T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588720 | |||||||
| chr7:130588726 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(109): Show |
114 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.737+22227C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588726 | |||||||
| chr7:130588762 | G | A | 92 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.737+22191C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588762 | |||||||
| chr7:130588768 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.737+22185G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588768 | |||||||
| chr7:130588799 | TA | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0246 others(13): Show |
16 | HG01099.hp2 HG02055.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.737+22153delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588799 | |||||||
| chr7:130588840 | A | G | 1 | a0001c0001t0001g0288 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.737+22113T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588840 | |||||||
| chr7:130588896 | T | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(204): Show |
209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.737+22057A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588896 | |||||||
| chr7:130588902 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.737+22051C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588902 | |||||||
| chr7:130589018 | A | G | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+21935T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130589018 | |||||||
| chr7:130589084 | C | T | 3 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0002t0001g0077 |
3 | NA19062.hp2 NA19064.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.737+21869G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130589084 | |||||||
| chr7:130589281 | CT | C | 15 | a0001c0001t0001g0020 a0001c0001t0001g0312 a0001c0001t0002g0162 others(12): Show |
15 | HG01975.hp2 HG02083.hp1 HG02683.hp1 others(12): Show |
intron_variant | MODIFIER | c.737+21671delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130589281 | |||||||
| chr7:130589361 | T | G | 1 | a0001c0001t0010g0003 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.737+21592A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130589361 | |||||||
| chr7:130589705 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(205): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.737+21248G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130589705 | |||||||
| chr7:130589911 | C | T | 93 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(90): Show |
93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.737+21042G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130589911 | |||||||
| chr7:130589929 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.737+21024C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130589929 | |||||||
| chr7:130590222 | T | TCTCTCCC others(16): Show |
4 | a0001c0001t0002g0166 a0001c0001t0002g0190 a0001c0001t0002g0224 others(1): Show |
4 | HG01167.hp2 HG01258.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+20708_737+2073 others(27): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590222 | |||||||
| chr7:130590336 | G | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0266 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.737+20617C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590336 | |||||||
| chr7:130590347 | A | T | 7 | a0001c0002t0001g0083 a0001c0002t0001g0085 a0001c0002t0001g0086 others(4): Show |
7 | NA18947.hp1 NA18955.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.737+20606T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590347 | |||||||
| chr7:130590391 | G | T | 5 | a0001c0001t0001g0246 a0001c0001t0001g0253 a0001c0001t0001g0257 others(2): Show |
5 | HG01099.hp2 HG02886.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+20562C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590391 | |||||||
| chr7:130590404 | C | T | 2 | a0001c0001t0002g0227 a0001c0001t0006g0226 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.737+20549G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590404 | |||||||
| chr7:130590501 | G | A | 1 | a0001c0001t0005g0250 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.737+20452C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590501 | |||||||
| chr7:130590545 | C | T | 320 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(317): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.737+20408G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590545 | |||||||
| chr7:130590549 | C | T | 1 | a0001c0002t0004g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.737+20404G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590549 | |||||||
| chr7:130590589 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.737+20364T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590589 | |||||||
| chr7:130590596 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.737+20357G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590596 | |||||||
| chr7:130590668 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+20285G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590668 | |||||||
| chr7:130590687 | G | C | 4 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 others(1): Show |
4 | HG01099.hp1 HG02257.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+20266C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590687 | |||||||
| chr7:130590776 | T | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+20177A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590776 | |||||||
| chr7:130590784 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(205): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.737+20169A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590784 | |||||||
| chr7:130590869 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.737+20084G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590869 | |||||||
| chr7:130590910 | GTCTGAGA others(33): Show |
G | 1 | a0003c0008t0001g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.737+20003_737+2004 others(44): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590910 | |||||||
| chr7:130590950 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(205): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.737+20003T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590950 | |||||||
| chr7:130590974 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.737+19979C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590974 | |||||||
| chr7:130590977 | C | T | 1 | a0001c0001t0002g0210 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.737+19976G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590977 | |||||||
| chr7:130591017 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.737+19936G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591017 | |||||||
| chr7:130591071 | C | T | 2 | a0001c0002t0001g0036 a0001c0002t0001g0037 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.737+19882G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591071 | |||||||
| chr7:130591091 | T | TG | 41 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(38): Show |
41 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.737+19861dupC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591091 | |||||||
| chr7:130591092 | G | C | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.737+19861C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591092 | |||||||
| chr7:130591109 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.737+19844C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591109 | |||||||
| chr7:130591120 | T | C | 40 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(37): Show |
40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19833A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591120 | |||||||
| chr7:130591123 | C | CCCGTCCG others(70): Show |
39 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(36): Show |
39 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.737+19829_737+1983 others(81): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591123 | |||||||
| chr7:130591132 | A | G | 40 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(37): Show |
40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19821T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591132 | |||||||
| chr7:130591134 | G | GGTGAGGG others(197): Show |
1 | a0001c0002t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.737+19818_737+1981 others(208): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591134 | |||||||
| chr7:130591140 | TG | T | 39 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(36): Show |
39 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.737+19812delC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591140 | |||||||
| chr7:130591143 | G | T | 1 | a0001c0001t0002g0219 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.737+19810C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591143 | |||||||
| chr7:130591147 | G | C | 39 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(36): Show |
39 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.737+19806C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591147 | |||||||
| chr7:130591159 | G | A | 1 | a0001c0002t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.737+19794C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591159 | |||||||
| chr7:130591163 | G | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+19790C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591163 | |||||||
| chr7:130591171 | G | A | 1 | a0001c0002t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.737+19782C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591171 | |||||||
| chr7:130591176 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.737+19777C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591176 | |||||||
| chr7:130591194 | G | A | 5 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(2): Show |
5 | HG00099.hp1 HG02572.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+19759C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591194 | |||||||
| chr7:130591211 | C | T | 1 | a0001c0002t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.737+19742G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591211 | |||||||
| chr7:130591223 | T | A | 1 | a0001c0002t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.737+19730A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591223 | |||||||
| chr7:130591228 | A | AG | 40 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(37): Show |
40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19724_737+1972 others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591228 | |||||||
| chr7:130591233 | T | TCTGCCCA others(498): Show |
1 | a0001c0002t0001g0102 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.737+19719_737+1972 others(509): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591233 | |||||||
| chr7:130591233 | T | TCTGCCCA others(498): Show |
1 | a0001c0002t0004g0103 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.737+19719_737+1972 others(509): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591233 | |||||||
| chr7:130591233 | T | TCTGCCCA others(496): Show |
3 | a0001c0002t0001g0093 a0001c0002t0001g0104 a0001c0002t0001g0105 |
3 | HG01884.hp1 HG04204.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.737+19719_737+1972 others(507): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591233 | |||||||
| chr7:130591233 | T | TCTGCCCA others(495): Show |
33 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(30): Show |
33 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.737+19719_737+1972 others(506): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591233 | |||||||
| chr7:130591235 | T | TGCCCAGC others(495): Show |
1 | a0001c0002t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.737+19717_737+1971 others(506): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591235 | |||||||
| chr7:130591239 | T | C | 40 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(37): Show |
40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19714A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591239 | |||||||
| chr7:130591247 | C | T | 1 | a0001c0002t0001g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.737+19706G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591247 | |||||||
| chr7:130591250 | T | C | 40 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(37): Show |
40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19703A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591250 | |||||||
| chr7:130591253 | G | A | 4 | a0001c0002t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0243 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+19700C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591253 | |||||||
| chr7:130591257 | G | A | 1 | a0001c0002t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.737+19696C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591257 | |||||||
| chr7:130591273 | C | G | 40 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(37): Show |
40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19680G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591273 | |||||||
| chr7:130591274 | G | A | 39 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(36): Show |
39 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.737+19679C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591274 | |||||||
| chr7:130591285 | G | A | 1 | a0001c0002t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.737+19668C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591285 | |||||||
| chr7:130591296 | C | T | 39 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(36): Show |
39 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.737+19657G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591296 | |||||||
| chr7:130591301 | C | CGTCCGGG others(371): Show |
1 | a0001c0002t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.737+19651_737+1965 others(382): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591301 | |||||||
| chr7:130591301 | C | T | 39 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(36): Show |
39 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.737+19652G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591301 | |||||||
| chr7:130591306 | G | A | 11 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0287 others(8): Show |
11 | HG02129.hp1 HG02155.hp1 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.737+19647C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591306 | |||||||
| chr7:130591319 | C | T | 40 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(37): Show |
40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19634G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591319 | |||||||
| chr7:130591367 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(245): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.737+19586T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591367 | |||||||
| chr7:130591369 | C | A | 40 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(37): Show |
40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19584G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591369 | |||||||
| chr7:130591383 | T | C | 40 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(37): Show |
40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19570A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591383 | |||||||
| chr7:130591387 | A | AAGGAGGT others(629): Show |
1 | a0001c0002t0003g0106 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(640): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(628): Show |
1 | a0001c0002t0003g0088 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(639): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(625): Show |
2 | a0001c0001t0004g0322 a0001c0002t0007g0239 |
2 | HG01192.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(624): Show |
1 | a0001c0002t0001g0055 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(626): Show |
1 | a0001c0001t0002g0207 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(637): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(623): Show |
1 | a0001c0001t0002g0204 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(634): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(625): Show |
1 | a0001c0001t0001g0310 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(624): Show |
2 | a0001c0001t0001g0131 a0001c0001t0001g0138 |
2 | HG02129.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(526): Show |
1 | a0001c0001t0001g0132 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(537): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(623): Show |
17 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0129 others(14): Show |
18 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.737+19565_737+1956 others(634): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(623): Show |
1 | a0001c0001t0004g0133 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(634): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(626): Show |
1 | a0001c0002t0001g0054 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(637): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(625): Show |
1 | a0001c0001t0002g0193 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(624): Show |
1 | a0001c0001t0004g0267 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(625): Show |
1 | a0001c0001t0006g0202 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(623): Show |
1 | a0001c0001t0002g0148 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(634): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(624): Show |
1 | a0001c0001t0002g0150 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(623): Show |
10 | a0001c0001t0002g0152 a0001c0001t0002g0162 a0001c0001t0002g0169 others(7): Show |
10 | HG00544.hp2 HG01192.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.737+19565_737+1956 others(634): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(397): Show |
1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(408): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(622): Show |
1 | a0001c0001t0002g0027 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(633): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(622): Show |
69 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(66): Show |
69 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.737+19565_737+1956 others(633): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(622): Show |
1 | a0001c0001t0002g0167 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(633): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(621): Show |
1 | a0001c0001t0002g0206 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(632): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(625): Show |
1 | a0001c0002t0003g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(626): Show |
1 | a0001c0002t0001g0056 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(637): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(625): Show |
1 | a0001c0001t0004g0245 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(625): Show |
1 | a0001c0001t0004g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(624): Show |
1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(625): Show |
1 | a0001c0002t0003g0123 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(624): Show |
1 | a0001c0002t0004g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(624): Show |
2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(625): Show |
3 | a0001c0002t0003g0111 a0001c0002t0003g0116 a0001c0002t0003g0120 |
3 | HG02148.hp1 NA19066.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(625): Show |
1 | a0001c0002t0001g0024 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(624): Show |
10 | a0001c0002t0003g0070 a0001c0002t0003g0081 a0001c0002t0003g0107 others(7): Show |
10 | HG00544.hp1 HG01952.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(624): Show |
21 | a0001c0001t0001g0017 a0001c0001t0001g0257 a0001c0001t0001g0271 others(18): Show |
21 | HG00140.hp1 HG01243.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(623): Show |
4 | a0001c0001t0001g0025 a0001c0002t0001g0128 a0001c0002t0003g0110 others(1): Show |
4 | HG00323.hp1 HG02809.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+19565_737+1956 others(634): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(623): Show |
1 | a0001c0001t0001g0309 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(634): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(624): Show |
1 | a0001c0001t0001g0297 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(622): Show |
2 | a0001c0001t0001g0302 a0001c0002t0001g0052 |
2 | HG00621.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.737+19565_737+1956 others(633): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(621): Show |
1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(632): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(571): Show |
4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+19565_737+1956 others(582): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(624): Show |
2 | a0001c0002t0003g0124 a0001c0002t0003g0125 |
2 | HG03490.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(624): Show |
2 | a0001c0005t0002g0011 a0001c0005t0002g0012 |
2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(625): Show |
1 | a0001c0001t0006g0215 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(397): Show |
1 | a0001c0001t0002g0260 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(408): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AAGGAGGT others(624): Show |
1 | a0001c0001t0002g0223 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591387 | A | AG | 40 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(37): Show |
40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19565dupC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | |||||||
| chr7:130591397 | G | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0314 |
2 | HG00639.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.737+19556C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591397 | |||||||
| chr7:130591411 | G | A | 1 | a0001c0002t0001g0038 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.737+19542C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591411 | |||||||
| chr7:130591414 | C | T | 1 | a0002c0003t0001g0242 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.737+19539G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591414 | |||||||
| chr7:130591416 | G | C | 20 | a0001c0002t0003g0070 a0001c0002t0003g0081 a0001c0002t0003g0088 others(17): Show |
20 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.737+19537C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591416 | |||||||
| chr7:130591430 | C | CA | 6 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0015 others(3): Show |
6 | HG01243.hp1 HG02258.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.737+19522_737+1952 others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591430 | |||||||
| chr7:130591453 | C | CCCCTGCC others(10): Show |
1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19499_737+1950 others(21): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591453 | |||||||
| chr7:130591454 | G | C | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19499C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591454 | |||||||
| chr7:130591462 | G | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0246 others(13): Show |
16 | HG01099.hp2 HG02055.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.737+19491C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591462 | |||||||
| chr7:130591476 | G | A | 1 | a0001c0002t0001g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.737+19477C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591476 | |||||||
| chr7:130591479 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19474C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591479 | |||||||
| chr7:130591485 | C | A | 1 | a0001c0012t0002g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.737+19468G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591485 | |||||||
| chr7:130591490 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.737+19463G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591490 | |||||||
| chr7:130591502 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19451G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591502 | |||||||
| chr7:130591503 | G | A | 2 | a0001c0002t0001g0092 a0001c0002t0001g0094 |
2 | NA18941.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.737+19450C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591503 | |||||||
| chr7:130591507 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19446G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591507 | |||||||
| chr7:130591508 | A | G | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19445T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591508 | |||||||
| chr7:130591511 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19442G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591511 | |||||||
| chr7:130591512 | G | A | 2 | a0001c0001t0001g0300 a0001c0001t0004g0286 |
2 | HG01496.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.737+19441C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591512 | |||||||
| chr7:130591573 | G | A | 1 | a0001c0002t0001g0059 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.737+19380C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591573 | |||||||
| chr7:130591575 | C | A | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19378G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591575 | |||||||
| chr7:130591579 | C | A | 10 | a0001c0002t0003g0081 a0001c0002t0003g0088 a0001c0002t0003g0111 others(7): Show |
10 | HG01261.hp2 HG01975.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.737+19374G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591579 | |||||||
| chr7:130591582 | C | T | 1 | a0001c0002t0001g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.737+19371G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591582 | |||||||
| chr7:130591585 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19368G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591585 | |||||||
| chr7:130591663 | G | A | 6 | a0001c0002t0003g0070 a0001c0002t0003g0106 a0001c0002t0003g0107 others(3): Show |
6 | HG00544.hp1 HG01952.hp2 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.737+19290C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591663 | |||||||
| chr7:130591711 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.737+19242G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591711 | |||||||
| chr7:130591730 | GGGGGTCA others(42): Show |
G | 1 | a0001c0001t0001g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.737+19174_737+1922 others(53): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591730 | |||||||
| chr7:130591731 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.737+19222C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591731 | |||||||
| chr7:130591813 | C | G | 10 | a0001c0002t0003g0081 a0001c0002t0003g0088 a0001c0002t0003g0111 others(7): Show |
10 | HG01261.hp2 HG01975.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.737+19140G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591813 | |||||||
| chr7:130591836 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(205): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.737+19117A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591836 | |||||||
| chr7:130592002 | G | A | 5 | a0001c0001t0002g0168 a0001c0001t0002g0204 a0001c0001t0002g0209 others(2): Show |
5 | HG01106.hp2 HG01192.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.737+18951C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130592002 | |||||||
| chr7:130592195 | T | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.737+18758A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130592195 | |||||||
| chr7:130592395 | C | CA | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(47): Show |
50 | HG00544.hp2 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.737+18557dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130592395 | |||||||
| chr7:130592454 | T | C | 2 | a0001c0002t0001g0047 a0001c0002t0001g0049 |
2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.737+18499A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130592454 | |||||||
| chr7:130592643 | C | T | 4 | a0001c0001t0001g0032 a0001c0002t0001g0052 a0001c0002t0001g0054 others(1): Show |
4 | HG00597.hp1 HG00621.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+18310G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130592643 | |||||||
| chr7:130592677 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.737+18276A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130592677 | |||||||
| chr7:130592763 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.737+18190C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130592763 | |||||||
| chr7:130592869 | C | T | 1 | a0001c0002t0001g0059 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.737+18084G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130592869 | |||||||
| chr7:130593157 | T | C | 1 | a0001c0002t0003g0124 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.737+17796A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130593157 | |||||||
| chr7:130593424 | T | C | 1 | a0001c0001t0002g0174 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.737+17529A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130593424 | |||||||
| chr7:130593728 | G | T | 1 | a0001c0001t0001g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.737+17225C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130593728 | |||||||
| chr7:130593764 | G | GA | 12 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0001g0135 others(9): Show |
12 | HG01891.hp1 HG01943.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.737+17188dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130593764 | |||||||
| chr7:130593764 | GA | G | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.737+17188delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130593764 | |||||||
| chr7:130593775 | T | A | 1 | a0001c0001t0001g0293 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.737+17178A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130593775 | |||||||
| chr7:130593870 | G | C | 1 | a0001c0001t0002g0169 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.737+17083C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130593870 | |||||||
| chr7:130594025 | CACATACA others(4): Show |
C | 1 | a0001c0002t0001g0126 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.737+16917_737+1692 others(15): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130594025 | |||||||
| chr7:130595733 | G | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+15220C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130595733 | |||||||
| chr7:130595803 | A | AC | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0137 others(54): Show |
57 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.737+15149dupG | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130595803 | |||||||
| chr7:130595803 | AC | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(54): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.737+15149delG | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130595803 | |||||||
| chr7:130595810 | C | G | 1 | a0001c0002t0001g0051 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.737+15143G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130595810 | |||||||
| chr7:130595811 | C | A | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.737+15142G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130595811 | |||||||
| chr7:130595811 | C | G | 1 | a0001c0001t0002g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.737+15142G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130595811 | |||||||
| chr7:130595870 | C | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(203): Show |
208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.737+15083G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130595870 | |||||||
| chr7:130596090 | T | TG | 4 | a0001c0002t0001g0052 a0001c0002t0001g0054 a0001c0002t0001g0055 others(1): Show |
4 | HG00597.hp1 HG00621.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+14862dupC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130596090 | |||||||
| chr7:130596105 | T | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.737+14848A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130596105 | |||||||
| chr7:130596210 | C | T | 2 | a0001c0005t0002g0011 a0001c0005t0002g0012 |
2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.737+14743G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130596210 | |||||||
| chr7:130596411 | T | C | 1 | a0001c0002t0001g0104 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.737+14542A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130596411 | |||||||
| chr7:130596522 | C | T | 1 | a0001c0001t0002g0026 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.737+14431G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130596522 | |||||||
| chr7:130596607 | G | C | 1 | a0005c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.737+14346C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130596607 | |||||||
| chr7:130596619 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.737+14334T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130596619 | |||||||
| chr7:130597032 | C | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+13921G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130597032 | |||||||
| chr7:130597111 | C | A | 1 | a0001c0001t0001g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.737+13842G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130597111 | |||||||
| chr7:130597114 | T | A | 1 | a0001c0001t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.737+13839A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130597114 | |||||||
| chr7:130597126 | C | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+13827G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130597126 | |||||||
| chr7:130597409 | C | G | 1 | a0001c0001t0001g0014 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.737+13544G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130597409 | |||||||
| chr7:130597513 | C | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.737+13440G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130597513 | |||||||
| chr7:130597947 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.737+13006C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130597947 | |||||||
| chr7:130598033 | G | A | 1 | a0001c0002t0001g0104 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.737+12920C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130598033 | |||||||
| chr7:130598106 | A | C | 1 | a0001c0001t0002g0158 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.737+12847T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130598106 | |||||||
| chr7:130598160 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.737+12793A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130598160 | |||||||
| chr7:130598241 | C | G | 1 | a0001c0002t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.737+12712G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130598241 | |||||||
| chr7:130598606 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.737+12347G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130598606 | |||||||
| chr7:130598865 | A | G | 1 | a0002c0003t0001g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.737+12088T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130598865 | |||||||
| chr7:130599047 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0144 |
3 | HG01069.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.737+11906G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599047 | |||||||
| chr7:130599320 | C | T | 3 | a0001c0002t0001g0060 a0001c0002t0001g0063 a0001c0002t0001g0064 |
3 | HG02280.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.737+11633G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599320 | |||||||
| chr7:130599434 | G | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.737+11519C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599434 | |||||||
| chr7:130599564 | C | T | 1 | a0001c0002t0007g0239 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.737+11389G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599564 | |||||||
| chr7:130599631 | T | A | 3 | a0001c0001t0002g0148 a0001c0001t0002g0163 a0001c0001t0002g0175 |
3 | HG00621.hp1 NA18954.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.737+11322A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599631 | |||||||
| chr7:130599684 | C | T | 13 | a0001c0001t0001g0246 a0001c0001t0001g0253 a0001c0001t0001g0254 others(10): Show |
13 | HG01099.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.737+11269G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599684 | |||||||
| chr7:130599797 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+11156G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599797 | |||||||
| chr7:130599839 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.737+11114C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599839 | |||||||
| chr7:130599953 | AT | A | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+10999delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599953 | |||||||
| chr7:130599960 | A | G | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+10993T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599960 | |||||||
| chr7:130600038 | A | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.737+10915T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600038 | |||||||
| chr7:130600078 | T | G | 1 | a0001c0001t0001g0302 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.737+10875A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600078 | |||||||
| chr7:130600217 | T | A | 1 | a0001c0001t0001g0132 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.737+10736A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600217 | |||||||
| chr7:130600284 | A | T | 4 | a0001c0001t0002g0148 a0001c0001t0002g0158 a0001c0001t0002g0163 others(1): Show |
4 | HG00438.hp2 HG00621.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+10669T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600284 | |||||||
| chr7:130600297 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.737+10656C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600297 | |||||||
| chr7:130600625 | C | T | 1 | a0001c0002t0001g0121 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.737+10328G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600625 | |||||||
| chr7:130600628 | G | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.737+10325C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600628 | |||||||
| chr7:130600776 | T | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.737+10177A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600776 | |||||||
| chr7:130600960 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.737+9993G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600960 | |||||||
| chr7:130601129 | G | A | 1 | a0001c0002t0003g0109 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.737+9824C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130601129 | |||||||
| chr7:130601283 | T | C | 1 | a0001c0002t0001g0039 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.737+9670A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130601283 | |||||||
| chr7:130601886 | AGAAG | A | 42 | a0001c0001t0001g0032 a0001c0002t0001g0004 a0001c0002t0001g0007 others(39): Show |
42 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.737+9063_737+9066d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130601886 | |||||||
| chr7:130601891 | GA | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.737+9061delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130601891 | |||||||
| chr7:130602037 | C | T | 1 | a0001c0002t0001g0105 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.737+8916G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602037 | |||||||
| chr7:130602038 | G | A | 1 | a0001c0002t0004g0082 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.737+8915C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602038 | |||||||
| chr7:130602228 | T | C | 1 | a0001c0002t0001g0068 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.737+8725A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602228 | |||||||
| chr7:130602330 | T | G | 42 | a0001c0001t0001g0273 a0001c0002t0001g0004 a0001c0002t0001g0007 others(39): Show |
42 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.737+8623A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602330 | |||||||
| chr7:130602357 | T | C | 1 | a0001c0002t0007g0237 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.737+8596A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602357 | |||||||
| chr7:130602417 | T | C | 6 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(3): Show |
6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.737+8536A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602417 | |||||||
| chr7:130602450 | T | C | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG00558.hp1 HG01934.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.737+8503A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602450 | |||||||
| chr7:130602693 | G | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0129 others(18): Show |
22 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.737+8260C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602693 | |||||||
| chr7:130602769 | G | A | 1 | a0001c0002t0003g0110 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.737+8184C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602769 | |||||||
| chr7:130602809 | G | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(7): Show |
10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.737+8144C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602809 | |||||||
| chr7:130602979 | A | T | 27 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(24): Show |
27 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.737+7974T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602979 | |||||||
| chr7:130603005 | T | C | 1 | a0001c0002t0001g0099 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.737+7948A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603005 | |||||||
| chr7:130603021 | T | C | 3 | a0001c0001t0001g0283 a0001c0001t0001g0300 a0001c0001t0004g0286 |
3 | HG01496.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.737+7932A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603021 | |||||||
| chr7:130603044 | C | T | 5 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(2): Show |
5 | HG01192.hp2 HG01993.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+7909G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603044 | |||||||
| chr7:130603105 | T | C | 3 | a0001c0001t0002g0151 a0001c0001t0002g0222 a0001c0002t0001g0057 |
3 | NA18964.hp2 NA19084.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.737+7848A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603105 | |||||||
| chr7:130603216 | C | T | 1 | a0001c0002t0001g0121 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.737+7737G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603216 | |||||||
| chr7:130603259 | G | T | 1 | a0001c0002t0001g0121 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.737+7694C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603259 | |||||||
| chr7:130603339 | A | G | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.737+7614T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603339 | |||||||
| chr7:130603375 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.737+7578A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603375 | |||||||
| chr7:130603589 | T | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+7364A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603589 | |||||||
| chr7:130603721 | C | CA | 99 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0275 others(96): Show |
99 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.737+7231dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603721 | |||||||
| chr7:130603721 | CA | C | 12 | a0001c0001t0001g0020 a0001c0001t0001g0073 a0001c0001t0001g0074 others(9): Show |
12 | HG01167.hp2 HG01168.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.737+7231delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603721 | |||||||
| chr7:130603721 | CAAAA | C | 9 | a0001c0001t0001g0274 a0001c0001t0001g0287 a0001c0001t0001g0288 others(6): Show |
9 | HG02129.hp1 HG02155.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.737+7228_737+7231d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603721 | |||||||
| chr7:130603746 | A | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0005t0002g0011 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+7207T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603746 | |||||||
| chr7:130603885 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.737+7068G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603885 | |||||||
| chr7:130604504 | G | A | 2 | a0001c0002t0001g0034 a0001c0002t0001g0035 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.737+6449C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130604504 | |||||||
| chr7:130604632 | G | A | 62 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(59): Show |
62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.737+6321C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130604632 | |||||||
| chr7:130604897 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.737+6056G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130604897 | |||||||
| chr7:130605175 | C | G | 1 | a0001c0001t0001g0287 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.737+5778G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130605175 | |||||||
| chr7:130605201 | T | A | 1 | a0001c0001t0001g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.737+5752A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130605201 | |||||||
| chr7:130605346 | A | G | 3 | a0001c0001t0001g0246 a0001c0001t0004g0245 a0001c0001t0004g0247 |
3 | HG01099.hp2 HG02886.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.737+5607T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130605346 | |||||||
| chr7:130605355 | G | A | 1 | a0001c0002t0001g0095 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.737+5598C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130605355 | |||||||
| chr7:130605605 | G | A | 2 | a0001c0001t0002g0159 a0001c0001t0002g0183 |
2 | NA18944.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.737+5348C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130605605 | |||||||
| chr7:130605937 | G | A | 1 | a0001c0002t0001g0104 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.737+5016C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130605937 | |||||||
| chr7:130606081 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(213): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.737+4872A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130606081 | |||||||
| chr7:130606240 | A | AAG | 68 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(65): Show |
69 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.737+4711_737+4712d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130606240 | |||||||
| chr7:130606240 | A | AAGAG | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.737+4709_737+4712d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130606240 | |||||||
| chr7:130606331 | A | T | 1 | a0001c0002t0001g0096 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.737+4622T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130606331 | |||||||
| chr7:130606429 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(215): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.737+4524A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130606429 | |||||||
| chr7:130606493 | G | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.737+4460C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130606493 | |||||||
| chr7:130606521 | T | C | 1 | a0001c0001t0002g0223 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.737+4432A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130606521 | |||||||
| chr7:130607129 | T | C | 4 | a0001c0002t0007g0236 a0001c0002t0007g0237 a0001c0002t0007g0238 others(1): Show |
4 | HG01192.hp2 HG01993.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+3824A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607129 | |||||||
| chr7:130607240 | C | CATAA | 24 | a0001c0001t0001g0025 a0001c0001t0001g0132 a0001c0001t0001g0208 others(21): Show |
24 | HG00621.hp1 HG01167.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.737+3709_737+3712d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607240 | |||||||
| chr7:130607240 | CATAA | C | 99 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(96): Show |
99 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.737+3709_737+3712d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607240 | |||||||
| chr7:130607240 | CATAAATA others(1): Show |
C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0032 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.737+3705_737+3712d others(10): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607240 | |||||||
| chr7:130607240 | CATAAATA others(5): Show |
C | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG00558.hp1 HG01934.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.737+3701_737+3712d others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607240 | |||||||
| chr7:130607339 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(213): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.737+3614A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607339 | |||||||
| chr7:130607380 | T | C | 3 | a0001c0001t0001g0283 a0001c0001t0001g0300 a0001c0001t0004g0286 |
3 | HG01496.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.737+3573A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607380 | |||||||
| chr7:130607660 | T | C | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.737+3293A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607660 | |||||||
| chr7:130607838 | G | C | 20 | a0001c0002t0003g0070 a0001c0002t0003g0081 a0001c0002t0003g0088 others(17): Show |
20 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.737+3115C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607838 | |||||||
| chr7:130607931 | C | T | 3 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0006g0215 |
3 | HG00639.hp1 HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.737+3022G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607931 | |||||||
| chr7:130607991 | G | A | 1 | a0001c0012t0002g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.737+2962C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607991 | |||||||
| chr7:130608005 | G | T | 7 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0002t0001g0093 others(4): Show |
7 | NA18941.hp1 NA18944.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.737+2948C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130608005 | |||||||
| chr7:130608100 | T | G | 2 | a0001c0001t0002g0227 a0001c0001t0006g0226 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.737+2853A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130608100 | |||||||
| chr7:130608121 | A | G | 1 | a0001c0001t0012g0201 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.737+2832T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130608121 | |||||||
| chr7:130608151 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.737+2802G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130608151 | |||||||
| chr7:130608426 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.737+2527G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130608426 | |||||||
| chr7:130608605 | G | C | 1 | a0001c0002t0001g0057 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.737+2348C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130608605 | |||||||
| chr7:130608718 | T | A | 3 | a0001c0002t0003g0123 a0001c0002t0003g0124 a0001c0002t0003g0125 |
3 | HG03490.hp2 HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.737+2235A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130608718 | |||||||
| chr7:130608920 | G | A | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG01167.hp1 HG02129.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.737+2033C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130608920 | |||||||
| chr7:130609333 | C | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.737+1620G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130609333 | |||||||
| chr7:130609477 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.737+1476A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130609477 | |||||||
| chr7:130609815 | G | T | 4 | a0001c0002t0001g0052 a0001c0002t0001g0054 a0001c0002t0001g0055 others(1): Show |
4 | HG00597.hp1 HG00621.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+1138C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130609815 | |||||||
| chr7:130610070 | C | G | 1 | a0001c0002t0001g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.737+883G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130610070 | |||||||
| chr7:130610119 | T | C | 1 | a0001c0002t0001g0030 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.737+834A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130610119 | |||||||
| chr7:130610451 | T | C | 10 | a0001c0002t0001g0241 a0001c0002t0007g0235 a0001c0002t0007g0236 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.737+502A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130610451 | |||||||
| chr7:130610654 | T | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(55): Show |
59 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.737+299A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130610654 | |||||||
| chr7:130610820 | T | A | 2 | a0001c0001t0001g0266 a0001c0001t0004g0267 |
2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.737+133A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130610820 | |||||||
| chr7:130610829 | G | A | 62 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(59): Show |
62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.737+124C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130610829 | |||||||
| chr7:130610900 | G | T | 6 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(3): Show |
6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.737+53C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130610900 | |||||||
| chr7:130611175 | T | C | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-65A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/23 | chr7 | 130611175 | |||||||
| chr7:130611385 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
55 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.580-275G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/23 | chr7 | 130611385 | |||||||
| chr7:130611432 | A | G | 12 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.580-322T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/23 | chr7 | 130611432 | |||||||
| chr7:130611612 | T | C | 1 | a0001c0001t0002g0210 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.580-502A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/23 | chr7 | 130611612 | |||||||
| chr7:130611657 | G | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0212 others(159): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.579+495C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/23 | chr7 | 130611657 | |||||||
| chr7:130611709 | A | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.579+443T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/23 | chr7 | 130611709 | |||||||
| chr7:130612078 | G | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(309): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.579+74C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/23 | chr7 | 130612078 | |||||||
| chr7:130612147 | A | C | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.579+5T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/23 | chr7 | 130612147 | |||||||
| chr7:130612248 | GA | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(213): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.493-11delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130612248 | |||||||
| chr7:130612360 | T | G | 5 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(2): Show |
5 | HG01192.hp2 HG01993.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-122A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130612360 | |||||||
| chr7:130612683 | C | T | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.493-445G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130612683 | |||||||
| chr7:130612725 | T | C | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.493-487A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130612725 | |||||||
| chr7:130612752 | T | C | 7 | a0001c0001t0005g0248 a0001c0001t0005g0250 a0001c0001t0005g0251 others(4): Show |
7 | HG02055.hp2 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.493-514A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130612752 | |||||||
| chr7:130613091 | A | T | 71 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.492+453T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130613091 | |||||||
| chr7:130613285 | G | A | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.492+259C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130613285 | |||||||
| chr7:130613390 | ACCCCTGC others(14): Show |
A | 10 | a0001c0002t0001g0241 a0001c0002t0007g0235 a0001c0002t0007g0236 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.492+133_492+153del others(21): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130613390 | |||||||
| chr7:130613484 | T | C | 3 | a0001c0002t0001g0060 a0001c0002t0001g0063 a0001c0002t0001g0064 |
3 | HG02280.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.492+60A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130613484 | |||||||
| chr7:130613538 | A | G | 1 | a0003c0008t0001g0117 | 1 | HG06807.hp1 | splice_region_variant&intron_variant | LOW | c.492+6T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130613538 | |||||||
| chr7:130613679 | C | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(213): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.400-43G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130613679 | |||||||
| chr7:130613811 | C | A | 6 | a0001c0001t0005g0250 a0001c0001t0005g0251 a0001c0001t0005g0255 others(3): Show |
6 | HG02055.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.400-175G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130613811 | |||||||
| chr7:130614738 | A | G | 1 | a0001c0001t0001g0282 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.400-1102T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130614738 | |||||||
| chr7:130614879 | G | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
55 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.400-1243C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130614879 | |||||||
| chr7:130615007 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.400-1371T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615007 | |||||||
| chr7:130615129 | T | C | 1 | a0001c0005t0002g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.400-1493A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615129 | |||||||
| chr7:130615321 | G | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.399+1669C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615321 | |||||||
| chr7:130615325 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(213): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.399+1665A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615325 | |||||||
| chr7:130615371 | G | T | 1 | a0001c0001t0004g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.399+1619C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615371 | |||||||
| chr7:130615399 | T | C | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.399+1591A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615399 | |||||||
| chr7:130615436 | T | C | 1 | a0001c0002t0001g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.399+1554A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615436 | |||||||
| chr7:130615495 | A | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(213): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.399+1495T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615495 | |||||||
| chr7:130615628 | A | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG01167.hp1 HG02129.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.399+1362T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615628 | |||||||
| chr7:130615651 | C | T | 1 | a0001c0001t0012g0201 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.399+1339G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615651 | |||||||
| chr7:130615933 | G | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.399+1057C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615933 | |||||||
| chr7:130615950 | T | A | 1 | a0001c0001t0002g0158 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.399+1040A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615950 | |||||||
| chr7:130615957 | T | A | 1 | a0001c0001t0002g0158 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.399+1033A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615957 | |||||||
| chr7:130616072 | T | C | 1 | a0001c0002t0001g0119 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.399+918A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616072 | |||||||
| chr7:130616194 | G | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(30): Show |
34 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.399+796C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616194 | |||||||
| chr7:130616221 | T | C | 2 | a0001c0001t0002g0162 a0005c0015t0001g0259 |
2 | HG02622.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.399+769A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616221 | |||||||
| chr7:130616278 | A | G | 6 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(3): Show |
6 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.399+712T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616278 | |||||||
| chr7:130616385 | A | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0129 others(18): Show |
22 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.399+605T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616385 | |||||||
| chr7:130616423 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.399+567G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616423 | |||||||
| chr7:130616584 | C | T | 3 | a0001c0002t0001g0021 a0001c0002t0001g0041 a0001c0002t0001g0042 |
3 | HG02004.hp1 HG03491.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.399+406G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616584 | |||||||
| chr7:130616635 | C | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.399+355G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616635 | |||||||
| chr7:130616778 | G | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0129 others(18): Show |
22 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.399+212C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616778 | |||||||
| chr7:130616805 | A | T | 1 | a0001c0002t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.399+185T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616805 | |||||||
| chr7:130617205 | T | C | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.324-140A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130617205 | |||||||
| chr7:130617216 | A | C | 14 | a0001c0002t0001g0040 a0001c0002t0001g0051 a0001c0002t0001g0052 others(11): Show |
14 | HG00597.hp1 HG00621.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.324-151T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130617216 | |||||||
| chr7:130617335 | C | T | 1 | a0001c0002t0001g0030 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.324-270G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130617335 | |||||||
| chr7:130617805 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.324-740A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130617805 | |||||||
| chr7:130617994 | G | C | 3 | a0001c0001t0001g0285 a0001c0001t0001g0311 a0001c0001t0001g0323 |
3 | HG00323.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.324-929C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130617994 | |||||||
| chr7:130618100 | C | CA | 12 | a0001c0002t0001g0058 a0001c0002t0001g0065 a0001c0002t0003g0081 others(9): Show |
12 | HG01975.hp1 HG01981.hp1 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.324-1036dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618100 | |||||||
| chr7:130618100 | C | CAAAAA | 51 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(48): Show |
52 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.324-1040_324-1036d others(7): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618100 | |||||||
| chr7:130618100 | C | CAAAAAA | 69 | a0001c0001t0001g0002 a0001c0001t0001g0132 a0001c0001t0001g0142 others(66): Show |
70 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.324-1041_324-1036d others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618100 | |||||||
| chr7:130618100 | C | CAAAAAAA | 72 | a0001c0001t0001g0005 a0001c0001t0001g0212 a0001c0001t0001g0281 others(69): Show |
72 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.324-1042_324-1036d others(9): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618100 | |||||||
| chr7:130618100 | C | CAAAAAAA others(1): Show |
23 | a0001c0001t0001g0032 a0001c0001t0001g0208 a0001c0001t0002g0027 others(20): Show |
23 | HG00140.hp2 HG00621.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.324-1043_324-1036d others(10): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618100 | |||||||
| chr7:130618100 | CA | C | 6 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0047 others(3): Show |
6 | HG02145.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-1036delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618100 | |||||||
| chr7:130618144 | CT | C | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.324-1080delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618144 | |||||||
| chr7:130618146 | T | C | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.324-1081A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618146 | |||||||
| chr7:130618221 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.324-1156C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618221 | |||||||
| chr7:130618343 | T | G | 1 | a0001c0001t0001g0287 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.324-1278A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618343 | |||||||
| chr7:130618503 | A | T | 1 | a0001c0001t0001g0287 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.324-1438T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618503 | |||||||
| chr7:130618522 | A | G | 1 | a0001c0002t0001g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.324-1457T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618522 | |||||||
| chr7:130619148 | G | C | 1 | a0001c0001t0006g0215 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.324-2083C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130619148 | |||||||
| chr7:130619228 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.324-2163A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130619228 | |||||||
| chr7:130619230 | T | C | 1 | a0001c0001t0001g0277 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.324-2165A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130619230 | |||||||
| chr7:130619472 | C | T | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.324-2407G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130619472 | |||||||
| chr7:130619624 | A | G | 3 | a0001c0001t0001g0283 a0001c0001t0001g0300 a0001c0001t0004g0286 |
3 | HG01496.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.324-2559T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130619624 | |||||||
| chr7:130619660 | C | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.324-2595G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130619660 | |||||||
| chr7:130619874 | T | C | 1 | a0001c0001t0005g0248 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324-2809A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130619874 | |||||||
| chr7:130619916 | T | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(3): Show |
6 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-2851A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130619916 | |||||||
| chr7:130620234 | A | C | 10 | a0001c0002t0001g0241 a0001c0002t0007g0235 a0001c0002t0007g0236 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.324-3169T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130620234 | |||||||
| chr7:130620363 | G | T | 3 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0038 |
3 | HG00099.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.324-3298C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130620363 | |||||||
| chr7:130620580 | A | G | 1 | a0001c0001t0005g0255 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-3515T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130620580 | |||||||
| chr7:130620608 | A | G | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.324-3543T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130620608 | |||||||
| chr7:130620765 | G | A | 1 | a0001c0002t0001g0065 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.324-3700C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130620765 | |||||||
| chr7:130621051 | C | T | 20 | a0001c0002t0003g0070 a0001c0002t0003g0081 a0001c0002t0003g0088 others(17): Show |
20 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.324-3986G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621051 | |||||||
| chr7:130621147 | G | A | 1 | a0001c0001t0002g0203 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.324-4082C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621147 | |||||||
| chr7:130621612 | C | T | 62 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(59): Show |
62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.324-4547G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621612 | |||||||
| chr7:130621745 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.324-4680G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621745 | |||||||
| chr7:130621845 | G | A | 1 | a0001c0002t0002g0089 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.324-4780C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621845 | |||||||
| chr7:130621942 | TC | T | 5 | a0001c0001t0002g0168 a0001c0001t0002g0204 a0001c0001t0002g0209 others(2): Show |
5 | HG01106.hp2 HG01192.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.324-4878delG | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621942 | |||||||
| chr7:130621943 | CA | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(59): Show |
63 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.324-4879delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621943 | |||||||
| chr7:130621943 | CAA | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(55): Show |
59 | HG01069.hp1 HG01070.hp1 HG01099.hp2 others(56): Show |
intron_variant | MODIFIER | c.324-4880_324-4879d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621943 | |||||||
| chr7:130621943 | CAAAAAAA others(4): Show |
C | 4 | a0001c0002t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0243 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-4889_324-4879d others(13): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621943 | |||||||
| chr7:130621944 | A | G | 5 | a0001c0001t0002g0168 a0001c0001t0002g0204 a0001c0001t0002g0209 others(2): Show |
5 | HG01106.hp2 HG01192.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.324-4879T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621944 | |||||||
| chr7:130622564 | C | T | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.324-5499G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130622564 | |||||||
| chr7:130622605 | G | A | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.324-5540C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130622605 | |||||||
| chr7:130623131 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
56 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.324-6066T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130623131 | |||||||
| chr7:130623504 | C | G | 22 | a0001c0002t0001g0128 a0001c0002t0003g0070 a0001c0002t0003g0081 others(19): Show |
22 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.324-6439G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130623504 | |||||||
| chr7:130623729 | C | T | 1 | a0001c0001t0002g0159 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.324-6664G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130623729 | |||||||
| chr7:130624165 | C | CCTT | 4 | a0001c0002t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0243 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-7101_324-7100i others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130624165 | |||||||
| chr7:130624168 | C | T | 4 | a0001c0002t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0243 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-7103G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130624168 | |||||||
| chr7:130624171 | A | T | 1 | a0001c0002t0003g0124 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.324-7106T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130624171 | |||||||
| chr7:130624177 | A | T | 6 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0002t0001g0093 others(3): Show |
6 | NA18941.hp1 NA18944.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-7112T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130624177 | |||||||
| chr7:130624346 | T | G | 10 | a0001c0002t0001g0241 a0001c0002t0007g0235 a0001c0002t0007g0236 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.324-7281A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130624346 | |||||||
| chr7:130625365 | A | C | 4 | a0001c0002t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0243 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-8300T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130625365 | |||||||
| chr7:130625672 | G | GT | 22 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
22 | HG01192.hp2 HG01243.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.324-8608dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130625672 | |||||||
| chr7:130625698 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.324-8633G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130625698 | |||||||
| chr7:130625755 | T | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.324-8690A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130625755 | |||||||
| chr7:130625953 | C | T | 1 | a0001c0001t0006g0170 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.324-8888G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130625953 | |||||||
| chr7:130625974 | T | C | 62 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(59): Show |
62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.324-8909A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130625974 | |||||||
| chr7:130626187 | T | C | 1 | a0001c0001t0001g0317 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.324-9122A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626187 | |||||||
| chr7:130626203 | A | G | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.324-9138T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626203 | |||||||
| chr7:130626252 | C | A | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.324-9187G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626252 | |||||||
| chr7:130626312 | C | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.324-9247G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626312 | |||||||
| chr7:130626354 | C | A | 3 | a0001c0002t0001g0021 a0001c0002t0001g0041 a0001c0002t0001g0042 |
3 | HG02004.hp1 HG03491.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.324-9289G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626354 | |||||||
| chr7:130626388 | C | T | 1 | a0001c0002t0003g0125 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.324-9323G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626388 | |||||||
| chr7:130626400 | AT | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
140 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.324-9336delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626400 | |||||||
| chr7:130626400 | ATT | A | 96 | a0001c0001t0001g0031 a0001c0001t0001g0134 a0001c0001t0001g0208 others(93): Show |
96 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.324-9337_324-9336d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626400 | |||||||
| chr7:130626400 | ATTT | A | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG02572.hp1 HG02735.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-9338_324-9336d others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626400 | |||||||
| chr7:130626421 | TC | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.324-9357delG | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626421 | |||||||
| chr7:130626515 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.324-9450G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626515 | |||||||
| chr7:130626580 | C | T | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.324-9515G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626580 | |||||||
| chr7:130626642 | G | C | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-9577C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626642 | |||||||
| chr7:130626946 | C | T | 3 | a0001c0002t0003g0123 a0001c0002t0003g0124 a0001c0002t0003g0125 |
3 | HG03490.hp2 HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.324-9881G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626946 | |||||||
| chr7:130627063 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.324-9998G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130627063 | |||||||
| chr7:130627083 | G | A | 1 | a0001c0001t0002g0192 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.324-10018C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130627083 | |||||||
| chr7:130627473 | A | T | 5 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0002t0001g0093 others(2): Show |
5 | NA18941.hp1 NA18944.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-10408T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130627473 | |||||||
| chr7:130627665 | C | T | 1 | a0001c0002t0001g0068 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.324-10600G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130627665 | |||||||
| chr7:130627941 | G | T | 1 | a0002c0003t0001g0242 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.324-10876C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130627941 | |||||||
| chr7:130628442 | T | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(3): Show |
6 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-11377A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130628442 | |||||||
| chr7:130628687 | A | G | 1 | a0001c0001t0002g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.324-11622T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130628687 | |||||||
| chr7:130628875 | T | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(278): Show |
283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.324-11810A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130628875 | |||||||
| chr7:130628935 | C | G | 2 | a0001c0001t0002g0210 a0001c0001t0002g0216 |
2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.324-11870G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130628935 | |||||||
| chr7:130629184 | T | G | 1 | a0001c0002t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.324-12119A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629184 | |||||||
| chr7:130629213 | T | A | 2 | a0001c0001t0002g0227 a0001c0001t0006g0226 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.324-12148A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629213 | |||||||
| chr7:130629229 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.324-12164G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629229 | |||||||
| chr7:130629231 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.324-12166C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629231 | |||||||
| chr7:130629283 | G | A | 4 | a0001c0001t0005g0250 a0001c0001t0005g0255 a0001c0001t0009g0252 others(1): Show |
4 | HG02055.hp2 HG02723.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.324-12218C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629283 | |||||||
| chr7:130629325 | G | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.324-12260C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629325 | |||||||
| chr7:130629399 | A | AT | 11 | a0001c0001t0001g0305 a0001c0001t0002g0194 a0001c0002t0001g0241 others(8): Show |
11 | HG01175.hp1 HG01192.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.324-12335dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629399 | |||||||
| chr7:130629399 | A | ATT | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.324-12336_324-1233 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629399 | |||||||
| chr7:130629459 | A | G | 4 | a0001c0001t0002g0159 a0001c0001t0002g0169 a0001c0001t0002g0183 others(1): Show |
4 | HG00544.hp2 HG00558.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.324-12394T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629459 | |||||||
| chr7:130629464 | G | A | 27 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(24): Show |
27 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.324-12399C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629464 | |||||||
| chr7:130629483 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.324-12418G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629483 | |||||||
| chr7:130630019 | G | A | 1 | a0005c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.324-12954C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630019 | |||||||
| chr7:130630052 | G | A | 2 | a0001c0002t0005g0078 a0001c0002t0005g0079 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.324-12987C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630052 | |||||||
| chr7:130630063 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.324-12998G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630063 | |||||||
| chr7:130630102 | G | A | 1 | a0001c0002t0001g0009 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.324-13037C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630102 | |||||||
| chr7:130630200 | C | T | 1 | a0001c0002t0001g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.324-13135G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630200 | |||||||
| chr7:130630207 | G | A | 10 | a0001c0002t0001g0241 a0001c0002t0007g0235 a0001c0002t0007g0236 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.324-13142C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630207 | |||||||
| chr7:130630420 | A | G | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.324-13355T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630420 | |||||||
| chr7:130630531 | A | C | 3 | a0001c0002t0001g0060 a0001c0002t0001g0063 a0001c0002t0001g0064 |
3 | HG02280.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.324-13466T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630531 | |||||||
| chr7:130630729 | T | A | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.324-13664A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630729 | |||||||
| chr7:130630820 | T | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.324-13755A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630820 | |||||||
| chr7:130631070 | G | A | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.324-14005C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631070 | |||||||
| chr7:130631078 | T | A | 1 | a0001c0002t0001g0105 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.324-14013A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631078 | |||||||
| chr7:130631081 | A | T | 1 | a0001c0002t0001g0055 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.324-14016T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631081 | |||||||
| chr7:130631089 | A | G | 4 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0047 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-14024T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631089 | |||||||
| chr7:130631172 | C | CT | 61 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(58): Show |
61 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.324-14108dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631172 | |||||||
| chr7:130631172 | CT | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.324-14108delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631172 | |||||||
| chr7:130631193 | ATGGAGAC others(18): Show |
A | 2 | a0001c0001t0002g0159 a0001c0001t0002g0183 |
2 | NA18944.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.324-14153_324-1412 others(29): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631193 | |||||||
| chr7:130631282 | C | T | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-14217G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631282 | |||||||
| chr7:130631484 | C | A | 8 | a0001c0002t0001g0021 a0001c0002t0001g0030 a0001c0002t0001g0036 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.324-14419G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631484 | |||||||
| chr7:130631513 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.324-14448A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631513 | |||||||
| chr7:130631573 | GT | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0129 others(17): Show |
21 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.324-14509delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631573 | |||||||
| chr7:130631744 | T | TAAGA | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(214): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.324-14680_324-1467 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631744 | |||||||
| chr7:130632557 | T | C | 1 | a0001c0001t0002g0199 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.324-15492A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130632557 | |||||||
| chr7:130632633 | T | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.324-15568A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130632633 | |||||||
| chr7:130632788 | G | A | 1 | a0005c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.324-15723C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130632788 | |||||||
| chr7:130632826 | C | T | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(310): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.324-15761G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130632826 | |||||||
| chr7:130632901 | C | A | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.324-15836G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130632901 | |||||||
| chr7:130633048 | T | G | 2 | a0001c0002t0001g0034 a0001c0002t0001g0035 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.324-15983A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633048 | |||||||
| chr7:130633149 | G | C | 10 | a0001c0002t0001g0241 a0001c0002t0007g0235 a0001c0002t0007g0236 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.324-16084C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633149 | |||||||
| chr7:130633266 | G | A | 20 | a0001c0002t0003g0070 a0001c0002t0003g0081 a0001c0002t0003g0088 others(17): Show |
20 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.324-16201C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633266 | |||||||
| chr7:130633431 | G | A | 3 | a0001c0002t0001g0060 a0001c0002t0001g0063 a0001c0002t0001g0064 |
3 | HG02280.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.324-16366C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633431 | |||||||
| chr7:130633516 | T | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(3): Show |
6 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-16451A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633516 | |||||||
| chr7:130633571 | G | A | 3 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 |
3 | HG01099.hp1 HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.324-16506C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633571 | |||||||
| chr7:130633624 | T | C | 1 | a0001c0001t0002g0232 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.324-16559A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633624 | |||||||
| chr7:130633727 | G | C | 1 | a0001c0001t0002g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.324-16662C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633727 | |||||||
| chr7:130633821 | G | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(3): Show |
6 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-16756C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633821 | |||||||
| chr7:130633967 | T | G | 3 | a0001c0001t0001g0246 a0001c0001t0004g0245 a0001c0001t0004g0247 |
3 | HG01099.hp2 HG02886.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.324-16902A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633967 | |||||||
| chr7:130634069 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.324-17004C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634069 | |||||||
| chr7:130634103 | C | T | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.324-17038G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634103 | |||||||
| chr7:130634104 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.324-17039C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634104 | |||||||
| chr7:130634105 | C | T | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-17040G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634105 | |||||||
| chr7:130634107 | G | A | 1 | a0001c0002t0001g0051 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.324-17042C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634107 | |||||||
| chr7:130634214 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.324-17149C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634214 | |||||||
| chr7:130634316 | T | C | 1 | a0001c0012t0002g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.324-17251A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634316 | |||||||
| chr7:130634613 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.324-17548C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634613 | |||||||
| chr7:130634664 | G | C | 1 | a0001c0002t0001g0086 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.324-17599C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634664 | |||||||
| chr7:130634780 | C | G | 5 | a0001c0001t0002g0168 a0001c0001t0002g0204 a0001c0001t0002g0209 others(2): Show |
5 | HG01106.hp2 HG01192.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.324-17715G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634780 | |||||||
| chr7:130635267 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(214): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.323+17602C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130635267 | |||||||
| chr7:130635298 | T | C | 1 | a0001c0002t0001g0004 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.323+17571A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130635298 | |||||||
| chr7:130635464 | T | C | 9 | a0001c0001t0002g0152 a0001c0001t0002g0155 a0001c0001t0002g0160 others(6): Show |
9 | HG02015.hp2 HG02523.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+17405A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130635464 | |||||||
| chr7:130635539 | G | GT | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+17329dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130635539 | |||||||
| chr7:130635653 | A | C | 9 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 others(6): Show |
9 | HG01167.hp2 HG01168.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+17216T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130635653 | |||||||
| chr7:130636043 | T | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0212 others(159): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.323+16826A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636043 | |||||||
| chr7:130636103 | G | A | 1 | a0001c0002t0004g0084 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.323+16766C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636103 | |||||||
| chr7:130636131 | A | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(216): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.323+16738T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636131 | |||||||
| chr7:130636152 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(214): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.323+16717A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636152 | |||||||
| chr7:130636325 | T | C | 1 | a0001c0002t0001g0049 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.323+16544A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636325 | |||||||
| chr7:130636508 | C | G | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG00558.hp1 HG01934.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.323+16361G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636508 | |||||||
| chr7:130636538 | G | GT | 7 | a0001c0002t0001g0022 a0001c0002t0001g0039 a0001c0002t0001g0045 others(4): Show |
7 | HG00597.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.323+16330dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636538 | |||||||
| chr7:130636538 | G | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.323+16331C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636538 | |||||||
| chr7:130636538 | GT | G | 71 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0032 others(68): Show |
71 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.323+16330delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636538 | |||||||
| chr7:130636538 | GTT | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(36): Show |
40 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.323+16329_323+1633 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636538 | |||||||
| chr7:130636538 | GTTT | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0212 a0001c0001t0001g0266 others(136): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.323+16328_323+1633 others(7): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636538 | |||||||
| chr7:130636626 | G | A | 1 | a0001c0001t0002g0187 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.323+16243C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636626 | |||||||
| chr7:130636705 | G | T | 1 | a0001c0001t0001g0277 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.323+16164C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636705 | |||||||
| chr7:130636890 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
56 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.323+15979A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636890 | |||||||
| chr7:130637023 | TTTTC | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(2): Show |
6 | NA18945.hp2 NA18963.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.323+15842_323+1584 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637023 | |||||||
| chr7:130637129 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.323+15740C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637129 | |||||||
| chr7:130637217 | C | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.323+15652G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637217 | |||||||
| chr7:130637310 | A | C | 1 | a0001c0002t0001g0068 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.323+15559T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637310 | |||||||
| chr7:130637405 | G | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0212 others(159): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.323+15464C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637405 | |||||||
| chr7:130637577 | G | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+15292C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637577 | |||||||
| chr7:130637628 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.323+15241G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637628 | |||||||
| chr7:130637691 | T | A | 1 | a0001c0002t0001g0121 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.323+15178A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637691 | |||||||
| chr7:130637985 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.323+14884C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637985 | |||||||
| chr7:130637994 | C | T | 1 | a0003c0008t0001g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.323+14875G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637994 | |||||||
| chr7:130638072 | T | C | 12 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.323+14797A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638072 | |||||||
| chr7:130638081 | G | C | 1 | a0001c0001t0002g0187 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.323+14788C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638081 | |||||||
| chr7:130638273 | CT | C | 10 | a0001c0002t0001g0241 a0001c0002t0007g0235 a0001c0002t0007g0236 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.323+14595delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638273 | |||||||
| chr7:130638295 | A | C | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.323+14574T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638295 | |||||||
| chr7:130638329 | G | A | 1 | a0001c0001t0002g0213 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.323+14540C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638329 | |||||||
| chr7:130638488 | G | A | 1 | a0001c0001t0001g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.323+14381C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638488 | |||||||
| chr7:130638711 | TCAGCCCC others(5): Show |
T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(55): Show |
59 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.323+14146_323+1415 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638711 | |||||||
| chr7:130638747 | C | T | 1 | a0001c0002t0007g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.323+14122G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638747 | |||||||
| chr7:130638803 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.323+14066C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638803 | |||||||
| chr7:130638862 | G | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+14007C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638862 | |||||||
| chr7:130639042 | A | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(216): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.323+13827T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130639042 | |||||||
| chr7:130639102 | T | C | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.323+13767A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130639102 | |||||||
| chr7:130639428 | C | G | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.323+13441G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130639428 | |||||||
| chr7:130639984 | C | G | 7 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0002t0001g0093 others(4): Show |
7 | NA18941.hp1 NA18944.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.323+12885G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130639984 | |||||||
| chr7:130640131 | G | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0212 others(159): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.323+12738C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640131 | |||||||
| chr7:130640158 | C | CT | 116 | a0001c0001t0001g0001 a0001c0001t0001g0134 a0001c0001t0001g0144 others(113): Show |
117 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.323+12710dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640158 | |||||||
| chr7:130640158 | C | CTT | 8 | a0001c0001t0002g0157 a0001c0001t0002g0191 a0001c0001t0002g0205 others(5): Show |
8 | HG00621.hp2 HG01952.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+12709_323+1271 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640158 | |||||||
| chr7:130640158 | CTT | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(54): Show |
58 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.323+12709_323+1271 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640158 | |||||||
| chr7:130640335 | T | C | 1 | a0001c0002t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.323+12534A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640335 | |||||||
| chr7:130640464 | T | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(55): Show |
59 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.323+12405A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640464 | |||||||
| chr7:130640580 | T | C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0246 others(12): Show |
15 | HG01099.hp2 HG02055.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.323+12289A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640580 | |||||||
| chr7:130640726 | G | T | 1 | a0001c0002t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.323+12143C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640726 | |||||||
| chr7:130640900 | A | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0310 |
4 | NA18945.hp2 NA18963.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+11969T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640900 | |||||||
| chr7:130640979 | T | C | 1 | a0001c0002t0001g0059 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.323+11890A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640979 | |||||||
| chr7:130640983 | C | G | 71 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.323+11886G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640983 | |||||||
| chr7:130641067 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.323+11802A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641067 | |||||||
| chr7:130641175 | C | CA | 88 | a0001c0001t0001g0032 a0001c0001t0001g0208 a0001c0001t0001g0212 others(85): Show |
88 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.323+11693dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641175 | |||||||
| chr7:130641175 | CA | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0025 others(61): Show |
65 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.323+11693delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641175 | |||||||
| chr7:130641402 | C | T | 40 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(37): Show |
40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.323+11467G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641402 | |||||||
| chr7:130641574 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.323+11295A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641574 | |||||||
| chr7:130641620 | T | C | 1 | a0001c0002t0007g0239 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.323+11249A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641620 | |||||||
| chr7:130641736 | G | A | 1 | a0001c0002t0007g0237 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.323+11133C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641736 | |||||||
| chr7:130641907 | C | T | 1 | a0001c0012t0002g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.323+10962G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641907 | |||||||
| chr7:130641968 | G | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(215): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.323+10901C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641968 | |||||||
| chr7:130642138 | T | G | 4 | a0001c0002t0003g0114 a0001c0002t0003g0115 a0001c0002t0003g0116 others(1): Show |
4 | NA19010.hp1 NA19066.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+10731A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130642138 | |||||||
| chr7:130642245 | C | CT | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(318): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.323+10623dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130642245 | |||||||
| chr7:130642571 | T | C | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.323+10298A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130642571 | |||||||
| chr7:130642676 | C | T | 90 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(87): Show |
90 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.323+10193G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130642676 | |||||||
| chr7:130642689 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
56 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.323+10180C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130642689 | |||||||
| chr7:130642699 | C | A | 1 | a0001c0002t0003g0120 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.323+10170G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130642699 | |||||||
| chr7:130642794 | G | A | 2 | a0001c0001t0001g0308 a0001c0001t0001g0318 |
2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.323+10075C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130642794 | |||||||
| chr7:130642967 | T | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
56 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.323+9902A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130642967 | |||||||
| chr7:130643067 | C | T | 2 | a0001c0002t0001g0126 a0001c0002t0001g0127 |
2 | HG01106.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.323+9802G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643067 | |||||||
| chr7:130643251 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.323+9618G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643251 | |||||||
| chr7:130643259 | C | T | 1 | a0001c0002t0003g0088 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.323+9610G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643259 | |||||||
| chr7:130643274 | G | C | 10 | a0001c0002t0001g0241 a0001c0002t0007g0235 a0001c0002t0007g0236 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.323+9595C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643274 | |||||||
| chr7:130643281 | C | T | 2 | a0001c0002t0005g0078 a0001c0002t0005g0079 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.323+9588G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643281 | |||||||
| chr7:130643294 | C | CA | 21 | a0001c0001t0001g0131 a0001c0001t0001g0143 a0001c0001t0001g0273 others(18): Show |
21 | HG00558.hp2 HG00639.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.323+9574dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643294 | |||||||
| chr7:130643425 | T | C | 1 | a0001c0001t0005g0248 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.323+9444A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643425 | |||||||
| chr7:130643554 | C | T | 1 | a0001c0002t0001g0066 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.323+9315G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643554 | |||||||
| chr7:130643623 | G | T | 1 | a0001c0001t0004g0306 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.323+9246C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643623 | |||||||
| chr7:130643816 | C | G | 10 | a0001c0002t0001g0241 a0001c0002t0007g0235 a0001c0002t0007g0236 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.323+9053G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643816 | |||||||
| chr7:130644044 | G | A | 1 | a0001c0001t0002g0189 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.323+8825C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644044 | |||||||
| chr7:130644141 | TAAAACAA | T | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.323+8721_323+8727d others(9): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644141 | |||||||
| chr7:130644180 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.323+8689C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644180 | |||||||
| chr7:130644446 | C | T | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG00558.hp1 HG01934.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.323+8423G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644446 | |||||||
| chr7:130644452 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.323+8417T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644452 | |||||||
| chr7:130644455 | T | C | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.323+8414A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644455 | |||||||
| chr7:130644524 | T | A | 1 | a0001c0001t0001g0321 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.323+8345A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644524 | |||||||
| chr7:130644621 | T | C | 1 | a0001c0002t0001g0118 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.323+8248A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644621 | |||||||
| chr7:130644659 | T | C | 1 | a0001c0002t0001g0119 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.323+8210A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644659 | |||||||
| chr7:130644828 | G | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+8041C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644828 | |||||||
| chr7:130644835 | G | A | 1 | a0001c0001t0002g0026 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.323+8034C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644835 | |||||||
| chr7:130644860 | G | A | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.323+8009C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644860 | |||||||
| chr7:130645037 | G | C | 10 | a0001c0002t0001g0241 a0001c0002t0007g0235 a0001c0002t0007g0236 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.323+7832C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645037 | |||||||
| chr7:130645062 | C | G | 1 | a0001c0001t0002g0162 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.323+7807G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645062 | |||||||
| chr7:130645068 | CA | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(184): Show |
189 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.323+7800delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645068 | |||||||
| chr7:130645298 | A | G | 1 | a0001c0005t0002g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.323+7571T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645298 | |||||||
| chr7:130645300 | G | A | 1 | a0001c0002t0001g0127 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.323+7569C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645300 | |||||||
| chr7:130645445 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
56 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.323+7424A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645445 | |||||||
| chr7:130645454 | C | T | 32 | a0001c0002t0001g0021 a0001c0002t0001g0030 a0001c0002t0001g0034 others(29): Show |
32 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.323+7415G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645454 | |||||||
| chr7:130645472 | C | T | 1 | a0001c0012t0002g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.323+7397G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645472 | |||||||
| chr7:130645534 | C | T | 3 | a0001c0002t0007g0236 a0001c0002t0007g0237 a0001c0002t0007g0238 |
3 | HG01993.hp1 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.323+7335G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645534 | |||||||
| chr7:130645586 | C | A | 1 | a0001c0002t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.323+7283G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645586 | |||||||
| chr7:130645623 | G | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+7246C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645623 | |||||||
| chr7:130645679 | A | C | 5 | a0001c0002t0001g0083 a0001c0002t0001g0085 a0001c0002t0001g0086 others(2): Show |
5 | NA18947.hp1 NA18955.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.323+7190T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645679 | |||||||
| chr7:130645747 | G | GAC | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(214): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.323+7120_323+7121d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645747 | |||||||
| chr7:130645888 | C | A | 62 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(59): Show |
62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.323+6981G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645888 | |||||||
| chr7:130646056 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.323+6813A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646056 | |||||||
| chr7:130646117 | A | T | 2 | a0001c0001t0001g0273 a0004c0011t0001g0276 |
2 | HG00099.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.323+6752T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646117 | |||||||
| chr7:130646197 | C | T | 1 | a0001c0002t0004g0082 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.323+6672G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646197 | |||||||
| chr7:130646218 | T | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.323+6651A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646218 | |||||||
| chr7:130646263 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.323+6606C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646263 | |||||||
| chr7:130646466 | AT | A | 10 | a0001c0002t0001g0241 a0001c0002t0007g0235 a0001c0002t0007g0236 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.323+6402delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646466 | |||||||
| chr7:130646467 | T | C | 1 | a0001c0001t0002g0223 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.323+6402A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646467 | |||||||
| chr7:130646471 | T | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+6398A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646471 | |||||||
| chr7:130646532 | C | T | 22 | a0001c0002t0001g0021 a0001c0002t0001g0030 a0001c0002t0001g0036 others(19): Show |
22 | HG00597.hp1 HG00621.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.323+6337G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646532 | |||||||
| chr7:130646623 | G | A | 1 | a0010c0009t0002g0217 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.323+6246C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646623 | |||||||
| chr7:130646749 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.323+6120C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646749 | |||||||
| chr7:130646813 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.323+6056G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646813 | |||||||
| chr7:130646828 | G | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0144 |
3 | HG01069.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.323+6041C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646828 | |||||||
| chr7:130646859 | G | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0230 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.323+6010C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646859 | |||||||
| chr7:130646865 | G | A | 90 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(87): Show |
90 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.323+6004C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646865 | |||||||
| chr7:130646921 | TTG | T | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.323+5946_323+5947d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646921 | |||||||
| chr7:130646943 | G | A | 3 | a0001c0001t0005g0251 a0001c0001t0005g0258 a0001c0002t0001g0065 |
3 | HG02630.hp2 HG02647.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.323+5926C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646943 | |||||||
| chr7:130646943 | GTA | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
54 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.323+5924_323+5925d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646943 | |||||||
| chr7:130646944 | T | C | 2 | a0001c0001t0005g0251 a0001c0001t0005g0258 |
2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.323+5925A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646944 | |||||||
| chr7:130646958 | CAT | C | 88 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(85): Show |
88 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.323+5909_323+5910d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646958 | |||||||
| chr7:130646958 | CATATATA others(21): Show |
C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(148): Show |
152 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.323+5883_323+5910d others(30): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646958 | |||||||
| chr7:130646958 | CATATATA others(23): Show |
C | 71 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.323+5881_323+5910d others(32): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646958 | |||||||
| chr7:130646967 | A | G | 3 | a0001c0001t0002g0151 a0001c0001t0002g0160 a0001c0001t0002g0222 |
3 | HG02015.hp2 NA18964.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.323+5902T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646967 | |||||||
| chr7:130646971 | G | A | 3 | a0001c0001t0002g0151 a0001c0001t0002g0160 a0001c0001t0002g0222 |
3 | HG02015.hp2 NA18964.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.323+5898C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646971 | |||||||
| chr7:130646973 | A | G | 2 | a0001c0001t0001g0253 a0001c0001t0001g0257 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.323+5896T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646973 | |||||||
| chr7:130646973 | ATATATAT others(19): Show |
A | 88 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(85): Show |
88 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.323+5870_323+5895d others(28): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646973 | |||||||
| chr7:130646983 | GTATATAT others(5): Show |
G | 1 | a0001c0001t0002g0222 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.323+5874_323+5885d others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646983 | |||||||
| chr7:130646983 | GTATATAT others(23): Show |
G | 4 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0047 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.323+5856_323+5885d others(32): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646983 | |||||||
| chr7:130646984 | T | C | 2 | a0001c0001t0001g0253 a0001c0001t0001g0257 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.323+5885A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646984 | |||||||
| chr7:130646986 | T | TATATATA others(5): Show |
1 | a0005c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.323+5882_323+5883i others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646986 | |||||||
| chr7:130646998 | T | C | 1 | a0005c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.323+5871A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646998 | |||||||
| chr7:130646999 | G | A | 1 | a0001c0001t0002g0222 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.323+5870C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646999 | |||||||
| chr7:130647001 | A | ATATATAT others(19): Show |
2 | a0001c0001t0001g0253 a0001c0001t0001g0257 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.323+5867_323+5868i others(28): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647001 | |||||||
| chr7:130647001 | A | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0246 others(11): Show |
14 | HG01099.hp2 HG02055.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.323+5868T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647001 | |||||||
| chr7:130647003 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0002g0160 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.323+5842_323+5865d others(26): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647003 | |||||||
| chr7:130647012 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.323+5857A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647012 | |||||||
| chr7:130647013 | A | G | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0002g0203 |
3 | HG02486.hp2 HG02717.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.323+5856T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647013 | |||||||
| chr7:130647023 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.323+5846T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647023 | |||||||
| chr7:130647029 | A | G | 1 | a0001c0002t0001g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.323+5840T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647029 | |||||||
| chr7:130647035 | A | T | 1 | a0001c0001t0002g0160 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.323+5834T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647035 | |||||||
| chr7:130647039 | T | A | 1 | a0001c0002t0001g0066 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.323+5830A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647039 | |||||||
| chr7:130647226 | G | C | 6 | a0001c0001t0005g0250 a0001c0001t0005g0251 a0001c0001t0005g0255 others(3): Show |
6 | HG02055.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.323+5643C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647226 | |||||||
| chr7:130647278 | C | T | 1 | a0001c0002t0007g0237 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.323+5591G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647278 | |||||||
| chr7:130647436 | C | G | 10 | a0001c0002t0001g0241 a0001c0002t0007g0235 a0001c0002t0007g0236 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.323+5433G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647436 | |||||||
| chr7:130647712 | A | G | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.323+5157T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647712 | |||||||
| chr7:130647730 | A | AT | 12 | a0001c0001t0001g0017 a0001c0001t0001g0032 a0001c0001t0001g0073 others(9): Show |
12 | HG00438.hp2 HG01243.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.323+5138dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647730 | |||||||
| chr7:130647730 | AT | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(59): Show |
63 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.323+5138delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647730 | |||||||
| chr7:130647747 | T | C | 2 | a0001c0002t0001g0033 a0001c0002t0001g0067 |
2 | HG03486.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.323+5122A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647747 | |||||||
| chr7:130647749 | G | C | 1 | a0001c0001t0001g0305 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.323+5120C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647749 | |||||||
| chr7:130647844 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.323+5025G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647844 | |||||||
| chr7:130647888 | G | A | 1 | a0001c0001t0002g0231 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.323+4981C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647888 | |||||||
| chr7:130647892 | A | G | 1 | a0001c0002t0001g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.323+4977T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647892 | |||||||
| chr7:130647951 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.323+4918G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647951 | |||||||
| chr7:130647966 | A | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+4903T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647966 | |||||||
| chr7:130647980 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.323+4889A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647980 | |||||||
| chr7:130647990 | A | C | 1 | a0001c0002t0001g0043 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.323+4879T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647990 | |||||||
| chr7:130648015 | C | A | 1 | a0001c0001t0002g0219 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.323+4854G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130648015 | |||||||
| chr7:130648396 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.323+4473G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130648396 | |||||||
| chr7:130649267 | T | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.323+3602A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649267 | |||||||
| chr7:130649368 | C | T | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.323+3501G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649368 | |||||||
| chr7:130649376 | C | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(214): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.323+3493G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649376 | |||||||
| chr7:130649525 | T | C | 1 | a0001c0001t0001g0324 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.323+3344A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649525 | |||||||
| chr7:130649535 | A | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(278): Show |
283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.323+3334T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649535 | |||||||
| chr7:130649727 | T | C | 1 | a0001c0001t0004g0306 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.323+3142A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649727 | |||||||
| chr7:130649799 | C | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0246 others(13): Show |
16 | HG01099.hp2 HG02055.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.323+3070G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649799 | |||||||
| chr7:130649951 | A | C | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.323+2918T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649951 | |||||||
| chr7:130649969 | T | G | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(278): Show |
283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.323+2900A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649969 | |||||||
| chr7:130650593 | C | T | 6 | a0001c0001t0002g0150 a0001c0001t0002g0197 a0001c0001t0002g0198 others(3): Show |
6 | HG01175.hp2 HG01515.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.323+2276G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130650593 | |||||||
| chr7:130650695 | C | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+2174G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130650695 | |||||||
| chr7:130650718 | A | T | 62 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(59): Show |
62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.323+2151T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130650718 | |||||||
| chr7:130650730 | G | A | 10 | a0001c0002t0001g0241 a0001c0002t0007g0235 a0001c0002t0007g0236 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.323+2139C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130650730 | |||||||
| chr7:130651059 | G | T | 1 | a0001c0001t0002g0196 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.323+1810C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651059 | |||||||
| chr7:130651184 | T | C | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.323+1685A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651184 | |||||||
| chr7:130651201 | T | C | 1 | a0001c0001t0002g0193 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.323+1668A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651201 | |||||||
| chr7:130651322 | G | GT | 68 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0262 others(65): Show |
69 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.323+1546dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651322 | |||||||
| chr7:130651379 | C | T | 1 | a0001c0002t0001g0024 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.323+1490G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651379 | |||||||
| chr7:130651393 | C | T | 2 | a0001c0001t0002g0157 a0001c0001t0002g0232 |
2 | HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.323+1476G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651393 | |||||||
| chr7:130651413 | C | T | 3 | a0001c0002t0001g0030 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG01070.hp2 HG01071.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.323+1456G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651413 | |||||||
| chr7:130651428 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.323+1441G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651428 | |||||||
| chr7:130651494 | A | AT | 13 | a0001c0002t0001g0034 a0001c0002t0001g0036 a0001c0002t0001g0037 others(10): Show |
13 | HG00099.hp1 HG00621.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.323+1374dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | |||||||
| chr7:130651494 | ATT | A | 24 | a0001c0001t0001g0208 a0001c0001t0002g0150 a0001c0001t0002g0152 others(21): Show |
24 | HG00544.hp2 HG01175.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.323+1373_323+1374d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | |||||||
| chr7:130651494 | ATTT | A | 71 | a0001c0001t0001g0212 a0001c0001t0002g0026 a0001c0001t0002g0028 others(68): Show |
71 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.323+1372_323+1374d others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | |||||||
| chr7:130651494 | ATTTT | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0129 a0001c0001t0001g0263 others(9): Show |
12 | HG00558.hp2 HG01168.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.323+1371_323+1374d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | |||||||
| chr7:130651494 | ATTTTT | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(38): Show |
41 | HG01175.hp1 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.323+1370_323+1374d others(7): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | |||||||
| chr7:130651494 | ATTTTTT | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0137 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.323+1369_323+1374d others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | |||||||
| chr7:130651494 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0254 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.323+1365_323+1374d others(12): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | |||||||
| chr7:130651494 | ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0002g0233 a0001c0001t0002g0234 |
2 | HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.323+1364_323+1374d others(13): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | |||||||
| chr7:130651494 | ATTTTTTT others(5): Show |
A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0144 a0001c0001t0002g0196 others(2): Show |
6 | HG01069.hp1 HG01515.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.323+1363_323+1374d others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | |||||||
| chr7:130651494 | ATTTTTTT others(6): Show |
A | 60 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0008 others(57): Show |
60 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.323+1362_323+1374d others(15): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | |||||||
| chr7:130651494 | ATTTTTTT others(7): Show |
A | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0002t0001g0092 |
3 | HG02486.hp2 HG02717.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.323+1361_323+1374d others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | |||||||
| chr7:130651533 | G | A | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.323+1336C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651533 | |||||||
| chr7:130651586 | G | A | 2 | a0001c0001t0009g0252 a0001c0001t0009g0256 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.323+1283C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651586 | |||||||
| chr7:130651605 | T | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+1264A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651605 | |||||||
| chr7:130651678 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.323+1191C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651678 | |||||||
| chr7:130651706 | C | T | 3 | a0001c0002t0001g0021 a0001c0002t0001g0041 a0001c0002t0001g0042 |
3 | HG02004.hp1 HG03491.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.323+1163G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651706 | |||||||
| chr7:130651716 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
56 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.323+1153G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651716 | |||||||
| chr7:130651754 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.323+1115C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651754 | |||||||
| chr7:130651795 | T | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+1074A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651795 | |||||||
| chr7:130651806 | G | A | 1 | a0001c0002t0001g0121 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.323+1063C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651806 | |||||||
| chr7:130651885 | G | A | 1 | a0001c0002t0001g0068 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.323+984C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651885 | |||||||
| chr7:130651902 | G | A | 2 | a0001c0006t0002g0153 a0001c0006t0002g0154 |
2 | NA18941.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.323+967C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651902 | |||||||
| chr7:130652123 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.323+746G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130652123 | |||||||
| chr7:130652288 | A | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+581T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130652288 | |||||||
| chr7:130652306 | A | G | 2 | a0001c0001t0001g0274 a0001c0001t0001g0307 |
2 | NA18967.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.323+563T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130652306 | |||||||
| chr7:130652419 | C | A | 1 | a0001c0002t0007g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.323+450G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130652419 | |||||||
| chr7:130652645 | G | C | 1 | a0001c0002t0003g0125 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.323+224C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130652645 | |||||||
| chr7:130652650 | A | G | 1 | a0001c0001t0002g0260 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.323+219T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130652650 | |||||||
| chr7:130652816 | A | T | 1 | a0001c0002t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.323+53T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130652816 | |||||||
| chr7:130653074 | CA | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.244-127delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130653074 | |||||||
| chr7:130653408 | C | G | 1 | a0001c0002t0001g0040 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.244-460G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130653408 | |||||||
| chr7:130653609 | G | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(3): Show |
6 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-661C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130653609 | |||||||
| chr7:130653729 | T | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0129 others(18): Show |
22 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.244-781A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130653729 | |||||||
| chr7:130653958 | C | T | 1 | a0001c0002t0001g0128 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.244-1010G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130653958 | |||||||
| chr7:130653968 | GA | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.244-1021delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130653968 | |||||||
| chr7:130654010 | C | T | 1 | a0001c0002t0001g0039 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.244-1062G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654010 | |||||||
| chr7:130654011 | G | GA | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.244-1064dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654011 | |||||||
| chr7:130654086 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.244-1138G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654086 | |||||||
| chr7:130654106 | G | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.244-1158C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654106 | |||||||
| chr7:130654309 | G | C | 3 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0009 |
3 | HG00438.hp1 NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.244-1361C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654309 | |||||||
| chr7:130654362 | T | A | 3 | a0001c0001t0008g0316 a0001c0001t0008g0319 a0001c0001t0008g0320 |
3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.244-1414A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654362 | |||||||
| chr7:130654603 | G | A | 4 | a0001c0002t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0243 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-1655C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654603 | |||||||
| chr7:130654644 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.244-1696C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654644 | |||||||
| chr7:130654666 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(214): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.244-1718A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654666 | |||||||
| chr7:130654675 | T | C | 1 | a0001c0001t0002g0194 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.244-1727A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654675 | |||||||
| chr7:130654692 | G | C | 10 | a0001c0002t0001g0241 a0001c0002t0007g0235 a0001c0002t0007g0236 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.244-1744C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654692 | |||||||
| chr7:130654699 | T | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.244-1751A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654699 | |||||||
| chr7:130654726 | A | T | 1 | a0001c0001t0002g0228 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.244-1778T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654726 | |||||||
| chr7:130654782 | C | T | 2 | a0001c0006t0002g0153 a0001c0006t0002g0154 |
2 | NA18941.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.244-1834G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654782 | |||||||
| chr7:130654833 | TTTTG | T | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.244-1889_244-1886d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654833 | |||||||
| chr7:130655148 | C | A | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(278): Show |
283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.244-2200G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130655148 | |||||||
| chr7:130655184 | G | A | 6 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(3): Show |
6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-2236C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130655184 | |||||||
| chr7:130655364 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.244-2416T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130655364 | |||||||
| chr7:130655475 | T | G | 6 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(3): Show |
6 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-2527A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130655475 | |||||||
| chr7:130655586 | C | G | 1 | a0001c0001t0004g0133 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.244-2638G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130655586 | |||||||
| chr7:130655628 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(214): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.244-2680A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130655628 | |||||||
| chr7:130655768 | G | GTGTCTCT others(8): Show |
1 | a0001c0002t0001g0024 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.244-2821_244-2820i others(17): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130655768 | |||||||
| chr7:130655921 | A | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0212 others(155): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.244-2973T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130655921 | |||||||
| chr7:130656011 | G | A | 1 | a0001c0002t0001g0071 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.244-3063C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130656011 | |||||||
| chr7:130656121 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.244-3173G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130656121 | |||||||
| chr7:130656160 | T | C | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-3212A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130656160 | |||||||
| chr7:130656207 | CT | C | 7 | a0001c0001t0002g0223 a0001c0002t0007g0235 a0001c0002t0007g0236 others(4): Show |
7 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.244-3260delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130656207 | |||||||
| chr7:130656388 | C | T | 91 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(88): Show |
91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.244-3440G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130656388 | |||||||
| chr7:130657193 | C | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(214): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.244-4245G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130657193 | |||||||
| chr7:130657376 | T | C | 1 | a0001c0001t0002g0220 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.244-4428A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130657376 | |||||||
| chr7:130657550 | AAT | A | 6 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(3): Show |
6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-4604_244-4603d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130657550 | |||||||
| chr7:130657603 | T | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
60 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.244-4655A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130657603 | |||||||
| chr7:130657686 | T | G | 3 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0038 |
3 | HG00099.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.244-4738A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130657686 | |||||||
| chr7:130657701 | T | C | 1 | a0001c0001t0004g0306 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.244-4753A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130657701 | |||||||
| chr7:130657758 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.244-4810G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130657758 | |||||||
| chr7:130657963 | T | C | 6 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(3): Show |
6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+5004A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130657963 | |||||||
| chr7:130658138 | A | G | 10 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(7): Show |
10 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.243+4829T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130658138 | |||||||
| chr7:130658201 | C | T | 3 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 |
3 | HG01099.hp1 HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.243+4766G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130658201 | |||||||
| chr7:130658389 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0257 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.243+4578C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130658389 | |||||||
| chr7:130658463 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.243+4504C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130658463 | |||||||
| chr7:130658670 | T | C | 1 | a0001c0001t0005g0258 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.243+4297A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130658670 | |||||||
| chr7:130658880 | C | T | 3 | a0001c0002t0005g0078 a0001c0002t0005g0079 a0001c0002t0005g0080 |
3 | HG01256.hp1 HG01258.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.243+4087G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130658880 | |||||||
| chr7:130659127 | G | A | 6 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(3): Show |
6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+3840C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659127 | |||||||
| chr7:130659152 | G | A | 1 | a0001c0002t0003g0122 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.243+3815C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659152 | |||||||
| chr7:130659171 | C | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.243+3796G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659171 | |||||||
| chr7:130659197 | T | C | 1 | a0001c0001t0010g0003 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.243+3770A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659197 | |||||||
| chr7:130659208 | A | G | 3 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0002t0001g0077 |
3 | NA19062.hp2 NA19064.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.243+3759T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659208 | |||||||
| chr7:130659224 | G | T | 1 | a0001c0001t0001g0302 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.243+3743C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659224 | |||||||
| chr7:130659354 | C | CAAAAAAA others(6): Show |
31 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(28): Show |
32 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.243+3600_243+3612d others(15): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659354 | |||||||
| chr7:130659354 | C | CAAAAAAA others(7): Show |
114 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(111): Show |
115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.243+3599_243+3612d others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659354 | |||||||
| chr7:130659354 | C | CAAAAAAA others(8): Show |
52 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(49): Show |
52 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.243+3612_243+3613i others(17): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659354 | |||||||
| chr7:130659354 | C | CAAAAAAA others(9): Show |
12 | a0001c0001t0001g0032 a0001c0001t0001g0317 a0001c0001t0001g0318 others(9): Show |
12 | HG01175.hp2 HG01515.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.243+3612_243+3613i others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659354 | |||||||
| chr7:130659354 | C | CAAAAAAA others(10): Show |
4 | a0001c0002t0007g0237 a0001c0002t0007g0238 a0001c0002t0007g0239 others(1): Show |
4 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+3612_243+3613i others(19): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659354 | |||||||
| chr7:130659356 | A | AAAAAAAA others(7): Show |
4 | a0001c0002t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0243 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.243+3610_243+3611i others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659356 | |||||||
| chr7:130659525 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.243+3442G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659525 | |||||||
| chr7:130659638 | G | T | 1 | a0001c0002t0001g0038 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.243+3329C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659638 | |||||||
| chr7:130659724 | C | T | 2 | a0001c0002t0001g0036 a0001c0002t0001g0037 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.243+3243G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659724 | |||||||
| chr7:130659887 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.243+3080C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659887 | |||||||
| chr7:130659926 | G | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
55 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.243+3041C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659926 | |||||||
| chr7:130660005 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.243+2962A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130660005 | |||||||
| chr7:130660023 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.243+2944C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130660023 | |||||||
| chr7:130660096 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(212): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.243+2871C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130660096 | |||||||
| chr7:130660370 | T | C | 3 | a0001c0002t0003g0123 a0001c0002t0003g0124 a0001c0002t0003g0125 |
3 | HG03490.hp2 HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.243+2597A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130660370 | |||||||
| chr7:130660925 | G | A | 2 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
2 | HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.243+2042C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130660925 | |||||||
| chr7:130660965 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.243+2002G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130660965 | |||||||
| chr7:130661027 | C | G | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.243+1940G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661027 | |||||||
| chr7:130661070 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.243+1897C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661070 | |||||||
| chr7:130661205 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.243+1762C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661205 | |||||||
| chr7:130661389 | A | C | 4 | a0001c0002t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0243 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.243+1578T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661389 | |||||||
| chr7:130661632 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(215): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.243+1335T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661632 | |||||||
| chr7:130661638 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): Show |
51 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.243+1329G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661638 | |||||||
| chr7:130661698 | G | A | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.243+1269C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661698 | |||||||
| chr7:130661713 | G | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(215): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.243+1254C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661713 | |||||||
| chr7:130661784 | T | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.243+1183A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661784 | |||||||
| chr7:130661898 | G | T | 4 | a0001c0002t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0243 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.243+1069C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661898 | |||||||
| chr7:130661977 | C | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.243+990G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661977 | |||||||
| chr7:130662022 | G | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.243+945C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662022 | |||||||
| chr7:130662031 | A | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.243+936T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662031 | |||||||
| chr7:130662119 | A | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.243+848T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662119 | |||||||
| chr7:130662187 | C | T | 6 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(3): Show |
6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+780G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662187 | |||||||
| chr7:130662371 | G | A | 10 | a0001c0002t0001g0241 a0001c0002t0007g0235 a0001c0002t0007g0236 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.243+596C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662371 | |||||||
| chr7:130662537 | T | C | 1 | a0001c0002t0001g0127 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.243+430A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662537 | |||||||
| chr7:130662785 | T | C | 1 | a0001c0001t0001g0321 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.243+182A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662785 | |||||||
| chr7:130662795 | A | G | 22 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0129 others(19): Show |
23 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.243+172T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662795 | |||||||
| chr7:130662847 | A | G | 10 | a0001c0002t0001g0241 a0001c0002t0007g0235 a0001c0002t0007g0236 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.243+120T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662847 | |||||||
| chr7:130662934 | TTTTCATC others(8): Show |
T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.243+18_243+32delTT others(13): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662934 | |||||||
| chr7:130662961 | A | T | 1 | a0001c0001t0002g0152 | 1 | NA18955.hp2 | splice_region_variant&intron_variant | LOW | c.243+6T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662961 | |||||||
| chr7:130663097 | C | A | 1 | a0001c0001t0004g0322 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.172-59G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663097 | |||||||
| chr7:130663204 | C | T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(217): Show |
222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.172-166G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663204 | |||||||
| chr7:130663283 | G | A | 2 | a0001c0002t0001g0126 a0001c0002t0001g0127 |
2 | HG01106.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.172-245C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663283 | |||||||
| chr7:130663324 | TG | T | 10 | a0001c0002t0001g0241 a0001c0002t0007g0235 a0001c0002t0007g0236 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.172-287delC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663324 | |||||||
| chr7:130663464 | A | C | 1 | a0001c0001t0002g0151 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.172-426T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663464 | |||||||
| chr7:130663576 | T | C | 2 | a0001c0001t0002g0227 a0001c0001t0006g0226 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.172-538A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663576 | |||||||
| chr7:130663714 | A | T | 2 | a0001c0001t0001g0266 a0001c0001t0004g0267 |
2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.172-676T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663714 | |||||||
| chr7:130663730 | CT | C | 157 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0074 others(154): Show |
157 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.172-693delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663730 | |||||||
| chr7:130663730 | CTT | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(51): Show |
55 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.172-694_172-693del others(2): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663730 | |||||||
| chr7:130663769 | C | T | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.172-731G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663769 | |||||||
| chr7:130663786 | T | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): Show |
51 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.172-748A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663786 | |||||||
| chr7:130663887 | C | T | 2 | a0001c0002t0001g0034 a0001c0002t0001g0035 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.172-849G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663887 | |||||||
| chr7:130663898 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0004g0130 |
2 | HG02723.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.172-860G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663898 | |||||||
| chr7:130664103 | G | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0262 a0001c0001t0001g0263 others(3): Show |
6 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-1065C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130664103 | |||||||
| chr7:130664160 | T | C | 4 | a0001c0002t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0243 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-1122A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130664160 | |||||||
| chr7:130664199 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(215): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.172-1161A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130664199 | |||||||
| chr7:130664326 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(215): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.172-1288T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130664326 | |||||||
| chr7:130664637 | T | A | 1 | a0001c0001t0002g0232 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.172-1599A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130664637 | |||||||
| chr7:130665010 | G | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): Show |
51 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.171+1839C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665010 | |||||||
| chr7:130665084 | AG | A | 101 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0002g0026 others(98): Show |
101 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.171+1764delC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665084 | |||||||
| chr7:130665167 | G | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0246 others(13): Show |
16 | HG01099.hp2 HG02055.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.171+1682C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665167 | |||||||
| chr7:130665276 | A | C | 2 | a0001c0001t0001g0031 a0001c0002t0001g0030 |
2 | HG04199.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.171+1573T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665276 | |||||||
| chr7:130665436 | T | A | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.171+1413A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665436 | |||||||
| chr7:130665441 | C | G | 3 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 |
3 | HG01168.hp1 HG01978.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.171+1408G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665441 | |||||||
| chr7:130665473 | T | C | 2 | a0001c0001t0002g0233 a0001c0001t0002g0234 |
2 | HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.171+1376A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665473 | |||||||
| chr7:130665610 | CTAAG | C | 6 | a0001c0002t0007g0235 a0001c0002t0007g0236 a0001c0002t0007g0237 others(3): Show |
6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+1235_171+1238d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665610 | |||||||
| chr7:130665668 | C | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+1181G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665668 | |||||||
| chr7:130666000 | C | T | 3 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 |
3 | HG01099.hp1 HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.171+849G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130666000 | |||||||
| chr7:130666436 | T | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.171+413A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130666436 | |||||||
| chr7:130666642 | G | A | 20 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0246 others(17): Show |
20 | HG01099.hp2 HG01433.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.171+207C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130666642 | |||||||
| chr7:130667044 | T | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.91-115A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 2/23 | chr7 | 130667044 | |||||||
| chr7:130667226 | A | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.90+256T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 2/23 | chr7 | 130667226 | |||||||
| chr7:130667725 | C | T | 1 | a0001c0002t0001g0021 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.38-191G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130667725 | |||||||
| chr7:130667816 | CACA | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.38-285_38-283delTG others(1): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130667816 | |||||||
| chr7:130667930 | A | C | 3 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0009 |
3 | HG00438.hp1 NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.38-396T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130667930 | |||||||
| chr7:130668084 | G | C | 1 | a0001c0001t0002g0260 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.37+548C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130668084 | |||||||
| chr7:130668239 | C | A | 1 | a0001c0002t0003g0261 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.37+393G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130668239 | |||||||
| chr7:130668351 | A | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.37+281T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130668351 | |||||||
| chr7:130668376 | AAG | A | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+254_37+255delCT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130668376 | |||||||
| chr7:130668380 | G | T | 1 | a0001c0002t0001g0004 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.37+252C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130668380 | |||||||
| chr7:130668391 | G | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0266 a0001c0001t0001g0268 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.37+241C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130668391 |