Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27132 |
| ensemblid | ENSG00000178773.15 |
| hgncid | 2320 |
| symbol | CPNE7 |
| name | copine 7 |
| refseq_nuc | NM_153636.3 |
| refseq_prot | NP_705900.1 |
| ensembl_nuc | ENST00000319518.13 |
| ensembl_prot | ENSP00000317374.8 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 89575758 |
| end | 89597246 |
| strand | + |
| ver | v1.2 |
| region | chr16:89575758-89597246 |
| region5000 | chr16:89570758-89602246 |
| regionname0 | CPNE7_chr16_89575758_89597246 |
| regionname5000 | CPNE7_chr16_89570758_89602246 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 558 | 277 | 88 | 56 | 80 | 13 | 38 | 60 | CPNE7_chr16_89570758_89602246 | CPNE7 | MSAGS others(553): Show |
chr16 | 89570758 | 89602246 |
| a0002 | 0/0 | 558 | 47 | 1 | 11 | 32 | 1 | 2 | 22 | CPNE7_chr16_89570758_89602246 | CPNE7 | MSAGS others(553): Show |
chr16 | 89570758 | 89602246 |
| a0003 | 0/0 | 558 | 14 | 0 | 0 | 14 | 0 | 0 | 9 | CPNE7_chr16_89570758_89602246 | CPNE7 | MSAGS others(553): Show |
chr16 | 89570758 | 89602246 |
| a0004 | 0/0 | 558 | 3 | 1 | 0 | 0 | 2 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | MSAGS others(553): Show |
chr16 | 89570758 | 89602246 |
| a0005 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | MSAGS others(553): Show |
chr16 | 89570758 | 89602246 |
| a0006 | 0/0 | 558 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | MSAGS others(553): Show |
chr16 | 89570758 | 89602246 |
| a0007 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | MSAGS others(553): Show |
chr16 | 89570758 | 89602246 |
| a0008 | 0/0 | 259 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | MSAGS others(254): Show |
chr16 | 89570758 | 89602246 |
| a0009 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | MSAGS others(553): Show |
chr16 | 89570758 | 89602246 |
| a0010 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | MSAGS others(553): Show |
chr16 | 89570758 | 89602246 |
| a0011 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | MSAGS others(553): Show |
chr16 | 89570758 | 89602246 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1674 | 123 | 31 | 35 | 18 | 11 | 27 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0001c0002 | 0/1 | 1674 | 104 | 29 | 8 | 55 | 2 | 9 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0001c0005 | 0/0 | 1674 | 18 | 0 | 11 | 6 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0001c0007 | 0/0 | 1674 | 13 | 13 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0001c0008 | 0/0 | 1674 | 6 | 5 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0001c0009 | 0/0 | 1674 | 3 | 2 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0001c0012 | 0/0 | 1674 | 2 | 1 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0001c0013 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0001c0015 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0001c0023 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0001c0024 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0001c0025 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0001c0027 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0001c0028 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0001c0029 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0002c0003 | 0/0 | 1674 | 26 | 0 | 1 | 24 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0002c0004 | 0/0 | 1674 | 18 | 1 | 9 | 6 | 1 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0002c0010 | 0/0 | 1674 | 2 | 0 | 1 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0002c0017 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0003c0006 | 0/0 | 1674 | 14 | 0 | 0 | 14 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0004c0011 | 0/0 | 1674 | 2 | 0 | 0 | 0 | 2 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0004c0020 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0005c0014 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0006c0018 | 0/0 | 1674 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0007c0026 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0008c0019 | 0/0 | 1655 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1650): Show |
chr16 | 89570758 | 89602246 | ||
| a0009c0022 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0010c0016 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 | ||
| a0011c0021 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ATGAG others(1669): Show |
chr16 | 89570758 | 89602246 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2442 | 121 | 31 | 35 | 17 | 11 | 26 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0001t0008 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0001t0012 | 0/0 | 2442 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0002t0001 | 0/0 | 2442 | 6 | 5 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0002t0002 | 0/1 | 2442 | 30 | 8 | 2 | 13 | 2 | 4 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0002t0003 | 0/0 | 2424 | 24 | 0 | 0 | 24 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2419): Show |
chr16 | 89570758 | 89602246 |
| a0001c0002t0004 | 0/0 | 2442 | 26 | 4 | 3 | 16 | 0 | 3 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0002t0005 | 0/0 | 2442 | 12 | 10 | 2 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0002t0007 | 0/0 | 2424 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2419): Show |
chr16 | 89570758 | 89602246 |
| a0001c0002t0009 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0002t0010 | 0/0 | 2424 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2419): Show |
chr16 | 89570758 | 89602246 |
| a0001c0002t0011 | 0/0 | 2442 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0002t0013 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0005t0002 | 0/0 | 2442 | 18 | 0 | 11 | 6 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0007t0006 | 0/0 | 2433 | 13 | 13 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2428): Show |
chr16 | 89570758 | 89602246 |
| a0001c0008t0001 | 0/0 | 2442 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0008t0002 | 0/0 | 2442 | 3 | 2 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0008t0005 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0009t0001 | 0/0 | 2442 | 3 | 2 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0012t0002 | 0/0 | 2442 | 2 | 1 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0013t0002 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0015t0001 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0023t0001 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0024t0001 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0025t0001 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0027t0005 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0028t0001 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0001c0029t0001 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0002c0003t0002 | 0/0 | 2442 | 3 | 0 | 0 | 3 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0002c0003t0003 | 0/0 | 2424 | 21 | 0 | 1 | 19 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2419): Show |
chr16 | 89570758 | 89602246 |
| a0002c0003t0004 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0002c0003t0007 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2419): Show |
chr16 | 89570758 | 89602246 |
| a0002c0004t0002 | 0/0 | 2442 | 17 | 1 | 9 | 5 | 1 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0002c0004t0014 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0002c0010t0001 | 0/0 | 2442 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0002c0010t0008 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0002c0017t0003 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2419): Show |
chr16 | 89570758 | 89602246 |
| a0003c0006t0003 | 0/0 | 2424 | 14 | 0 | 0 | 14 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2419): Show |
chr16 | 89570758 | 89602246 |
| a0004c0011t0001 | 0/0 | 2442 | 2 | 0 | 0 | 0 | 2 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0004c0020t0001 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0005c0014t0001 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0006c0018t0002 | 0/0 | 2442 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0007c0026t0001 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0008c0019t0002 | 0/0 | 2423 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2418): Show |
chr16 | 89570758 | 89602246 |
| a0009c0022t0004 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| a0010c0016t0003 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2419): Show |
chr16 | 89570758 | 89602246 |
| a0011c0021t0001 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | ACGTG others(2437): Show |
chr16 | 89570758 | 89602246 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0275 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0008g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0001t0012g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0062 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0005g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0007g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0009g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0010g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0011g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0002t0013g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0005t0002g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0005t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0005t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0005t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0005t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0005t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0005t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0005t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0005t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0005t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0005t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0005t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0005t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0005t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0007t0006g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0007t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0007t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0007t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0007t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0007t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0007t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0007t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0007t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0007t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0007t0006g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0007t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0008t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0008t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0008t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0008t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0008t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0008t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0009t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0009t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0009t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0012t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0012t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0013t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0015t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0023t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0024t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0025t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0027t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0028t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0001c0029t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0003t0007g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0004t0002g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0004t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0004t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0004t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0004t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0004t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0004t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0004t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0004t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0004t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0004t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0004t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0004t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0004t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0004t0014g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0010t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0010t0008g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0002c0017t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0003c0006t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0003c0006t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0003c0006t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0003c0006t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0003c0006t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0003c0006t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0003c0006t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0003c0006t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0003c0006t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0003c0006t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0003c0006t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0003c0006t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0003c0006t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0004c0011t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0004c0011t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0004c0020t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0005c0014t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0006c0018t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0007c0026t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0008c0019t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0009c0022t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0010c0016t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| a0011c0021t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | GBR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0333 | EUR | GBR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | GBR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0190 | EUR | FIN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | FIN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | FIN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | FIN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00423 | hp2 | a0002 | c0003 | t0002 | g0119 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00438 | hp1 | a0001 | c0005 | t0002 | g0294 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00438 | hp2 | a0001 | c0002 | t0003 | g0230 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00544 | hp1 | a0001 | c0002 | t0004 | g0126 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00544 | hp2 | a0001 | c0002 | t0003 | g0282 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0307 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00597 | hp1 | a0002 | c0003 | t0002 | g0132 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00597 | hp2 | a0003 | c0006 | t0003 | g0150 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00609 | hp1 | a0001 | c0002 | t0004 | g0137 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00609 | hp2 | a0002 | c0017 | t0003 | g0142 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00621 | hp1 | a0003 | c0006 | t0003 | g0334 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00621 | hp2 | a0002 | c0003 | t0004 | g0301 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0276 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00642 | hp2 | a0002 | c0003 | t0003 | g0141 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00673 | hp1 | a0001 | c0001 | t0008 | g0050 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00673 | hp2 | a0002 | c0004 | t0002 | g0302 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01070 | hp2 | a0001 | c0005 | t0002 | g0001 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01071 | hp1 | a0001 | c0005 | t0002 | g0001 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01074 | hp1 | a0002 | c0004 | t0002 | g0303 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01081 | hp2 | a0001 | c0008 | t0002 | g0019 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0087 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01167 | hp2 | a0001 | c0012 | t0002 | g0289 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01168 | hp2 | a0002 | c0004 | t0002 | g0002 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01169 | hp1 | a0002 | c0004 | t0002 | g0002 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01192 | hp2 | a0001 | c0002 | t0005 | g0312 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01243 | hp2 | a0001 | c0002 | t0005 | g0182 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01257 | hp2 | a0001 | c0005 | t0002 | g0001 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01258 | hp1 | a0002 | c0004 | t0002 | g0002 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01258 | hp2 | a0001 | c0005 | t0002 | g0001 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01261 | hp1 | a0001 | c0005 | t0002 | g0076 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0270 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01346 | hp2 | a0002 | c0004 | t0002 | g0305 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01361 | hp2 | a0002 | c0004 | t0002 | g0309 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01496 | hp2 | a0001 | c0005 | t0002 | g0202 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0045 | EUR | IBS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01891 | hp1 | a0005 | c0014 | t0001 | g0012 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01928 | hp1 | a0002 | c0010 | t0001 | g0239 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01943 | hp1 | a0001 | c0002 | t0004 | g0139 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01943 | hp2 | a0002 | c0004 | t0002 | g0296 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01952 | hp1 | a0001 | c0002 | t0004 | g0135 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01975 | hp2 | a0002 | c0004 | t0002 | g0304 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01978 | hp1 | a0001 | c0005 | t0002 | g0001 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01993 | hp2 | a0001 | c0005 | t0002 | g0203 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02027 | hp1 | a0002 | c0003 | t0003 | g0167 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02027 | hp2 | a0001 | c0002 | t0004 | g0125 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02071 | hp1 | a0002 | c0003 | t0003 | g0116 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02080 | hp1 | a0001 | c0002 | t0004 | g0215 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02080 | hp2 | a0003 | c0006 | t0003 | g0227 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02083 | hp1 | a0001 | c0002 | t0004 | g0217 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02083 | hp2 | a0003 | c0006 | t0003 | g0228 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02129 | hp1 | a0002 | c0003 | t0003 | g0077 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02129 | hp2 | a0001 | c0002 | t0004 | g0218 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02132 | hp1 | a0001 | c0005 | t0002 | g0308 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02132 | hp2 | a0001 | c0002 | t0004 | g0219 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02148 | hp2 | a0001 | c0005 | t0002 | g0234 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02155 | hp1 | a0001 | c0005 | t0002 | g0306 | EAS | CDX | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02155 | hp2 | a0002 | c0003 | t0007 | g0290 | EAS | CDX | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02165 | hp1 | a0001 | c0002 | t0004 | g0118 | EAS | CDX | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02165 | hp2 | a0002 | c0003 | t0003 | g0129 | EAS | CDX | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02257 | hp1 | a0001 | c0025 | t0001 | g0193 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02258 | hp1 | a0001 | c0002 | t0004 | g0321 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02273 | hp1 | a0001 | c0005 | t0002 | g0109 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02273 | hp2 | a0001 | c0002 | t0004 | g0136 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02280 | hp1 | a0001 | c0007 | t0006 | g0154 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02280 | hp2 | a0001 | c0009 | t0001 | g0017 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02293 | hp1 | a0006 | c0018 | t0002 | g0001 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02293 | hp2 | a0002 | c0004 | t0002 | g0002 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02300 | hp1 | a0001 | c0005 | t0002 | g0243 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02602 | hp1 | a0002 | c0004 | t0002 | g0271 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02615 | hp1 | a0001 | c0002 | t0005 | g0284 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02615 | hp2 | a0007 | c0026 | t0001 | g0021 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02622 | hp1 | a0001 | c0012 | t0002 | g0288 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02622 | hp2 | a0001 | c0029 | t0001 | g0263 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0323 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02723 | hp2 | a0001 | c0007 | t0006 | g0068 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02735 | hp2 | a0001 | c0002 | t0004 | g0138 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02738 | hp2 | a0001 | c0002 | t0011 | g0195 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02809 | hp1 | a0001 | c0002 | t0005 | g0283 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02809 | hp2 | a0004 | c0020 | t0001 | g0332 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02818 | hp1 | a0001 | c0002 | t0005 | g0158 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02818 | hp2 | a0001 | c0007 | t0006 | g0159 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02896 | hp2 | a0001 | c0002 | t0004 | g0320 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02922 | hp1 | a0001 | c0002 | t0005 | g0287 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02922 | hp2 | a0001 | c0008 | t0001 | g0014 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02970 | hp1 | a0001 | c0002 | t0005 | g0024 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0329 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02976 | hp2 | a0001 | c0002 | t0005 | g0280 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03017 | hp1 | a0001 | c0009 | t0001 | g0065 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03041 | hp1 | a0001 | c0008 | t0001 | g0009 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03041 | hp2 | a0001 | c0013 | t0002 | g0010 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0313 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03098 | hp2 | a0001 | c0007 | t0006 | g0156 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0264 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03139 | hp2 | a0001 | c0008 | t0002 | g0013 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03195 | hp1 | a0001 | c0007 | t0006 | g0162 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03195 | hp2 | a0001 | c0007 | t0006 | g0006 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03209 | hp1 | a0001 | c0007 | t0006 | g0274 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0257 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03225 | hp1 | a0001 | c0007 | t0006 | g0157 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03225 | hp2 | a0001 | c0007 | t0006 | g0075 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0098 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0163 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03453 | hp2 | a0001 | c0008 | t0005 | g0018 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0319 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0314 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03579 | hp2 | a0001 | c0015 | t0001 | g0322 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03669 | hp2 | a0001 | c0001 | t0012 | g0147 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0235 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03927 | hp1 | a0002 | c0003 | t0003 | g0133 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03927 | hp2 | a0001 | c0005 | t0002 | g0295 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03942 | hp1 | a0001 | c0002 | t0004 | g0261 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0200 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG04228 | hp2 | a0001 | c0002 | t0010 | g0210 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18522 | hp1 | a0001 | c0007 | t0006 | g0006 | AFR | YRI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0330 | AFR | YRI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18612 | hp1 | a0003 | c0006 | t0003 | g0151 | EAS | CHB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | CHB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18747 | hp1 | a0001 | c0002 | t0004 | g0224 | EAS | CHB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18747 | hp2 | a0008 | c0019 | t0002 | g0246 | EAS | CHB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18906 | hp1 | a0001 | c0007 | t0006 | g0285 | AFR | YRI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18906 | hp2 | a0001 | c0007 | t0006 | g0155 | AFR | YRI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18940 | hp1 | a0003 | c0006 | t0003 | g0152 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18940 | hp2 | a0001 | c0002 | t0004 | g0056 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18941 | hp1 | a0002 | c0003 | t0003 | g0143 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18941 | hp2 | a0001 | c0002 | t0003 | g0035 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18942 | hp2 | a0002 | c0003 | t0003 | g0004 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18943 | hp1 | a0002 | c0003 | t0003 | g0222 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18943 | hp2 | a0003 | c0006 | t0003 | g0005 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18944 | hp1 | a0001 | c0002 | t0003 | g0080 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18944 | hp2 | a0009 | c0022 | t0004 | g0281 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18945 | hp1 | a0002 | c0003 | t0003 | g0131 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18945 | hp2 | a0001 | c0002 | t0004 | g0057 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18946 | hp1 | a0003 | c0006 | t0003 | g0267 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18946 | hp2 | a0001 | c0002 | t0003 | g0047 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18947 | hp1 | a0001 | c0005 | t0002 | g0043 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18947 | hp2 | a0001 | c0002 | t0003 | g0229 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18950 | hp2 | a0002 | c0004 | t0002 | g0316 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18952 | hp1 | a0010 | c0016 | t0003 | g0114 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18952 | hp2 | a0001 | c0002 | t0007 | g0007 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18959 | hp1 | a0002 | c0003 | t0003 | g0221 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18959 | hp2 | a0002 | c0003 | t0003 | g0004 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18962 | hp1 | a0001 | c0002 | t0004 | g0153 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18964 | hp1 | a0001 | c0002 | t0003 | g0038 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18966 | hp1 | a0001 | c0002 | t0004 | g0231 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18970 | hp1 | a0001 | c0002 | t0003 | g0188 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18977 | hp1 | a0001 | c0002 | t0003 | g0022 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18977 | hp2 | a0001 | c0002 | t0003 | g0037 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18979 | hp2 | a0002 | c0004 | t0002 | g0020 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18980 | hp1 | a0002 | c0004 | t0014 | g0300 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18980 | hp2 | a0001 | c0002 | t0003 | g0044 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18982 | hp1 | a0001 | c0024 | t0001 | g0208 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0173 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18983 | hp1 | a0002 | c0003 | t0003 | g0128 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18990 | hp1 | a0003 | c0006 | t0003 | g0226 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18994 | hp1 | a0001 | c0005 | t0002 | g0315 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18994 | hp2 | a0003 | c0006 | t0003 | g0149 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18995 | hp1 | a0002 | c0003 | t0003 | g0123 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18995 | hp2 | a0001 | c0002 | t0003 | g0201 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18998 | hp1 | a0001 | c0002 | t0003 | g0176 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA18998 | hp2 | a0002 | c0003 | t0003 | g0140 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19004 | hp2 | a0002 | c0003 | t0003 | g0134 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19005 | hp1 | a0002 | c0003 | t0003 | g0113 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19005 | hp2 | a0002 | c0004 | t0002 | g0324 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19009 | hp2 | a0002 | c0003 | t0003 | g0144 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19010 | hp1 | a0002 | c0003 | t0002 | g0310 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19011 | hp2 | a0003 | c0006 | t0003 | g0268 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19012 | hp1 | a0002 | c0003 | t0003 | g0130 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19030 | hp1 | a0001 | c0023 | t0001 | g0223 | AFR | LWK | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19030 | hp2 | a0001 | c0002 | t0013 | g0189 | AFR | LWK | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | LWK | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19054 | hp2 | a0002 | c0010 | t0008 | g0127 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19055 | hp1 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19057 | hp1 | a0011 | c0021 | t0001 | g0216 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19057 | hp2 | a0001 | c0002 | t0003 | g0266 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19064 | hp1 | a0001 | c0002 | t0004 | g0165 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19064 | hp2 | a0001 | c0002 | t0003 | g0148 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19065 | hp1 | a0001 | c0002 | t0003 | g0298 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19065 | hp2 | a0001 | c0002 | t0003 | g0253 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19066 | hp2 | a0003 | c0006 | t0003 | g0260 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19067 | hp1 | a0001 | c0002 | t0003 | g0177 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19067 | hp2 | a0001 | c0002 | t0003 | g0049 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19070 | hp1 | a0001 | c0002 | t0003 | g0054 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19070 | hp2 | a0001 | c0002 | t0003 | g0220 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19074 | hp2 | a0003 | c0006 | t0003 | g0005 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19080 | hp1 | a0002 | c0003 | t0003 | g0124 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19080 | hp2 | a0001 | c0002 | t0007 | g0007 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19082 | hp1 | a0001 | c0005 | t0002 | g0042 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19082 | hp2 | a0001 | c0002 | t0003 | g0225 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19084 | hp1 | a0002 | c0004 | t0002 | g0299 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19084 | hp2 | a0001 | c0002 | t0004 | g0117 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19085 | hp1 | a0001 | c0002 | t0004 | g0055 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19087 | hp1 | a0002 | c0003 | t0003 | g0166 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19087 | hp2 | a0003 | c0006 | t0003 | g0164 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19240 | hp1 | a0001 | c0027 | t0005 | g0161 | AFR | YRI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA19240 | hp2 | a0001 | c0028 | t0001 | g0160 | AFR | YRI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA20129 | hp1 | a0001 | c0002 | t0005 | g0191 | AFR | ASW | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA20129 | hp2 | a0001 | c0009 | t0001 | g0015 | AFR | ASW | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA20752 | hp1 | a0004 | c0011 | t0001 | g0081 | EUR | TSI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA20752 | hp2 | a0002 | c0004 | t0002 | g0293 | EUR | TSI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA20805 | hp1 | a0004 | c0011 | t0001 | g0106 | EUR | TSI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | TSI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0199 | SAS | GIH | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA20905 | hp2 | a0001 | c0002 | t0004 | g0112 | SAS | GIH | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02109 | hp1 | a0001 | c0008 | t0002 | g0016 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02486 | hp1 | a0001 | c0002 | t0005 | g0078 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02559 | hp1 | a0001 | c0007 | t0006 | g0252 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG02559 | hp2 | a0001 | c0002 | t0005 | g0183 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03471 | hp1 | a0001 | c0002 | t0004 | g0317 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | USA | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| HG06807 | hp2 | a0001 | c0002 | t0005 | g0023 | AFR | USA | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | USA | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA20300 | hp2 | a0002 | c0004 | t0002 | g0297 | AFR | USA | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA21309 | hp1 | a0001 | c0002 | t0009 | g0318 | AFR | LWK | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0062 | REF | REF | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0275 | REF | REF | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89577593 | T | C | 2 | a0002 a0010 |
48 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(45): Show |
missense_variant | MODERATE | c.229T>C | p.Phe77Leu | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/15 | 369/2442 | 229/1677 | 77/558 | chr16 | 89577593 | |||
| chr16:89577698 | G | A | 1 | a0006 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.334G>A | p.Gly112Ser | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/15 | 474/2442 | 334/1677 | 112/558 | chr16 | 89577698 | |||
| chr16:89585766 | AGGCCTTT others(67): Show |
A | 1 | a0008 | 1 | NA18747.hp2 | frameshift_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.768_780+61delTGAGG others(69): Show |
p.Phe256fs | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/15 | 908/2442 | 768/1677 | 256/558 | INFO_REALIGN_3_PRIME | chr16 | 89585766 | ||
| chr16:89586712 | C | T | 1 | a0007 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.823C>T | p.Arg275Cys | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/15 | 963/2442 | 823/1677 | 275/558 | chr16 | 89586712 | |||
| chr16:89588712 | G | A | 1 | a0004 | 3 | HG02809.hp2 NA20752.hp1 NA20805.hp1 |
missense_variant | MODERATE | c.965G>A | p.Arg322Gln | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/15 | 1105/2442 | 965/1677 | 322/558 | chr16 | 89588712 | |||
| chr16:89591252 | A | G | 1 | a0005 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.1294A>G | p.Lys432Glu | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/15 | 1434/2442 | 1294/1677 | 432/558 | chr16 | 89591252 | |||
| chr16:89595425 | G | A | 1 | a0009 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.1361G>A | p.Arg454Gln | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/15 | 1501/2442 | 1361/1677 | 454/558 | chr16 | 89595425 | |||
| chr16:89595428 | A | G | 1 | a0011 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.1364A>G | p.Glu455Gly | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/15 | 1504/2442 | 1364/1677 | 455/558 | chr16 | 89595428 | |||
| chr16:89596617 | C | T | 2 | a0003 a0010 |
15 | HG00597.hp2 HG00621.hp1 HG02080.hp2 others(12): Show |
missense_variant | MODERATE | c.1673C>T | p.Pro558Leu | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 1813/2442 | 1673/1677 | 558/558 | chr16 | 89596617 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89576050 | G | A | 4 | a0001c0008 a0001c0009 a0001c0013 others(1): Show |
11 | HG01081.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
synonymous_variant | LOW | c.153G>A | p.Gln51Gln | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/15 | 293/2442 | 153/1677 | 51/558 | chr16 | 89576050 | |||
| chr16:89577589 | G | A | 1 | a0001c0015 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.225G>A | p.Lys75Lys | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/15 | 365/2442 | 225/1677 | 75/558 | chr16 | 89577589 | |||
| chr16:89584791 | C | T | 1 | a0001c0029 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.525C>T | p.Ser175Ser | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/15 | 665/2442 | 525/1677 | 175/558 | chr16 | 89584791 | |||
| chr16:89584800 | C | T | 2 | a0001c0027 a0001c0028 |
2 | NA19240.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.534C>T | p.Phe178Phe | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/15 | 674/2442 | 534/1677 | 178/558 | chr16 | 89584800 | |||
| chr16:89591137 | C | T | 1 | a0001c0025 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1179C>T | p.Gly393Gly | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/15 | 1319/2442 | 1179/1677 | 393/558 | chr16 | 89591137 | |||
| chr16:89591173 | C | A | 1 | a0011c0021 | 1 | NA19057.hp1 | synonymous_variant | LOW | c.1215C>A | p.Val405Val | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/15 | 1355/2442 | 1215/1677 | 405/558 | chr16 | 89591173 | |||
| chr16:89595381 | G | C | 1 | a0001c0007 | 13 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(10): Show |
synonymous_variant | LOW | c.1317G>C | p.Leu439Leu | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/15 | 1457/2442 | 1317/1677 | 439/558 | chr16 | 89595381 | |||
| chr16:89595396 | C | T | 2 | a0001c0012 a0001c0013 |
3 | HG01167.hp2 HG02622.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.1332C>T | p.Asp444Asp | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/15 | 1472/2442 | 1332/1677 | 444/558 | chr16 | 89595396 | |||
| chr16:89595399 | C | T | 4 | a0001c0005 a0001c0024 a0002c0004 others(1): Show |
38 | HG00438.hp1 HG00673.hp2 HG01070.hp2 others(35): Show |
synonymous_variant | LOW | c.1335C>T | p.Gly445Gly | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/15 | 1475/2442 | 1335/1677 | 445/558 | chr16 | 89595399 | |||
| chr16:89595429 | G | A | 1 | a0011c0021 | 1 | NA19057.hp1 | synonymous_variant | LOW | c.1365G>A | p.Glu455Glu | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/15 | 1505/2442 | 1365/1677 | 455/558 | chr16 | 89595429 | |||
| chr16:89595519 | C | T | 1 | a0002c0017 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.1455C>T | p.Gly485Gly | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/15 | 1595/2442 | 1455/1677 | 485/558 | chr16 | 89595519 | |||
| chr16:89596495 | G | A | 1 | a0001c0023 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1551G>A | p.Ala517Ala | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 1691/2442 | 1551/1677 | 517/558 | chr16 | 89596495 | |||
| chr16:89596582 | T | C | 19 | a0001c0002 a0001c0005 a0001c0007 others(16): Show |
211 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(208): Show |
synonymous_variant | LOW | c.1638T>C | p.Gly546Gly | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 1778/2442 | 1638/1677 | 546/558 | chr16 | 89596582 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89575795 | G | A | 1 | a0001c0002t0009 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-103G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/15 | 103 | chr16 | 89575795 | ||||||
| chr16:89575872 | C | G | 1 | a0002c0004t0014 | 1 | NA18980.hp1 | 5_prime_UTR_variant | MODIFIER | c.-26C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/15 | 26 | chr16 | 89575872 | ||||||
| chr16:89596664 | G | A | 19 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0005 others(16): Show |
121 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*43G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 43 | chr16 | 89596664 | ||||||
| chr16:89596735 | C | A | 1 | a0001c0001t0012 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 114 | chr16 | 89596735 | ||||||
| chr16:89596782 | C | T | 4 | a0001c0002t0004 a0001c0002t0011 a0002c0003t0004 others(1): Show |
29 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*161C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 161 | chr16 | 89596782 | ||||||
| chr16:89596924 | A | G | 1 | a0001c0001t0012 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*303A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 303 | chr16 | 89596924 | ||||||
| chr16:89596959 | G | A | 3 | a0001c0002t0005 a0001c0008t0005 a0001c0027t0005 |
14 | HG01192.hp2 HG01243.hp2 HG02486.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*338G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 338 | chr16 | 89596959 | ||||||
| chr16:89597005 | C | T | 2 | a0001c0002t0007 a0002c0003t0007 |
3 | HG02155.hp2 NA18952.hp2 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*384C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 384 | chr16 | 89597005 | ||||||
| chr16:89597066 | C | T | 1 | a0001c0002t0011 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*445C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 445 | chr16 | 89597066 | ||||||
| chr16:89597157 | A | G | 1 | a0001c0002t0013 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*536A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 536 | chr16 | 89597157 | ||||||
| chr16:89597158 | TGGGGTCT others(2): Show |
T | 1 | a0001c0007t0006 | 13 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*556_*564delGGGGTC others(3): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 556 | INFO_REALIGN_3_PRIME | chr16 | 89597158 | |||||
| chr16:89597158 | TGGGGTCT others(11): Show |
T | 8 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0010 others(5): Show |
65 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*547_*564delGGGGTC others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 547 | INFO_REALIGN_3_PRIME | chr16 | 89597158 | |||||
| chr16:89597189 | G | T | 2 | a0001c0001t0008 a0002c0010t0008 |
2 | HG00673.hp1 NA19054.hp2 |
3_prime_UTR_variant | MODIFIER | c.*568G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 568 | chr16 | 89597189 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89576088 | G | C | 11 | a0001c0001t0001g0011 a0001c0008t0001g0009 a0001c0008t0001g0014 others(8): Show |
11 | HG01081.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.174+17G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576088 | |||||||
| chr16:89576095 | G | T | 1 | a0003c0006t0003g0334 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.174+24G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576095 | |||||||
| chr16:89576299 | G | A | 1 | a0002c0004t0002g0020 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.174+228G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576299 | |||||||
| chr16:89576417 | G | T | 1 | a0001c0001t0001g0333 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.174+346G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576417 | |||||||
| chr16:89576606 | C | A | 45 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0031 others(42): Show |
45 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.174+535C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576606 | |||||||
| chr16:89576673 | T | A | 1 | a0001c0001t0001g0066 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.174+602T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576673 | |||||||
| chr16:89576702 | C | T | 1 | a0001c0009t0001g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.174+631C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576702 | |||||||
| chr16:89576720 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.174+649C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576720 | |||||||
| chr16:89576752 | A | G | 1 | a0001c0009t0001g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.174+681A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576752 | |||||||
| chr16:89576839 | C | T | 40 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(37): Show |
40 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.175-700C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576839 | |||||||
| chr16:89576913 | G | A | 4 | a0001c0002t0001g0029 a0001c0002t0002g0026 a0001c0002t0002g0027 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-626G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576913 | |||||||
| chr16:89577056 | C | G | 47 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0031 others(44): Show |
47 | HG00323.hp2 HG00673.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.175-483C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577056 | |||||||
| chr16:89577124 | T | C | 50 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0031 others(47): Show |
50 | HG00323.hp2 HG00673.hp1 HG01261.hp1 others(47): Show |
intron_variant | MODIFIER | c.175-415T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577124 | |||||||
| chr16:89577193 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.175-346C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577193 | |||||||
| chr16:89577226 | T | G | 1 | a0001c0002t0003g0080 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.175-313T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577226 | |||||||
| chr16:89577268 | G | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0082 a0001c0001t0001g0083 others(28): Show |
32 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.175-271G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577268 | |||||||
| chr16:89577268 | G | T | 1 | a0002c0004t0002g0324 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.175-271G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577268 | |||||||
| chr16:89577292 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.175-247C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577292 | |||||||
| chr16:89577338 | G | A | 1 | a0001c0005t0002g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.175-201G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577338 | |||||||
| chr16:89577410 | A | C | 1 | a0001c0001t0001g0079 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.175-129A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577410 | |||||||
| chr16:89577452 | C | T | 2 | a0001c0002t0005g0023 a0001c0002t0005g0024 |
2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.175-87C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577452 | |||||||
| chr16:89577463 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG02602.hp2 HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.175-76G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577463 | |||||||
| chr16:89577770 | C | A | 70 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0070 others(67): Show |
73 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.357+49C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89577770 | |||||||
| chr16:89577796 | A | G | 1 | a0002c0003t0003g0167 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.357+75A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89577796 | |||||||
| chr16:89577952 | G | A | 3 | a0001c0001t0001g0168 a0001c0002t0001g0029 a0004c0011t0001g0081 |
3 | HG03540.hp1 HG03834.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.357+231G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89577952 | |||||||
| chr16:89578052 | C | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0328 |
3 | HG02723.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.357+331C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578052 | |||||||
| chr16:89578067 | C | CT | 16 | a0001c0001t0001g0331 a0001c0002t0001g0323 a0001c0002t0002g0319 others(13): Show |
16 | HG01081.hp2 HG01109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.357+361dupT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89578067 | ||||||
| chr16:89578067 | CT | C | 197 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(194): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.357+361delT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89578067 | ||||||
| chr16:89578127 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.357+406T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578127 | |||||||
| chr16:89578167 | C | T | 4 | a0001c0002t0001g0314 a0001c0002t0002g0313 a0001c0002t0005g0078 others(1): Show |
4 | HG01192.hp2 HG02486.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+446C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578167 | |||||||
| chr16:89578288 | A | C | 2 | a0001c0001t0001g0331 a0004c0020t0001g0332 |
2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.357+567A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578288 | |||||||
| chr16:89578309 | T | C | 3 | a0001c0001t0001g0331 a0001c0002t0001g0029 a0004c0020t0001g0332 |
3 | HG01109.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.357+588T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578309 | |||||||
| chr16:89578314 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.357+593T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578314 | |||||||
| chr16:89578363 | C | T | 2 | a0001c0001t0001g0331 a0004c0020t0001g0332 |
2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.357+642C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578363 | |||||||
| chr16:89578399 | T | C | 7 | a0001c0001t0001g0171 a0001c0008t0001g0009 a0001c0008t0002g0016 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.357+678T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578399 | |||||||
| chr16:89578408 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.357+687C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578408 | |||||||
| chr16:89578418 | C | T | 2 | a0001c0008t0001g0009 a0001c0009t0001g0065 |
2 | HG03017.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.357+697C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578418 | |||||||
| chr16:89578452 | A | G | 14 | a0001c0001t0001g0331 a0001c0002t0001g0029 a0001c0002t0001g0323 others(11): Show |
14 | HG01081.hp2 HG01109.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.357+731A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578452 | |||||||
| chr16:89578525 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.357+804C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578525 | |||||||
| chr16:89578657 | G | A | 1 | a0001c0002t0004g0112 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.357+936G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578657 | |||||||
| chr16:89578675 | G | A | 3 | a0002c0003t0003g0004 a0002c0003t0003g0113 a0010c0016t0003g0114 |
4 | NA18942.hp2 NA18952.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+954G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578675 | |||||||
| chr16:89578759 | C | CA | 9 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0331 others(6): Show |
9 | HG01109.hp2 HG02071.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.357+1057dupA | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89578759 | ||||||
| chr16:89578759 | CA | C | 8 | a0001c0001t0001g0034 a0001c0001t0001g0175 a0001c0002t0001g0029 others(5): Show |
8 | HG02615.hp2 HG02738.hp1 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.357+1057delA | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89578759 | ||||||
| chr16:89578759 | CAA | C | 196 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(193): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.357+1056_357+1057d others(4): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89578759 | ||||||
| chr16:89578759 | CAAA | C | 29 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0063 others(26): Show |
32 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.357+1055_357+1057d others(5): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89578759 | ||||||
| chr16:89578898 | T | A | 3 | a0001c0002t0001g0029 a0001c0002t0002g0026 a0001c0008t0001g0009 |
3 | HG03041.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.357+1177T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578898 | |||||||
| chr16:89578913 | C | T | 17 | a0001c0002t0001g0163 a0001c0002t0002g0313 a0001c0002t0005g0078 others(14): Show |
18 | HG01192.hp2 HG02280.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.357+1192C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578913 | |||||||
| chr16:89578928 | C | T | 1 | a0001c0002t0002g0270 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.357+1207C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578928 | |||||||
| chr16:89578937 | C | A | 2 | a0001c0001t0001g0331 a0004c0020t0001g0332 |
2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.357+1216C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578937 | |||||||
| chr16:89578952 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0286 |
2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.357+1231G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578952 | |||||||
| chr16:89578960 | C | G | 2 | a0001c0002t0001g0323 a0001c0015t0001g0322 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.357+1239C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578960 | |||||||
| chr16:89578966 | T | G | 1 | a0001c0008t0001g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.357+1245T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578966 | |||||||
| chr16:89578976 | G | A | 2 | a0001c0002t0001g0029 a0001c0002t0002g0026 |
2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.357+1255G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578976 | |||||||
| chr16:89579029 | G | T | 199 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(196): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.357+1308G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579029 | |||||||
| chr16:89579067 | G | A | 6 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0002t0005g0023 others(3): Show |
6 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.357+1346G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579067 | |||||||
| chr16:89579162 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.357+1441C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579162 | |||||||
| chr16:89579163 | G | A | 1 | a0001c0008t0001g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.357+1442G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579163 | |||||||
| chr16:89579289 | C | CA | 13 | a0001c0001t0001g0171 a0001c0001t0001g0184 a0001c0001t0001g0185 others(10): Show |
13 | HG02109.hp1 HG02451.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.357+1583dupA | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89579289 | ||||||
| chr16:89579289 | CA | C | 6 | a0001c0001t0001g0108 a0001c0001t0001g0272 a0001c0001t0001g0331 others(3): Show |
6 | HG01109.hp2 HG01168.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.357+1583delA | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89579289 | ||||||
| chr16:89579339 | G | A | 1 | a0001c0002t0005g0287 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.357+1618G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579339 | |||||||
| chr16:89579438 | C | T | 240 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(237): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.357+1717C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579438 | |||||||
| chr16:89579475 | G | A | 2 | a0001c0002t0001g0314 a0005c0014t0001g0012 |
2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.357+1754G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579475 | |||||||
| chr16:89579484 | G | A | 3 | a0001c0001t0001g0067 a0001c0007t0006g0068 a0001c0007t0006g0274 |
3 | HG02723.hp2 HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.357+1763G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579484 | |||||||
| chr16:89579487 | C | T | 61 | a0001c0001t0001g0082 a0001c0001t0001g0115 a0001c0001t0001g0120 others(58): Show |
63 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.357+1766C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579487 | |||||||
| chr16:89579549 | G | C | 248 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(245): Show |
258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.357+1828G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579549 | |||||||
| chr16:89579615 | C | T | 211 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(208): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.357+1894C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579615 | |||||||
| chr16:89579671 | ATCACATG others(18): Show |
A | 8 | a0001c0001t0001g0171 a0001c0002t0001g0323 a0001c0008t0001g0009 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.357+1967_357+1991d others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89579671 | ||||||
| chr16:89579676 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.357+1955A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579676 | |||||||
| chr16:89579717 | C | G | 1 | a0001c0002t0001g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.357+1996C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579717 | |||||||
| chr16:89579722 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.357+2001C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579722 | |||||||
| chr16:89579746 | CACACAGA others(513): Show |
C | 1 | a0001c0001t0001g0085 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.357+2076_357+2595d others(2): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89579746 | ||||||
| chr16:89579781 | CGTCACCC others(237): Show |
C | 1 | a0001c0002t0002g0098 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.357+2108_357+2351d others(2): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89579781 | ||||||
| chr16:89579797 | G | A | 1 | a0001c0005t0002g0203 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.357+2076G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579797 | |||||||
| chr16:89579797 | GGAACATC others(467): Show |
G | 1 | a0001c0001t0001g0095 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.357+2090_357+2563d others(2): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89579797 | ||||||
| chr16:89579811 | GTCACACG others(421): Show |
G | 209 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(206): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.357+2108_357+2535d others(2): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89579811 | ||||||
| chr16:89579836 | C | G | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2115C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579836 | |||||||
| chr16:89579841 | G | A | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2120G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579841 | |||||||
| chr16:89579872 | G | A | 2 | a0001c0002t0001g0314 a0005c0014t0001g0012 |
2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.357+2151G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579872 | |||||||
| chr16:89579878 | T | C | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2157T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579878 | |||||||
| chr16:89579887 | G | A | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2166G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579887 | |||||||
| chr16:89579901 | A | G | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2180A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579901 | |||||||
| chr16:89579907 | C | T | 3 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0330 |
3 | HG01891.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.357+2186C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579907 | |||||||
| chr16:89579918 | G | A | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2197G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579918 | |||||||
| chr16:89579928 | G | C | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2207G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579928 | |||||||
| chr16:89579933 | A | G | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2212A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579933 | |||||||
| chr16:89579964 | G | A | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2243G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579964 | |||||||
| chr16:89579971 | G | A | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2250G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579971 | |||||||
| chr16:89579988 | A | G | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2267A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579988 | |||||||
| chr16:89579992 | C | G | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2271C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579992 | |||||||
| chr16:89579993 | A | C | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2272A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579993 | |||||||
| chr16:89579995 | G | A | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2274G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579995 | |||||||
| chr16:89579996 | G | T | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2275G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579996 | |||||||
| chr16:89579997 | A | C | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2276A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579997 | |||||||
| chr16:89580009 | A | G | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2288A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580009 | |||||||
| chr16:89580016 | G | A | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2295G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580016 | |||||||
| chr16:89580025 | T | C | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2304T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580025 | |||||||
| chr16:89580026 | G | T | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2305G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580026 | |||||||
| chr16:89580033 | G | A | 8 | a0001c0001t0001g0171 a0001c0002t0001g0323 a0001c0008t0001g0009 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.357+2312G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580033 | |||||||
| chr16:89580034 | C | A | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2313C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580034 | |||||||
| chr16:89580036 | G | C | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2315G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580036 | |||||||
| chr16:89580040 | C | T | 2 | a0001c0002t0005g0280 a0001c0008t0001g0014 |
2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.357+2319C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580040 | |||||||
| chr16:89580055 | G | A | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2334G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580055 | |||||||
| chr16:89580060 | A | C | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2339A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580060 | |||||||
| chr16:89580062 | G | A | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2341G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580062 | |||||||
| chr16:89580063 | G | T | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2342G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580063 | |||||||
| chr16:89580064 | A | C | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2343A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580064 | |||||||
| chr16:89580078 | T | C | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2357T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580078 | |||||||
| chr16:89580081 | A | T | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2360A>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580081 | |||||||
| chr16:89580082 | G | C | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2361G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580082 | |||||||
| chr16:89580086 | C | T | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2365C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580086 | |||||||
| chr16:89580087 | G | A | 3 | a0001c0002t0002g0098 a0001c0008t0001g0009 a0002c0004t0002g0020 |
3 | HG03041.hp1 HG03239.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.357+2366G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580087 | |||||||
| chr16:89580107 | C | T | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2386C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580107 | |||||||
| chr16:89580108 | A | G | 10 | a0001c0001t0001g0171 a0001c0002t0001g0323 a0001c0002t0002g0098 others(7): Show |
10 | HG02109.hp1 HG02451.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.357+2387A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580108 | |||||||
| chr16:89580109 | G | A | 25 | a0001c0001t0001g0311 a0001c0002t0002g0307 a0001c0002t0003g0298 others(22): Show |
28 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.357+2388G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580109 | |||||||
| chr16:89580122 | C | T | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2401C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580122 | |||||||
| chr16:89580124 | C | T | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2403C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580124 | |||||||
| chr16:89580128 | G | C | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2407G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580128 | |||||||
| chr16:89580132 | C | T | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2411C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580132 | |||||||
| chr16:89580133 | A | G | 30 | a0001c0001t0001g0311 a0001c0002t0001g0033 a0001c0002t0001g0314 others(27): Show |
33 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.357+2412A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580133 | |||||||
| chr16:89580147 | G | A | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2426G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580147 | |||||||
| chr16:89580163 | CGTCACCC others(153): Show |
C | 1 | a0001c0002t0002g0098 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.357+2443_357+2602d others(2): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580163 | |||||||
| chr16:89580164 | G | A | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2443G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580164 | |||||||
| chr16:89580172 | C | A | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2451C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580172 | |||||||
| chr16:89580174 | G | C | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2453G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580174 | |||||||
| chr16:89580192 | C | T | 1 | a0002c0004t0002g0305 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.357+2471C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580192 | |||||||
| chr16:89580193 | G | A | 1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2472G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580193 | |||||||
| chr16:89580193 | G | GTCACACG others(39): Show |
3 | a0002c0003t0002g0132 a0002c0003t0003g0124 a0002c0003t0003g0167 |
3 | HG00597.hp1 HG02027.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.357+2489_357+2534d others(48): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580193 | ||||||
| chr16:89580235 | C | A | 38 | a0001c0001t0001g0171 a0001c0001t0001g0311 a0001c0002t0001g0033 others(35): Show |
41 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.357+2514C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580235 | |||||||
| chr16:89580239 | A | G | 41 | a0001c0001t0001g0171 a0001c0001t0001g0311 a0001c0001t0001g0331 others(38): Show |
44 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.357+2518A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580239 | |||||||
| chr16:89580245 | C | T | 2 | a0001c0001t0001g0291 a0001c0008t0002g0013 |
2 | HG00741.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.357+2524C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580245 | |||||||
| chr16:89580271 | A | G | 8 | a0001c0001t0001g0171 a0001c0002t0001g0323 a0001c0008t0001g0009 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.357+2550A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580271 | |||||||
| chr16:89580285 | A | G | 8 | a0001c0001t0001g0171 a0001c0002t0001g0323 a0001c0008t0001g0009 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.357+2564A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580285 | |||||||
| chr16:89580302 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.357+2581G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580302 | |||||||
| chr16:89580320 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.357+2599A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580320 | |||||||
| chr16:89580324 | C | A | 1 | a0001c0002t0002g0098 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.357+2603C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580324 | |||||||
| chr16:89580331 | G | GTCACACG others(591): Show |
1 | a0001c0008t0001g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.357+2626_357+2627i others(600): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580331 | ||||||
| chr16:89580331 | G | GTCACACG others(1445): Show |
1 | a0001c0015t0001g0322 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.357+2626_357+2627i others(1454): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580331 | ||||||
| chr16:89580331 | G | GTCACACG others(591): Show |
5 | a0001c0001t0001g0171 a0001c0008t0002g0016 a0001c0008t0005g0018 others(2): Show |
5 | HG02109.hp1 HG02451.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.357+2626_357+2627i others(600): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580331 | ||||||
| chr16:89580331 | G | GTCACACG others(1445): Show |
1 | a0001c0002t0001g0323 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.357+2626_357+2627i others(1454): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580331 | ||||||
| chr16:89580338 | G | A | 1 | a0001c0002t0005g0023 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.357+2617G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580338 | |||||||
| chr16:89580348 | ATCACCCG others(153): Show |
A | 1 | a0001c0001t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.357+2682_357+2841d others(2): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580348 | ||||||
| chr16:89580355 | G | A | 2 | a0001c0002t0001g0314 a0005c0014t0001g0012 |
2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.357+2634G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580355 | |||||||
| chr16:89580361 | C | T | 1 | a0001c0002t0002g0098 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.357+2640C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580361 | |||||||
| chr16:89580369 | C | T | 2 | a0001c0002t0002g0319 a0001c0002t0009g0318 |
2 | HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.357+2648C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580369 | |||||||
| chr16:89580379 | G | A | 1 | a0001c0027t0005g0161 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.357+2658G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580379 | |||||||
| chr16:89580385 | T | C | 2 | a0001c0001t0001g0331 a0004c0020t0001g0332 |
2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.357+2664T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580385 | |||||||
| chr16:89580396 | ATCACCCG others(38): Show |
A | 1 | a0001c0009t0001g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.357+2682_357+2726d others(47): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580396 | ||||||
| chr16:89580403 | G | A | 210 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(207): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.357+2682G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580403 | |||||||
| chr16:89580420 | ATCACCCA others(14): Show |
A | 1 | a0001c0002t0001g0314 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.357+2713_357+2733d others(23): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580420 | ||||||
| chr16:89580434 | A | AGAACATC others(14): Show |
1 | a0009c0022t0004g0281 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.357+2742_357+2762d others(23): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580434 | ||||||
| chr16:89580434 | A | G | 239 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(236): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.357+2713A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580434 | |||||||
| chr16:89580473 | C | G | 1 | a0001c0002t0004g0137 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.357+2752C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580473 | |||||||
| chr16:89580485 | C | A | 1 | a0001c0001t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.357+2764C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580485 | |||||||
| chr16:89580516 | T | C | 2 | a0001c0001t0001g0331 a0004c0020t0001g0332 |
2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.357+2795T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580516 | |||||||
| chr16:89580545 | T | C | 2 | a0001c0002t0003g0035 a0001c0002t0003g0038 |
2 | NA18941.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.357+2824T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580545 | |||||||
| chr16:89580556 | ATCACCCA others(14): Show |
A | 1 | a0001c0002t0013g0189 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.357+2857_357+2877d others(23): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580556 | ||||||
| chr16:89580607 | C | T | 214 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(211): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.357+2886C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580607 | |||||||
| chr16:89580623 | CTCACCTG others(697): Show |
C | 2 | a0001c0001t0001g0331 a0004c0020t0001g0332 |
2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.357+2908_358-2365d others(2): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580623 | ||||||
| chr16:89580629 | T | C | 252 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(249): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.357+2908T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580629 | |||||||
| chr16:89580659 | A | G | 1 | a0001c0001t0008g0050 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.357+2938A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580659 | |||||||
| chr16:89580713 | C | T | 8 | a0001c0001t0001g0171 a0001c0002t0001g0323 a0001c0008t0001g0009 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.358-2984C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580713 | |||||||
| chr16:89580793 | CACACGGA others(17): Show |
C | 1 | a0001c0002t0005g0287 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.358-2883_358-2860d others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580793 | ||||||
| chr16:89580832 | G | A | 25 | a0001c0001t0001g0311 a0001c0002t0002g0307 a0001c0002t0003g0298 others(22): Show |
28 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.358-2865G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580832 | |||||||
| chr16:89580839 | ATCACACG others(17): Show |
A | 1 | a0001c0001t0001g0089 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.358-2844_358-2821d others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580839 | ||||||
| chr16:89580889 | C | T | 1 | a0001c0002t0001g0314 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.358-2808C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580889 | |||||||
| chr16:89580893 | C | T | 2 | a0001c0002t0004g0117 a0001c0002t0004g0126 |
2 | HG00544.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.358-2804C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580893 | |||||||
| chr16:89580917 | T | TGGAACAT others(14): Show |
3 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0330 |
3 | HG01891.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.358-2771_358-2751d others(23): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580917 | ||||||
| chr16:89580938 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.358-2759C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580938 | |||||||
| chr16:89580963 | T | C | 1 | a0001c0008t0001g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.358-2734T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580963 | |||||||
| chr16:89580978 | A | G | 326 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(323): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.358-2719A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580978 | |||||||
| chr16:89581019 | G | A | 1 | a0001c0009t0001g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.358-2678G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581019 | |||||||
| chr16:89581033 | G | A | 1 | a0001c0002t0009g0318 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.358-2664G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581033 | |||||||
| chr16:89581131 | A | G | 1 | a0001c0008t0002g0019 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.358-2566A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581131 | |||||||
| chr16:89581180 | C | T | 2 | a0001c0002t0001g0033 a0007c0026t0001g0021 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.358-2517C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581180 | |||||||
| chr16:89581196 | G | A | 2 | a0001c0002t0001g0033 a0007c0026t0001g0021 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.358-2501G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581196 | |||||||
| chr16:89581219 | T | TGGAACAT others(42): Show |
25 | a0001c0001t0001g0311 a0001c0002t0002g0307 a0001c0002t0003g0298 others(22): Show |
28 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.358-2436_358-2435i others(51): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89581219 | ||||||
| chr16:89581261 | C | T | 1 | a0001c0002t0001g0314 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.358-2436C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581261 | |||||||
| chr16:89581268 | C | T | 202 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(199): Show |
209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.358-2429C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581268 | |||||||
| chr16:89581273 | C | T | 1 | a0001c0025t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.358-2424C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581273 | |||||||
| chr16:89581297 | C | T | 218 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(215): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.358-2400C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581297 | |||||||
| chr16:89581351 | G | A | 2 | a0001c0001t0001g0331 a0004c0020t0001g0332 |
2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.358-2346G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581351 | |||||||
| chr16:89581364 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.358-2333C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581364 | |||||||
| chr16:89581424 | C | T | 2 | a0003c0006t0003g0267 a0003c0006t0003g0268 |
2 | NA18946.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.358-2273C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581424 | |||||||
| chr16:89581519 | C | T | 2 | a0001c0001t0001g0331 a0004c0020t0001g0332 |
2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.358-2178C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581519 | |||||||
| chr16:89581543 | G | C | 254 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(251): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.358-2154G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581543 | |||||||
| chr16:89581615 | G | C | 1 | a0001c0002t0002g0190 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.358-2082G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581615 | |||||||
| chr16:89581873 | C | T | 55 | a0001c0001t0001g0082 a0001c0001t0001g0115 a0001c0001t0001g0120 others(52): Show |
57 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.358-1824C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581873 | |||||||
| chr16:89581883 | G | A | 25 | a0001c0001t0001g0311 a0001c0002t0002g0307 a0001c0002t0003g0298 others(22): Show |
28 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.358-1814G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581883 | |||||||
| chr16:89581992 | G | A | 1 | a0001c0002t0005g0191 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.358-1705G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581992 | |||||||
| chr16:89582023 | C | T | 1 | a0001c0002t0001g0314 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.358-1674C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582023 | |||||||
| chr16:89582078 | C | G | 9 | a0001c0001t0001g0171 a0001c0002t0001g0163 a0001c0002t0001g0323 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.358-1619C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582078 | |||||||
| chr16:89582095 | T | C | 4 | a0001c0001t0001g0086 a0001c0001t0001g0107 a0001c0001t0001g0326 others(1): Show |
4 | HG00733.hp1 HG01106.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-1602T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582095 | |||||||
| chr16:89582172 | C | T | 75 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0031 others(72): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.358-1525C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582172 | |||||||
| chr16:89582245 | A | C | 5 | a0001c0001t0001g0171 a0001c0008t0002g0016 a0001c0008t0005g0018 others(2): Show |
5 | HG02109.hp1 HG02451.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.358-1452A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582245 | |||||||
| chr16:89582396 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.358-1301G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582396 | |||||||
| chr16:89582406 | T | A | 5 | a0001c0002t0002g0313 a0001c0002t0005g0078 a0001c0002t0005g0283 others(2): Show |
5 | HG01192.hp2 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.358-1291T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582406 | |||||||
| chr16:89582412 | C | T | 1 | a0001c0002t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.358-1285C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582412 | |||||||
| chr16:89582443 | C | A | 1 | a0001c0001t0001g0327 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.358-1254C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582443 | |||||||
| chr16:89582568 | C | T | 38 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0031 others(35): Show |
38 | HG00323.hp2 HG00673.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.358-1129C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582568 | |||||||
| chr16:89582571 | G | T | 1 | a0001c0001t0001g0251 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.358-1126G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582571 | |||||||
| chr16:89582629 | T | G | 1 | a0001c0001t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.358-1068T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582629 | |||||||
| chr16:89582656 | G | T | 2 | a0001c0002t0001g0314 a0005c0014t0001g0012 |
2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.358-1041G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582656 | |||||||
| chr16:89582761 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.358-936G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582761 | |||||||
| chr16:89582774 | C | G | 2 | a0001c0002t0001g0314 a0005c0014t0001g0012 |
2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.358-923C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582774 | |||||||
| chr16:89582814 | G | A | 1 | a0001c0025t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.358-883G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582814 | |||||||
| chr16:89582837 | A | G | 210 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(207): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.358-860A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582837 | |||||||
| chr16:89583140 | C | T | 1 | a0001c0025t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.358-557C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89583140 | |||||||
| chr16:89583227 | G | A | 218 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(215): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.358-470G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89583227 | |||||||
| chr16:89583267 | G | A | 219 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(216): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.358-430G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89583267 | |||||||
| chr16:89583276 | G | C | 25 | a0001c0001t0001g0311 a0001c0002t0002g0307 a0001c0002t0003g0298 others(22): Show |
28 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.358-421G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89583276 | |||||||
| chr16:89583384 | G | A | 1 | a0001c0002t0002g0194 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.358-313G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89583384 | |||||||
| chr16:89583471 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.358-226G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89583471 | |||||||
| chr16:89583591 | G | A | 1 | a0001c0007t0006g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.358-106G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89583591 | |||||||
| chr16:89583609 | T | C | 2 | a0001c0002t0001g0323 a0001c0015t0001g0322 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.358-88T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89583609 | |||||||
| chr16:89583797 | C | A | 2 | a0001c0008t0005g0018 a0001c0009t0001g0015 |
2 | HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.432+26C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 3/14 | chr16 | 89583797 | |||||||
| chr16:89583861 | G | A | 1 | a0001c0002t0011g0195 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.432+90G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 3/14 | chr16 | 89583861 | |||||||
| chr16:89583963 | T | G | 260 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(257): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.433-65T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 3/14 | chr16 | 89583963 | |||||||
| chr16:89583974 | G | A | 4 | a0001c0001t0001g0079 a0001c0002t0002g0194 a0001c0002t0002g0196 others(1): Show |
4 | HG00423.hp1 NA19012.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-54G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 3/14 | chr16 | 89583974 | |||||||
| chr16:89584010 | C | T | 5 | a0001c0001t0001g0171 a0001c0008t0002g0016 a0001c0008t0005g0018 others(2): Show |
5 | HG02109.hp1 HG02451.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-18C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 3/14 | chr16 | 89584010 | |||||||
| chr16:89584123 | C | T | 3 | a0001c0002t0004g0317 a0001c0002t0004g0320 a0001c0002t0004g0321 |
3 | HG02258.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.507+21C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584123 | |||||||
| chr16:89584152 | G | A | 2 | a0001c0002t0001g0314 a0005c0014t0001g0012 |
2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.507+50G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584152 | |||||||
| chr16:89584189 | C | T | 7 | a0001c0001t0001g0171 a0001c0001t0001g0180 a0001c0001t0001g0181 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.507+87C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584189 | |||||||
| chr16:89584218 | G | A | 2 | a0001c0001t0001g0331 a0004c0020t0001g0332 |
2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.507+116G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584218 | |||||||
| chr16:89584258 | C | T | 1 | a0001c0002t0001g0323 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.507+156C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584258 | |||||||
| chr16:89584273 | C | T | 1 | a0004c0011t0001g0081 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.507+171C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584273 | |||||||
| chr16:89584398 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.507+296G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584398 | |||||||
| chr16:89584422 | C | T | 27 | a0001c0001t0001g0311 a0001c0002t0002g0307 a0001c0002t0002g0319 others(24): Show |
30 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.507+320C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584422 | |||||||
| chr16:89584436 | C | G | 1 | a0001c0002t0001g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.507+334C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584436 | |||||||
| chr16:89584485 | T | A | 1 | a0001c0009t0001g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.508-289T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584485 | |||||||
| chr16:89584510 | G | C | 1 | a0001c0001t0001g0327 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.508-264G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584510 | |||||||
| chr16:89584593 | A | G | 12 | a0001c0001t0001g0079 a0001c0002t0002g0008 a0001c0002t0002g0190 others(9): Show |
13 | HG00280.hp1 HG00423.hp1 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.508-181A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584593 | |||||||
| chr16:89584634 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.508-140G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584634 | |||||||
| chr16:89584671 | C | T | 1 | a0001c0002t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.508-103C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584671 | |||||||
| chr16:89584729 | C | T | 2 | a0001c0001t0001g0245 a0001c0002t0002g0329 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.508-45C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584729 | |||||||
| chr16:89584762 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | NA18971.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.508-12G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584762 | |||||||
| chr16:89584767 | T | TC | 25 | a0001c0001t0001g0311 a0001c0002t0002g0307 a0001c0002t0003g0298 others(22): Show |
28 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(25): Show |
splice_acceptor_variant&intron_variant | HIGH | c.508-3dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 89584767 | ||||||
| chr16:89584862 | G | C | 1 | a0001c0002t0003g0253 | 1 | NA19065.hp2 | splice_region_variant&intron_variant | LOW | c.591+5G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/14 | chr16 | 89584862 | |||||||
| chr16:89584913 | C | T | 2 | a0001c0002t0001g0314 a0005c0014t0001g0012 |
2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.591+56C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/14 | chr16 | 89584913 | |||||||
| chr16:89585027 | C | T | 1 | a0001c0008t0001g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.591+170C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/14 | chr16 | 89585027 | |||||||
| chr16:89585095 | C | G | 1 | a0001c0002t0003g0148 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.591+238C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/14 | chr16 | 89585095 | |||||||
| chr16:89585205 | G | A | 1 | a0001c0002t0002g0199 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.592-259G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/14 | chr16 | 89585205 | |||||||
| chr16:89585239 | G | A | 2 | a0001c0002t0004g0264 a0001c0029t0001g0263 |
2 | HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.592-225G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/14 | chr16 | 89585239 | |||||||
| chr16:89585409 | C | G | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG03688.hp1 HG03704.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.592-55C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/14 | chr16 | 89585409 | |||||||
| chr16:89585628 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.682-59C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 6/14 | chr16 | 89585628 | |||||||
| chr16:89585629 | G | A | 1 | a0002c0004t0002g0293 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.682-58G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 6/14 | chr16 | 89585629 | |||||||
| chr16:89585802 | A | AG | 86 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0040 others(83): Show |
86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.780+22dupG | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89585802 | ||||||
| chr16:89585838 | G | A | 12 | a0001c0001t0001g0111 a0001c0002t0005g0158 a0001c0007t0006g0006 others(9): Show |
13 | HG02280.hp1 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.780+53G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89585838 | |||||||
| chr16:89585871 | T | TG | 19 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(16): Show |
19 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.780+93dupG | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89585871 | ||||||
| chr16:89585907 | TG | T | 34 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(31): Show |
38 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.780+128delG | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89585907 | ||||||
| chr16:89585966 | G | C | 69 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(66): Show |
73 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.780+181G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89585966 | |||||||
| chr16:89585971 | T | C | 77 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(74): Show |
81 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.780+186T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89585971 | |||||||
| chr16:89586046 | AGGGAGGG others(20): Show |
A | 35 | a0001c0001t0001g0058 a0001c0001t0001g0105 a0001c0001t0001g0115 others(32): Show |
35 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.780+278_780+304del others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89586046 | ||||||
| chr16:89586071 | C | G | 1 | a0003c0006t0003g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.780+286C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89586071 | |||||||
| chr16:89586388 | G | C | 29 | a0001c0001t0001g0058 a0001c0001t0001g0171 a0001c0002t0002g0307 others(26): Show |
29 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.781-282G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89586388 | |||||||
| chr16:89586406 | GC | G | 66 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(63): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.781-261delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89586406 | ||||||
| chr16:89586409 | C | G | 66 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(63): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.781-261C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89586409 | |||||||
| chr16:89586544 | G | GCCCTC | 6 | a0001c0002t0001g0314 a0001c0002t0004g0317 a0001c0002t0004g0320 others(3): Show |
6 | HG02258.hp1 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.781-112_781-108dup others(5): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89586544 | ||||||
| chr16:89586557 | C | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG01074.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.781-113C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89586557 | |||||||
| chr16:89586597 | G | T | 1 | a0001c0002t0013g0189 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.781-73G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89586597 | |||||||
| chr16:89586624 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(129): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.781-46G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89586624 | |||||||
| chr16:89586765 | T | C | 63 | a0001c0001t0001g0079 a0001c0001t0001g0120 a0001c0001t0001g0121 others(60): Show |
65 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.867+9T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586765 | |||||||
| chr16:89586767 | G | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0291 |
2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.867+11G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586767 | |||||||
| chr16:89586768 | C | T | 1 | a0001c0015t0001g0322 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.867+12C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586768 | |||||||
| chr16:89586776 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | NA18962.hp2 NA18990.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.867+20G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586776 | |||||||
| chr16:89586797 | G | C | 2 | a0001c0002t0002g0028 a0001c0002t0002g0330 |
2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.867+41G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586797 | |||||||
| chr16:89586896 | C | G | 50 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0120 others(47): Show |
51 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.867+140C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586896 | |||||||
| chr16:89586898 | A | G | 1 | a0001c0005t0002g0243 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.867+142A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586898 | |||||||
| chr16:89586964 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.868-79G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586964 | |||||||
| chr16:89586993 | T | C | 5 | a0001c0002t0001g0314 a0001c0002t0004g0264 a0001c0008t0001g0009 others(2): Show |
5 | HG01081.hp2 HG02615.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.868-50T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586993 | |||||||
| chr16:89587011 | C | T | 4 | a0001c0001t0001g0265 a0001c0002t0003g0054 a0001c0002t0003g0266 others(1): Show |
4 | HG01928.hp2 HG02809.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-32C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89587011 | |||||||
| chr16:89587111 | A | ATGGCCCC others(148): Show |
1 | a0001c0015t0001g0322 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.927+52_927+53insTC others(153): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587111 | ||||||
| chr16:89587112 | T | C | 12 | a0001c0001t0001g0171 a0001c0002t0001g0314 a0001c0002t0004g0264 others(9): Show |
12 | HG01081.hp2 HG02109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.927+10T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587112 | |||||||
| chr16:89587116 | C | CCCGCCCC others(3): Show |
105 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(102): Show |
110 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.927+22_927+31dupAT others(8): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587116 | ||||||
| chr16:89587124 | A | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0168 a0004c0020t0001g0332 |
3 | HG02809.hp2 HG03834.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.927+22A>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587124 | |||||||
| chr16:89587125 | T | C | 3 | a0001c0001t0001g0064 a0001c0001t0001g0168 a0004c0020t0001g0332 |
3 | HG02809.hp2 HG03834.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.927+23T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587125 | |||||||
| chr16:89587125 | T | G | 5 | a0001c0002t0002g0313 a0001c0002t0005g0078 a0001c0002t0005g0283 others(2): Show |
5 | HG01192.hp2 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+23T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587125 | |||||||
| chr16:89587126 | G | C | 3 | a0001c0001t0001g0064 a0001c0001t0001g0168 a0004c0020t0001g0332 |
3 | HG02809.hp2 HG03834.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.927+24G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587126 | |||||||
| chr16:89587126 | G | GCCGCCCC others(34): Show |
1 | a0003c0006t0003g0152 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.927+31_927+32insAT others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587126 | ||||||
| chr16:89587126 | G | GCCGCCCC others(126): Show |
2 | a0001c0002t0007g0007 a0002c0003t0007g0290 |
3 | HG02155.hp2 NA18952.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.927+31_927+32insAT others(131): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587126 | ||||||
| chr16:89587126 | G | GCCGCCCC others(279): Show |
1 | a0001c0002t0003g0022 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+31_927+32insAT others(284): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587126 | ||||||
| chr16:89587129 | G | GCCCCATG others(4): Show |
1 | a0001c0001t0001g0244 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.927+31_927+32insAT others(9): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587129 | ||||||
| chr16:89587134 | C | A | 3 | a0001c0002t0002g0027 a0001c0002t0013g0189 a0001c0025t0001g0193 |
3 | HG02145.hp1 HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.927+32C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587134 | |||||||
| chr16:89587135 | TCAGTCCG others(14): Show |
T | 3 | a0001c0002t0002g0027 a0001c0002t0013g0189 a0001c0025t0001g0193 |
3 | HG02145.hp1 HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.927+35_927+55delAG others(19): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587135 | ||||||
| chr16:89587141 | C | T | 4 | a0001c0001t0001g0064 a0001c0002t0003g0022 a0003c0006t0003g0152 others(1): Show |
4 | HG02809.hp2 HG03834.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+39C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587141 | |||||||
| chr16:89587154 | C | A | 14 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0204 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.927+52C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587154 | |||||||
| chr16:89587155 | G | A | 1 | a0001c0002t0002g0250 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.927+53G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587155 | |||||||
| chr16:89587155 | G | C | 1 | a0001c0001t0001g0256 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.927+53G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587155 | |||||||
| chr16:89587155 | G | T | 262 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(259): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.927+53G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587155 | |||||||
| chr16:89587156 | C | T | 1 | a0001c0002t0002g0250 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.927+54C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587156 | |||||||
| chr16:89587157 | C | G | 4 | a0001c0002t0002g0027 a0001c0002t0002g0250 a0001c0002t0013g0189 others(1): Show |
4 | HG02145.hp1 HG02257.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+55C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587157 | |||||||
| chr16:89587159 | C | T | 2 | a0001c0002t0007g0007 a0002c0003t0007g0290 |
3 | HG02155.hp2 NA18952.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.927+57C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587159 | |||||||
| chr16:89587160 | G | GC | 7 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0205 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+63dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587160 | ||||||
| chr16:89587172 | C | T | 117 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(114): Show |
123 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.927+70C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587172 | |||||||
| chr16:89587185 | C | A | 114 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(111): Show |
119 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.927+83C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587185 | |||||||
| chr16:89587186 | T | G | 27 | a0001c0002t0003g0080 a0001c0002t0003g0148 a0001c0002t0003g0173 others(24): Show |
27 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.927+84T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587186 | |||||||
| chr16:89587186 | T | TC | 6 | a0001c0001t0001g0089 a0001c0001t0001g0111 a0001c0002t0002g0200 others(3): Show |
6 | HG02080.hp1 HG02738.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+88dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587186 | ||||||
| chr16:89587191 | GC | G | 23 | a0001c0001t0001g0058 a0001c0002t0002g0307 a0001c0005t0002g0294 others(20): Show |
26 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.927+94delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587191 | ||||||
| chr16:89587192 | C | G | 3 | a0001c0002t0004g0317 a0001c0002t0004g0320 a0001c0002t0004g0321 |
3 | HG02258.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.927+90C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587192 | |||||||
| chr16:89587203 | T | A | 1 | a0001c0001t0001g0331 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.927+101T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587203 | |||||||
| chr16:89587203 | T | C | 117 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(114): Show |
122 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.927+101T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587203 | |||||||
| chr16:89587216 | A | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(224): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.927+114A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587216 | |||||||
| chr16:89587217 | T | A | 1 | a0009c0022t0004g0281 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.927+115T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587217 | |||||||
| chr16:89587217 | T | C | 1 | a0003c0006t0003g0152 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.927+115T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587217 | |||||||
| chr16:89587217 | TC | T | 95 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0059 others(92): Show |
100 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.927+119delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587217 | ||||||
| chr16:89587218 | C | T | 1 | a0009c0022t0004g0281 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.927+116C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587218 | |||||||
| chr16:89587219 | C | G | 1 | a0009c0022t0004g0281 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.927+117C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587219 | |||||||
| chr16:89587221 | C | G | 8 | a0001c0001t0001g0031 a0001c0001t0001g0082 a0001c0001t0001g0089 others(5): Show |
8 | HG00544.hp2 HG01099.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+119C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587221 | |||||||
| chr16:89587221 | C | T | 10 | a0001c0001t0001g0171 a0001c0002t0001g0314 a0001c0002t0004g0264 others(7): Show |
10 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.927+119C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587221 | |||||||
| chr16:89587222 | G | C | 8 | a0001c0001t0001g0031 a0001c0001t0001g0082 a0001c0001t0001g0089 others(5): Show |
8 | HG00544.hp2 HG01099.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+120G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587222 | |||||||
| chr16:89587222 | GC | G | 41 | a0001c0001t0001g0064 a0001c0001t0001g0120 a0001c0001t0001g0121 others(38): Show |
41 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.927+125delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587222 | ||||||
| chr16:89587234 | C | T | 112 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(109): Show |
117 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.927+132C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587234 | |||||||
| chr16:89587235 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.927+133G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587235 | |||||||
| chr16:89587246 | C | CA | 95 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(92): Show |
100 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.927+144_927+145ins others(1): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587246 | |||||||
| chr16:89587247 | C | A | 9 | a0001c0001t0001g0083 a0001c0001t0001g0174 a0001c0002t0001g0323 others(6): Show |
9 | HG01516.hp2 HG01891.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.927+145C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587247 | |||||||
| chr16:89587247 | C | CA | 10 | a0001c0001t0001g0171 a0001c0002t0001g0314 a0001c0002t0004g0264 others(7): Show |
10 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.927+145_927+146ins others(1): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587247 | |||||||
| chr16:89587248 | T | C | 109 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(106): Show |
114 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.927+146T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587248 | |||||||
| chr16:89587248 | T | TC | 116 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(113): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.927+149dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587248 | ||||||
| chr16:89587251 | C | CT | 5 | a0001c0001t0001g0064 a0002c0004t0002g0309 a0003c0006t0003g0152 others(2): Show |
5 | HG01361.hp2 HG02809.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+149_927+150ins others(1): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587251 | |||||||
| chr16:89587252 | G | C | 4 | a0001c0001t0001g0168 a0001c0007t0006g0075 a0001c0023t0001g0223 others(1): Show |
4 | HG03225.hp2 HG03834.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+150G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587252 | |||||||
| chr16:89587252 | G | GC | 7 | a0001c0001t0001g0175 a0001c0001t0001g0244 a0001c0002t0005g0182 others(4): Show |
7 | HG00621.hp1 HG01243.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+155dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587252 | ||||||
| chr16:89587253 | C | G | 2 | a0001c0001t0001g0168 a0001c0007t0006g0075 |
2 | HG03225.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.927+151C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587253 | |||||||
| chr16:89587264 | T | A | 5 | a0001c0001t0001g0171 a0001c0008t0002g0016 a0001c0008t0005g0018 others(2): Show |
5 | HG02109.hp1 HG02451.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+162T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587264 | |||||||
| chr16:89587264 | T | C | 126 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(123): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.927+162T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587264 | |||||||
| chr16:89587275 | C | CCCCTCCA | 4 | a0001c0002t0001g0314 a0001c0002t0004g0264 a0001c0008t0001g0009 others(1): Show |
4 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+174_927+175ins others(7): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587275 | ||||||
| chr16:89587277 | A | C | 225 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(222): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.927+175A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587277 | |||||||
| chr16:89587278 | T | C | 13 | a0001c0001t0001g0171 a0001c0002t0001g0314 a0001c0002t0002g0027 others(10): Show |
14 | HG02109.hp1 HG02145.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.927+176T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587278 | |||||||
| chr16:89587278 | T | G | 1 | a0004c0020t0001g0332 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.927+176T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587278 | |||||||
| chr16:89587278 | T | TCCCCGCC others(24): Show |
1 | a0002c0003t0003g0113 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.927+185_927+186ins others(31): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587278 | ||||||
| chr16:89587279 | C | CGGGA | 4 | a0001c0002t0001g0314 a0001c0002t0004g0264 a0001c0008t0001g0009 others(1): Show |
4 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+177_927+178ins others(4): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587279 | |||||||
| chr16:89587279 | C | CTCCACAC others(5): Show |
2 | a0001c0008t0005g0018 a0001c0009t0001g0015 |
2 | HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.927+177_927+178ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587279 | |||||||
| chr16:89587280 | C | T | 2 | a0001c0001t0001g0171 a0001c0008t0002g0016 |
2 | HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.927+178C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587280 | |||||||
| chr16:89587281 | C | A | 1 | a0001c0008t0002g0019 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.927+179C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587281 | |||||||
| chr16:89587282 | C | T | 110 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(107): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.927+180C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587282 | |||||||
| chr16:89587283 | G | A | 3 | a0001c0001t0001g0171 a0001c0008t0002g0016 a0001c0008t0002g0019 |
3 | HG01081.hp2 HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.927+181G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587283 | |||||||
| chr16:89587283 | G | C | 1 | a0001c0013t0002g0010 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+181G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587283 | |||||||
| chr16:89587283 | GC | G | 80 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0034 others(77): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.927+186delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587283 | ||||||
| chr16:89587285 | C | A | 3 | a0001c0001t0001g0171 a0001c0008t0002g0016 a0001c0013t0002g0010 |
3 | HG02109.hp1 HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.927+183C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587285 | |||||||
| chr16:89587287 | C | A | 1 | a0001c0013t0002g0010 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+185C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587287 | |||||||
| chr16:89587287 | C | CCCG | 6 | a0001c0002t0001g0314 a0001c0002t0004g0264 a0001c0008t0001g0009 others(3): Show |
6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+186_927+187ins others(3): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587287 | ||||||
| chr16:89587288 | C | G | 2 | a0001c0001t0001g0171 a0001c0008t0002g0016 |
2 | HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.927+186C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587288 | |||||||
| chr16:89587289 | T | C | 7 | a0001c0002t0001g0314 a0001c0002t0004g0264 a0001c0008t0001g0009 others(4): Show |
7 | HG02615.hp2 HG03041.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+187T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587289 | |||||||
| chr16:89587289 | T | G | 3 | a0001c0001t0001g0171 a0001c0008t0002g0016 a0001c0008t0002g0019 |
3 | HG01081.hp2 HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.927+187T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587289 | |||||||
| chr16:89587290 | C | G | 3 | a0001c0001t0001g0171 a0001c0008t0002g0016 a0001c0013t0002g0010 |
3 | HG02109.hp1 HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.927+188C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587290 | |||||||
| chr16:89587291 | A | G | 1 | a0001c0013t0002g0010 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+189A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587291 | |||||||
| chr16:89587291 | A | T | 1 | a0001c0025t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.927+189A>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587291 | |||||||
| chr16:89587292 | G | C | 6 | a0001c0002t0001g0314 a0001c0002t0004g0264 a0001c0008t0001g0009 others(3): Show |
6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+190G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587292 | |||||||
| chr16:89587293 | T | A | 1 | a0001c0013t0002g0010 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+191T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587293 | |||||||
| chr16:89587293 | T | C | 8 | a0001c0001t0001g0171 a0001c0002t0001g0314 a0001c0002t0004g0264 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.927+191T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587293 | |||||||
| chr16:89587295 | T | C | 156 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(153): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.927+193T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587295 | |||||||
| chr16:89587295 | T | G | 6 | a0001c0002t0001g0314 a0001c0002t0004g0264 a0001c0008t0001g0009 others(3): Show |
6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+193T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587295 | |||||||
| chr16:89587296 | G | C | 1 | a0001c0013t0002g0010 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+194G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587296 | |||||||
| chr16:89587297 | T | A | 6 | a0001c0002t0001g0314 a0001c0002t0004g0264 a0001c0008t0001g0009 others(3): Show |
6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+195T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587297 | |||||||
| chr16:89587297 | T | G | 1 | a0001c0013t0002g0010 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+195T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587297 | |||||||
| chr16:89587298 | G | C | 3 | a0001c0001t0001g0171 a0001c0008t0002g0016 a0001c0013t0002g0010 |
3 | HG02109.hp1 HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.927+196G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587298 | |||||||
| chr16:89587299 | G | C | 4 | a0001c0001t0001g0171 a0001c0008t0002g0016 a0001c0008t0002g0019 others(1): Show |
4 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+197G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587299 | |||||||
| chr16:89587299 | G | GAGGAA | 6 | a0001c0002t0001g0314 a0001c0002t0004g0264 a0001c0008t0001g0009 others(3): Show |
6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+197_927+198ins others(5): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587299 | |||||||
| chr16:89587302 | C | A | 6 | a0001c0002t0001g0314 a0001c0002t0004g0264 a0001c0008t0001g0009 others(3): Show |
6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+200C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587302 | |||||||
| chr16:89587303 | C | G | 6 | a0001c0002t0001g0314 a0001c0002t0004g0264 a0001c0008t0001g0009 others(3): Show |
6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+201C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587303 | |||||||
| chr16:89587304 | G | GC | 5 | a0001c0001t0001g0032 a0001c0001t0001g0083 a0001c0001t0001g0102 others(2): Show |
5 | HG00639.hp2 HG01516.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+205dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587304 | ||||||
| chr16:89587306 | C | CA | 6 | a0001c0002t0001g0314 a0001c0002t0004g0264 a0001c0008t0001g0009 others(3): Show |
6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+204_927+205ins others(1): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587306 | |||||||
| chr16:89587307 | C | G | 6 | a0001c0002t0001g0314 a0001c0002t0004g0264 a0001c0008t0001g0009 others(3): Show |
6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+205C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587307 | |||||||
| chr16:89587308 | A | ACCCGGAG others(28): Show |
2 | a0001c0008t0002g0019 a0001c0013t0002g0010 |
2 | HG01081.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.927+206_927+207ins others(35): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587308 | |||||||
| chr16:89587308 | A | C | 256 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(253): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.927+206A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587308 | |||||||
| chr16:89587309 | T | A | 4 | a0001c0001t0001g0102 a0001c0001t0001g0168 a0001c0001t0001g0179 others(1): Show |
4 | HG00639.hp2 HG03225.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+207T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587309 | |||||||
| chr16:89587309 | T | C | 6 | a0001c0001t0001g0171 a0001c0008t0002g0016 a0001c0008t0002g0019 others(3): Show |
6 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+207T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587309 | |||||||
| chr16:89587309 | T | G | 105 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(102): Show |
110 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.927+207T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587309 | |||||||
| chr16:89587310 | C | A | 6 | a0001c0002t0001g0314 a0001c0002t0004g0264 a0001c0008t0001g0009 others(3): Show |
6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+208C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587310 | |||||||
| chr16:89587311 | C | CGGAGGAG others(31): Show |
2 | a0001c0001t0001g0171 a0001c0008t0002g0016 |
2 | HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.927+209_927+210ins others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587311 | |||||||
| chr16:89587311 | C | T | 1 | a0004c0020t0001g0332 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.927+209C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587311 | |||||||
| chr16:89587312 | C | CTGGAGT | 4 | a0001c0002t0004g0264 a0001c0008t0001g0009 a0001c0008t0005g0018 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+210_927+211ins others(6): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587312 | |||||||
| chr16:89587313 | C | A | 2 | a0001c0002t0001g0314 a0007c0026t0001g0021 |
2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.927+211C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587313 | |||||||
| chr16:89587313 | C | CACACCGG others(48): Show |
1 | a0004c0020t0001g0332 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.927+211_927+212ins others(55): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587313 | |||||||
| chr16:89587313 | C | T | 135 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(132): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.927+211C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587313 | |||||||
| chr16:89587314 | G | C | 4 | a0001c0002t0004g0264 a0001c0008t0001g0009 a0001c0008t0005g0018 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+212G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587314 | |||||||
| chr16:89587315 | C | T | 3 | a0001c0002t0001g0314 a0004c0020t0001g0332 a0007c0026t0001g0021 |
3 | HG02615.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.927+213C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587315 | |||||||
| chr16:89587317 | C | G | 2 | a0001c0008t0002g0019 a0001c0013t0002g0010 |
2 | HG01081.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.927+215C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587317 | |||||||
| chr16:89587320 | T | C | 10 | a0001c0001t0001g0171 a0001c0002t0001g0314 a0001c0007t0006g0006 others(7): Show |
11 | HG01081.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+218T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587320 | |||||||
| chr16:89587320 | T | G | 4 | a0001c0002t0004g0264 a0001c0008t0001g0009 a0001c0008t0005g0018 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+218T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587320 | |||||||
| chr16:89587322 | A | C | 10 | a0001c0001t0001g0171 a0001c0002t0001g0314 a0001c0002t0004g0264 others(7): Show |
10 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.927+220A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587322 | |||||||
| chr16:89587322 | A | T | 1 | a0001c0013t0002g0010 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+220A>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587322 | |||||||
| chr16:89587324 | T | C | 11 | a0001c0001t0001g0171 a0001c0002t0001g0314 a0001c0002t0004g0264 others(8): Show |
11 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+222T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587324 | |||||||
| chr16:89587325 | CCGT | C | 3 | a0001c0002t0001g0314 a0004c0020t0001g0332 a0007c0026t0001g0021 |
3 | HG02615.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.927+224_927+226del others(3): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587325 | |||||||
| chr16:89587326 | C | A | 4 | a0001c0001t0001g0102 a0001c0001t0001g0168 a0001c0001t0001g0179 others(1): Show |
4 | HG00639.hp2 HG03225.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+224C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587326 | |||||||
| chr16:89587326 | C | T | 49 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0255 others(46): Show |
54 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.927+224C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587326 | |||||||
| chr16:89587327 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+225G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587327 | |||||||
| chr16:89587327 | G | C | 7 | a0001c0001t0001g0171 a0001c0008t0001g0009 a0001c0008t0002g0016 others(4): Show |
7 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+225G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587327 | |||||||
| chr16:89587328 | T | C | 5 | a0001c0001t0001g0171 a0001c0008t0001g0009 a0001c0008t0002g0016 others(2): Show |
5 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+226T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587328 | |||||||
| chr16:89587330 | G | C | 10 | a0001c0001t0001g0171 a0001c0002t0001g0314 a0001c0008t0001g0009 others(7): Show |
10 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.927+228G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587330 | |||||||
| chr16:89587330 | G | GCCCCCGC others(179): Show |
1 | a0001c0005t0002g0294 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.927+232_927+233ins others(186): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(168): Show |
5 | a0002c0003t0003g0004 a0002c0003t0003g0140 a0002c0003t0003g0141 others(2): Show |
6 | HG00609.hp2 HG00642.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+236_927+237ins others(175): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(122): Show |
1 | a0001c0001t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(129): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(120): Show |
1 | a0001c0005t0002g0043 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(127): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(119): Show |
1 | a0001c0001t0001g0093 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(126): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(120): Show |
1 | a0001c0001t0001g0273 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(127): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(120): Show |
1 | a0001c0001t0001g0256 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(127): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(127): Show |
1 | a0001c0001t0001g0060 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(134): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(119): Show |
1 | a0004c0011t0001g0081 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(126): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(137): Show |
1 | a0001c0002t0002g0194 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(144): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(113): Show |
1 | a0001c0001t0001g0170 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(120): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(126): Show |
1 | a0001c0002t0003g0044 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(133): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(119): Show |
59 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(56): Show |
60 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(126): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(120): Show |
3 | a0001c0001t0001g0090 a0001c0001t0001g0333 a0001c0002t0003g0038 |
3 | HG00140.hp1 HG00642.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.927+237_927+238ins others(127): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(125): Show |
8 | a0001c0001t0001g0061 a0001c0001t0001g0069 a0001c0001t0001g0070 others(5): Show |
8 | HG00280.hp1 HG01243.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(132): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(126): Show |
2 | a0001c0002t0002g0196 a0001c0002t0003g0037 |
2 | HG00423.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.927+237_927+238ins others(133): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(169): Show |
1 | a0002c0004t0002g0299 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(176): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(182): Show |
1 | a0002c0004t0002g0309 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(189): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(178): Show |
1 | a0002c0004t0002g0271 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(185): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(164): Show |
1 | a0002c0004t0014g0300 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(171): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(176): Show |
1 | a0002c0004t0002g0020 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(183): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(176): Show |
1 | a0002c0003t0004g0301 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(183): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(131): Show |
2 | a0002c0004t0002g0303 a0002c0004t0002g0304 |
2 | HG01074.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.927+237_927+238ins others(138): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(164): Show |
1 | a0001c0001t0001g0058 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(171): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(176): Show |
3 | a0002c0004t0002g0002 a0002c0004t0002g0296 a0002c0004t0002g0297 |
6 | HG01168.hp2 HG01169.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(183): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(164): Show |
2 | a0002c0004t0002g0293 a0002c0004t0002g0316 |
2 | NA18950.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.927+237_927+238ins others(171): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(170): Show |
1 | a0002c0004t0002g0324 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(177): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(163): Show |
1 | a0002c0004t0002g0302 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(170): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(172): Show |
1 | a0002c0004t0002g0305 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(179): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(175): Show |
1 | a0001c0005t0002g0306 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(182): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(174): Show |
1 | a0001c0005t0002g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(181): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(114): Show |
1 | a0001c0002t0004g0321 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(121): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(113): Show |
2 | a0001c0002t0004g0317 a0001c0002t0004g0320 |
2 | HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.927+237_927+238ins others(120): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(125): Show |
1 | a0001c0002t0002g0197 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(132): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(76): Show |
8 | a0001c0001t0001g0032 a0001c0001t0001g0063 a0001c0001t0001g0207 others(5): Show |
8 | HG02602.hp2 HG03579.hp1 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+238_927+239ins others(83): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(94): Show |
1 | a0001c0001t0001g0206 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.927+238_927+239ins others(101): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(100): Show |
1 | a0001c0002t0002g0235 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.927+238_927+239ins others(107): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(82): Show |
2 | a0001c0001t0001g0083 a0001c0009t0001g0065 |
2 | HG01516.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.927+238_927+239ins others(89): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(113): Show |
1 | a0001c0002t0001g0323 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.927+238_927+239ins others(120): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(88): Show |
4 | a0001c0001t0001g0102 a0001c0001t0001g0168 a0001c0001t0001g0179 others(1): Show |
4 | HG00639.hp2 HG03225.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+238_927+239ins others(95): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(114): Show |
1 | a0001c0008t0002g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.927+243_927+244ins others(121): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(145): Show |
1 | a0001c0015t0001g0322 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.927+243_927+244ins others(152): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(125): Show |
1 | a0001c0002t0005g0078 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.927+243_927+244ins others(132): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(86): Show |
1 | a0001c0025t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(93): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(107): Show |
1 | a0001c0002t0002g0027 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(114): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(161): Show |
1 | a0001c0002t0005g0284 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(168): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(145): Show |
1 | a0001c0002t0005g0283 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(152): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(124): Show |
1 | a0001c0002t0005g0312 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(131): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(125): Show |
1 | a0001c0002t0002g0313 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(132): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(219): Show |
1 | a0001c0002t0002g0247 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(226): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(218): Show |
1 | a0001c0002t0002g0292 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(225): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(218): Show |
5 | a0001c0002t0002g0008 a0001c0002t0002g0248 a0001c0002t0002g0249 others(2): Show |
6 | NA18612.hp2 NA18747.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(225): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(397): Show |
4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG00323.hp2 HG02300.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(404): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(335): Show |
1 | a0001c0001t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(342): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(186): Show |
1 | a0001c0001t0001g0255 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(193): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(151): Show |
1 | a0001c0001t0001g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(158): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(156): Show |
1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(163): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(192): Show |
1 | a0001c0002t0002g0028 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(199): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(185): Show |
1 | a0001c0002t0005g0280 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(192): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(191): Show |
1 | a0001c0002t0002g0330 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(198): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(137): Show |
30 | a0001c0002t0003g0080 a0001c0002t0003g0148 a0001c0002t0003g0173 others(27): Show |
30 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(144): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(138): Show |
2 | a0001c0002t0004g0125 a0002c0003t0003g0124 |
2 | HG02027.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.927+237_927+238ins others(145): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(163): Show |
1 | a0001c0001t0001g0120 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(170): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(143): Show |
3 | a0001c0002t0004g0135 a0001c0002t0004g0136 a0001c0002t0004g0224 |
3 | HG01952.hp1 HG02273.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.927+237_927+238ins others(150): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(155): Show |
1 | a0001c0001t0001g0122 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(162): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(161): Show |
1 | a0001c0001t0001g0121 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(168): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(167): Show |
4 | a0001c0007t0006g0006 a0001c0007t0006g0155 a0001c0007t0006g0252 others(1): Show |
5 | HG02559.hp1 HG03195.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(174): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(181): Show |
1 | a0001c0007t0006g0156 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(188): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(179): Show |
7 | a0001c0001t0001g0066 a0001c0001t0001g0277 a0001c0001t0001g0278 others(4): Show |
7 | HG00639.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(186): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(185): Show |
2 | a0001c0002t0005g0158 a0001c0007t0006g0162 |
2 | HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.927+237_927+238ins others(192): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(191): Show |
4 | a0001c0007t0006g0068 a0001c0007t0006g0157 a0001c0007t0006g0274 others(1): Show |
4 | HG02723.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(198): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(203): Show |
1 | a0001c0007t0006g0154 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(210): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587330 | G | GCCCCGCC others(185): Show |
1 | a0001c0001t0001g0327 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(192): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | ||||||
| chr16:89587332 | C | CCCGCCCC others(102): Show |
1 | a0001c0001t0001g0111 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(109): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587332 | ||||||
| chr16:89587332 | C | CCCGCCCC others(71): Show |
1 | a0001c0002t0003g0230 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.927+238_927+239ins others(78): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587332 | ||||||
| chr16:89587332 | C | CCCGCCCC others(71): Show |
4 | a0001c0001t0001g0175 a0001c0002t0003g0022 a0001c0005t0002g0076 others(1): Show |
4 | HG00621.hp1 HG01261.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+238_927+239ins others(78): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587332 | ||||||
| chr16:89587332 | C | CCCGCCCC others(70): Show |
69 | a0001c0001t0001g0030 a0001c0001t0001g0059 a0001c0001t0001g0067 others(66): Show |
74 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.927+238_927+239ins others(77): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587332 | ||||||
| chr16:89587332 | C | CCCGCCCC others(109): Show |
1 | a0005c0014t0001g0012 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.927+243_927+244ins others(116): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587332 | ||||||
| chr16:89587332 | C | CCCGCCCC others(109): Show |
1 | a0001c0023t0001g0223 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.927+243_927+244ins others(116): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587332 | ||||||
| chr16:89587332 | C | CCCGCCCC others(101): Show |
4 | a0001c0002t0007g0007 a0001c0002t0013g0189 a0002c0003t0007g0290 others(1): Show |
5 | HG02155.hp2 NA18940.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(108): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587332 | ||||||
| chr16:89587334 | C | CGCCCCAC others(107): Show |
1 | a0004c0011t0001g0106 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(114): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587334 | ||||||
| chr16:89587334 | C | CGCCCCCG others(108): Show |
2 | a0001c0002t0002g0319 a0001c0002t0009g0318 |
2 | HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.927+243_927+244ins others(115): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587334 | ||||||
| chr16:89587335 | G | GCCCCACC others(121): Show |
1 | a0001c0001t0001g0092 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(128): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | ||||||
| chr16:89587335 | G | GCCCCACC others(123): Show |
1 | a0001c0005t0002g0042 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(130): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | ||||||
| chr16:89587335 | G | GCCCCACC others(120): Show |
2 | a0001c0001t0001g0094 a0001c0002t0002g0036 |
2 | HG00741.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.927+237_927+238ins others(127): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | ||||||
| chr16:89587335 | G | GCCCCACC others(177): Show |
1 | a0001c0005t0002g0315 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(184): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | ||||||
| chr16:89587335 | G | GCCCCACC others(133): Show |
1 | a0001c0002t0002g0307 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(140): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | ||||||
| chr16:89587335 | G | GCCCCCCT others(72): Show |
3 | a0001c0002t0003g0225 a0001c0002t0011g0195 a0001c0005t0002g0234 |
3 | HG02148.hp2 HG02738.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.927+238_927+239ins others(79): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | ||||||
| chr16:89587335 | G | GCCCCCCT others(72): Show |
1 | a0001c0002t0004g0215 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.927+238_927+239ins others(79): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | ||||||
| chr16:89587335 | G | GCCCCCCT others(71): Show |
5 | a0001c0001t0001g0072 a0001c0001t0001g0082 a0001c0002t0003g0176 others(2): Show |
5 | HG01099.hp2 HG02080.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+238_927+239ins others(78): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | ||||||
| chr16:89587335 | G | GCCCCCCT others(78): Show |
1 | a0001c0001t0001g0031 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.927+238_927+239ins others(85): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | ||||||
| chr16:89587335 | G | GCCCCCCT others(108): Show |
1 | a0001c0002t0002g0270 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.927+238_927+239ins others(115): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | ||||||
| chr16:89587335 | G | GCCCCTCC others(138): Show |
1 | a0002c0003t0003g0113 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(145): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | ||||||
| chr16:89587336 | C | CCCCACCC others(184): Show |
1 | a0001c0005t0002g0295 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(191): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587336 | ||||||
| chr16:89587340 | C | A | 1 | a0001c0005t0002g0295 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.927+238C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587340 | |||||||
| chr16:89587340 | C | CCCCCACA others(71): Show |
1 | a0001c0001t0001g0205 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.927+238_927+239ins others(78): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587340 | |||||||
| chr16:89587340 | C | CCTCCACA others(72): Show |
1 | a0001c0005t0002g0202 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.927+238_927+239ins others(79): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587340 | |||||||
| chr16:89587340 | C | CCTCCACA others(71): Show |
3 | a0001c0001t0001g0232 a0001c0029t0001g0263 a0003c0006t0003g0150 |
3 | HG00597.hp2 HG01175.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.927+238_927+239ins others(78): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587340 | |||||||
| chr16:89587340 | C | CCTCCACA others(71): Show |
1 | a0001c0001t0001g0242 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.927+238_927+239ins others(78): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587340 | |||||||
| chr16:89587341 | G | C | 7 | a0001c0001t0001g0205 a0001c0001t0001g0232 a0001c0001t0001g0242 others(4): Show |
7 | HG00558.hp2 HG00597.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+239G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587341 | |||||||
| chr16:89587341 | G | GC | 7 | a0001c0001t0001g0180 a0001c0002t0005g0312 a0001c0005t0002g0042 others(4): Show |
7 | HG01192.hp2 HG02055.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+244dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587341 | ||||||
| chr16:89587344 | C | G | 1 | a0001c0002t0002g0307 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.927+242C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587344 | |||||||
| chr16:89587347 | G | GC | 12 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0092 others(9): Show |
12 | HG00597.hp2 HG01192.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.927+250dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587347 | ||||||
| chr16:89587408 | G | A | 99 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(96): Show |
101 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.927+306G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587408 | |||||||
| chr16:89587473 | T | A | 3 | a0001c0002t0004g0055 a0001c0002t0004g0056 a0001c0002t0004g0057 |
3 | NA18940.hp2 NA18945.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.927+371T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587473 | |||||||
| chr16:89587521 | C | T | 7 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0002t0005g0023 others(4): Show |
7 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+419C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587521 | |||||||
| chr16:89587535 | C | T | 29 | a0001c0001t0001g0241 a0001c0005t0002g0001 a0001c0005t0002g0076 others(26): Show |
36 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.927+433C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587535 | |||||||
| chr16:89587591 | TTGAG | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0034 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.927+493_927+496del others(4): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587591 | ||||||
| chr16:89587600 | C | G | 1 | a0001c0002t0004g0118 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.927+498C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587600 | |||||||
| chr16:89587634 | C | T | 2 | a0001c0002t0002g0313 a0001c0002t0005g0312 |
2 | HG01192.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.927+532C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587634 | |||||||
| chr16:89587665 | CCGCAGAC others(19): Show |
C | 1 | a0001c0008t0002g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.927+568_927+593del others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587665 | ||||||
| chr16:89587670 | G | C | 1 | a0002c0004t0002g0305 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.927+568G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587670 | |||||||
| chr16:89587677 | C | T | 1 | a0002c0004t0002g0305 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.927+575C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587677 | |||||||
| chr16:89587685 | A | C | 1 | a0002c0004t0002g0305 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.927+583A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587685 | |||||||
| chr16:89587686 | T | C | 1 | a0002c0004t0002g0305 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.927+584T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587686 | |||||||
| chr16:89587688 | G | T | 1 | a0002c0004t0002g0305 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.927+586G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587688 | |||||||
| chr16:89587697 | A | ACCCCGTG others(79): Show |
1 | a0001c0001t0001g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.927+619_927+620ins others(86): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587697 | ||||||
| chr16:89587705 | TCACCCCC others(4): Show |
T | 1 | a0002c0003t0003g0167 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.927+611_927+621del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587705 | ||||||
| chr16:89587707 | A | ACCCACAG others(387): Show |
1 | a0001c0008t0002g0016 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.927+608_927+609ins others(394): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587707 | ||||||
| chr16:89587707 | A | ACCCCCCA others(234): Show |
1 | a0001c0001t0001g0090 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.927+610_927+611ins others(241): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587707 | ||||||
| chr16:89587707 | ACCCCCAT others(94): Show |
A | 1 | a0001c0001t0001g0079 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.927+611_927+711del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587707 | ||||||
| chr16:89587711 | C | A | 1 | a0002c0004t0002g0305 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.927+609C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587711 | |||||||
| chr16:89587713 | A | ATGTCACC others(30): Show |
1 | a0001c0001t0001g0238 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.927+612_927+613ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587713 | ||||||
| chr16:89587713 | A | G | 5 | a0001c0001t0001g0090 a0001c0001t0001g0212 a0001c0002t0001g0314 others(2): Show |
5 | HG00642.hp1 HG01243.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+611A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587713 | |||||||
| chr16:89587713 | ATAGCACC others(94): Show |
A | 1 | a0001c0001t0001g0061 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.927+613_927+713del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587713 | ||||||
| chr16:89587713 | ATAGCACC others(403): Show |
A | 1 | a0001c0002t0002g0098 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.927+613_928-551del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587713 | ||||||
| chr16:89587715 | A | G | 80 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(77): Show |
82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.927+613A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587715 | |||||||
| chr16:89587716 | G | GCACCCGC others(31): Show |
1 | a0002c0004t0002g0316 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.927+619_927+620ins others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587716 | ||||||
| chr16:89587716 | G | GCACCCGC others(69): Show |
1 | a0001c0002t0001g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.927+619_927+620ins others(76): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587716 | ||||||
| chr16:89587716 | G | GCACCCGC others(111): Show |
1 | a0001c0015t0001g0322 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.927+619_927+620ins others(118): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587716 | ||||||
| chr16:89587716 | G | T | 80 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(77): Show |
82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.927+614G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587716 | |||||||
| chr16:89587716 | GCACCCCC others(30): Show |
G | 1 | a0001c0001t0001g0233 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.927+620_927+656del others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587716 | ||||||
| chr16:89587716 | GCACCCCC others(94): Show |
G | 1 | a0001c0012t0002g0288 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+620_927+720del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587716 | ||||||
| chr16:89587716 | GCACCCCC others(403): Show |
G | 1 | a0001c0001t0001g0025 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.927+620_928-544del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587716 | ||||||
| chr16:89587718 | A | ACCCCCGT others(20): Show |
1 | a0001c0002t0002g0200 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.927+621_927+647dup others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | ||||||
| chr16:89587718 | A | ACCCCCGT others(2461): Show |
1 | a0001c0002t0001g0163 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(2468): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | ||||||
| chr16:89587718 | A | ACCCCCGT others(120): Show |
1 | a0001c0001t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(127): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | ||||||
| chr16:89587718 | A | ACCCCCGT others(520): Show |
1 | a0001c0001t0001g0286 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.927+656_927+657ins others(527): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | ||||||
| chr16:89587718 | A | ACCCGCGT others(241): Show |
1 | a0001c0001t0001g0120 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.927+619_927+620ins others(248): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | ||||||
| chr16:89587718 | A | ACCCGCGT others(19): Show |
1 | a0001c0013t0002g0010 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+619_927+620ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | ||||||
| chr16:89587718 | A | ACCCGCGT others(20): Show |
1 | a0003c0006t0003g0152 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.927+619_927+620ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | ||||||
| chr16:89587718 | ACCCCCGT others(56): Show |
A | 4 | a0001c0002t0001g0276 a0001c0002t0004g0224 a0001c0002t0005g0023 others(1): Show |
4 | HG00639.hp1 HG03041.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+648_927+710del others(63): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | ||||||
| chr16:89587718 | ACCCCCGT others(366): Show |
A | 3 | a0001c0001t0001g0101 a0001c0002t0002g0249 a0001c0002t0005g0158 |
3 | HG01099.hp1 HG02818.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.927+673_928-528del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | ||||||
| chr16:89587721 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0060 others(2): Show |
5 | HG02602.hp2 HG03688.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+619C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587721 | |||||||
| chr16:89587722 | C | CCGTGTCA others(541): Show |
1 | a0001c0001t0001g0206 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.927+635_927+636ins others(548): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587722 | ||||||
| chr16:89587722 | C | CCGTGTCA others(95): Show |
1 | a0001c0002t0005g0024 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.927+647_927+648ins others(102): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587722 | ||||||
| chr16:89587722 | C | CCGTGTCA others(1381): Show |
1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.927+656_927+657ins others(1388): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587722 | ||||||
| chr16:89587722 | C | CCGTGTCA others(108): Show |
2 | a0001c0001t0001g0187 a0011c0021t0001g0216 |
2 | NA18970.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.927+656_927+657ins others(115): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587722 | ||||||
| chr16:89587722 | C | CCGTGTCA others(56): Show |
2 | a0001c0001t0001g0067 a0001c0002t0004g0215 |
2 | HG02080.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.927+656_927+657ins others(63): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587722 | ||||||
| chr16:89587722 | C | G | 120 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(117): Show |
122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.927+620C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587722 | |||||||
| chr16:89587722 | C | T | 3 | a0001c0007t0006g0159 a0001c0007t0006g0162 a0001c0007t0006g0274 |
3 | HG02818.hp2 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.927+620C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587722 | |||||||
| chr16:89587722 | CCGTGTCA others(313): Show |
C | 1 | a0001c0025t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.927+648_928-606del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587722 | ||||||
| chr16:89587722 | CCGTGTCA others(403): Show |
C | 1 | a0001c0001t0001g0082 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.927+673_928-491del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587722 | ||||||
| chr16:89587725 | T | C | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+623T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587725 | |||||||
| chr16:89587728 | C | T | 3 | a0001c0002t0001g0323 a0001c0007t0006g0285 a0002c0003t0003g0124 |
3 | HG02717.hp2 NA18906.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.927+626C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587728 | |||||||
| chr16:89587728 | CACCCACA others(120): Show |
C | 4 | a0001c0001t0001g0104 a0001c0002t0002g0329 a0001c0002t0003g0049 others(1): Show |
4 | HG01109.hp1 HG02970.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+648_927+774del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587728 | ||||||
| chr16:89587728 | CACCCACA others(340): Show |
C | 1 | a0002c0010t0008g0127 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.927+657_928-570del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587728 | ||||||
| chr16:89587731 | C | CCACAGAT others(741): Show |
1 | a0001c0002t0002g0307 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.927+647_927+648ins others(748): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587731 | ||||||
| chr16:89587734 | C | T | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+632C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587734 | |||||||
| chr16:89587738 | T | A | 27 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0001g0122 others(24): Show |
27 | HG00423.hp2 HG02080.hp2 HG02155.hp2 others(24): Show |
intron_variant | MODIFIER | c.927+636T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587738 | |||||||
| chr16:89587738 | TACACGGC others(30): Show |
T | 2 | a0001c0002t0003g0266 a0002c0003t0003g0124 |
2 | NA19057.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.927+657_927+693del others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587738 | ||||||
| chr16:89587741 | A | G | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+639A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587741 | |||||||
| chr16:89587741 | ACGGCCCC others(55): Show |
A | 1 | a0001c0002t0003g0022 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+640_927+701del others(62): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587741 | |||||||
| chr16:89587742 | C | T | 1 | a0001c0002t0004g0321 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.927+640C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587742 | |||||||
| chr16:89587743 | G | A | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+641G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587743 | |||||||
| chr16:89587744 | G | C | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+642G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587744 | |||||||
| chr16:89587744 | G | GC | 106 | a0001c0001t0001g0039 a0001c0001t0001g0052 a0001c0001t0001g0058 others(103): Show |
107 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.927+647dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCCG others(32): Show |
2 | a0002c0003t0003g0004 a0010c0016t0003g0114 |
3 | NA18942.hp2 NA18952.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.927+647_927+648ins others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCCG others(123): Show |
1 | a0001c0002t0003g0148 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.927+647_927+648ins others(130): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCCG others(32): Show |
3 | a0001c0002t0003g0173 a0003c0006t0003g0267 a0003c0006t0003g0268 |
3 | NA18946.hp1 NA18982.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.927+647_927+648ins others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCCG others(69): Show |
1 | a0001c0001t0001g0048 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.927+647_927+648ins others(76): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCCG others(145): Show |
1 | a0002c0003t0003g0077 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.927+647_927+648ins others(152): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCCG others(58): Show |
1 | a0002c0003t0002g0119 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.927+647_927+648ins others(65): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCCG others(208): Show |
1 | a0001c0001t0001g0066 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.927+647_927+648ins others(215): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCGT others(20): Show |
1 | a0001c0001t0001g0279 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCGT others(46): Show |
1 | a0003c0006t0003g0260 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.927+656_927+657ins others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCGT others(573): Show |
1 | a0001c0024t0001g0208 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(580): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCGT others(200): Show |
1 | a0001c0002t0004g0125 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.927+656_927+657ins others(207): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCGT others(57): Show |
1 | a0001c0012t0002g0289 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.927+656_927+657ins others(64): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCGT others(372): Show |
1 | a0002c0004t0014g0300 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(379): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCGT others(20): Show |
1 | a0003c0006t0003g0151 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCGT others(325): Show |
1 | a0001c0001t0001g0205 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(332): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCGT others(31): Show |
1 | a0003c0006t0003g0226 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.927+672_927+673ins others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCGT others(169): Show |
1 | a0001c0001t0001g0255 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.927+672_927+673ins others(176): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587744 | G | GCCCCCGT others(20): Show |
1 | a0001c0001t0001g0121 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.927+651_927+652ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | ||||||
| chr16:89587745 | C | A | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+643C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587745 | |||||||
| chr16:89587745 | C | T | 3 | a0002c0004t0002g0271 a0002c0004t0002g0304 a0002c0004t0002g0309 |
3 | HG01361.hp2 HG01975.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.927+643C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587745 | |||||||
| chr16:89587745 | CCCCCGTG others(29): Show |
C | 2 | a0001c0002t0004g0139 a0001c0007t0006g0159 |
2 | HG01943.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.927+648_927+683del others(36): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587745 | ||||||
| chr16:89587745 | CCCCCGTG others(365): Show |
C | 2 | a0001c0001t0001g0110 a0001c0008t0005g0018 |
2 | HG03453.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.927+648_928-554del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587745 | ||||||
| chr16:89587745 | CCCCCGTG others(402): Show |
C | 1 | a0007c0026t0001g0021 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.927+648_928-517del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587745 | ||||||
| chr16:89587748 | CCGTGTCA others(4): Show |
C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0240 others(3): Show |
7 | HG00597.hp2 HG01516.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+657_927+667del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587748 | ||||||
| chr16:89587748 | CCGTGTCA others(169): Show |
C | 1 | a0002c0003t0003g0116 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.927+657_928-741del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587748 | ||||||
| chr16:89587749 | CGTGTCAC others(67): Show |
C | 1 | a0001c0007t0006g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.927+648_927+721del others(74): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587749 | |||||||
| chr16:89587754 | C | T | 9 | a0001c0001t0001g0121 a0001c0001t0001g0178 a0001c0001t0001g0209 others(6): Show |
9 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(6): Show |
intron_variant | MODIFIER | c.927+652C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587754 | |||||||
| chr16:89587754 | CACCCGCG others(249): Show |
C | 1 | a0001c0001t0001g0175 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.927+657_928-661del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587754 | ||||||
| chr16:89587755 | A | ACCCACAG others(8): Show |
3 | a0002c0003t0003g0133 a0002c0003t0004g0301 a0003c0006t0003g0005 |
3 | HG00621.hp2 HG03927.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.927+656_927+657ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587755 | ||||||
| chr16:89587755 | A | ACCCACAG others(9): Show |
1 | a0001c0001t0001g0327 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587755 | ||||||
| chr16:89587755 | A | ACCCACAG others(10): Show |
1 | a0001c0002t0002g0027 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(17): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587755 | ||||||
| chr16:89587755 | A | ACCCACAG others(34): Show |
1 | a0001c0007t0006g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.927+656_927+657ins others(41): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587755 | ||||||
| chr16:89587755 | A | ACCCACAG others(73): Show |
1 | a0001c0001t0008g0050 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(80): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587755 | ||||||
| chr16:89587755 | A | ACCCACAG others(82): Show |
1 | a0001c0001t0001g0207 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(89): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587755 | ||||||
| chr16:89587755 | ACCCGCGT others(19): Show |
A | 5 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0107 others(2): Show |
5 | HG01074.hp1 HG01074.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+657_927+682del others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587755 | ||||||
| chr16:89587755 | ACCCGCGT others(83): Show |
A | 1 | a0004c0011t0001g0106 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.927+657_927+746del others(90): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587755 | ||||||
| chr16:89587759 | G | A | 1 | a0001c0008t0002g0019 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.927+657G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587759 | |||||||
| chr16:89587759 | G | C | 19 | a0001c0001t0001g0040 a0001c0001t0001g0085 a0001c0001t0001g0102 others(16): Show |
19 | HG00558.hp2 HG00621.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.927+657G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587759 | |||||||
| chr16:89587759 | G | GCGTGTCA others(287): Show |
1 | a0002c0003t0003g0131 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.927+672_927+673ins others(294): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587759 | ||||||
| chr16:89587759 | G | GCGTGTCA others(95): Show |
1 | a0001c0002t0003g0220 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.927+672_927+673ins others(102): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587759 | ||||||
| chr16:89587759 | G | GCGTGTCA others(383): Show |
1 | a0001c0001t0001g0070 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.927+672_927+673ins others(390): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587759 | ||||||
| chr16:89587759 | G | GCGTGTCA others(104): Show |
1 | a0001c0001t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.927+672_927+673ins others(111): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587759 | ||||||
| chr16:89587759 | GCGTGTCA others(19): Show |
G | 8 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0094 others(5): Show |
8 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+673_927+698del others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587759 | ||||||
| chr16:89587759 | GCGTGTCA others(329): Show |
G | 2 | a0001c0002t0005g0280 a0001c0028t0001g0160 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.927+673_928-565del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587759 | ||||||
| chr16:89587761 | G | A | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+659G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587761 | |||||||
| chr16:89587763 | G | A | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+661G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587763 | |||||||
| chr16:89587764 | T | G | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+662T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587764 | |||||||
| chr16:89587765 | C | CACCCACA others(20): Show |
1 | a0001c0001t0001g0122 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.927+672_927+673ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587765 | ||||||
| chr16:89587765 | C | T | 4 | a0001c0001t0001g0003 a0001c0002t0002g0027 a0002c0003t0003g0004 others(1): Show |
6 | HG01516.hp1 HG01517.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+663C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587765 | |||||||
| chr16:89587765 | CACCCACA others(83): Show |
C | 6 | a0001c0001t0001g0115 a0001c0002t0003g0035 a0001c0002t0003g0046 others(3): Show |
6 | HG02155.hp2 HG03195.hp2 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+673_927+762del others(90): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587765 | ||||||
| chr16:89587765 | CACCCACA others(185): Show |
C | 1 | a0001c0002t0004g0136 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.927+673_928-709del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587765 | ||||||
| chr16:89587765 | CACCCACA others(238): Show |
C | 7 | a0001c0001t0001g0245 a0001c0007t0006g0006 a0001c0007t0006g0075 others(4): Show |
7 | HG02280.hp1 HG02451.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+673_928-656del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587765 | ||||||
| chr16:89587765 | CACCCACA others(303): Show |
C | 3 | a0001c0002t0002g0008 a0001c0002t0002g0036 a0001c0002t0002g0247 |
4 | NA18950.hp1 NA19000.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+673_928-591del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587765 | ||||||
| chr16:89587767 | C | CCCACAGA others(19): Show |
1 | a0001c0008t0002g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.927+672_927+673ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587767 | ||||||
| chr16:89587767 | C | G | 2 | a0001c0002t0001g0314 a0002c0003t0003g0133 |
2 | HG03516.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.927+665C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587767 | |||||||
| chr16:89587770 | A | G | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+668A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587770 | |||||||
| chr16:89587775 | A | AACACGGC others(195): Show |
1 | a0001c0002t0004g0219 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.927+684_927+685ins others(202): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587775 | ||||||
| chr16:89587775 | A | AACACGGC others(321): Show |
1 | a0002c0003t0003g0140 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.927+688_927+689ins others(328): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587775 | ||||||
| chr16:89587775 | A | AACACGGC others(120): Show |
1 | a0001c0001t0001g0073 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.927+688_927+689ins others(127): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587775 | ||||||
| chr16:89587775 | A | T | 215 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0031 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.927+673A>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587775 | |||||||
| chr16:89587775 | AACACGGC others(19): Show |
A | 1 | a0001c0002t0002g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.927+685_927+710del others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587775 | ||||||
| chr16:89587775 | AACACGGC others(83): Show |
A | 1 | a0001c0001t0001g0254 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.927+685_927+774del others(90): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587775 | ||||||
| chr16:89587775 | AACACGGC others(303): Show |
A | 1 | a0001c0001t0001g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.927+711_928-553del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587775 | ||||||
| chr16:89587779 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.927+677C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587779 | |||||||
| chr16:89587781 | G | GC | 24 | a0001c0001t0001g0040 a0001c0001t0001g0069 a0001c0001t0001g0105 others(21): Show |
24 | HG00544.hp1 HG00621.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.927+684dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | ||||||
| chr16:89587781 | G | GCCCCCCG others(5): Show |
4 | a0001c0001t0001g0090 a0001c0001t0001g0097 a0001c0024t0001g0208 others(1): Show |
4 | HG00642.hp1 HG01071.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+684_927+685ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | ||||||
| chr16:89587781 | G | GCCCCCCG others(903): Show |
1 | a0001c0002t0001g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.927+684_927+685ins others(910): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | ||||||
| chr16:89587781 | G | GCCCCCCG others(392): Show |
1 | a0001c0002t0004g0153 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(399): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | ||||||
| chr16:89587781 | G | GCCCCCCG others(32): Show |
1 | a0002c0003t0003g0113 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | ||||||
| chr16:89587781 | G | GCCCCCGT others(4): Show |
1 | a0001c0001t0001g0269 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.927+683_927+693dup others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | ||||||
| chr16:89587781 | G | GCCCCCGT others(318): Show |
1 | a0003c0006t0003g0152 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.927+710_927+711ins others(325): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | ||||||
| chr16:89587781 | G | GCCCCCGT others(209): Show |
1 | a0002c0004t0002g0302 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.927+710_927+711ins others(216): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | ||||||
| chr16:89587781 | G | GCCCCCGT others(106): Show |
1 | a0001c0001t0001g0326 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(113): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | ||||||
| chr16:89587781 | G | GCCCCCGT others(964): Show |
1 | a0001c0001t0001g0184 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(971): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | ||||||
| chr16:89587781 | G | GCCCCCGT others(575): Show |
1 | a0001c0002t0002g0200 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(582): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | ||||||
| chr16:89587781 | GCCCCCGT others(20): Show |
G | 5 | a0001c0001t0001g0108 a0001c0002t0002g0087 a0001c0002t0003g0225 others(2): Show |
5 | HG01106.hp2 HG01346.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+694_927+720del others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | ||||||
| chr16:89587781 | GCCCCCGT others(84): Show |
G | 4 | a0001c0001t0001g0146 a0001c0001t0001g0272 a0001c0002t0004g0056 others(1): Show |
4 | HG01168.hp1 NA18940.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+694_927+784del others(91): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | ||||||
| chr16:89587781 | GCCCCCGT others(239): Show |
G | 1 | a0001c0001t0001g0259 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.927+694_928-634del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | ||||||
| chr16:89587782 | CCCCCGTG others(120): Show |
C | 2 | a0001c0001t0001g0088 a0001c0002t0002g0026 |
2 | HG01978.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.927+685_928-762del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587782 | ||||||
| chr16:89587782 | CCCCCGTG others(328): Show |
C | 2 | a0001c0001t0001g0064 a0001c0002t0004g0264 |
2 | HG03139.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.927+685_928-554del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587782 | ||||||
| chr16:89587782 | CCCCCGTG others(365): Show |
C | 1 | a0001c0007t0006g0155 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.927+685_928-517del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587782 | ||||||
| chr16:89587782 | CCCCCGTG others(402): Show |
C | 1 | a0001c0002t0009g0318 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.927+685_928-480del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587782 | ||||||
| chr16:89587785 | C | CCCCGTGT others(17): Show |
1 | a0001c0002t0011g0195 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.927+684_927+685ins others(24): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCCGTGTC others(95): Show |
1 | a0001c0001t0001g0074 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(102): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCCGTGTC others(58): Show |
1 | a0001c0001t0001g0213 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.927+684_927+685ins others(65): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCCGTGTC others(231): Show |
1 | a0001c0001t0001g0172 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(238): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCCGTGTC others(5): Show |
19 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0093 others(16): Show |
20 | HG00544.hp2 HG00558.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.927+684_927+685ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCCGTGTC others(301): Show |
1 | a0001c0002t0004g0231 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(308): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCCGTGTC others(208): Show |
1 | a0001c0001t0001g0059 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(215): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCCGTGTC others(43): Show |
2 | a0003c0006t0003g0164 a0003c0006t0003g0227 |
2 | HG02080.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.927+684_927+685ins others(50): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCCGTGTC others(194): Show |
1 | a0001c0002t0004g0217 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(201): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCCGTGTC others(42): Show |
1 | a0001c0001t0001g0011 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.927+684_927+685ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCCGTGTC others(301): Show |
1 | a0001c0001t0001g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.927+684_927+685ins others(308): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCCGTGTC others(68): Show |
1 | a0005c0014t0001g0012 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(75): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCCGTGTT others(5): Show |
4 | a0001c0001t0008g0050 a0001c0002t0004g0215 a0002c0003t0003g0134 others(1): Show |
4 | HG00673.hp1 HG02080.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+684_927+685ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCCGTGTT others(42): Show |
1 | a0002c0003t0003g0144 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.927+684_927+685ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCGTGTCA others(820): Show |
1 | a0001c0001t0001g0185 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.927+698_927+699ins others(827): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCGTGTCA others(41): Show |
1 | a0001c0001t0001g0192 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.927+693_927+694ins others(48): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCGTGTCA others(116): Show |
1 | a0002c0004t0002g0293 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.927+693_927+694ins others(123): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCGTGTCA others(4): Show |
20 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0095 others(17): Show |
20 | HG00323.hp2 HG01257.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.927+693_927+694ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCGTGTCA others(67): Show |
1 | a0001c0002t0005g0191 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(74): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCGTGTCA others(42): Show |
1 | a0001c0001t0001g0328 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCGTGTCA others(79): Show |
3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0063 |
3 | HG02602.hp2 HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.927+693_927+694ins others(86): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCGTGTCA others(105): Show |
1 | a0001c0001t0001g0206 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.927+693_927+694ins others(112): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCGTGTCA others(267): Show |
1 | a0004c0011t0001g0081 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(274): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCGTGTCA others(78): Show |
1 | a0001c0001t0001g0237 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(85): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCGTGTCA others(78): Show |
1 | a0001c0001t0001g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(85): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCGTGTCA others(169): Show |
1 | a0001c0002t0002g0270 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.927+693_927+694ins others(176): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCGTGTCA others(31): Show |
1 | a0001c0002t0004g0137 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.927+690_927+691ins others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCGTGTTA others(637): Show |
1 | a0001c0001t0001g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.927+688_927+689ins others(644): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCGTGTTA others(31): Show |
1 | a0002c0017t0003g0142 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.927+688_927+689ins others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCGTGTTA others(285): Show |
1 | a0001c0002t0002g0330 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.927+688_927+689ins others(292): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | CCGTGTTA others(155): Show |
1 | a0001c0002t0003g0229 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.927+688_927+689ins others(162): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | C | G | 2 | a0001c0002t0001g0276 a0001c0002t0004g0224 |
2 | HG00639.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.927+683C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587785 | |||||||
| chr16:89587785 | CCGTGTCA others(95): Show |
C | 1 | a0001c0001t0001g0311 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.927+711_928-761del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587785 | CCGTGTCA others(250): Show |
C | 1 | a0001c0002t0004g0135 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.927+716_928-601del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | ||||||
| chr16:89587786 | C | CGTGTCAC others(251): Show |
1 | a0002c0003t0003g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(258): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587786 | ||||||
| chr16:89587786 | CGTGTCAC others(30): Show |
C | 1 | a0001c0002t0003g0038 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.927+685_927+721del others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587786 | |||||||
| chr16:89587786 | CGTGTCAC others(249): Show |
C | 1 | a0001c0002t0002g0292 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.927+685_928-633del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587786 | |||||||
| chr16:89587788 | T | C | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+686T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587788 | |||||||
| chr16:89587791 | C | T | 38 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0072 others(35): Show |
39 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.927+689C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587791 | |||||||
| chr16:89587792 | ACCCACAG others(46): Show |
A | 15 | a0001c0001t0001g0052 a0001c0001t0001g0091 a0001c0001t0001g0092 others(12): Show |
15 | HG00140.hp1 HG00639.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.927+694_927+746del others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587792 | ||||||
| chr16:89587792 | ACCCACAG others(292): Show |
A | 8 | a0001c0001t0001g0040 a0001c0001t0001g0085 a0001c0001t0001g0105 others(5): Show |
8 | HG01070.hp1 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+694_928-581del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587792 | ||||||
| chr16:89587793 | C | CCCACAGA others(294): Show |
1 | a0002c0004t0002g0309 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.927+710_927+711ins others(301): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587793 | ||||||
| chr16:89587793 | C | CCCGCGTG others(31): Show |
1 | a0001c0008t0002g0019 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.927+693_927+694ins others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587793 | ||||||
| chr16:89587793 | C | CCCGCGTG others(30): Show |
1 | a0002c0004t0002g0316 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.927+693_927+694ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587793 | ||||||
| chr16:89587793 | C | G | 13 | a0001c0001t0001g0073 a0001c0001t0001g0179 a0001c0001t0001g0273 others(10): Show |
13 | HG00423.hp1 HG01361.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.927+691C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587793 | |||||||
| chr16:89587797 | C | T | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+695C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587797 | |||||||
| chr16:89587801 | T | A | 8 | a0001c0001t0001g0089 a0001c0001t0001g0206 a0001c0001t0001g0211 others(5): Show |
8 | HG02615.hp1 HG03239.hp2 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.927+699T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587801 | |||||||
| chr16:89587804 | A | G | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+702A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587804 | |||||||
| chr16:89587805 | C | T | 9 | a0001c0001t0001g0111 a0001c0001t0001g0180 a0001c0008t0002g0013 others(6): Show |
9 | HG00597.hp2 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.927+703C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587805 | |||||||
| chr16:89587807 | G | A | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+705G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587807 | |||||||
| chr16:89587807 | GC | G | 79 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0051 others(76): Show |
86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.927+711delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587807 | ||||||
| chr16:89587807 | GCCCCCCG others(58): Show |
G | 1 | a0004c0020t0001g0332 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.927+711_927+775del others(65): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587807 | ||||||
| chr16:89587807 | GCCCCCCG others(186): Show |
G | 1 | a0001c0002t0002g0319 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.927+711_928-670del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587807 | ||||||
| chr16:89587808 | C | CCCCCCGT others(452): Show |
1 | a0002c0004t0002g0324 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.927+720_927+721ins others(459): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | ||||||
| chr16:89587808 | C | CCCCCGTG others(18): Show |
1 | a0001c0002t0010g0210 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.927+710_927+711ins others(25): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | ||||||
| chr16:89587808 | C | CCCCCGTG others(108): Show |
1 | a0001c0001t0001g0071 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.927+710_927+711ins others(115): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | ||||||
| chr16:89587808 | C | CCCCCGTG others(40): Show |
1 | a0001c0002t0002g0190 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.927+710_927+711ins others(47): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | ||||||
| chr16:89587808 | C | CCCCCGTG others(29): Show |
1 | a0001c0001t0001g0265 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.927+710_927+711ins others(36): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | ||||||
| chr16:89587808 | C | CCCCCGTG others(617): Show |
1 | a0001c0002t0004g0165 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.927+710_927+711ins others(624): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | ||||||
| chr16:89587808 | C | CCCCCGTG others(179): Show |
1 | a0001c0001t0001g0066 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.927+710_927+711ins others(186): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | ||||||
| chr16:89587808 | C | CCCCCGTG others(18): Show |
1 | a0001c0002t0004g0137 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.927+710_927+711ins others(25): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | ||||||
| chr16:89587808 | C | CCCCCGTG others(757): Show |
1 | a0002c0004t0002g0271 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.927+710_927+711ins others(764): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | ||||||
| chr16:89587808 | C | CCCCCGTG others(56): Show |
1 | a0002c0003t0003g0141 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.927+710_927+711ins others(63): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | ||||||
| chr16:89587808 | CCCCCCGT others(302): Show |
C | 1 | a0001c0002t0005g0182 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.927+753_928-512del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | ||||||
| chr16:89587809 | C | A | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+707C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587809 | |||||||
| chr16:89587811 | CCCGTGTC others(5): Show |
C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0211 a0001c0001t0001g0233 others(2): Show |
5 | HG01361.hp1 HG02071.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+711_927+722del others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587811 | ||||||
| chr16:89587811 | CCCGTGTC others(69): Show |
C | 2 | a0001c0002t0003g0188 a0001c0005t0002g0306 |
2 | HG02155.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.927+711_927+786del others(76): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587811 | ||||||
| chr16:89587811 | CCCGTGTC others(106): Show |
C | 1 | a0002c0004t0002g0304 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.927+711_928-750del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587811 | ||||||
| chr16:89587812 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.927+710C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587812 | |||||||
| chr16:89587812 | CCGTGTCA others(223): Show |
C | 1 | a0001c0002t0005g0312 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.927+721_928-623del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587812 | ||||||
| chr16:89587812 | CCGTGTCA others(387): Show |
C | 1 | a0001c0002t0007g0007 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.927+721_928-459del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587812 | ||||||
| chr16:89587818 | C | T | 24 | a0001c0001t0001g0072 a0001c0001t0001g0120 a0001c0001t0001g0122 others(21): Show |
24 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.927+716C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587818 | |||||||
| chr16:89587818 | CACCCGCG others(30): Show |
C | 1 | a0001c0002t0003g0201 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.927+721_927+757del others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587818 | ||||||
| chr16:89587819 | A | ACCCACAG others(8): Show |
2 | a0001c0001t0001g0169 a0001c0002t0003g0080 |
2 | NA18944.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.927+720_927+721ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587819 | ||||||
| chr16:89587819 | A | ACCCACAG others(9): Show |
1 | a0001c0001t0001g0209 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.927+720_927+721ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587819 | ||||||
| chr16:89587819 | A | ACCCACAG others(34): Show |
2 | a0001c0001t0001g0069 a0001c0007t0006g0068 |
2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.927+720_927+721ins others(41): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587819 | ||||||
| chr16:89587819 | A | ACCCACAG others(60): Show |
1 | a0001c0001t0001g0111 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.927+720_927+721ins others(67): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587819 | ||||||
| chr16:89587819 | A | AGCCACAG others(9): Show |
1 | a0001c0005t0002g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.927+717_927+718ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587819 | |||||||
| chr16:89587819 | A | AGCCACAG others(274): Show |
1 | a0002c0004t0002g0020 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.927+717_927+718ins others(281): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587819 | |||||||
| chr16:89587819 | A | AGCCACAG others(706): Show |
1 | a0001c0005t0002g0043 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.927+717_927+718ins others(713): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587819 | |||||||
| chr16:89587819 | A | AGCCACAG others(197): Show |
1 | a0001c0005t0002g0042 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.927+717_927+718ins others(204): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587819 | |||||||
| chr16:89587819 | A | AGCCACAG others(34): Show |
1 | a0002c0003t0004g0301 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.927+717_927+718ins others(41): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587819 | |||||||
| chr16:89587823 | G | C | 14 | a0001c0001t0001g0069 a0001c0001t0001g0095 a0001c0001t0001g0111 others(11): Show |
14 | HG00558.hp1 HG00621.hp2 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.927+721G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587823 | |||||||
| chr16:89587823 | G | GCGTGTCA others(251): Show |
1 | a0001c0001t0001g0089 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.927+736_927+737ins others(258): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587823 | ||||||
| chr16:89587823 | G | GCGTGTCA others(270): Show |
1 | a0002c0004t0002g0305 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.927+736_927+737ins others(277): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587823 | ||||||
| chr16:89587823 | GCGTGTCA others(265): Show |
G | 1 | a0001c0002t0002g0313 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.927+753_928-549del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587823 | ||||||
| chr16:89587829 | C | CACCCACA others(20): Show |
2 | a0003c0006t0003g0267 a0003c0006t0003g0268 |
2 | NA18946.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.927+748_927+749ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587829 | ||||||
| chr16:89587829 | C | T | 1 | a0001c0002t0004g0218 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.927+727C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587829 | |||||||
| chr16:89587829 | CACCCACA others(19): Show |
C | 5 | a0001c0001t0001g0103 a0001c0001t0001g0121 a0001c0002t0002g0045 others(2): Show |
5 | HG00099.hp2 HG01517.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+749_927+774del others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587829 | ||||||
| chr16:89587831 | C | G | 2 | a0001c0001t0001g0273 a0001c0002t0013g0189 |
2 | HG01361.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.927+729C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587831 | |||||||
| chr16:89587834 | A | C | 1 | a0001c0002t0003g0080 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.927+732A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587834 | |||||||
| chr16:89587835 | C | T | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+733C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587835 | |||||||
| chr16:89587837 | G | T | 1 | a0001c0002t0003g0080 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.927+735G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587837 | |||||||
| chr16:89587839 | T | A | 25 | a0001c0001t0001g0059 a0001c0001t0001g0067 a0001c0001t0001g0084 others(22): Show |
25 | HG00323.hp1 HG00733.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.927+737T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587839 | |||||||
| chr16:89587839 | T | TACACGGC others(131): Show |
1 | a0002c0003t0003g0130 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.927+752_927+753ins others(138): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587839 | ||||||
| chr16:89587840 | A | G | 1 | a0001c0002t0003g0080 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.927+738A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587840 | |||||||
| chr16:89587843 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0238 a0001c0008t0001g0014 others(1): Show |
4 | HG01123.hp1 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+741C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587843 | |||||||
| chr16:89587845 | G | GC | 36 | a0001c0001t0001g0058 a0001c0001t0001g0083 a0001c0001t0001g0100 others(33): Show |
37 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.927+748dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587845 | ||||||
| chr16:89587845 | G | GCCCCCCG others(5): Show |
1 | a0001c0001t0001g0097 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.927+748_927+749ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587845 | ||||||
| chr16:89587845 | G | GCCCCCCG others(785): Show |
1 | a0002c0003t0003g0129 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.927+748_927+749ins others(792): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587845 | ||||||
| chr16:89587845 | G | GCCCCCCG others(32): Show |
1 | a0002c0003t0003g0128 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.927+748_927+749ins others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587845 | ||||||
| chr16:89587845 | G | GCCCCCGT others(4): Show |
3 | a0001c0001t0001g0269 a0001c0001t0001g0326 a0001c0002t0005g0284 |
3 | HG00733.hp1 HG02615.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.927+752_927+753ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587845 | ||||||
| chr16:89587845 | G | GCCCCCGT others(481): Show |
1 | a0001c0002t0003g0282 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.927+752_927+753ins others(488): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587845 | ||||||
| chr16:89587845 | GCCCCCGT others(20): Show |
G | 7 | a0001c0001t0001g0039 a0001c0001t0001g0094 a0001c0001t0001g0145 others(4): Show |
7 | HG00597.hp2 HG00741.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+753_927+779del others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587845 | ||||||
| chr16:89587845 | GCCCCCGT others(148): Show |
G | 1 | a0001c0002t0004g0117 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.928-760_928-606del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587845 | ||||||
| chr16:89587846 | CCCCCGTG others(264): Show |
C | 2 | a0001c0002t0003g0298 a0001c0007t0006g0159 |
2 | HG02818.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.927+749_928-554del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587846 | ||||||
| chr16:89587849 | C | CCCCGTGT others(6): Show |
2 | a0001c0001t0001g0090 a0001c0002t0013g0189 |
2 | HG00642.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.927+748_927+749ins others(13): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | ||||||
| chr16:89587849 | C | CCCGTGTC others(5): Show |
12 | a0001c0001t0001g0070 a0001c0001t0001g0171 a0001c0001t0001g0172 others(9): Show |
12 | HG00099.hp1 HG00558.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.927+748_927+749ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | ||||||
| chr16:89587849 | C | CCCGTGTC others(119): Show |
1 | a0001c0002t0003g0177 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.927+748_927+749ins others(126): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | ||||||
| chr16:89587849 | C | CCCGTGTC others(569): Show |
1 | a0001c0001t0001g0242 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.927+748_927+749ins others(576): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | ||||||
| chr16:89587849 | C | CCCGTGTC others(42): Show |
2 | a0001c0001t0001g0180 a0001c0001t0001g0207 |
2 | HG02055.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.927+748_927+749ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | ||||||
| chr16:89587849 | C | CCCGTGTC others(270): Show |
1 | a0001c0001t0001g0278 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.927+748_927+749ins others(277): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | ||||||
| chr16:89587849 | C | CCCGTGTT others(5): Show |
6 | a0001c0001t0001g0122 a0001c0002t0004g0218 a0002c0003t0003g0131 others(3): Show |
6 | HG02129.hp2 NA18945.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+748_927+749ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | ||||||
| chr16:89587849 | C | CCCGTGTT others(230): Show |
1 | a0001c0001t0001g0238 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.927+748_927+749ins others(237): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | ||||||
| chr16:89587849 | C | CCGTGTCA others(57): Show |
1 | a0002c0004t0002g0309 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.927+752_927+753ins others(64): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | ||||||
| chr16:89587849 | C | CCGTGTCA others(4): Show |
19 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0034 others(16): Show |
20 | HG01081.hp2 HG01175.hp1 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.927+752_927+753ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | ||||||
| chr16:89587849 | C | CCGTGTCA others(67): Show |
1 | a0001c0013t0002g0010 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+752_927+753ins others(74): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | ||||||
| chr16:89587849 | C | CCGTGTCA others(367): Show |
1 | a0003c0006t0003g0005 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.927+752_927+753ins others(374): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | ||||||
| chr16:89587849 | C | G | 17 | a0001c0001t0001g0052 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00140.hp1 HG00639.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.927+747C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587849 | |||||||
| chr16:89587850 | CGTGTTAC others(30): Show |
C | 1 | a0001c0005t0002g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.927+749_927+785del others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587850 | |||||||
| chr16:89587851 | G | A | 2 | a0001c0001t0001g0244 a0001c0002t0002g0200 |
2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.927+749G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587851 | |||||||
| chr16:89587855 | T | C | 193 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0030 others(190): Show |
202 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.927+753T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587855 | |||||||
| chr16:89587855 | T | TACCCGCG others(4): Show |
1 | a0001c0002t0001g0314 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.927+757_927+758ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587855 | ||||||
| chr16:89587856 | ACCCACAG others(228): Show |
A | 1 | a0001c0002t0004g0321 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.927+758_928-581del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587856 | ||||||
| chr16:89587857 | C | CCCGCGTG others(56): Show |
1 | a0001c0002t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.927+757_927+758ins others(63): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587857 | ||||||
| chr16:89587857 | C | G | 20 | a0001c0001t0001g0063 a0001c0001t0001g0073 a0001c0001t0001g0079 others(17): Show |
20 | HG00621.hp2 HG00673.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.927+755C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587857 | |||||||
| chr16:89587865 | T | A | 11 | a0001c0001t0001g0070 a0001c0001t0001g0084 a0001c0001t0001g0090 others(8): Show |
11 | HG00099.hp1 HG00558.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+763T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587865 | |||||||
| chr16:89587869 | C | T | 9 | a0001c0001t0001g0179 a0001c0001t0001g0181 a0001c0001t0001g0265 others(6): Show |
9 | HG01928.hp2 HG03195.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.927+767C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587869 | |||||||
| chr16:89587871 | GC | G | 68 | a0001c0001t0001g0030 a0001c0001t0001g0051 a0001c0001t0001g0052 others(65): Show |
69 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.927+775delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587871 | ||||||
| chr16:89587871 | GCCCCCCG others(187): Show |
G | 1 | a0001c0002t0002g0197 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.927+775_928-605del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587871 | ||||||
| chr16:89587872 | C | CCCCCCGT others(82): Show |
1 | a0001c0001t0001g0251 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.928-755_928-754ins others(89): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587872 | ||||||
| chr16:89587872 | C | CCCCCGTG others(3): Show |
1 | a0001c0002t0002g0248 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.927+774_927+775ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587872 | ||||||
| chr16:89587872 | C | CCCCCGTG others(18): Show |
1 | a0001c0002t0002g0330 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.927+774_927+775ins others(25): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587872 | ||||||
| chr16:89587872 | C | CCCCCGTG others(66): Show |
1 | a0001c0005t0002g0295 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.927+774_927+775ins others(73): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587872 | ||||||
| chr16:89587872 | C | CCCCCGTG others(29): Show |
1 | a0001c0001t0001g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.927+774_927+775ins others(36): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587872 | ||||||
| chr16:89587872 | C | CCCCCGTG others(56): Show |
1 | a0001c0002t0004g0138 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.927+774_927+775ins others(63): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587872 | ||||||
| chr16:89587872 | CCCCCCGT others(94): Show |
C | 1 | a0001c0002t0004g0139 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.927+785_928-688del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587872 | ||||||
| chr16:89587875 | CCCGTGTC others(5): Show |
C | 10 | a0001c0001t0001g0100 a0001c0001t0001g0240 a0001c0002t0001g0314 others(7): Show |
10 | HG01123.hp2 HG01891.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.927+775_927+786del others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587875 | ||||||
| chr16:89587875 | CCCGTGTC others(42): Show |
C | 1 | a0002c0004t0002g0303 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.927+775_928-750del others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587875 | ||||||
| chr16:89587876 | C | T | 2 | a0001c0002t0003g0037 a0001c0002t0003g0044 |
2 | NA18977.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.927+774C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587876 | |||||||
| chr16:89587876 | CCGTGTCA others(4): Show |
C | 4 | a0001c0001t0001g0058 a0001c0001t0001g0122 a0002c0003t0003g0221 others(1): Show |
4 | NA18942.hp1 NA18959.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+785_928-778del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587876 | ||||||
| chr16:89587877 | CGTGTCAC others(3): Show |
C | 1 | a0001c0002t0003g0230 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.927+776_927+785del others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587877 | |||||||
| chr16:89587878 | G | A | 2 | a0001c0002t0002g0248 a0001c0002t0004g0219 |
2 | HG02132.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.927+776G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587878 | |||||||
| chr16:89587882 | C | T | 9 | a0001c0001t0001g0178 a0001c0001t0001g0331 a0001c0001t0008g0050 others(6): Show |
9 | HG00673.hp1 HG01109.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.927+780C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587882 | |||||||
| chr16:89587883 | A | ACCCACAG others(8): Show |
1 | a0002c0003t0003g0222 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.927+784_927+785ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587883 | ||||||
| chr16:89587883 | A | ACCCACAG others(9): Show |
2 | a0001c0001t0001g0120 a0002c0004t0002g0299 |
2 | NA18990.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.927+784_927+785ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587883 | ||||||
| chr16:89587883 | A | ACCCACAG others(36): Show |
1 | a0001c0001t0001g0184 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.927+784_927+785ins others(43): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587883 | ||||||
| chr16:89587883 | A | ACCCACAG others(141): Show |
1 | a0002c0004t0002g0020 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.927+784_927+785ins others(148): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587883 | ||||||
| chr16:89587883 | A | ACCCACAG others(115): Show |
1 | a0001c0005t0002g0202 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.927+784_927+785ins others(122): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587883 | ||||||
| chr16:89587883 | A | ACCCACAG others(61): Show |
1 | a0001c0001t0001g0186 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.927+784_927+785ins others(68): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587883 | ||||||
| chr16:89587883 | A | ACCCACAG others(45): Show |
1 | a0001c0007t0006g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.927+784_927+785ins others(52): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587883 | ||||||
| chr16:89587883 | A | ACCCACAG others(62): Show |
1 | a0002c0004t0002g0271 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.927+784_927+785ins others(69): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587883 | ||||||
| chr16:89587883 | A | AGCCACAG others(8): Show |
2 | a0001c0001t0001g0072 a0002c0003t0004g0301 |
2 | HG00621.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.927+781_927+782ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587883 | |||||||
| chr16:89587883 | A | AGCCACAG others(9): Show |
1 | a0001c0005t0002g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.927+781_927+782ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587883 | |||||||
| chr16:89587883 | A | AGCCACAG others(146): Show |
1 | a0001c0005t0002g0294 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.927+781_927+782ins others(153): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587883 | |||||||
| chr16:89587883 | A | AGCCACAG others(88): Show |
9 | a0001c0001t0001g0241 a0001c0005t0002g0001 a0001c0005t0002g0076 others(6): Show |
14 | HG01070.hp2 HG01071.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.927+781_927+782ins others(95): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587883 | |||||||
| chr16:89587887 | G | A | 1 | a0001c0002t0002g0329 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.927+785G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587887 | |||||||
| chr16:89587887 | G | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0072 a0001c0001t0001g0083 others(24): Show |
33 | HG00438.hp1 HG00621.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.927+785G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587887 | |||||||
| chr16:89587887 | G | GCGTGTCA others(308): Show |
1 | a0001c0001t0001g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.928-773_928-772ins others(315): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587887 | ||||||
| chr16:89587887 | G | GCGTGTCA others(19): Show |
3 | a0001c0002t0002g0190 a0001c0002t0004g0126 a0001c0007t0006g0156 |
3 | HG00280.hp1 HG00544.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.928-777_928-752dup others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587887 | ||||||
| chr16:89587887 | G | GCGTGTCA others(72): Show |
1 | a0002c0004t0002g0305 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.928-752_928-751ins others(79): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587887 | ||||||
| chr16:89587887 | G | GCGTGTCA others(407): Show |
1 | a0001c0001t0001g0237 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.928-769_928-768ins others(414): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587887 | ||||||
| chr16:89587887 | GCGTGTCA others(83): Show |
G | 2 | a0001c0002t0004g0055 a0001c0002t0004g0317 |
2 | HG03471.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.928-760_928-671del others(90): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587887 | ||||||
| chr16:89587887 | GCGTGTCA others(201): Show |
G | 1 | a0001c0002t0002g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.928-723_928-516del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587887 | ||||||
| chr16:89587893 | C | T | 4 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0002t0004g0112 others(1): Show |
4 | HG02080.hp1 NA18962.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-782C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587893 | |||||||
| chr16:89587895 | C | G | 4 | a0001c0001t0001g0072 a0001c0005t0002g0306 a0001c0005t0002g0315 others(1): Show |
4 | HG02145.hp2 HG02155.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-780C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587895 | |||||||
| chr16:89587903 | T | A | 9 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0001c0001t0001g0209 others(6): Show |
9 | HG00558.hp1 HG00733.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.928-772T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587903 | |||||||
| chr16:89587907 | C | T | 9 | a0001c0001t0001g0059 a0001c0001t0001g0073 a0001c0001t0001g0192 others(6): Show |
9 | HG00140.hp2 HG00741.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.928-768C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587907 | |||||||
| chr16:89587909 | G | GC | 78 | a0001c0001t0001g0039 a0001c0001t0001g0058 a0001c0001t0001g0059 others(75): Show |
78 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.928-761dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | ||||||
| chr16:89587909 | G | GCCCCCCG others(21): Show |
2 | a0001c0002t0001g0163 a0003c0006t0003g0228 |
2 | HG02083.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.928-761_928-760ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | ||||||
| chr16:89587909 | G | GCCCCCCG others(21): Show |
2 | a0001c0001t0001g0277 a0001c0001t0001g0327 |
2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.928-761_928-760ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | ||||||
| chr16:89587909 | G | GCCCCCCG others(236): Show |
1 | a0002c0003t0003g0004 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.928-761_928-760ins others(243): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | ||||||
| chr16:89587909 | G | GCCCCCGT others(20): Show |
2 | a0001c0002t0003g0176 a0001c0002t0004g0125 |
2 | HG02027.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.928-752_928-751ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | ||||||
| chr16:89587909 | G | GCCCCCGT others(177): Show |
2 | a0001c0001t0001g0187 a0011c0021t0001g0216 |
2 | NA18970.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.928-752_928-751ins others(184): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | ||||||
| chr16:89587909 | G | GCCCCCGT others(196): Show |
1 | a0003c0006t0003g0151 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.928-752_928-751ins others(203): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | ||||||
| chr16:89587909 | G | GCCCCCGT others(46): Show |
1 | a0001c0002t0002g0027 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.928-752_928-751ins others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | ||||||
| chr16:89587909 | G | GCCCCCGT others(20): Show |
1 | a0001c0002t0011g0195 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.928-755_928-754ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | ||||||
| chr16:89587909 | G | GCCCCCGT others(20): Show |
1 | a0001c0001t0001g0089 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.928-757_928-756ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | ||||||
| chr16:89587909 | G | GCCCCCGT others(427): Show |
1 | a0001c0001t0001g0279 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.928-757_928-756ins others(434): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | ||||||
| chr16:89587909 | GCCCCCGT others(4): Show |
G | 1 | a0002c0003t0003g0128 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.928-762_928-752del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | ||||||
| chr16:89587910 | CCCCCGTG others(274): Show |
C | 1 | a0001c0001t0001g0083 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.928-760_928-480del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587910 | ||||||
| chr16:89587913 | C | CCCGTGTC others(166): Show |
1 | a0001c0001t0001g0209 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.928-761_928-760ins others(173): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587913 | ||||||
| chr16:89587913 | CCGTGTCA others(4): Show |
C | 9 | a0001c0001t0001g0060 a0001c0001t0001g0120 a0001c0002t0003g0080 others(6): Show |
9 | HG00597.hp2 HG02486.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.928-751_928-741del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587913 | ||||||
| chr16:89587913 | CCGTGTCA others(122): Show |
C | 3 | a0001c0002t0002g0194 a0001c0002t0002g0196 a0002c0003t0002g0310 |
3 | HG00423.hp1 NA19010.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.928-751_928-623del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587913 | ||||||
| chr16:89587913 | CCGTGTCA others(212): Show |
C | 1 | a0001c0002t0002g0235 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.928-751_928-533del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587913 | ||||||
| chr16:89587913 | CCGTGTCA others(286): Show |
C | 1 | a0001c0001t0001g0084 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.928-751_928-459del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587913 | ||||||
| chr16:89587914 | CGTGTCAC others(3): Show |
C | 8 | a0001c0001t0001g0122 a0001c0001t0001g0178 a0001c0001t0001g0236 others(5): Show |
8 | HG00323.hp1 HG02155.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-760_928-751del others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587914 | |||||||
| chr16:89587915 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.928-760G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587915 | |||||||
| chr16:89587919 | C | T | 13 | a0001c0001t0001g0089 a0001c0001t0001g0192 a0001c0001t0001g0269 others(10): Show |
13 | HG00140.hp2 HG00642.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.928-756C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587919 | |||||||
| chr16:89587919 | CACCCGCG others(84): Show |
C | 3 | a0001c0001t0001g0168 a0001c0002t0004g0118 a0008c0019t0002g0246 |
3 | HG02165.hp1 HG03834.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.928-751_928-661del others(91): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587919 | ||||||
| chr16:89587919 | CACCCGCG others(149): Show |
C | 1 | a0001c0001t0001g0079 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.928-751_928-596del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587919 | ||||||
| chr16:89587920 | A | ACCCACAG others(35): Show |
1 | a0001c0001t0001g0058 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.928-752_928-751ins others(42): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587920 | ||||||
| chr16:89587920 | A | ACCCACAG others(8): Show |
5 | a0001c0001t0001g0269 a0001c0002t0003g0230 a0002c0003t0003g0143 others(2): Show |
5 | HG00438.hp2 HG00621.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.928-752_928-751ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587920 | ||||||
| chr16:89587920 | A | ACCCACAG others(9): Show |
6 | a0001c0001t0001g0205 a0001c0002t0003g0220 a0001c0002t0004g0153 others(3): Show |
7 | HG01257.hp2 HG01258.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-752_928-751ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587920 | ||||||
| chr16:89587920 | A | ACCCACAG others(46): Show |
2 | a0003c0006t0003g0267 a0003c0006t0003g0268 |
2 | NA18946.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.928-752_928-751ins others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587920 | ||||||
| chr16:89587920 | A | AGCCACAG others(9): Show |
1 | a0002c0004t0002g0020 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.928-755_928-754ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587920 | |||||||
| chr16:89587920 | A | AGCCACAG others(47): Show |
1 | a0001c0002t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.928-755_928-754ins others(54): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587920 | |||||||
| chr16:89587924 | G | C | 28 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0001g0086 others(25): Show |
29 | HG00438.hp2 HG00621.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.928-751G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587924 | |||||||
| chr16:89587924 | GCGTGTCA others(164): Show |
G | 4 | a0001c0001t0001g0053 a0001c0001t0001g0061 a0001c0001t0001g0091 others(1): Show |
4 | HG00323.hp2 HG01106.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-723_928-553del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587924 | ||||||
| chr16:89587926 | G | A | 1 | a0001c0002t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-749G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587926 | |||||||
| chr16:89587930 | C | T | 3 | a0001c0001t0001g0178 a0001c0002t0004g0126 a0001c0002t0004g0261 |
3 | HG00544.hp1 HG02257.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.928-745C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587930 | |||||||
| chr16:89587930 | CACCCACA others(20): Show |
C | 4 | a0001c0001t0001g0115 a0001c0001t0001g0146 a0001c0002t0003g0022 others(1): Show |
4 | NA18966.hp2 NA18970.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-723_928-697del others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587930 | ||||||
| chr16:89587930 | CACCCACA others(73): Show |
C | 6 | a0001c0001t0001g0145 a0001c0002t0002g0087 a0001c0002t0003g0035 others(3): Show |
6 | HG01106.hp2 NA18941.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-718_928-639del others(80): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587930 | ||||||
| chr16:89587930 | CACCCACA others(138): Show |
C | 1 | a0001c0001t0001g0258 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.928-723_928-579del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587930 | ||||||
| chr16:89587932 | C | CCCACAGA others(19): Show |
1 | a0002c0004t0002g0316 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.928-724_928-723ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587932 | ||||||
| chr16:89587932 | C | G | 5 | a0001c0005t0002g0001 a0001c0008t0001g0009 a0002c0003t0004g0301 others(2): Show |
6 | HG00621.hp2 HG01074.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-743C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587932 | |||||||
| chr16:89587933 | C | T | 1 | a0001c0002t0002g0307 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.928-742C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587933 | |||||||
| chr16:89587935 | A | G | 1 | a0001c0002t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-740A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587935 | |||||||
| chr16:89587940 | T | A | 31 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0070 others(28): Show |
36 | HG00140.hp2 HG00609.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.928-735T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587940 | |||||||
| chr16:89587944 | C | T | 2 | a0001c0001t0001g0111 a0001c0002t0001g0163 |
2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.928-731C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587944 | |||||||
| chr16:89587946 | GC | G | 72 | a0001c0001t0001g0032 a0001c0001t0001g0051 a0001c0001t0001g0060 others(69): Show |
72 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.928-723delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587946 | ||||||
| chr16:89587946 | GCCCCCCG others(47): Show |
G | 1 | a0001c0001t0001g0333 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.928-723_928-670del others(54): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587946 | ||||||
| chr16:89587946 | GCCCCCCG others(74): Show |
G | 8 | a0001c0001t0001g0052 a0001c0001t0001g0102 a0001c0002t0002g0041 others(5): Show |
8 | HG00639.hp2 HG01928.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-723_928-643del others(81): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587946 | ||||||
| chr16:89587947 | C | A | 1 | a0001c0002t0004g0137 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.928-728C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587947 | |||||||
| chr16:89587947 | C | CCCCCCCG others(20): Show |
1 | a0001c0005t0002g0076 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.928-723_928-722ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | ||||||
| chr16:89587947 | C | CCCCCCGT others(4): Show |
1 | a0001c0008t0002g0016 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.928-719_928-718ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | ||||||
| chr16:89587947 | C | CCCCCCGT others(19): Show |
7 | a0001c0001t0001g0241 a0001c0005t0002g0001 a0001c0005t0002g0202 others(4): Show |
9 | HG01070.hp2 HG01071.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.928-719_928-718ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | ||||||
| chr16:89587947 | C | CCCCCCGT others(104): Show |
1 | a0001c0002t0003g0173 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.928-719_928-718ins others(111): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | ||||||
| chr16:89587947 | C | CCCCCGTG others(3): Show |
1 | a0001c0001t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.928-724_928-723ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | ||||||
| chr16:89587947 | C | CCCCCGTG others(29): Show |
1 | a0001c0002t0005g0191 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.928-724_928-723ins others(36): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | ||||||
| chr16:89587947 | C | CCCCCGTG others(409): Show |
1 | a0001c0001t0001g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-724_928-723ins others(416): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | ||||||
| chr16:89587947 | C | CCCCCGTG others(251): Show |
1 | a0001c0002t0004g0165 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.928-724_928-723ins others(258): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | ||||||
| chr16:89587947 | C | CCCCCGTG others(98): Show |
1 | a0002c0004t0002g0302 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.928-724_928-723ins others(105): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | ||||||
| chr16:89587947 | C | CCCCTCGT others(4): Show |
1 | a0001c0001t0001g0048 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.928-725_928-724ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | ||||||
| chr16:89587947 | C | CCTCCCGT others(4): Show |
1 | a0001c0008t0002g0019 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.928-727_928-726ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | ||||||
| chr16:89587947 | CCCCCCGT others(163): Show |
C | 4 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0007t0006g0006 others(1): Show |
4 | HG01109.hp1 HG03195.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-718_928-549del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | ||||||
| chr16:89587947 | CCCCCCGT others(200): Show |
C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0108 |
2 | HG00099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.928-718_928-512del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | ||||||
| chr16:89587950 | CCCGTGTT others(175): Show |
C | 1 | a0004c0020t0001g0332 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.928-723_928-542del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587950 | ||||||
| chr16:89587951 | C | CCATGTCA others(4): Show |
2 | a0001c0001t0001g0187 a0011c0021t0001g0216 |
2 | NA18970.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.928-723_928-722ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | ||||||
| chr16:89587951 | C | CCCGTGTC others(43): Show |
1 | a0003c0006t0003g0149 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.928-723_928-722ins others(50): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | ||||||
| chr16:89587951 | C | CCGTGTCA others(31): Show |
2 | a0001c0002t0003g0229 a0001c0002t0004g0138 |
2 | HG02735.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.928-719_928-718ins others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | ||||||
| chr16:89587951 | C | CCGTGTCA others(95): Show |
1 | a0001c0002t0004g0125 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.928-719_928-718ins others(102): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | ||||||
| chr16:89587951 | C | CCGTGTCA others(43): Show |
1 | a0001c0001t0001g0090 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.928-719_928-718ins others(50): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | ||||||
| chr16:89587951 | C | CCGTGTCA others(4): Show |
17 | a0001c0001t0001g0171 a0001c0001t0001g0237 a0001c0001t0001g0325 others(14): Show |
17 | HG01952.hp2 HG02027.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.928-719_928-718ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | ||||||
| chr16:89587951 | C | CCGTGTCA others(639): Show |
1 | a0002c0004t0002g0293 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.928-719_928-718ins others(646): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | ||||||
| chr16:89587951 | C | CCGTGTCA others(42): Show |
1 | a0001c0001t0001g0185 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.928-719_928-718ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | ||||||
| chr16:89587951 | C | CCGTGTCA others(42): Show |
3 | a0002c0003t0002g0119 a0003c0006t0003g0226 a0003c0006t0003g0334 |
3 | HG00423.hp2 HG00621.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.928-719_928-718ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | ||||||
| chr16:89587951 | C | CCGTGTCA others(199): Show |
1 | a0003c0006t0003g0005 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.928-719_928-718ins others(206): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | ||||||
| chr16:89587951 | C | CCGTGTCA others(41): Show |
2 | a0002c0003t0003g0113 a0010c0016t0003g0114 |
2 | NA18952.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.928-719_928-718ins others(48): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | ||||||
| chr16:89587951 | C | CCGTGTTA others(4): Show |
1 | a0001c0001t0001g0242 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.928-714_928-713ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | ||||||
| chr16:89587951 | C | CGTGTCAC others(30): Show |
2 | a0001c0002t0002g0200 a0001c0007t0006g0068 |
2 | HG02723.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.928-724_928-723ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | |||||||
| chr16:89587951 | C | CGTGTCAC others(158): Show |
1 | a0001c0002t0004g0217 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.928-724_928-723ins others(165): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | |||||||
| chr16:89587951 | C | CGTGTCAC others(30): Show |
1 | a0001c0002t0004g0218 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.928-724_928-723ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | |||||||
| chr16:89587951 | C | CGTGTCAC others(193): Show |
1 | a0001c0002t0002g0307 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.928-724_928-723ins others(200): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | |||||||
| chr16:89587951 | C | CGTGTCAC others(3): Show |
28 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(25): Show |
28 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.928-724_928-723ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | |||||||
| chr16:89587951 | C | CGTGTCAC others(67): Show |
1 | a0001c0001t0001g0071 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.928-724_928-723ins others(74): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | |||||||
| chr16:89587951 | C | CGTGTCAC others(79): Show |
1 | a0003c0006t0003g0005 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.928-724_928-723ins others(86): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | |||||||
| chr16:89587951 | C | CGTGTCAG others(313): Show |
1 | a0002c0004t0002g0299 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.928-724_928-723ins others(320): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | |||||||
| chr16:89587951 | C | CGTGTCAG others(68): Show |
1 | a0001c0001t0001g0073 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.928-724_928-723ins others(75): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | |||||||
| chr16:89587951 | C | CGTGTTAC others(320): Show |
1 | a0001c0001t0001g0031 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.928-724_928-723ins others(327): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | |||||||
| chr16:89587951 | C | CGTGTTAC others(3): Show |
1 | a0002c0003t0003g0077 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.928-724_928-723ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | |||||||
| chr16:89587951 | C | G | 2 | a0001c0001t0001g0048 a0001c0008t0002g0019 |
2 | HG01081.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.928-724C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | |||||||
| chr16:89587951 | C | T | 3 | a0001c0001t0001g0093 a0001c0002t0003g0049 a0001c0002t0010g0210 |
3 | HG00733.hp2 HG04228.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.928-724C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | |||||||
| chr16:89587951 | CCGTGTTA others(174): Show |
C | 1 | a0001c0002t0002g0329 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.928-718_928-538del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | ||||||
| chr16:89587953 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0244 |
2 | HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.928-722G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587953 | |||||||
| chr16:89587954 | T | C | 1 | a0001c0002t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-721T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587954 | |||||||
| chr16:89587957 | T | C | 195 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0030 others(192): Show |
204 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.928-718T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587957 | |||||||
| chr16:89587957 | T | TACCCACA others(371): Show |
1 | a0001c0001t0008g0050 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.928-697_928-696ins others(378): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587957 | ||||||
| chr16:89587957 | T | TACCCACA others(460): Show |
1 | a0003c0006t0003g0268 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.928-666_928-665ins others(467): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587957 | ||||||
| chr16:89587957 | T | TACCCCGC others(5): Show |
1 | a0001c0001t0001g0291 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.928-714_928-713ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587957 | ||||||
| chr16:89587957 | T | TACCCGCG others(4): Show |
1 | a0001c0001t0001g0331 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.928-714_928-713ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587957 | ||||||
| chr16:89587957 | T | TACCCGCG others(261): Show |
1 | a0002c0003t0003g0140 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.928-714_928-713ins others(268): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587957 | ||||||
| chr16:89587958 | ACCCACAG others(8): Show |
A | 11 | a0001c0001t0001g0030 a0001c0001t0001g0097 a0001c0001t0001g0213 others(8): Show |
11 | HG00597.hp2 HG01071.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.928-713_928-699del others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587958 | ||||||
| chr16:89587958 | ACCCACAG others(35): Show |
A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0086 others(11): Show |
15 | HG00733.hp2 HG01081.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.928-713_928-672del others(42): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587958 | ||||||
| chr16:89587958 | ACCCACAG others(126): Show |
A | 8 | a0001c0001t0001g0051 a0001c0001t0001g0092 a0001c0001t0001g0211 others(5): Show |
8 | HG01175.hp2 HG01192.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-713_928-581del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587958 | ||||||
| chr16:89587959 | C | G | 9 | a0001c0001t0001g0072 a0001c0001t0001g0262 a0001c0001t0001g0273 others(6): Show |
9 | HG00621.hp2 HG00673.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.928-716C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587959 | |||||||
| chr16:89587963 | C | T | 1 | a0001c0002t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-712C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587963 | |||||||
| chr16:89587967 | T | A | 10 | a0001c0001t0001g0058 a0001c0001t0001g0269 a0001c0001t0012g0147 others(7): Show |
10 | HG00423.hp2 HG00544.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.928-708T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587967 | |||||||
| chr16:89587970 | A | G | 1 | a0001c0002t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-705A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587970 | |||||||
| chr16:89587971 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0111 a0001c0008t0001g0009 others(1): Show |
4 | HG02896.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-704C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587971 | |||||||
| chr16:89587972 | G | A | 1 | a0001c0002t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-703G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587972 | |||||||
| chr16:89587973 | G | C | 1 | a0001c0002t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-702G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587973 | |||||||
| chr16:89587973 | G | GC | 25 | a0001c0001t0001g0048 a0001c0001t0001g0089 a0001c0001t0001g0181 others(22): Show |
25 | HG00558.hp2 HG01074.hp1 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.928-697dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587973 | ||||||
| chr16:89587973 | G | GCCCCCCG others(5): Show |
2 | a0001c0008t0002g0016 a0002c0004t0002g0271 |
2 | HG02109.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.928-697_928-696ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587973 | ||||||
| chr16:89587973 | G | GCCCCCCG others(74): Show |
1 | a0002c0004t0002g0020 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(81): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587973 | ||||||
| chr16:89587973 | G | GCCCCCCG others(26): Show |
1 | a0001c0001t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(33): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587973 | ||||||
| chr16:89587973 | G | GCCCCCGT others(4): Show |
3 | a0001c0001t0001g0066 a0001c0001t0001g0096 a0001c0001t0001g0325 |
3 | HG01257.hp1 HG01952.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.928-698_928-688dup others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587973 | ||||||
| chr16:89587973 | GCCCCCGT others(47): Show |
G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0311 a0001c0007t0006g0285 |
3 | NA18906.hp1 NA19054.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.928-687_928-634del others(54): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587973 | ||||||
| chr16:89587974 | C | A | 1 | a0001c0002t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-701C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587974 | |||||||
| chr16:89587974 | CCCCCGTG others(210): Show |
C | 1 | a0001c0002t0004g0224 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.928-696_928-480del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587974 | ||||||
| chr16:89587975 | C | A | 1 | a0002c0003t0003g0134 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.928-700C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587975 | |||||||
| chr16:89587977 | C | CCATGTCA others(41): Show |
1 | a0001c0001t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.928-697_928-696ins others(48): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCCGTGTC others(5): Show |
17 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(14): Show |
17 | HG00323.hp1 HG00597.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.928-697_928-696ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCCGTGTC others(371): Show |
1 | a0001c0001t0001g0172 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.928-697_928-696ins others(378): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCCGTGTC others(256): Show |
1 | a0001c0001t0001g0206 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(263): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCCGTGTC others(433): Show |
1 | a0002c0004t0014g0300 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.928-697_928-696ins others(440): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCCGTGTC others(198): Show |
1 | a0002c0004t0002g0309 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(205): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCCGTGTC others(386): Show |
1 | a0002c0003t0003g0141 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(393): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCCGTGTC others(207): Show |
1 | a0001c0002t0003g0148 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(214): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCCGTGTT others(5): Show |
6 | a0001c0001t0001g0204 a0001c0002t0003g0173 a0002c0003t0003g0123 others(3): Show |
6 | HG00609.hp2 HG02083.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-697_928-696ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCCGTGTT others(208): Show |
1 | a0003c0006t0003g0260 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(215): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCCGTGTT others(42): Show |
1 | a0002c0003t0003g0131 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.928-697_928-696ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCCGTGTT others(145): Show |
1 | a0002c0003t0003g0004 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(152): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCGTGTCA others(4): Show |
1 | a0001c0008t0002g0019 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.928-696_928-686dup others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCGTGTCA others(881): Show |
1 | a0001c0001t0001g0074 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.928-671_928-670ins others(888): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCGTGTCA others(31): Show |
1 | a0001c0001t0001g0244 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.928-679_928-678ins others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCGTGTCA others(4): Show |
20 | a0001c0001t0001g0060 a0001c0001t0001g0063 a0001c0001t0001g0262 others(17): Show |
20 | HG00438.hp2 HG00741.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.928-688_928-687ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCGTGTCA others(105): Show |
1 | a0001c0001t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.928-688_928-687ins others(112): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCGTGTCA others(681): Show |
1 | a0003c0006t0003g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.928-688_928-687ins others(688): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCGTGTCA others(80): Show |
1 | a0001c0002t0003g0176 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.928-688_928-687ins others(87): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCGTGTCA others(1153): Show |
1 | a0002c0003t0003g0129 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.928-688_928-687ins others(1160): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCGTGTCA others(79): Show |
1 | a0001c0002t0001g0163 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.928-688_928-687ins others(86): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | CCTGTGTC others(5): Show |
1 | a0001c0002t0001g0314 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587977 | C | G | 12 | a0001c0001t0001g0030 a0001c0001t0001g0097 a0001c0001t0001g0213 others(9): Show |
12 | HG00597.hp2 HG01071.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.928-698C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587977 | |||||||
| chr16:89587977 | CCGTGTCA others(185): Show |
C | 1 | a0001c0002t0002g0028 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.928-670_928-479del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | ||||||
| chr16:89587979 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.928-696G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587979 | |||||||
| chr16:89587979 | G | T | 1 | a0001c0002t0001g0314 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.928-696G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587979 | |||||||
| chr16:89587983 | C | CACCCGCG others(191): Show |
1 | a0001c0001t0001g0242 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.928-688_928-687ins others(198): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587983 | ||||||
| chr16:89587983 | C | T | 3 | a0001c0001t0001g0269 a0001c0002t0002g0027 a0001c0007t0006g0156 |
3 | HG02145.hp1 HG03098.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.928-692C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587983 | |||||||
| chr16:89587983 | CACCCACA others(20): Show |
C | 2 | a0001c0002t0007g0007 a0002c0003t0007g0290 |
2 | HG02155.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.928-665_928-639del others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587983 | ||||||
| chr16:89587983 | CACCCACA others(85): Show |
C | 1 | a0001c0001t0001g0272 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.928-670_928-579del others(92): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587983 | ||||||
| chr16:89587984 | ACCCACAG others(9): Show |
A | 10 | a0001c0001t0001g0100 a0001c0001t0001g0115 a0001c0001t0001g0174 others(7): Show |
10 | HG00639.hp1 HG01123.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.928-687_928-672del others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587984 | ||||||
| chr16:89587984 | ACCCACAG others(100): Show |
A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0094 |
2 | HG00741.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.928-687_928-581del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587984 | ||||||
| chr16:89587985 | C | CCCACAGA others(19): Show |
1 | a0001c0005t0002g0001 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.928-671_928-670ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587985 | ||||||
| chr16:89587985 | C | G | 11 | a0001c0001t0001g0059 a0001c0001t0001g0073 a0001c0001t0001g0192 others(8): Show |
11 | HG00140.hp2 HG00438.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.928-690C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587985 | |||||||
| chr16:89587988 | A | C | 1 | a0001c0002t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-687A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587988 | |||||||
| chr16:89587991 | G | T | 1 | a0001c0002t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-684G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587991 | |||||||
| chr16:89587993 | T | A | 11 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0096 others(8): Show |
11 | HG01123.hp1 HG01257.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-682T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587993 | |||||||
| chr16:89587997 | C | T | 9 | a0001c0001t0001g0072 a0001c0001t0001g0178 a0001c0001t0001g0205 others(6): Show |
9 | HG01928.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.928-678C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587997 | |||||||
| chr16:89587999 | G | C | 2 | a0001c0002t0002g0026 a0001c0002t0004g0137 |
2 | HG00609.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.928-676G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587999 | |||||||
| chr16:89587999 | GC | G | 61 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0069 others(58): Show |
66 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.928-670delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587999 | ||||||
| chr16:89587999 | GCCCCCCG others(21): Show |
G | 1 | a0001c0002t0003g0188 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.928-670_928-643del others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587999 | ||||||
| chr16:89588000 | C | A | 1 | a0001c0002t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-675C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588000 | |||||||
| chr16:89588000 | C | CCCCCCGT others(4): Show |
1 | a0001c0001t0001g0326 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.928-666_928-665ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588000 | ||||||
| chr16:89588000 | C | CCCCCCGT others(206): Show |
1 | a0001c0001t0001g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.928-666_928-665ins others(213): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588000 | ||||||
| chr16:89588000 | C | CCCCCCGT others(832): Show |
1 | a0003c0006t0003g0267 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.928-666_928-665ins others(839): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588000 | ||||||
| chr16:89588000 | C | CCCCCCGT others(30): Show |
2 | a0001c0002t0003g0080 a0001c0002t0003g0177 |
2 | NA18944.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.928-666_928-665ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588000 | ||||||
| chr16:89588000 | C | CCCCCGTG others(3): Show |
4 | a0001c0001t0001g0034 a0001c0001t0001g0096 a0001c0001t0001g0237 others(1): Show |
4 | HG01257.hp1 HG01952.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-671_928-670ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588000 | ||||||
| chr16:89588000 | C | CCCCCGTG others(507): Show |
1 | a0001c0001t0001g0111 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.928-671_928-670ins others(514): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588000 | ||||||
| chr16:89588000 | C | CCCCCGTG others(67): Show |
1 | a0001c0001t0001g0059 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.928-671_928-670ins others(74): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588000 | ||||||
| chr16:89588000 | C | CCCCCGTG others(18): Show |
1 | a0002c0003t0004g0301 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.928-671_928-670ins others(25): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588000 | ||||||
| chr16:89588003 | CCCGTGTT others(32): Show |
C | 1 | a0001c0001t0001g0170 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.928-670_928-632del others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588003 | ||||||
| chr16:89588004 | C | CCCGTGTC others(107): Show |
1 | a0003c0006t0003g0149 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.928-670_928-669ins others(114): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588004 | ||||||
| chr16:89588004 | C | CCGTGTCA others(4): Show |
23 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0060 others(20): Show |
23 | HG00741.hp2 HG01071.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.928-666_928-665ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588004 | ||||||
| chr16:89588004 | C | CCGTGTCA others(171): Show |
1 | a0002c0004t0002g0316 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.928-666_928-665ins others(178): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588004 | ||||||
| chr16:89588004 | C | CCGTGTCA others(79): Show |
1 | a0001c0001t0001g0074 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.928-666_928-665ins others(86): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588004 | ||||||
| chr16:89588004 | C | CCGTGTCA others(190): Show |
1 | a0003c0006t0003g0005 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.928-666_928-665ins others(197): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588004 | ||||||
| chr16:89588004 | C | CGTGTCAC others(14): Show |
1 | a0001c0002t0002g0190 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.928-671_928-670ins others(21): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | |||||||
| chr16:89588004 | C | CGTGTCAC others(3): Show |
23 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0001g0071 others(20): Show |
23 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.928-671_928-670ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | |||||||
| chr16:89588004 | C | CGTGTCAC others(230): Show |
1 | a0001c0001t0001g0286 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.928-671_928-670ins others(237): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | |||||||
| chr16:89588004 | C | CGTGTCAC others(167): Show |
1 | a0001c0001t0001g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.928-671_928-670ins others(174): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | |||||||
| chr16:89588004 | C | CGTGTCAC others(214): Show |
1 | a0001c0001t0001g0032 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.928-671_928-670ins others(221): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | |||||||
| chr16:89588004 | C | CGTGTCAC others(79): Show |
1 | a0001c0002t0004g0137 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.928-671_928-670ins others(86): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | |||||||
| chr16:89588004 | C | CGTGTCAC others(131): Show |
1 | a0001c0024t0001g0208 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.928-671_928-670ins others(138): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | |||||||
| chr16:89588004 | C | CGTGTCAC others(67): Show |
1 | a0001c0002t0001g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.928-671_928-670ins others(74): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | |||||||
| chr16:89588004 | C | G | 22 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0093 others(19): Show |
23 | HG00639.hp1 HG00733.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.928-671C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | |||||||
| chr16:89588005 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.928-670C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588005 | |||||||
| chr16:89588006 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.928-669G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588006 | |||||||
| chr16:89588010 | T | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0030 others(181): Show |
193 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.928-665T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588010 | |||||||
| chr16:89588010 | T | TACCCGCG others(4): Show |
4 | a0001c0001t0001g0048 a0001c0002t0004g0215 a0002c0003t0003g0144 others(1): Show |
4 | HG02080.hp1 NA19009.hp2 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-661_928-660ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588010 | ||||||
| chr16:89588011 | ACCCACAG others(9): Show |
A | 1 | a0001c0002t0002g0248 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.928-660_928-645del others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588011 | ||||||
| chr16:89588012 | C | CCCGCGTG others(30): Show |
1 | a0001c0001t0001g0331 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.928-661_928-660ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588012 | ||||||
| chr16:89588012 | C | G | 17 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0089 others(14): Show |
19 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.928-663C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588012 | |||||||
| chr16:89588020 | T | A | 10 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0001g0093 others(7): Show |
10 | HG00558.hp1 HG00733.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.928-655T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588020 | |||||||
| chr16:89588024 | C | T | 7 | a0001c0001t0001g0073 a0001c0002t0001g0033 a0001c0002t0002g0319 others(4): Show |
7 | HG00673.hp2 HG01884.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-651C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588024 | |||||||
| chr16:89588025 | G | A | 1 | a0008c0019t0002g0246 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.928-650G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588025 | |||||||
| chr16:89588026 | GC | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0060 others(82): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.928-643delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588026 | ||||||
| chr16:89588026 | GCCCCCCG others(5): Show |
G | 2 | a0002c0003t0003g0134 a0002c0003t0003g0166 |
2 | NA19004.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.928-645_928-634del others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588026 | ||||||
| chr16:89588027 | C | CCCCCGTG others(109): Show |
2 | a0001c0005t0002g0042 a0001c0005t0002g0043 |
2 | NA18947.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.928-644_928-643ins others(116): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588027 | ||||||
| chr16:89588030 | CCCGTGTC others(5): Show |
C | 5 | a0001c0001t0001g0180 a0001c0002t0001g0314 a0001c0005t0002g0109 others(2): Show |
5 | HG02027.hp1 HG02055.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-643_928-632del others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588030 | ||||||
| chr16:89588031 | C | T | 6 | a0001c0001t0001g0262 a0001c0002t0003g0035 a0001c0002t0003g0037 others(3): Show |
6 | HG03669.hp1 NA18941.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-644C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588031 | |||||||
| chr16:89588031 | CCGTGTCA others(4): Show |
C | 3 | a0001c0005t0002g0306 a0001c0005t0002g0308 a0001c0005t0002g0315 |
3 | HG02132.hp1 HG02155.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.928-633_928-623del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588031 | ||||||
| chr16:89588033 | G | A | 2 | a0001c0002t0002g0248 a0001c0002t0004g0217 |
2 | HG02083.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.928-642G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588033 | |||||||
| chr16:89588037 | C | CACCCGCG others(68): Show |
1 | a0002c0003t0003g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.928-606_928-605ins others(75): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588037 | ||||||
| chr16:89588037 | C | T | 12 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(9): Show |
12 | HG01361.hp1 HG01517.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.928-638C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588037 | |||||||
| chr16:89588038 | A | ACCCACAG others(8): Show |
2 | a0001c0001t0001g0241 a0002c0003t0003g0222 |
2 | HG01975.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.928-634_928-633ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588038 | ||||||
| chr16:89588038 | A | ACCCACAG others(9): Show |
3 | a0001c0001t0001g0072 a0001c0005t0002g0294 a0002c0004t0002g0020 |
3 | HG00438.hp1 HG02145.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.928-634_928-633ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588038 | ||||||
| chr16:89588038 | A | ACCCACAG others(352): Show |
1 | a0001c0001t0001g0186 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.928-634_928-633ins others(359): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588038 | ||||||
| chr16:89588038 | A | ACCCACAG others(34): Show |
7 | a0001c0005t0002g0001 a0001c0005t0002g0076 a0001c0005t0002g0202 others(4): Show |
9 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.928-634_928-633ins others(41): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588038 | ||||||
| chr16:89588038 | A | ACCCACAG others(34): Show |
1 | a0001c0008t0002g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.928-634_928-633ins others(41): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588038 | ||||||
| chr16:89588038 | A | AGCCACAG others(34): Show |
2 | a0002c0004t0002g0002 a0002c0004t0002g0296 |
5 | HG01168.hp2 HG01169.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-637_928-636ins others(41): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588038 | |||||||
| chr16:89588038 | ACCCGCGT others(46): Show |
A | 1 | a0001c0001t0001g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.928-633_928-581del others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588038 | ||||||
| chr16:89588042 | G | A | 1 | a0010c0016t0003g0114 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.928-633G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588042 | |||||||
| chr16:89588042 | G | C | 19 | a0001c0001t0001g0011 a0001c0001t0001g0072 a0001c0001t0001g0100 others(16): Show |
24 | HG00438.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.928-633G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588042 | |||||||
| chr16:89588042 | G | GCGTGTCA others(19): Show |
1 | a0001c0002t0004g0153 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.928-631_928-606dup others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588042 | ||||||
| chr16:89588042 | GCGTGTCA others(46): Show |
G | 1 | a0001c0001t0001g0175 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.928-605_928-553del others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588042 | ||||||
| chr16:89588043 | C | T | 1 | a0001c0002t0002g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.928-632C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588043 | |||||||
| chr16:89588048 | CACCCACA others(20): Show |
C | 6 | a0001c0001t0001g0236 a0001c0002t0002g0292 a0001c0002t0003g0266 others(3): Show |
6 | HG00323.hp1 HG00597.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.928-605_928-579del others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588048 | ||||||
| chr16:89588050 | C | G | 8 | a0001c0005t0002g0001 a0001c0005t0002g0076 a0001c0005t0002g0109 others(5): Show |
10 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.928-625C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588050 | |||||||
| chr16:89588058 | T | A | 22 | a0001c0001t0001g0031 a0001c0001t0001g0086 a0001c0001t0001g0093 others(19): Show |
23 | HG00733.hp2 HG01106.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.928-617T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588058 | |||||||
| chr16:89588058 | T | TACACGGC others(82): Show |
1 | a0001c0001t0012g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(89): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588058 | ||||||
| chr16:89588062 | C | T | 8 | a0001c0001t0001g0089 a0001c0001t0001g0238 a0001c0001t0001g0291 others(5): Show |
8 | HG00741.hp2 HG01123.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-613C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588062 | |||||||
| chr16:89588064 | GC | G | 79 | a0001c0001t0001g0052 a0001c0001t0001g0066 a0001c0001t0001g0100 others(76): Show |
82 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.928-605delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588064 | ||||||
| chr16:89588065 | C | CCCCCCAT others(30): Show |
2 | a0001c0001t0001g0187 a0011c0021t0001g0216 |
2 | NA18970.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.928-605_928-604ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | ||||||
| chr16:89588065 | C | CCCCCCGT others(4): Show |
1 | a0001c0001t0001g0003 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.928-601_928-600ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | ||||||
| chr16:89588065 | C | CCCCCCGT others(131): Show |
1 | a0001c0002t0011g0195 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.928-601_928-600ins others(138): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | ||||||
| chr16:89588065 | C | CCCCCCGT others(30): Show |
1 | a0002c0003t0003g0128 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.928-601_928-600ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | ||||||
| chr16:89588065 | C | CCCCCCGT others(82): Show |
1 | a0001c0001t0001g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-601_928-600ins others(89): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | ||||||
| chr16:89588065 | C | CCCCCGTG others(3): Show |
1 | a0001c0008t0002g0016 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.928-606_928-605ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | ||||||
| chr16:89588065 | C | CCCCCGTG others(83): Show |
1 | a0001c0002t0004g0218 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(90): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | ||||||
| chr16:89588065 | C | CCCCCGTG others(120): Show |
1 | a0001c0002t0004g0219 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(127): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | ||||||
| chr16:89588065 | CCCCCCGT others(19): Show |
C | 1 | a0001c0002t0001g0323 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.928-600_928-575del others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | ||||||
| chr16:89588065 | CCCCCCGT others(45): Show |
C | 6 | a0001c0001t0001g0145 a0001c0002t0004g0136 a0001c0007t0006g0075 others(3): Show |
6 | HG02071.hp1 HG02273.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.928-600_928-549del others(52): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | ||||||
| chr16:89588068 | CCCGTGTT others(57): Show |
C | 6 | a0001c0001t0001g0245 a0001c0001t0001g0254 a0001c0002t0001g0276 others(3): Show |
6 | HG00639.hp1 HG01081.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-605_928-542del others(64): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588068 | ||||||
| chr16:89588068 | CCCGTGTT others(131): Show |
C | 2 | a0001c0002t0002g0026 a0001c0002t0003g0022 |
2 | HG03579.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.928-605_928-468del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588068 | ||||||
| chr16:89588069 | C | CCCGTGTC others(5): Show |
1 | a0001c0001t0001g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.928-605_928-604ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | ||||||
| chr16:89588069 | C | CCGTGTCA others(229): Show |
1 | a0001c0002t0003g0173 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.928-601_928-600ins others(236): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | ||||||
| chr16:89588069 | C | CCGTGTCA others(130): Show |
1 | a0001c0001t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.928-601_928-600ins others(137): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | ||||||
| chr16:89588069 | C | CCGTGTCA others(4): Show |
14 | a0001c0001t0001g0058 a0001c0001t0001g0063 a0001c0001t0001g0097 others(11): Show |
14 | HG00099.hp1 HG00438.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.928-601_928-600ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | ||||||
| chr16:89588069 | C | CCGTGTCA others(91): Show |
1 | a0001c0001t0001g0178 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.928-601_928-600ins others(98): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | ||||||
| chr16:89588069 | C | CCGTGTCA others(196): Show |
1 | a0001c0001t0001g0089 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.928-601_928-600ins others(203): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | ||||||
| chr16:89588069 | C | CCGTGTCA others(197): Show |
1 | a0010c0016t0003g0114 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.928-601_928-600ins others(204): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | ||||||
| chr16:89588069 | C | CCGTGTCA others(263): Show |
1 | a0002c0003t0003g0140 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.928-601_928-600ins others(270): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | ||||||
| chr16:89588069 | C | CCGTGTCA others(155): Show |
1 | a0001c0001t0001g0048 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.928-601_928-600ins others(162): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | ||||||
| chr16:89588069 | C | CCGTGTTA others(4): Show |
1 | a0001c0001t0001g0242 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.928-596_928-595ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | ||||||
| chr16:89588069 | C | CGTGTCAC others(3): Show |
1 | a0001c0008t0002g0019 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | |||||||
| chr16:89588069 | C | CGTGTCAC others(67): Show |
1 | a0002c0004t0002g0324 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(74): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | |||||||
| chr16:89588069 | C | CGTGTCAC others(30): Show |
1 | a0002c0003t0003g0077 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.928-606_928-605ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | |||||||
| chr16:89588069 | C | CGTGTCAC others(158): Show |
1 | a0002c0003t0002g0119 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(165): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | |||||||
| chr16:89588069 | C | CGTGTCAC others(29): Show |
2 | a0001c0001t0001g0059 a0001c0002t0004g0138 |
2 | HG02735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.928-606_928-605ins others(36): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | |||||||
| chr16:89588069 | C | CGTGTCAC others(232): Show |
1 | a0001c0001t0001g0326 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.928-606_928-605ins others(239): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | |||||||
| chr16:89588069 | C | CGTGTCAC others(697): Show |
1 | a0001c0005t0002g0295 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(704): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | |||||||
| chr16:89588069 | C | CGTGTCAC others(41): Show |
1 | a0001c0001t0001g0096 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.928-606_928-605ins others(48): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | |||||||
| chr16:89588069 | C | CGTGTCAC others(4): Show |
1 | a0001c0001t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.928-606_928-605ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | |||||||
| chr16:89588069 | C | CGTGTCAC others(3): Show |
26 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0060 others(23): Show |
26 | HG00140.hp2 HG01167.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.928-606_928-605ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | |||||||
| chr16:89588069 | C | CGTGTCAC others(41): Show |
1 | a0001c0001t0001g0090 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.928-606_928-605ins others(48): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | |||||||
| chr16:89588069 | C | CGTGTCAC others(192): Show |
1 | a0001c0001t0001g0071 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(199): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | |||||||
| chr16:89588069 | C | CGTGTTAC others(92): Show |
1 | a0001c0001t0001g0032 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(99): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | |||||||
| chr16:89588069 | C | CGTGTTAC others(3): Show |
1 | a0001c0001t0001g0233 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | |||||||
| chr16:89588069 | C | T | 1 | a0001c0002t0003g0044 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.928-606C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | |||||||
| chr16:89588075 | T | C | 203 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(200): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.928-600T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588075 | |||||||
| chr16:89588075 | T | TACCCGCG others(4): Show |
4 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0002t0002g0270 others(1): Show |
4 | HG01261.hp2 HG01346.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-596_928-595ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588075 | ||||||
| chr16:89588075 | T | TACCCGCG others(79): Show |
1 | a0001c0001t0001g0238 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.928-596_928-595ins others(86): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588075 | ||||||
| chr16:89588075 | T | TACCCGCG others(2867): Show |
1 | a0001c0002t0003g0148 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.928-596_928-595ins others(2874): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588075 | ||||||
| chr16:89588075 | T | TACCCGCG others(42): Show |
1 | a0001c0002t0003g0177 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.928-596_928-595ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588075 | ||||||
| chr16:89588075 | T | TACCCGCG others(1087): Show |
1 | a0001c0001t0001g0291 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.928-596_928-595ins others(1094): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588075 | ||||||
| chr16:89588075 | TACCCACA others(45): Show |
T | 2 | a0001c0002t0004g0057 a0002c0010t0001g0239 |
2 | HG01928.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.928-595_928-544del others(52): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588075 | ||||||
| chr16:89588076 | ACCCACAG others(8): Show |
A | 37 | a0001c0001t0001g0039 a0001c0001t0001g0052 a0001c0001t0001g0086 others(34): Show |
37 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.928-595_928-581del others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588076 | ||||||
| chr16:89588077 | C | G | 7 | a0001c0001t0001g0241 a0001c0001t0001g0251 a0001c0001t0001g0262 others(4): Show |
10 | HG01168.hp2 HG01169.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.928-598C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588077 | |||||||
| chr16:89588085 | T | A | 8 | a0001c0001t0001g0066 a0001c0001t0001g0089 a0001c0001t0001g0178 others(5): Show |
8 | HG00423.hp2 HG02257.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-590T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588085 | |||||||
| chr16:89588089 | C | T | 5 | a0001c0001t0001g0169 a0001c0002t0004g0320 a0001c0008t0002g0013 others(2): Show |
5 | HG00673.hp2 HG02896.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.928-586C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588089 | |||||||
| chr16:89588091 | G | GC | 38 | a0001c0001t0001g0058 a0001c0001t0001g0073 a0001c0001t0001g0096 others(35): Show |
41 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.928-579dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588091 | ||||||
| chr16:89588091 | G | GCCCCCCG others(5): Show |
2 | a0001c0002t0003g0176 a0001c0008t0002g0016 |
2 | HG02109.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.928-579_928-578ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588091 | ||||||
| chr16:89588091 | G | GCCCCCCG others(84): Show |
1 | a0002c0003t0003g0143 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.928-579_928-578ins others(91): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588091 | ||||||
| chr16:89588091 | G | GCCCCCCG others(682): Show |
1 | a0002c0003t0003g0129 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.928-579_928-578ins others(689): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588091 | ||||||
| chr16:89588091 | G | GCCCCCGT others(4): Show |
2 | a0001c0001t0001g0325 a0005c0014t0001g0012 |
2 | HG01891.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.928-580_928-570dup others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588091 | ||||||
| chr16:89588091 | G | GCCCCCGT others(461): Show |
1 | a0001c0002t0003g0220 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.928-570_928-569ins others(468): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588091 | ||||||
| chr16:89588091 | G | GCCCCCGT others(625): Show |
1 | a0001c0013t0002g0010 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.928-570_928-569ins others(632): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588091 | ||||||
| chr16:89588092 | CCCCCGTG others(18): Show |
C | 4 | a0001c0002t0004g0112 a0001c0002t0004g0135 a0001c0002t0004g0261 others(1): Show |
4 | HG01952.hp1 HG03942.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-578_928-554del others(25): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588092 | ||||||
| chr16:89588092 | CCCCCGTG others(55): Show |
C | 5 | a0001c0002t0003g0035 a0001c0002t0003g0038 a0001c0007t0006g0162 others(2): Show |
5 | HG03195.hp1 HG03209.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-578_928-517del others(62): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588092 | ||||||
| chr16:89588095 | C | CCCGTGTC others(5): Show |
10 | a0001c0001t0001g0090 a0001c0001t0001g0169 a0001c0002t0002g0270 others(7): Show |
10 | HG00642.hp1 HG00673.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.928-579_928-578ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | ||||||
| chr16:89588095 | C | CCCGTGTC others(70): Show |
1 | a0002c0003t0003g0004 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.928-579_928-578ins others(77): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | ||||||
| chr16:89588095 | C | CCCGTGTC others(42): Show |
1 | a0001c0001t0001g0048 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.928-579_928-578ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | ||||||
| chr16:89588095 | C | CCCGTGTT others(32): Show |
1 | a0002c0003t0003g0141 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.928-579_928-578ins others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | ||||||
| chr16:89588095 | C | CCCGTGTT others(571): Show |
1 | a0001c0002t0003g0229 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.928-579_928-578ins others(578): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | ||||||
| chr16:89588095 | C | CCCGTGTT others(5): Show |
5 | a0001c0002t0004g0137 a0002c0003t0003g0131 a0002c0003t0003g0133 others(2): Show |
5 | HG00609.hp1 HG03927.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-579_928-578ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | ||||||
| chr16:89588095 | C | CCGTGTCA others(30): Show |
1 | a0001c0001t0001g0066 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.928-463_928-427dup others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | ||||||
| chr16:89588095 | C | CCGTGTCA others(15): Show |
1 | a0001c0002t0002g0190 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.928-570_928-569ins others(22): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | ||||||
| chr16:89588095 | C | CCGTGTCA others(189): Show |
1 | a0001c0001t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.928-570_928-569ins others(196): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | ||||||
| chr16:89588095 | C | CCGTGTCA others(4): Show |
29 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0031 others(26): Show |
30 | HG00140.hp2 HG01346.hp2 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.928-570_928-569ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | ||||||
| chr16:89588095 | C | CCGTGTCA others(42): Show |
1 | a0001c0001t0001g0111 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.928-570_928-569ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | ||||||
| chr16:89588095 | C | CCGTGTCA others(118): Show |
1 | a0003c0006t0003g0005 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.928-570_928-569ins others(125): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | ||||||
| chr16:89588095 | C | CCGTGTCA others(107): Show |
1 | a0003c0006t0003g0260 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.928-570_928-569ins others(114): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | ||||||
| chr16:89588095 | C | CCGTGTCA others(41): Show |
2 | a0001c0002t0002g0307 a0001c0002t0005g0283 |
2 | HG00558.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.928-570_928-569ins others(48): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | ||||||
| chr16:89588095 | C | G | 57 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0051 others(54): Show |
57 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.928-580C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588095 | |||||||
| chr16:89588095 | CCGTGTCA others(67): Show |
C | 1 | a0001c0002t0002g0319 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.928-500_928-427del others(74): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | ||||||
| chr16:89588096 | CGTGTCAC others(66): Show |
C | 3 | a0001c0002t0004g0117 a0001c0002t0004g0139 a0001c0002t0007g0007 |
3 | HG01943.hp1 NA18952.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.928-578_928-506del others(73): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588096 | |||||||
| chr16:89588097 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0213 |
2 | HG02109.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.928-578G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588097 | |||||||
| chr16:89588101 | C | CACCCGCG others(442): Show |
1 | a0001c0001t0001g0242 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.928-570_928-569ins others(449): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588101 | ||||||
| chr16:89588101 | C | T | 13 | a0001c0001t0001g0096 a0001c0001t0001g0204 a0001c0002t0003g0080 others(10): Show |
13 | HG00609.hp2 HG01257.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.928-574C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588101 | |||||||
| chr16:89588103 | C | G | 6 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0001g0272 others(3): Show |
6 | HG01168.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-572C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588103 | |||||||
| chr16:89588111 | T | A | 6 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0111 others(3): Show |
6 | HG00741.hp1 HG01106.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.928-564T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588111 | |||||||
| chr16:89588115 | C | T | 4 | a0001c0002t0003g0266 a0001c0002t0004g0321 a0001c0005t0002g0295 others(1): Show |
4 | HG02258.hp1 HG03927.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-560C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588115 | |||||||
| chr16:89588117 | G | C | 1 | a0001c0002t0002g0250 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.928-558G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588117 | |||||||
| chr16:89588117 | G | GC | 80 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0048 others(77): Show |
81 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.928-553dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | ||||||
| chr16:89588117 | G | GCCCCCCG others(21): Show |
1 | a0002c0004t0002g0271 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.928-553_928-552ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | ||||||
| chr16:89588117 | G | GCCCCCCG others(58): Show |
1 | a0001c0001t0001g0328 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.928-553_928-552ins others(65): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | ||||||
| chr16:89588117 | G | GCCCCCCG others(32): Show |
1 | a0001c0012t0002g0289 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.928-553_928-552ins others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | ||||||
| chr16:89588117 | G | GCCCCCCG others(21): Show |
2 | a0001c0007t0006g0068 a0002c0003t0003g0140 |
2 | HG02723.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.928-553_928-552ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | ||||||
| chr16:89588117 | G | GCCCCCGT others(174): Show |
1 | a0001c0001t0001g0205 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.928-544_928-543ins others(181): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | ||||||
| chr16:89588117 | G | GCCCCCGT others(57): Show |
2 | a0001c0005t0002g0042 a0001c0005t0002g0043 |
2 | NA18947.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.928-528_928-527ins others(64): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | ||||||
| chr16:89588117 | G | GCCCCCGT others(31): Show |
3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0327 |
3 | HG02258.hp2 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.928-553_928-516dup others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | ||||||
| chr16:89588117 | G | GCCCCCGT others(68): Show |
1 | a0001c0001t0001g0277 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.928-553_928-479dup others(75): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | ||||||
| chr16:89588117 | G | GCCCCCGT others(20): Show |
1 | a0002c0004t0002g0309 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.928-547_928-546ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | ||||||
| chr16:89588117 | G | GCCCCCGT others(403): Show |
1 | a0001c0001t0001g0244 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.928-547_928-546ins others(410): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | ||||||
| chr16:89588121 | C | CT | 5 | a0001c0001t0001g0175 a0001c0002t0003g0049 a0001c0002t0003g0054 others(2): Show |
5 | HG01346.hp2 HG02027.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.928-554_928-553ins others(1): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588121 | |||||||
| chr16:89588121 | CCGTGTCA others(4): Show |
C | 10 | a0001c0001t0001g0100 a0001c0001t0001g0233 a0001c0001t0001g0240 others(7): Show |
10 | HG00544.hp1 HG01123.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.928-543_928-533del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588121 | ||||||
| chr16:89588122 | CGTGTCAC others(3): Show |
C | 12 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0170 others(9): Show |
12 | HG00438.hp2 HG00597.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.928-552_928-543del others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588122 | |||||||
| chr16:89588123 | G | GTGTCACC others(130): Show |
1 | a0001c0002t0002g0190 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.928-523_928-522ins others(137): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588123 | ||||||
| chr16:89588127 | C | CACCCGCG others(57): Show |
1 | a0001c0001t0001g0269 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.928-528_928-527ins others(64): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588127 | ||||||
| chr16:89588127 | C | T | 5 | a0001c0001t0001g0212 a0001c0002t0005g0182 a0002c0003t0003g0131 others(2): Show |
5 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-548C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588127 | |||||||
| chr16:89588128 | A | ACCCACAG others(8): Show |
7 | a0001c0001t0001g0072 a0001c0001t0001g0241 a0001c0002t0005g0023 others(4): Show |
7 | HG00438.hp1 HG01975.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-544_928-543ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588128 | ||||||
| chr16:89588128 | A | ACCCACAG others(9): Show |
7 | a0001c0001t0001g0181 a0001c0001t0001g0204 a0001c0002t0003g0080 others(4): Show |
7 | HG02129.hp2 HG02132.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-544_928-543ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588128 | ||||||
| chr16:89588128 | A | ACCCACAG others(35): Show |
1 | a0001c0001t0001g0073 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.928-544_928-543ins others(42): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588128 | ||||||
| chr16:89588128 | A | ACCCACAG others(36): Show |
1 | a0001c0001t0001g0122 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.928-544_928-543ins others(43): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588128 | ||||||
| chr16:89588128 | A | ACCCACAG others(88): Show |
1 | a0001c0002t0004g0217 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.928-544_928-543ins others(95): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588128 | ||||||
| chr16:89588128 | A | ACCCACAG others(46): Show |
1 | a0001c0001t0001g0209 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.928-544_928-543ins others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588128 | ||||||
| chr16:89588128 | A | ACCCACAG others(98): Show |
2 | a0002c0004t0002g0002 a0002c0004t0002g0296 |
5 | HG01168.hp2 HG01169.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-544_928-543ins others(105): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588128 | ||||||
| chr16:89588128 | A | ACCCACAG others(255): Show |
1 | a0001c0005t0002g0001 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.928-544_928-543ins others(262): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588128 | ||||||
| chr16:89588128 | A | AGCCACAG others(9): Show |
2 | a0001c0005t0002g0109 a0003c0006t0003g0267 |
2 | HG02273.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.928-547_928-546ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588128 | |||||||
| chr16:89588128 | A | AGCCACAG others(73): Show |
1 | a0001c0005t0002g0001 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.928-547_928-546ins others(80): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588128 | |||||||
| chr16:89588128 | A | AGCCACAG others(72): Show |
7 | a0001c0005t0002g0001 a0001c0005t0002g0076 a0001c0005t0002g0202 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-547_928-546ins others(79): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588128 | |||||||
| chr16:89588132 | G | A | 1 | a0001c0008t0002g0019 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.928-543G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588132 | |||||||
| chr16:89588132 | G | C | 32 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0122 others(29): Show |
39 | HG00438.hp1 HG00558.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.928-543G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588132 | |||||||
| chr16:89588132 | G | GCGTGTCA others(19): Show |
2 | a0001c0002t0001g0033 a0001c0015t0001g0322 |
2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.928-532_928-507dup others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588132 | ||||||
| chr16:89588132 | G | GCGTGTCA others(20): Show |
3 | a0001c0001t0008g0050 a0001c0002t0002g0199 a0001c0002t0004g0138 |
3 | HG00673.hp1 HG02735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.928-542_928-516dup others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588132 | ||||||
| chr16:89588132 | G | GCGTGTCA others(391): Show |
1 | a0001c0001t0001g0184 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.928-516_928-515ins others(398): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588132 | ||||||
| chr16:89588132 | G | GCGTGTCA others(93): Show |
1 | a0001c0001t0001g0032 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.928-532_928-433dup others(100): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588132 | ||||||
| chr16:89588138 | C | CACCCACA others(46): Show |
1 | a0002c0003t0003g0128 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.928-528_928-527ins others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588138 | ||||||
| chr16:89588138 | C | T | 8 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(5): Show |
8 | HG01928.hp1 HG02165.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-537C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588138 | |||||||
| chr16:89588140 | C | CCCACAGA others(19): Show |
1 | a0001c0002t0004g0317 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.928-524_928-523ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588140 | ||||||
| chr16:89588140 | C | G | 4 | a0001c0001t0001g0100 a0001c0001t0001g0233 a0001c0001t0001g0240 others(1): Show |
4 | HG01123.hp2 HG02071.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-535C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588140 | |||||||
| chr16:89588148 | T | A | 23 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0089 others(20): Show |
30 | HG00323.hp1 HG00621.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.928-527T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588148 | |||||||
| chr16:89588152 | C | T | 1 | a0001c0025t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.928-523C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588152 | |||||||
| chr16:89588153 | G | A | 9 | a0001c0001t0001g0079 a0001c0002t0002g0190 a0001c0002t0002g0194 others(6): Show |
9 | HG00280.hp1 HG00423.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.928-522G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588153 | |||||||
| chr16:89588154 | G | GC | 104 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0031 others(101): Show |
111 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.928-516dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | ||||||
| chr16:89588154 | G | GCCCCCCG others(21): Show |
1 | a0002c0004t0002g0299 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.928-516_928-515ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | ||||||
| chr16:89588154 | G | GCCCCCCG others(59): Show |
1 | a0003c0006t0003g0228 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.928-516_928-515ins others(66): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | ||||||
| chr16:89588154 | G | GCCCCCCG others(2922): Show |
1 | a0001c0002t0003g0148 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.928-516_928-515ins others(2929): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | ||||||
| chr16:89588154 | G | GCCCCCCG others(21): Show |
1 | a0001c0007t0006g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.928-516_928-515ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | ||||||
| chr16:89588154 | G | GCCCCCGT others(20): Show |
2 | a0002c0003t0004g0301 a0002c0004t0002g0302 |
2 | HG00621.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.928-507_928-506ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | ||||||
| chr16:89588154 | G | GCCCCCGT others(20): Show |
3 | a0001c0001t0001g0089 a0002c0004t0014g0300 a0003c0006t0003g0149 |
3 | HG03831.hp2 NA18980.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.928-507_928-506ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | ||||||
| chr16:89588154 | G | GCCCCCGT others(47): Show |
1 | a0001c0002t0004g0125 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.928-507_928-506ins others(54): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | ||||||
| chr16:89588154 | G | GCCCCCGT others(20): Show |
1 | a0001c0001t0001g0265 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.928-507_928-506ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | ||||||
| chr16:89588154 | G | GCCCGCGT others(84): Show |
1 | a0002c0003t0003g0144 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.928-518_928-517ins others(91): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | ||||||
| chr16:89588154 | G | GCCCGCGT others(202): Show |
1 | a0002c0003t0003g0004 | 2 | NA18942.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.928-518_928-517ins others(209): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | ||||||
| chr16:89588158 | C | G | 1 | a0002c0003t0003g0133 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.928-517C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588158 | |||||||
| chr16:89588158 | CCGTGTCA others(4): Show |
C | 14 | a0001c0001t0001g0052 a0001c0001t0001g0093 a0001c0001t0001g0212 others(11): Show |
14 | HG00597.hp1 HG00733.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.928-506_928-496del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588158 | ||||||
| chr16:89588158 | CCGTGTCA others(41): Show |
C | 2 | a0001c0002t0003g0188 a0001c0009t0001g0017 |
2 | HG02280.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.928-506_928-459del others(48): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588158 | ||||||
| chr16:89588159 | CGTGTCAC others(3): Show |
C | 2 | a0001c0002t0004g0057 a0002c0003t0007g0290 |
2 | HG02155.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.928-515_928-506del others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588159 | |||||||
| chr16:89588160 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.928-515G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588160 | |||||||
| chr16:89588164 | C | CACCCACA others(58): Show |
1 | a0001c0001t0001g0238 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.928-507_928-506ins others(65): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588164 | ||||||
| chr16:89588164 | C | T | 2 | a0001c0002t0004g0055 a0001c0002t0005g0284 |
2 | HG02615.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.928-511C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588164 | |||||||
| chr16:89588165 | A | ACCCACAG others(74): Show |
1 | a0002c0003t0003g0133 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.928-507_928-506ins others(81): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | ||||||
| chr16:89588165 | A | ACCCACAG others(8): Show |
6 | a0001c0001t0001g0213 a0001c0002t0003g0282 a0001c0002t0004g0218 others(3): Show |
6 | HG00544.hp2 HG01346.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-507_928-506ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | ||||||
| chr16:89588165 | A | ACCCACAG others(9): Show |
4 | a0002c0003t0003g0130 a0002c0003t0003g0222 a0003c0006t0003g0005 others(1): Show |
4 | NA18940.hp1 NA18943.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-507_928-506ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | ||||||
| chr16:89588165 | A | ACCCACAG others(748): Show |
1 | a0002c0003t0003g0131 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.928-507_928-506ins others(755): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | ||||||
| chr16:89588165 | A | ACCCACAG others(1789): Show |
1 | a0001c0002t0004g0231 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.928-507_928-506ins others(1796): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | ||||||
| chr16:89588165 | A | ACCCACAG others(110): Show |
1 | a0001c0002t0011g0195 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.928-507_928-506ins others(117): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | ||||||
| chr16:89588165 | A | ACCCACAG others(99): Show |
1 | a0001c0001t0001g0331 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.928-507_928-506ins others(106): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | ||||||
| chr16:89588165 | A | ACCCACAG others(61): Show |
1 | a0002c0017t0003g0142 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.928-507_928-506ins others(68): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | ||||||
| chr16:89588165 | A | ACCCACAG others(306): Show |
1 | a0003c0006t0003g0268 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.928-507_928-506ins others(313): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | ||||||
| chr16:89588165 | A | ACCCACAG others(36): Show |
1 | a0001c0002t0004g0153 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.928-507_928-506ins others(43): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | ||||||
| chr16:89588165 | A | AGCCACAG others(9): Show |
1 | a0001c0001t0001g0241 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.928-510_928-509ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588165 | |||||||
| chr16:89588165 | A | AGCCACAG others(138): Show |
1 | a0001c0002t0005g0024 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.928-510_928-509ins others(145): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588165 | |||||||
| chr16:89588169 | G | C | 25 | a0001c0001t0001g0086 a0001c0001t0001g0107 a0001c0001t0001g0213 others(22): Show |
25 | HG00544.hp2 HG00609.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.928-506G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588169 | |||||||
| chr16:89588169 | G | GCGTGTCA others(137): Show |
1 | a0003c0006t0003g0228 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.928-470_928-469ins others(144): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588169 | ||||||
| chr16:89588170 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.928-505C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588170 | |||||||
| chr16:89588171 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0213 |
2 | HG00099.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.928-504G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588171 | |||||||
| chr16:89588175 | C | T | 11 | a0001c0001t0001g0048 a0001c0001t0001g0238 a0001c0002t0004g0056 others(8): Show |
11 | HG00597.hp1 HG01123.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-500C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588175 | |||||||
| chr16:89588177 | C | CCCACAGA others(19): Show |
1 | a0001c0001t0001g0070 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.928-473_928-472ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588177 | ||||||
| chr16:89588177 | C | G | 1 | a0001c0002t0004g0261 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.928-498C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588177 | |||||||
| chr16:89588185 | T | A | 11 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
11 | HG01257.hp1 HG01361.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-490T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588185 | |||||||
| chr16:89588189 | C | T | 4 | a0001c0001t0001g0212 a0001c0002t0002g0319 a0001c0008t0002g0013 others(1): Show |
4 | HG01243.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-486C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588189 | |||||||
| chr16:89588190 | G | A | 1 | a0001c0002t0002g0248 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.928-485G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588190 | |||||||
| chr16:89588191 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.928-484G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588191 | |||||||
| chr16:89588191 | G | GC | 102 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0070 others(99): Show |
111 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.928-479dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCCG others(85): Show |
1 | a0001c0001t0001g0255 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.928-479_928-478ins others(92): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCCG others(21): Show |
1 | a0001c0002t0004g0125 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.928-479_928-478ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCCG others(70): Show |
1 | a0001c0001t0001g0003 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.928-479_928-478ins others(77): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCCG others(146): Show |
1 | a0001c0001t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.928-479_928-478ins others(153): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCCG others(250): Show |
1 | a0001c0002t0004g0137 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.928-479_928-478ins others(257): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCCG others(58): Show |
1 | a0001c0008t0002g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.928-479_928-478ins others(65): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCCG others(21): Show |
2 | a0001c0002t0004g0055 a0002c0003t0003g0113 |
2 | NA19005.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.928-479_928-478ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCCG others(1119): Show |
1 | a0002c0003t0003g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.928-479_928-478ins others(1126): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCCG others(84): Show |
1 | a0001c0002t0003g0173 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.928-479_928-478ins others(91): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCGT others(20): Show |
3 | a0001c0002t0002g0200 a0001c0008t0002g0016 a0002c0003t0002g0119 |
3 | HG00423.hp2 HG02109.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.928-470_928-469ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCGT others(871): Show |
1 | a0001c0002t0003g0220 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.928-470_928-469ins others(878): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCGT others(201): Show |
1 | a0003c0006t0003g0267 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(208): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCGT others(74): Show |
1 | a0001c0002t0003g0080 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(81): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCGT others(100): Show |
1 | a0001c0001t0001g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.928-470_928-469ins others(107): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCGT others(57): Show |
1 | a0001c0002t0005g0191 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(64): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCGT others(916): Show |
1 | a0001c0001t0001g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(923): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCGT others(95): Show |
1 | a0001c0001t0001g0031 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(102): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588191 | G | GCCCCCGT others(281): Show |
1 | a0001c0001t0001g0063 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.928-427_928-426ins others(288): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | ||||||
| chr16:89588195 | C | CCGTGTCA others(142): Show |
1 | a0001c0001t0008g0050 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.928-427_928-426ins others(149): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588195 | ||||||
| chr16:89588195 | CCGTGTCA others(4): Show |
C | 77 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0061 others(74): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.928-469_928-459del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588195 | ||||||
| chr16:89588196 | CGTGTCAC others(3): Show |
C | 17 | a0001c0001t0001g0040 a0001c0001t0001g0058 a0001c0001t0001g0091 others(14): Show |
17 | HG01106.hp1 HG01243.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.928-478_928-469del others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588196 | |||||||
| chr16:89588201 | C | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0089 a0002c0003t0003g0077 |
3 | HG02129.hp1 HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.928-474C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588201 | |||||||
| chr16:89588202 | A | ACCCACAG others(8): Show |
3 | a0001c0001t0001g0269 a0001c0002t0001g0033 a0002c0004t0002g0324 |
3 | HG02572.hp2 HG03239.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.928-470_928-469ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | ||||||
| chr16:89588202 | A | ACCCACAG others(137): Show |
1 | a0003c0006t0003g0149 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.928-470_928-469ins others(144): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | ||||||
| chr16:89588202 | A | ACCCACAG others(46): Show |
2 | a0001c0001t0001g0089 a0001c0002t0004g0217 |
2 | HG02083.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.928-470_928-469ins others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | ||||||
| chr16:89588202 | A | ACCCACAG others(47): Show |
1 | a0001c0001t0001g0060 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(54): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | ||||||
| chr16:89588202 | A | ACCCACAG others(147): Show |
1 | a0001c0001t0001g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-470_928-469ins others(154): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | ||||||
| chr16:89588202 | A | ACCCACAG others(190): Show |
1 | a0010c0016t0003g0114 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(197): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | ||||||
| chr16:89588202 | A | ACCCACAG others(136): Show |
1 | a0001c0001t0001g0185 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.928-470_928-469ins others(143): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | ||||||
| chr16:89588202 | A | ACCCACAG others(124): Show |
1 | a0001c0002t0004g0215 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(131): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | ||||||
| chr16:89588202 | A | ACCCACAG others(71): Show |
2 | a0001c0001t0001g0011 a0003c0006t0003g0334 |
2 | HG00621.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.928-470_928-469ins others(78): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | ||||||
| chr16:89588202 | A | ACCCACAG others(485): Show |
1 | a0001c0001t0001g0237 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(492): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | ||||||
| chr16:89588202 | A | ACCCACAG others(45): Show |
1 | a0001c0001t0001g0209 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(52): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | ||||||
| chr16:89588202 | A | ACCCACAG others(774): Show |
1 | a0001c0024t0001g0208 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(781): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | ||||||
| chr16:89588202 | A | ACCCCCCG others(59): Show |
1 | a0001c0001t0001g0090 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(66): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | ||||||
| chr16:89588202 | A | AGCCACAG others(9): Show |
1 | a0001c0005t0002g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.928-473_928-472ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588202 | |||||||
| chr16:89588202 | A | AGCCACAG others(88): Show |
1 | a0002c0004t0002g0297 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.928-473_928-472ins others(95): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588202 | |||||||
| chr16:89588202 | A | AGCCACAG others(46): Show |
2 | a0001c0001t0001g0069 a0001c0001t0001g0111 |
2 | HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.928-473_928-472ins others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588202 | |||||||
| chr16:89588202 | A | AGCCACAG others(1344): Show |
1 | a0001c0002t0001g0163 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.928-473_928-472ins others(1351): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588202 | |||||||
| chr16:89588202 | A | AGCCACAG others(2535): Show |
1 | a0001c0008t0001g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.928-473_928-472ins others(2542): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588202 | |||||||
| chr16:89588202 | A | AGCCACAG others(327): Show |
1 | a0001c0001t0001g0244 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.928-473_928-472ins others(334): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588202 | |||||||
| chr16:89588202 | A | AGCCGCGT others(57): Show |
1 | a0001c0001t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.928-473_928-472ins others(64): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588202 | |||||||
| chr16:89588206 | G | C | 27 | a0001c0001t0001g0011 a0001c0001t0001g0060 a0001c0001t0001g0069 others(24): Show |
27 | HG00558.hp1 HG00621.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.928-469G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588206 | |||||||
| chr16:89588206 | G | GCGTGTCA others(310): Show |
1 | a0001c0002t0013g0189 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.928-454_928-453ins others(317): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(209): Show |
1 | a0001c0001t0001g0326 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.928-454_928-453ins others(216): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(94): Show |
1 | a0001c0001t0001g0242 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.928-454_928-453ins others(101): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(122): Show |
1 | a0001c0001t0001g0241 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.928-454_928-453ins others(129): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(82): Show |
1 | a0002c0003t0003g0143 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.928-449_928-448ins others(89): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(19): Show |
27 | a0001c0001t0001g0051 a0001c0001t0001g0093 a0001c0001t0001g0180 others(24): Show |
27 | HG00544.hp2 HG00558.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.928-458_928-433dup others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(20): Show |
21 | a0001c0002t0005g0024 a0001c0005t0002g0001 a0001c0005t0002g0042 others(18): Show |
28 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.928-468_928-442dup others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(21): Show |
1 | a0001c0005t0002g0295 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(237): Show |
1 | a0001c0001t0001g0186 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.928-442_928-441ins others(244): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(1467): Show |
1 | a0001c0002t0004g0138 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(1474): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(2084): Show |
1 | a0001c0002t0003g0177 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.928-442_928-441ins others(2091): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(386): Show |
1 | a0001c0002t0002g0270 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(393): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(799): Show |
1 | a0003c0006t0003g0226 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.928-442_928-441ins others(806): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(234): Show |
1 | a0003c0006t0003g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(241): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(196): Show |
1 | a0003c0006t0003g0005 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(203): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(232): Show |
1 | a0001c0001t0001g0074 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.928-442_928-441ins others(239): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(604): Show |
1 | a0011c0021t0001g0216 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.928-442_928-441ins others(611): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(174): Show |
1 | a0002c0003t0003g0077 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.928-442_928-441ins others(181): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(109): Show |
1 | a0001c0001t0001g0071 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(116): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(2604): Show |
1 | a0001c0001t0001g0291 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(2611): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(45): Show |
2 | a0001c0002t0002g0200 a0001c0002t0002g0330 |
2 | HG04204.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.928-433_928-432ins others(52): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(227): Show |
1 | a0003c0006t0003g0151 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.928-433_928-432ins others(234): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(71): Show |
1 | a0001c0001t0001g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.928-433_928-432ins others(78): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(135): Show |
1 | a0001c0001t0001g0328 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.928-433_928-432ins others(142): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(173): Show |
1 | a0001c0001t0001g0187 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.928-433_928-432ins others(180): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(390): Show |
1 | a0001c0001t0001g0206 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.928-433_928-432ins others(397): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(364): Show |
1 | a0002c0004t0002g0316 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.928-433_928-432ins others(371): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(56): Show |
1 | a0001c0001t0001g0192 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.928-427_928-426ins others(63): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(966): Show |
1 | a0001c0001t0001g0207 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.928-427_928-426ins others(973): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(269): Show |
1 | a0004c0011t0001g0081 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.928-427_928-426ins others(276): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(296): Show |
1 | a0001c0001t0001g0059 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.928-450_928-449ins others(303): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(169): Show |
1 | a0001c0001t0001g0325 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-450_928-449ins others(176): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GCGTGTCA others(94): Show |
1 | a0001c0002t0002g0027 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.928-451_928-450ins others(101): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | ||||||
| chr16:89588206 | G | GTGTGTCA others(195): Show |
1 | a0001c0001t0001g0097 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.928-469_928-468ins others(202): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588206 | |||||||
| chr16:89588208 | G | A | 1 | a0001c0009t0001g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.928-467G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588208 | |||||||
| chr16:89588212 | C | CACCCACA others(19): Show |
1 | a0002c0003t0003g0131 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.928-438_928-437ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588212 | ||||||
| chr16:89588212 | C | T | 4 | a0001c0001t0001g0060 a0001c0007t0006g0157 a0002c0003t0002g0132 others(1): Show |
4 | HG00597.hp1 HG02071.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-463C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588212 | |||||||
| chr16:89588214 | C | CCCACAGA others(19): Show |
1 | a0001c0001t0001g0070 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.928-436_928-435ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588214 | ||||||
| chr16:89588214 | C | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0111 |
2 | HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.928-461C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588214 | |||||||
| chr16:89588228 | G | GC | 8 | a0001c0002t0002g0313 a0001c0002t0005g0078 a0001c0002t0005g0312 others(5): Show |
8 | HG01192.hp2 HG02486.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-442dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588228 | ||||||
| chr16:89588228 | G | GCCCCCCG others(21): Show |
1 | a0002c0004t0002g0020 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588228 | ||||||
| chr16:89588228 | G | GCCCCCCG others(32): Show |
1 | a0001c0002t0005g0284 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.928-442_928-441ins others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588228 | ||||||
| chr16:89588228 | G | GCCCCCCG others(132): Show |
1 | a0001c0002t0005g0283 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.928-442_928-441ins others(139): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588228 | ||||||
| chr16:89588228 | G | GCCCCCGT others(20): Show |
1 | a0001c0002t0005g0191 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.928-433_928-432ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588228 | ||||||
| chr16:89588236 | G | A | 2 | a0001c0005t0002g0294 a0001c0005t0002g0315 |
2 | HG00438.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.928-439G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588236 | |||||||
| chr16:89588239 | A | ACCCACAG others(20): Show |
1 | a0001c0001t0001g0205 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.928-433_928-432ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588239 | ||||||
| chr16:89588245 | G | A | 1 | a0001c0002t0003g0266 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.928-430G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588245 | |||||||
| chr16:89588258 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.928-417A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588258 | |||||||
| chr16:89588262 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-413G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588262 | |||||||
| chr16:89588270 | G | A | 1 | a0002c0003t0003g0140 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.928-405G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588270 | |||||||
| chr16:89588352 | C | T | 3 | a0001c0002t0005g0158 a0001c0027t0005g0161 a0001c0028t0001g0160 |
3 | HG02818.hp1 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.928-323C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588352 | |||||||
| chr16:89588392 | C | T | 53 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0067 others(50): Show |
53 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.928-283C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588392 | |||||||
| chr16:89588393 | G | A | 4 | a0001c0002t0004g0215 a0001c0002t0004g0217 a0001c0002t0004g0218 others(1): Show |
4 | HG02080.hp1 HG02083.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-282G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588393 | |||||||
| chr16:89588413 | G | A | 1 | a0001c0002t0002g0270 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.928-262G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588413 | |||||||
| chr16:89588421 | C | T | 106 | a0001c0001t0001g0039 a0001c0001t0001g0083 a0001c0001t0001g0110 others(103): Show |
110 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.928-254C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588421 | |||||||
| chr16:89588503 | C | T | 1 | a0001c0013t0002g0010 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.928-172C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588503 | |||||||
| chr16:89588599 | G | A | 4 | a0001c0001t0001g0238 a0001c0001t0001g0242 a0001c0001t0001g0325 others(1): Show |
4 | HG01123.hp1 HG01496.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-76G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588599 | |||||||
| chr16:89588629 | G | A | 3 | a0001c0002t0005g0158 a0001c0027t0005g0161 a0001c0028t0001g0160 |
3 | HG02818.hp1 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.928-46G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588629 | |||||||
| chr16:89588813 | G | A | 96 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0083 others(93): Show |
99 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
splice_region_variant&intron_variant | LOW | c.1061+5G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89588813 | |||||||
| chr16:89588816 | C | T | 1 | a0004c0020t0001g0332 | 1 | HG02809.hp2 | splice_region_variant&intron_variant | LOW | c.1061+8C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89588816 | |||||||
| chr16:89588865 | G | A | 3 | a0001c0012t0002g0288 a0001c0012t0002g0289 a0001c0013t0002g0010 |
3 | HG01167.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1061+57G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89588865 | |||||||
| chr16:89588940 | C | T | 4 | a0001c0002t0001g0276 a0001c0002t0001g0323 a0001c0015t0001g0322 others(1): Show |
4 | HG00639.hp1 HG02717.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1061+132C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89588940 | |||||||
| chr16:89588953 | C | T | 1 | a0001c0002t0002g0307 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1061+145C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89588953 | |||||||
| chr16:89588966 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1061+158G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89588966 | |||||||
| chr16:89589013 | C | T | 100 | a0001c0001t0001g0083 a0001c0001t0001g0110 a0001c0001t0001g0120 others(97): Show |
103 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1061+205C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589013 | |||||||
| chr16:89589014 | G | A | 1 | a0001c0001t0012g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1061+206G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589014 | |||||||
| chr16:89589153 | G | A | 38 | a0001c0001t0001g0171 a0001c0001t0001g0241 a0001c0005t0002g0001 others(35): Show |
45 | HG00438.hp1 HG00673.hp2 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.1061+345G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589153 | |||||||
| chr16:89589175 | C | T | 1 | a0001c0002t0003g0282 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1061+367C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589175 | |||||||
| chr16:89589206 | C | T | 1 | a0002c0004t0002g0297 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1061+398C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589206 | |||||||
| chr16:89589207 | A | G | 224 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0039 others(221): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1061+399A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589207 | |||||||
| chr16:89589218 | G | A | 3 | a0001c0001t0001g0232 a0001c0001t0001g0273 a0001c0001t0001g0291 |
3 | HG00741.hp2 HG01175.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1061+410G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589218 | |||||||
| chr16:89589219 | G | A | 189 | a0001c0001t0001g0039 a0001c0001t0001g0060 a0001c0001t0001g0061 others(186): Show |
201 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.1061+411G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589219 | |||||||
| chr16:89589287 | G | A | 1 | a0004c0020t0001g0332 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1061+479G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589287 | |||||||
| chr16:89589303 | ACT | A | 3 | a0001c0002t0001g0029 a0001c0002t0001g0163 a0001c0008t0001g0014 |
3 | HG02922.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1061+498_1061+499d others(4): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 89589303 | ||||||
| chr16:89589328 | C | T | 1 | a0005c0014t0001g0012 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1061+520C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589328 | |||||||
| chr16:89589358 | C | T | 6 | a0001c0002t0002g0257 a0001c0002t0002g0319 a0001c0002t0002g0329 others(3): Show |
6 | HG01891.hp1 HG02970.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1062-539C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589358 | |||||||
| chr16:89589468 | C | T | 1 | a0001c0002t0001g0323 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1062-429C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589468 | |||||||
| chr16:89589469 | C | T | 2 | a0001c0001t0001g0083 a0001c0009t0001g0065 |
2 | HG01516.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1062-428C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589469 | |||||||
| chr16:89589553 | C | A | 5 | a0001c0002t0002g0257 a0001c0002t0002g0319 a0001c0002t0002g0329 others(2): Show |
5 | HG02970.hp2 HG03139.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1062-344C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589553 | |||||||
| chr16:89589611 | C | T | 28 | a0001c0002t0003g0035 a0001c0002t0003g0037 a0001c0002t0003g0038 others(25): Show |
29 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1062-286C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589611 | |||||||
| chr16:89589661 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1062-236C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589661 | |||||||
| chr16:89589702 | G | A | 5 | a0001c0002t0002g0257 a0001c0002t0002g0319 a0001c0002t0002g0329 others(2): Show |
5 | HG02970.hp2 HG03139.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1062-195G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589702 | |||||||
| chr16:89589754 | C | T | 12 | a0001c0001t0001g0241 a0001c0005t0002g0001 a0001c0005t0002g0076 others(9): Show |
19 | HG01070.hp2 HG01071.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1062-143C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589754 | |||||||
| chr16:89589755 | A | G | 199 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(196): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1062-142A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589755 | |||||||
| chr16:89589814 | G | A | 1 | a0001c0008t0002g0016 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1062-83G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589814 | |||||||
| chr16:89589843 | T | C | 197 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(194): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1062-54T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589843 | |||||||
| chr16:89590016 | C | A | 100 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0079 others(97): Show |
103 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1116+65C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590016 | |||||||
| chr16:89590016 | C | T | 1 | a0005c0014t0001g0012 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1116+65C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590016 | |||||||
| chr16:89590089 | G | A | 1 | a0001c0002t0004g0165 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1116+138G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590089 | |||||||
| chr16:89590137 | T | G | 19 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0051 others(16): Show |
19 | HG00323.hp2 HG00673.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.1116+186T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590137 | |||||||
| chr16:89590169 | C | T | 29 | a0001c0002t0003g0035 a0001c0002t0003g0037 a0001c0002t0003g0038 others(26): Show |
30 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1116+218C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590169 | |||||||
| chr16:89590223 | A | G | 195 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(192): Show |
205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1116+272A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590223 | |||||||
| chr16:89590301 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1116+350G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590301 | |||||||
| chr16:89590396 | A | G | 5 | a0001c0002t0002g0257 a0001c0002t0002g0319 a0001c0002t0002g0329 others(2): Show |
5 | HG02970.hp2 HG03139.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1116+445A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590396 | |||||||
| chr16:89590454 | G | A | 1 | a0001c0025t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1116+503G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590454 | |||||||
| chr16:89590589 | G | T | 1 | a0001c0002t0003g0229 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1117-418G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590589 | |||||||
| chr16:89590645 | C | T | 2 | a0001c0002t0002g0028 a0001c0002t0002g0330 |
2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1117-362C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590645 | |||||||
| chr16:89590750 | C | CGGGGGAG others(32): Show |
4 | a0001c0002t0004g0136 a0001c0002t0004g0137 a0001c0002t0004g0139 others(1): Show |
4 | HG00609.hp1 HG01943.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1117-202_1117-164d others(41): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 89590750 | ||||||
| chr16:89590750 | C | T | 1 | a0001c0002t0001g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1117-257C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590750 | |||||||
| chr16:89590750 | CGGGGGAG others(32): Show |
C | 51 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0059 others(48): Show |
51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1117-202_1117-164d others(41): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 89590750 | ||||||
| chr16:89590776 | GGGGGCCG others(31): Show |
G | 1 | a0001c0001t0001g0031 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1117-226_1117-189d others(40): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 89590776 | ||||||
| chr16:89590789 | G | A | 1 | a0001c0002t0002g0235 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1117-218G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590789 | |||||||
| chr16:89590789 | GGGGGGAG others(31): Show |
G | 1 | a0001c0001t0001g0233 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1117-212_1117-175d others(40): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 89590789 | ||||||
| chr16:89590839 | C | G | 1 | a0001c0002t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1117-168C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590839 | |||||||
| chr16:89590862 | C | T | 24 | a0001c0001t0001g0262 a0001c0002t0002g0045 a0001c0002t0002g0087 others(21): Show |
24 | HG01106.hp2 HG01192.hp2 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.1117-145C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590862 | |||||||
| chr16:89590975 | G | A | 1 | a0003c0006t0003g0228 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1117-32G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590975 | |||||||
| chr16:89591102 | C | T | 29 | a0001c0002t0003g0022 a0001c0002t0003g0080 a0001c0002t0003g0176 others(26): Show |
31 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1169-25C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 12/14 | chr16 | 89591102 | |||||||
| chr16:89591311 | T | A | 71 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0110 others(68): Show |
73 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1302+51T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591311 | |||||||
| chr16:89591321 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1302+61C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591321 | |||||||
| chr16:89591420 | G | A | 2 | a0001c0002t0002g0087 a0001c0002t0002g0098 |
2 | HG01106.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1302+160G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591420 | |||||||
| chr16:89591445 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1302+185C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591445 | |||||||
| chr16:89591506 | T | A | 1 | a0001c0002t0002g0190 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1302+246T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591506 | |||||||
| chr16:89591534 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1302+274C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591534 | |||||||
| chr16:89591536 | C | T | 3 | a0001c0002t0005g0158 a0001c0027t0005g0161 a0001c0028t0001g0160 |
3 | HG02818.hp1 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1302+276C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591536 | |||||||
| chr16:89591541 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1302+281A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591541 | |||||||
| chr16:89591547 | A | G | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1302+287A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591547 | |||||||
| chr16:89591628 | T | A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0286 |
3 | HG02630.hp2 HG02886.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1302+368T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591628 | |||||||
| chr16:89591634 | C | G | 8 | a0001c0002t0001g0276 a0001c0002t0001g0323 a0001c0002t0004g0264 others(5): Show |
8 | HG00639.hp1 HG01081.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1302+374C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591634 | |||||||
| chr16:89591704 | C | G | 1 | a0001c0025t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1302+444C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591704 | |||||||
| chr16:89591723 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1302+463A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591723 | |||||||
| chr16:89591739 | A | C | 4 | a0001c0001t0001g0170 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
4 | HG02055.hp1 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+479A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591739 | |||||||
| chr16:89591741 | C | A | 8 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(5): Show |
8 | HG01109.hp2 HG02451.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.1302+481C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591741 | |||||||
| chr16:89591767 | C | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0073 others(1): Show |
4 | HG01884.hp1 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+507C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591767 | |||||||
| chr16:89591786 | G | C | 10 | a0001c0001t0001g0277 a0001c0002t0001g0276 a0001c0002t0001g0323 others(7): Show |
10 | HG00639.hp1 HG01081.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1302+526G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591786 | |||||||
| chr16:89591793 | G | A | 2 | a0001c0002t0002g0026 a0004c0020t0001g0332 |
2 | HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1302+533G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591793 | |||||||
| chr16:89591801 | C | A | 21 | a0001c0001t0001g0011 a0001c0001t0001g0072 a0001c0001t0001g0074 others(18): Show |
21 | HG00639.hp1 HG01081.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1302+541C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591801 | |||||||
| chr16:89591801 | C | T | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG00323.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1302+541C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591801 | |||||||
| chr16:89591804 | C | A | 21 | a0001c0001t0001g0011 a0001c0001t0001g0072 a0001c0001t0001g0074 others(18): Show |
21 | HG00639.hp1 HG01081.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1302+544C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591804 | |||||||
| chr16:89591814 | C | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0072 a0001c0001t0001g0074 others(5): Show |
8 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+554C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591814 | |||||||
| chr16:89591826 | A | G | 84 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0030 others(81): Show |
86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.1302+566A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591826 | |||||||
| chr16:89591829 | G | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0031 others(71): Show |
76 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(73): Show |
intron_variant | MODIFIER | c.1302+569G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591829 | |||||||
| chr16:89591838 | C | T | 166 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0025 others(163): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1302+578C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591838 | |||||||
| chr16:89591845 | C | T | 95 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0051 others(92): Show |
98 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1302+585C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591845 | |||||||
| chr16:89591846 | G | A | 4 | a0001c0001t0001g0277 a0001c0002t0001g0276 a0001c0002t0001g0323 others(1): Show |
4 | HG00639.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+586G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591846 | |||||||
| chr16:89591846 | G | T | 126 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0039 others(123): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.1302+586G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591846 | |||||||
| chr16:89591858 | T | G | 1 | a0001c0002t0001g0314 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1302+598T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591858 | |||||||
| chr16:89591859 | T | C | 1 | a0001c0002t0001g0314 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1302+599T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591859 | |||||||
| chr16:89591861 | T | C | 1 | a0001c0002t0001g0314 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1302+601T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591861 | |||||||
| chr16:89591900 | C | T | 3 | a0001c0002t0001g0029 a0001c0002t0001g0163 a0001c0008t0001g0014 |
3 | HG02922.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1302+640C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591900 | |||||||
| chr16:89591916 | G | A | 8 | a0001c0001t0001g0110 a0001c0001t0001g0184 a0001c0001t0001g0185 others(5): Show |
8 | HG01109.hp2 HG02451.hp2 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+656G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591916 | |||||||
| chr16:89591935 | A | G | 1 | a0001c0002t0001g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1302+675A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591935 | |||||||
| chr16:89591935 | ATGATCCA others(308): Show |
A | 1 | a0001c0009t0001g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1302+718_1302+1032 others(3): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89591935 | ||||||
| chr16:89591995 | G | A | 200 | a0001c0001t0001g0011 a0001c0001t0001g0072 a0001c0001t0001g0073 others(197): Show |
211 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.1302+735G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591995 | |||||||
| chr16:89592001 | C | G | 54 | a0001c0001t0001g0241 a0001c0002t0002g0008 a0001c0002t0002g0036 others(51): Show |
62 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1302+741C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592001 | |||||||
| chr16:89592010 | G | T | 4 | a0001c0002t0004g0264 a0001c0002t0004g0317 a0001c0002t0004g0320 others(1): Show |
4 | HG02258.hp1 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+750G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592010 | |||||||
| chr16:89592013 | G | GT | 71 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0051 others(68): Show |
71 | HG00323.hp2 HG00673.hp1 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.1302+765dupT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89592013 | ||||||
| chr16:89592016 | T | G | 4 | a0001c0002t0004g0264 a0001c0002t0004g0317 a0001c0002t0004g0320 others(1): Show |
4 | HG02258.hp1 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+756T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592016 | |||||||
| chr16:89592031 | G | A | 3 | a0001c0002t0005g0158 a0001c0027t0005g0161 a0001c0028t0001g0160 |
3 | HG02818.hp1 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1302+771G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592031 | |||||||
| chr16:89592039 | G | A | 43 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0262 others(40): Show |
43 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1302+779G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592039 | |||||||
| chr16:89592051 | A | C | 5 | a0001c0001t0001g0115 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
5 | HG01928.hp2 NA18966.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+791A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592051 | |||||||
| chr16:89592053 | G | A | 5 | a0001c0001t0001g0115 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
5 | HG01928.hp2 NA18966.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+793G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592053 | |||||||
| chr16:89592063 | T | C | 261 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0034 others(258): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1302+803T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592063 | |||||||
| chr16:89592069 | C | T | 207 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0110 others(204): Show |
219 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.1302+809C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592069 | |||||||
| chr16:89592091 | C | T | 4 | a0001c0002t0004g0264 a0001c0002t0004g0317 a0001c0002t0004g0320 others(1): Show |
4 | HG02258.hp1 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+831C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592091 | |||||||
| chr16:89592095 | C | A | 194 | a0001c0001t0001g0011 a0001c0001t0001g0072 a0001c0001t0001g0073 others(191): Show |
206 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.1302+835C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592095 | |||||||
| chr16:89592108 | G | A | 45 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0262 others(42): Show |
45 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1302+848G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592108 | |||||||
| chr16:89592109 | C | T | 44 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0262 others(41): Show |
44 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1302+849C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592109 | |||||||
| chr16:89592110 | G | A | 44 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0262 others(41): Show |
44 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1302+850G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592110 | |||||||
| chr16:89592113 | A | T | 43 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0262 others(40): Show |
43 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1302+853A>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592113 | |||||||
| chr16:89592175 | A | AT | 99 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0039 others(96): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1302+927dupT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89592175 | ||||||
| chr16:89592175 | A | ATTTTTTT others(311): Show |
1 | a0001c0002t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1302+927_1302+928i others(320): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89592175 | ||||||
| chr16:89592215 | C | T | 1 | a0001c0025t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1302+955C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592215 | |||||||
| chr16:89592223 | C | T | 4 | a0001c0002t0001g0029 a0001c0002t0001g0163 a0001c0008t0001g0014 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+963C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592223 | |||||||
| chr16:89592249 | C | T | 2 | a0001c0001t0001g0171 a0001c0002t0005g0287 |
2 | HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1302+989C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592249 | |||||||
| chr16:89592280 | CTGGGATT others(796): Show |
C | 1 | a0001c0002t0002g0027 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1302+1046_1302+184 others(4): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89592280 | ||||||
| chr16:89592306 | G | A | 54 | a0001c0001t0001g0241 a0001c0002t0002g0008 a0001c0002t0002g0036 others(51): Show |
62 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1302+1046G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592306 | |||||||
| chr16:89592366 | C | T | 40 | a0001c0001t0001g0262 a0001c0002t0001g0276 a0001c0002t0001g0323 others(37): Show |
40 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1302+1106C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592366 | |||||||
| chr16:89592395 | G | C | 4 | a0001c0002t0004g0264 a0001c0002t0004g0317 a0001c0002t0004g0320 others(1): Show |
4 | HG02258.hp1 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+1135G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592395 | |||||||
| chr16:89592448 | A | AT | 56 | a0001c0001t0001g0053 a0001c0001t0001g0241 a0001c0002t0001g0033 others(53): Show |
64 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1302+1205dupT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89592448 | ||||||
| chr16:89592448 | AT | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0103 others(11): Show |
14 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(11): Show |
intron_variant | MODIFIER | c.1302+1205delT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89592448 | ||||||
| chr16:89592471 | A | G | 28 | a0001c0001t0001g0082 a0001c0001t0001g0096 a0001c0001t0001g0172 others(25): Show |
29 | HG00099.hp1 HG01099.hp2 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.1302+1211A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592471 | |||||||
| chr16:89592505 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0198 |
2 | HG04199.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1302+1245C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592505 | |||||||
| chr16:89592658 | G | C | 1 | a0001c0002t0001g0323 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1302+1398G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592658 | |||||||
| chr16:89592732 | G | A | 1 | a0001c0002t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1302+1472G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592732 | |||||||
| chr16:89592743 | A | C | 1 | a0001c0001t0001g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1302+1483A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592743 | |||||||
| chr16:89592805 | C | A | 1 | a0004c0011t0001g0106 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1302+1545C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592805 | |||||||
| chr16:89592810 | C | CT | 99 | a0001c0001t0001g0082 a0001c0001t0001g0110 a0001c0001t0001g0172 others(96): Show |
108 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1302+1569dupT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89592810 | ||||||
| chr16:89592810 | C | CTT | 36 | a0001c0001t0001g0262 a0001c0002t0002g0026 a0001c0002t0002g0045 others(33): Show |
36 | HG00609.hp1 HG00621.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.1302+1568_1302+156 others(6): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89592810 | ||||||
| chr16:89592814 | T | TC | 55 | a0001c0002t0003g0022 a0001c0002t0003g0035 a0001c0002t0003g0037 others(52): Show |
58 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1302+1554_1302+155 others(5): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592814 | |||||||
| chr16:89592815 | T | C | 5 | a0001c0002t0003g0044 a0001c0002t0003g0046 a0001c0002t0003g0054 others(2): Show |
5 | HG02083.hp2 NA18980.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1302+1555T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592815 | |||||||
| chr16:89592848 | T | C | 4 | a0001c0002t0005g0023 a0001c0002t0005g0024 a0001c0002t0005g0182 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+1588T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592848 | |||||||
| chr16:89592914 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1302+1654G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592914 | |||||||
| chr16:89592950 | G | C | 1 | a0001c0008t0001g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1302+1690G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592950 | |||||||
| chr16:89592961 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1302+1701C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592961 | |||||||
| chr16:89592975 | G | C | 1 | a0001c0002t0001g0314 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1302+1715G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592975 | |||||||
| chr16:89592998 | G | C | 62 | a0001c0002t0003g0022 a0001c0002t0003g0035 a0001c0002t0003g0037 others(59): Show |
65 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1302+1738G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592998 | |||||||
| chr16:89593042 | C | A | 37 | a0001c0001t0001g0262 a0001c0002t0002g0028 a0001c0002t0002g0045 others(34): Show |
37 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1302+1782C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593042 | |||||||
| chr16:89593071 | C | T | 4 | a0001c0002t0004g0264 a0001c0002t0004g0317 a0001c0002t0004g0320 others(1): Show |
4 | HG02258.hp1 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+1811C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593071 | |||||||
| chr16:89593103 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1302+1843C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593103 | |||||||
| chr16:89593130 | T | A | 204 | a0001c0001t0001g0082 a0001c0001t0001g0096 a0001c0001t0001g0172 others(201): Show |
216 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.1302+1870T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593130 | |||||||
| chr16:89593214 | C | G | 61 | a0001c0002t0003g0022 a0001c0002t0003g0035 a0001c0002t0003g0037 others(58): Show |
64 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1302+1954C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593214 | |||||||
| chr16:89593240 | T | A | 3 | a0001c0002t0002g0319 a0001c0002t0009g0318 a0001c0008t0002g0013 |
3 | HG03139.hp2 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1302+1980T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593240 | |||||||
| chr16:89593292 | C | G | 1 | a0001c0002t0013g0189 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1302+2032C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593292 | |||||||
| chr16:89593292 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1302+2032C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593292 | |||||||
| chr16:89593294 | C | T | 14 | a0001c0002t0005g0023 a0001c0002t0005g0024 a0001c0002t0005g0078 others(11): Show |
14 | HG01192.hp2 HG01243.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1302+2034C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593294 | |||||||
| chr16:89593310 | G | A | 2 | a0001c0002t0001g0314 a0001c0002t0002g0026 |
2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1302+2050G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593310 | |||||||
| chr16:89593358 | A | AT | 82 | a0001c0001t0001g0082 a0001c0001t0001g0096 a0001c0001t0001g0172 others(79): Show |
86 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1303-1996dupT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89593358 | ||||||
| chr16:89593365 | T | C | 3 | a0001c0001t0001g0232 a0001c0001t0001g0273 a0001c0001t0001g0291 |
3 | HG00741.hp2 HG01175.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1303-2002T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593365 | |||||||
| chr16:89593404 | G | C | 1 | a0001c0024t0001g0208 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1303-1963G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593404 | |||||||
| chr16:89593462 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1303-1905C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593462 | |||||||
| chr16:89593519 | A | AT | 60 | a0001c0002t0003g0022 a0001c0002t0003g0035 a0001c0002t0003g0037 others(57): Show |
63 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1303-1842dupT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89593519 | ||||||
| chr16:89593553 | T | C | 3 | a0001c0002t0001g0314 a0001c0002t0002g0026 a0001c0008t0002g0013 |
3 | HG03139.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1303-1814T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593553 | |||||||
| chr16:89593554 | G | A | 1 | a0001c0002t0001g0314 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1303-1813G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593554 | |||||||
| chr16:89593642 | G | A | 1 | a0001c0002t0001g0314 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1303-1725G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593642 | |||||||
| chr16:89593661 | C | G | 1 | a0001c0002t0002g0045 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1303-1706C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593661 | |||||||
| chr16:89593809 | T | A | 1 | a0005c0014t0001g0012 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1303-1558T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593809 | |||||||
| chr16:89593826 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1303-1541T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593826 | |||||||
| chr16:89593895 | C | T | 1 | a0001c0002t0002g0098 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1303-1472C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593895 | |||||||
| chr16:89593907 | G | T | 40 | a0001c0001t0001g0262 a0001c0002t0002g0027 a0001c0002t0002g0028 others(37): Show |
40 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1303-1460G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593907 | |||||||
| chr16:89593935 | G | A | 19 | a0001c0001t0001g0059 a0001c0001t0001g0067 a0001c0001t0001g0071 others(16): Show |
19 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1303-1432G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593935 | |||||||
| chr16:89594101 | A | G | 82 | a0001c0001t0001g0082 a0001c0001t0001g0096 a0001c0001t0001g0172 others(79): Show |
86 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1303-1266A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594101 | |||||||
| chr16:89594103 | C | G | 112 | a0001c0001t0001g0262 a0001c0002t0001g0276 a0001c0002t0001g0323 others(109): Show |
120 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.1303-1264C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594103 | |||||||
| chr16:89594140 | G | A | 5 | a0001c0002t0005g0078 a0001c0002t0005g0191 a0001c0002t0005g0284 others(2): Show |
5 | HG01192.hp2 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303-1227G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594140 | |||||||
| chr16:89594192 | C | T | 7 | a0001c0002t0001g0029 a0001c0002t0001g0033 a0001c0002t0001g0163 others(4): Show |
7 | HG00639.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1303-1175C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594192 | |||||||
| chr16:89594227 | G | C | 2 | a0001c0001t0008g0050 a0002c0010t0008g0127 |
2 | HG00673.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1303-1140G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594227 | |||||||
| chr16:89594270 | G | A | 1 | a0002c0003t0003g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1303-1097G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594270 | |||||||
| chr16:89594367 | G | C | 1 | a0001c0002t0002g0045 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1303-1000G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594367 | |||||||
| chr16:89594376 | G | A | 4 | a0001c0002t0001g0029 a0001c0002t0001g0033 a0001c0002t0001g0163 others(1): Show |
4 | HG02572.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303-991G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594376 | |||||||
| chr16:89594378 | G | A | 1 | a0001c0002t0005g0023 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1303-989G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594378 | |||||||
| chr16:89594442 | C | A | 13 | a0001c0007t0006g0006 a0001c0007t0006g0068 a0001c0007t0006g0075 others(10): Show |
14 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1303-925C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594442 | |||||||
| chr16:89594473 | C | T | 1 | a0001c0002t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1303-894C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594473 | |||||||
| chr16:89594560 | G | A | 5 | a0003c0006t0003g0226 a0003c0006t0003g0260 a0003c0006t0003g0267 others(2): Show |
5 | NA18946.hp1 NA18952.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303-807G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594560 | |||||||
| chr16:89594624 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1303-743T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594624 | |||||||
| chr16:89594642 | C | CT | 32 | a0001c0001t0001g0011 a0001c0001t0001g0048 a0001c0001t0001g0059 others(29): Show |
32 | HG00099.hp2 HG00558.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1303-696dupT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | ||||||
| chr16:89594642 | C | CTT | 44 | a0001c0002t0003g0022 a0001c0002t0003g0035 a0001c0002t0003g0038 others(41): Show |
46 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1303-697_1303-696d others(4): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | ||||||
| chr16:89594642 | C | CTTT | 13 | a0001c0002t0003g0037 a0001c0002t0003g0176 a0001c0002t0003g0177 others(10): Show |
14 | HG00597.hp2 HG02129.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.1303-698_1303-696d others(5): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | ||||||
| chr16:89594642 | CTTTTTTT | C | 10 | a0001c0002t0001g0033 a0001c0002t0002g0027 a0001c0002t0004g0261 others(7): Show |
10 | HG00438.hp1 HG01361.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.1303-702_1303-696d others(9): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | ||||||
| chr16:89594642 | CTTTTTTT others(1): Show |
C | 90 | a0001c0001t0001g0262 a0001c0002t0001g0276 a0001c0002t0001g0314 others(87): Show |
98 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1303-703_1303-696d others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | ||||||
| chr16:89594642 | CTTTTTTT others(2): Show |
C | 19 | a0001c0001t0001g0067 a0001c0002t0004g0215 a0001c0002t0004g0320 others(16): Show |
19 | HG01192.hp2 HG01243.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.1303-704_1303-696d others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | ||||||
| chr16:89594642 | CTTTTTTT others(3): Show |
C | 1 | a0001c0024t0001g0208 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1303-705_1303-696d others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | ||||||
| chr16:89594642 | CTTTTTTT others(6): Show |
C | 3 | a0001c0002t0001g0029 a0001c0002t0001g0163 a0001c0008t0001g0014 |
3 | HG02922.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1303-708_1303-696d others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | ||||||
| chr16:89594642 | CTTTTTTT others(7): Show |
C | 15 | a0001c0002t0013g0189 a0001c0007t0006g0006 a0001c0007t0006g0068 others(12): Show |
16 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.1303-709_1303-696d others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | ||||||
| chr16:89594668 | T | G | 8 | a0001c0001t0001g0262 a0001c0002t0002g0045 a0001c0002t0002g0087 others(5): Show |
8 | HG01106.hp2 HG01261.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.1303-699T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594668 | |||||||
| chr16:89594691 | C | T | 13 | a0001c0007t0006g0006 a0001c0007t0006g0068 a0001c0007t0006g0075 others(10): Show |
14 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1303-676C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594691 | |||||||
| chr16:89594715 | G | A | 61 | a0001c0002t0003g0022 a0001c0002t0003g0035 a0001c0002t0003g0037 others(58): Show |
64 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1303-652G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594715 | |||||||
| chr16:89594726 | A | T | 3 | a0001c0002t0001g0276 a0001c0002t0001g0323 a0001c0015t0001g0322 |
3 | HG00639.hp1 HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1303-641A>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594726 | |||||||
| chr16:89594769 | A | G | 1 | a0001c0008t0001g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1303-598A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594769 | |||||||
| chr16:89594830 | T | C | 62 | a0001c0002t0003g0022 a0001c0002t0003g0035 a0001c0002t0003g0037 others(59): Show |
65 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1303-537T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594830 | |||||||
| chr16:89594899 | G | A | 1 | a0003c0006t0003g0149 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1303-468G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594899 | |||||||
| chr16:89595098 | A | G | 199 | a0001c0001t0001g0262 a0001c0002t0001g0029 a0001c0002t0001g0033 others(196): Show |
211 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.1303-269A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89595098 | |||||||
| chr16:89595129 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0172 |
2 | HG00099.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.1303-238G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89595129 | |||||||
| chr16:89595267 | C | T | 26 | a0001c0002t0004g0055 a0001c0002t0004g0056 a0001c0002t0004g0057 others(23): Show |
26 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.1303-100C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89595267 | |||||||
| chr16:89595362 | C | T | 30 | a0001c0002t0004g0055 a0001c0002t0004g0056 a0001c0002t0004g0057 others(27): Show |
30 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(27): Show |
splice_region_variant&intron_variant | LOW | c.1303-5C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89595362 | |||||||
| chr16:89595635 | G | A | 1 | a0001c0002t0001g0314 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1539+32G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595635 | |||||||
| chr16:89595655 | T | C | 32 | a0001c0002t0003g0022 a0001c0002t0003g0080 a0001c0002t0003g0176 others(29): Show |
34 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.1539+52T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595655 | |||||||
| chr16:89595741 | C | T | 1 | a0001c0008t0001g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1539+138C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595741 | |||||||
| chr16:89595824 | A | T | 3 | a0001c0002t0001g0276 a0001c0002t0001g0323 a0001c0015t0001g0322 |
3 | HG00639.hp1 HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1539+221A>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595824 | |||||||
| chr16:89595879 | G | A | 2 | a0001c0001t0001g0120 a0001c0002t0002g0199 |
2 | NA18990.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1539+276G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595879 | |||||||
| chr16:89595911 | C | T | 29 | a0001c0002t0004g0055 a0001c0002t0004g0056 a0001c0002t0004g0057 others(26): Show |
29 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.1539+308C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595911 | |||||||
| chr16:89595942 | G | A | 1 | a0001c0002t0002g0028 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1539+339G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595942 | |||||||
| chr16:89595953 | A | G | 1 | a0001c0002t0002g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1539+350A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595953 | |||||||
| chr16:89595955 | C | G | 1 | a0001c0002t0004g0219 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1539+352C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595955 | |||||||
| chr16:89595976 | G | A | 3 | a0001c0002t0001g0276 a0001c0002t0001g0323 a0001c0015t0001g0322 |
3 | HG00639.hp1 HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1539+373G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595976 | |||||||
| chr16:89595979 | GAGACGCA others(28): Show |
G | 4 | a0001c0001t0001g0170 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
4 | HG02055.hp1 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1539+381_1539+415d others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 89595979 | ||||||
| chr16:89595980 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1539+377A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595980 | |||||||
| chr16:89596014 | A | G | 196 | a0001c0002t0001g0029 a0001c0002t0001g0033 a0001c0002t0001g0163 others(193): Show |
208 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.1539+411A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596014 | |||||||
| chr16:89596045 | G | T | 1 | a0007c0026t0001g0021 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1540-439G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596045 | |||||||
| chr16:89596052 | G | C | 1 | a0007c0026t0001g0021 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1540-432G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596052 | |||||||
| chr16:89596063 | A | G | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
6 | HG02602.hp2 HG02738.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.1540-421A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596063 | |||||||
| chr16:89596082 | C | G | 6 | a0001c0001t0001g0238 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
6 | HG01123.hp1 HG01496.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-402C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596082 | |||||||
| chr16:89596113 | C | T | 12 | a0001c0007t0006g0006 a0001c0007t0006g0068 a0001c0007t0006g0075 others(9): Show |
13 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1540-371C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596113 | |||||||
| chr16:89596122 | G | A | 1 | a0002c0004t0002g0020 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1540-362G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596122 | |||||||
| chr16:89596208 | G | A | 1 | a0001c0023t0001g0223 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1540-276G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596208 | |||||||
| chr16:89596238 | AG | A | 12 | a0001c0007t0006g0006 a0001c0007t0006g0068 a0001c0007t0006g0075 others(9): Show |
13 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1540-244delG | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 89596238 | ||||||
| chr16:89596419 | G | A | 1 | a0001c0001t0012g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1540-65G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596419 | |||||||
| chr16:89596429 | C | T | 52 | a0001c0002t0002g0008 a0001c0002t0002g0036 a0001c0002t0002g0041 others(49): Show |
60 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1540-55C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596429 | |||||||
| chr16:89596467 | G | C | 79 | a0001c0002t0001g0029 a0001c0002t0001g0163 a0001c0002t0003g0022 others(76): Show |
83 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.1540-17G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596467 | |||||||
| chr16:89596472 | C | G | 1 | a0001c0002t0013g0189 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1540-12C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596472 |