Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8506 |
| ensemblid | ENSG00000108797.12 |
| hgncid | 8011 |
| symbol | CNTNAP1 |
| name | contactin associated protein 1 |
| refseq_nuc | NM_003632.3 |
| refseq_prot | NP_003623.1 |
| ensembl_nuc | ENST00000264638.9 |
| ensembl_prot | ENSP00000264638.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 42682531 |
| end | 42699993 |
| strand | + |
| ver | v1.2 |
| region | chr17:42682531-42699993 |
| region5000 | chr17:42677531-42704993 |
| regionname0 | CNTNAP1_chr17_42682531_42699993 |
| regionname5000 | CNTNAP1_chr17_42677531_42704993 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1384 | 338 | 75 | 64 | 144 | 10 | 43 | 107 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | MMHLR others(1379): Show |
chr17 | 42677531 | 42704993 |
| a0002 | 0/0 | 1384 | 20 | 16 | 4 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | MMHLR others(1379): Show |
chr17 | 42677531 | 42704993 |
| a0003 | 0/0 | 1384 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | MMHLR others(1379): Show |
chr17 | 42677531 | 42704993 |
| a0004 | 0/0 | 1384 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | MMHLR others(1379): Show |
chr17 | 42677531 | 42704993 |
| a0005 | 0/0 | 1384 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | MMHLR others(1379): Show |
chr17 | 42677531 | 42704993 |
| a0006 | 0/0 | 1384 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | MMHLR others(1379): Show |
chr17 | 42677531 | 42704993 |
| a0007 | 0/0 | 1384 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | MMHLR others(1379): Show |
chr17 | 42677531 | 42704993 |
| a0008 | 0/0 | 1384 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | MMHLR others(1379): Show |
chr17 | 42677531 | 42704993 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4152 | 165 | 50 | 25 | 61 | 5 | 24 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0001c0002 | 1/1 | 4152 | 146 | 21 | 31 | 75 | 4 | 13 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0001c0004 | 0/0 | 4152 | 8 | 0 | 7 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0001c0005 | 0/0 | 4152 | 7 | 0 | 0 | 5 | 0 | 2 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0001c0009 | 0/0 | 4152 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0001c0010 | 0/0 | 4152 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0001c0011 | 0/0 | 4152 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0001c0016 | 0/0 | 4152 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0001c0018 | 0/0 | 4152 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0001c0019 | 0/0 | 4152 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0001c0020 | 0/0 | 4152 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0001c0021 | 0/0 | 4152 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0001c0022 | 0/0 | 4152 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0001c0023 | 0/0 | 4152 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0001c0024 | 0/0 | 4152 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0001c0026 | 0/0 | 4152 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0002c0003 | 0/0 | 4152 | 17 | 13 | 4 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0002c0006 | 0/0 | 4152 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0002c0007 | 0/0 | 4152 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0002c0014 | 0/0 | 4152 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0003c0015 | 0/0 | 4152 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0004c0008 | 0/0 | 4152 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0005c0013 | 0/0 | 4152 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0006c0017 | 0/0 | 4152 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0007c0012 | 0/0 | 4152 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 | ||
| a0008c0025 | 0/0 | 4152 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | ATGAT others(4147): Show |
chr17 | 42677531 | 42704993 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5537 | 14 | 12 | 1 | 0 | 1 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0001t0002 | 0/0 | 5537 | 142 | 33 | 24 | 58 | 4 | 23 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0001t0003 | 0/0 | 5537 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0001t0004 | 0/0 | 5537 | 4 | 4 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0001t0005 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0001t0006 | 0/0 | 5537 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0001t0007 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0001t0009 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0002t0001 | 1/1 | 5537 | 143 | 21 | 28 | 75 | 4 | 13 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0002t0003 | 0/0 | 5537 | 3 | 0 | 3 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0004t0001 | 0/0 | 5537 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0004t0002 | 0/0 | 5537 | 7 | 0 | 6 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0005t0002 | 0/0 | 5537 | 7 | 0 | 0 | 5 | 0 | 2 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0009t0001 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0010t0001 | 0/0 | 5537 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0011t0001 | 0/0 | 5537 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0016t0002 | 0/0 | 5537 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0018t0002 | 0/0 | 5537 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0019t0002 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0020t0001 | 0/0 | 5537 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0021t0002 | 0/0 | 5537 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0022t0002 | 0/0 | 5537 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0023t0001 | 0/0 | 5537 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0024t0002 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0001c0026t0008 | 0/0 | 5537 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0002c0003t0001 | 0/0 | 5537 | 17 | 13 | 4 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0002c0006t0001 | 0/0 | 5537 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0002c0007t0001 | 0/0 | 5537 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0002c0014t0010 | 0/0 | 5537 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0003c0015t0002 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0004c0008t0001 | 0/0 | 5537 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0005c0013t0001 | 0/0 | 5537 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0006c0017t0002 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0007c0012t0001 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| a0008c0025t0002 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | GAAAC others(5532): Show |
chr17 | 42677531 | 42704993 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0003 | 0/0 | 11 | 0 | 1 | 7 | 1 | 2 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0004 | 0/0 | 8 | 3 | 4 | 0 | 1 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0005 | 0/0 | 7 | 6 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0006 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0016 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0026 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0001t0009g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0001 | 0/0 | 39 | 1 | 13 | 17 | 1 | 7 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0002 | 0/1 | 22 | 1 | 6 | 10 | 2 | 2 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0012 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0013 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0019 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0020 | 1/0 | 3 | 0 | 0 | 2 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0003g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0004t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0004t0002g0010 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0004t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0005t0002g0023 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0005t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0005t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0005t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0005t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0009t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0010t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0011t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0016t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0018t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0019t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0020t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0021t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0022t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0023t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0024t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0001c0026t0008g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0002c0003t0001g0011 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0002c0003t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0002c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0002c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0002c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0002c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0002c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0002c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0002c0003t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0002c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0002c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0002c0006t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0002c0007t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0002c0014t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0003c0015t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0004c0008t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0005c0013t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0006c0017t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0007c0012t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| a0008c0025t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0027 | EUR | GBR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | GBR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00140 | hp1 | a0001 | c0016 | t0002 | g0027 | EUR | GBR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | FIN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0082 | EUR | FIN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | FIN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | FIN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00423 | hp2 | a0001 | c0024 | t0002 | g0164 | EAS | CHS | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | CHS | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | CHS | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | CHS | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | CHS | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | CHS | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0078 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01109 | hp1 | a0001 | c0004 | t0002 | g0010 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01109 | hp2 | a0002 | c0003 | t0001 | g0045 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01167 | hp2 | a0002 | c0003 | t0001 | g0011 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01169 | hp2 | a0002 | c0003 | t0001 | g0011 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01192 | hp2 | a0001 | c0026 | t0008 | g0006 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01243 | hp2 | a0002 | c0003 | t0001 | g0011 | AMR | PUR | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01257 | hp2 | a0001 | c0002 | t0003 | g0031 | AMR | CLM | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01258 | hp1 | a0001 | c0002 | t0003 | g0031 | AMR | CLM | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01361 | hp1 | a0001 | c0004 | t0001 | g0056 | AMR | CLM | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0127 | EUR | IBS | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01943 | hp2 | a0001 | c0004 | t0002 | g0010 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01978 | hp2 | a0001 | c0004 | t0002 | g0125 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02004 | hp1 | a0001 | c0004 | t0002 | g0010 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02055 | hp1 | a0002 | c0003 | t0001 | g0107 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02056 | hp1 | a0003 | c0015 | t0002 | g0040 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02132 | hp1 | a0001 | c0005 | t0002 | g0118 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02145 | hp1 | a0001 | c0011 | t0001 | g0192 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | CDX | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | CDX | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02273 | hp2 | a0001 | c0004 | t0002 | g0010 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02293 | hp2 | a0001 | c0004 | t0002 | g0010 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0011 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0098 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | KHV | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02572 | hp1 | a0002 | c0003 | t0001 | g0028 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0105 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0191 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02683 | hp2 | a0001 | c0018 | t0002 | g0123 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0070 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0060 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0106 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0189 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02886 | hp2 | a0002 | c0003 | t0001 | g0196 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02895 | hp1 | a0002 | c0003 | t0001 | g0187 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0100 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02922 | hp1 | a0002 | c0003 | t0001 | g0188 | AFR | ESN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ESN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02970 | hp2 | a0002 | c0003 | t0001 | g0011 | AFR | ESN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | ESN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0076 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0194 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | MSL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | MSL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03130 | hp1 | a0001 | c0021 | t0002 | g0185 | AFR | ESN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | ESN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | ESN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ESN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | ESN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03209 | hp1 | a0002 | c0003 | t0001 | g0197 | AFR | MSL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03209 | hp2 | a0001 | c0010 | t0001 | g0103 | AFR | MSL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03225 | hp2 | a0002 | c0006 | t0001 | g0045 | AFR | MSL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03453 | hp1 | a0002 | c0014 | t0010 | g0149 | AFR | MSL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03486 | hp1 | a0004 | c0008 | t0001 | g0193 | AFR | MSL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03486 | hp2 | a0002 | c0007 | t0001 | g0195 | AFR | MSL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0190 | AFR | ESN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ESN | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03579 | hp1 | a0002 | c0003 | t0001 | g0028 | AFR | MSL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | MSL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | STU | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03704 | hp1 | a0001 | c0005 | t0002 | g0023 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03831 | hp1 | a0005 | c0013 | t0001 | g0141 | SAS | BEB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | BEB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | BEB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | BEB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03927 | hp2 | a0001 | c0005 | t0002 | g0112 | SAS | BEB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | BEB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | STU | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | STU | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | BEB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG04199 | hp1 | a0001 | c0023 | t0001 | g0058 | SAS | STU | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG04199 | hp2 | a0001 | c0022 | t0002 | g0132 | SAS | STU | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG04204 | hp1 | a0001 | c0004 | t0002 | g0054 | SAS | STU | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | CHB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | CHB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | CHB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | YRI | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18948 | hp1 | a0001 | c0005 | t0002 | g0023 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18954 | hp1 | a0006 | c0017 | t0002 | g0027 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18963 | hp2 | a0001 | c0005 | t0002 | g0023 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18965 | hp1 | a0001 | c0001 | t0007 | g0050 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18968 | hp2 | a0007 | c0012 | t0001 | g0062 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18977 | hp2 | a0001 | c0005 | t0002 | g0120 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19001 | hp2 | a0008 | c0025 | t0002 | g0048 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19003 | hp2 | a0001 | c0019 | t0002 | g0035 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19005 | hp1 | a0001 | c0001 | t0009 | g0018 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19010 | hp1 | a0001 | c0005 | t0002 | g0119 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | LWK | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0028 | AFR | LWK | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19059 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19066 | hp1 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19087 | hp1 | a0001 | c0009 | t0001 | g0090 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | YRI | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ASW | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ASW | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0163 | SAS | GIH | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | GIH | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | CLM | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | MSL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | USA | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | USA | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | USA | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | USA | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | LWK | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| NA21309 | hp2 | a0001 | c0020 | t0001 | g0053 | AFR | LWK | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0002 | REF | REF | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0020 | REF | REF | CNTNAP1_chr17_42677531_42704993 | CNTNAP1 | chr17 | 42677531 | 42704993 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:42684147 | G | T | 1 | a0007 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.281G>T | p.Trp94Leu | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 3/24 | 580/5537 | 281/4155 | 94/1384 | chr17 | 42684147 | |||
| chr17:42685390 | G | C | 1 | a0005 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.685G>C | p.Gly229Arg | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 5/24 | 984/5537 | 685/4155 | 229/1384 | chr17 | 42685390 | |||
| chr17:42688537 | A | G | 1 | a0008 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.1382A>G | p.Asp461Gly | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 9/24 | 1681/5537 | 1382/4155 | 461/1384 | chr17 | 42688537 | |||
| chr17:42688983 | G | C | 2 | a0002 a0004 |
21 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
missense_variant | MODERATE | c.1564G>C | p.Val522Leu | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 10/24 | 1863/5537 | 1564/4155 | 522/1384 | chr17 | 42688983 | |||
| chr17:42690756 | G | C | 1 | a0003 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.1873G>C | p.Val625Leu | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 13/24 | 2172/5537 | 1873/4155 | 625/1384 | chr17 | 42690756 | |||
| chr17:42691917 | C | T | 1 | a0004 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.2456C>T | p.Ser819Leu | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 16/24 | 2755/5537 | 2456/4155 | 819/1384 | chr17 | 42691917 | |||
| chr17:42693341 | G | A | 1 | a0006 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.2797G>A | p.Ala933Thr | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/24 | 3096/5537 | 2797/4155 | 933/1384 | chr17 | 42693341 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:42683904 | A | C | 17 | a0001c0001 a0001c0004 a0001c0005 others(14): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
synonymous_variant | LOW | c.151A>C | p.Arg51Arg | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 2/24 | 450/5537 | 151/4155 | 51/1384 | chr17 | 42683904 | |||
| chr17:42684193 | C | T | 1 | a0001c0011 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.327C>T | p.Asp109Asp | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 3/24 | 626/5537 | 327/4155 | 109/1384 | chr17 | 42684193 | |||
| chr17:42686006 | C | T | 1 | a0001c0026 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.765C>T | p.Gly255Gly | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/24 | 1064/5537 | 765/4155 | 255/1384 | chr17 | 42686006 | |||
| chr17:42687028 | T | C | 1 | a0002c0006 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.1026T>C | p.His342His | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 7/24 | 1325/5537 | 1026/4155 | 342/1384 | chr17 | 42687028 | |||
| chr17:42688913 | C | T | 1 | a0001c0024 | 1 | HG00423.hp2 | synonymous_variant | LOW | c.1494C>T | p.Ser498Ser | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 10/24 | 1793/5537 | 1494/4155 | 498/1384 | chr17 | 42688913 | |||
| chr17:42690122 | C | T | 1 | a0001c0023 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.1770C>T | p.Leu590Leu | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 12/24 | 2069/5537 | 1770/4155 | 590/1384 | chr17 | 42690122 | |||
| chr17:42690744 | C | A | 1 | a0001c0004 | 8 | HG01109.hp1 HG01361.hp1 HG01943.hp2 others(5): Show |
synonymous_variant | LOW | c.1861C>A | p.Arg621Arg | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 13/24 | 2160/5537 | 1861/4155 | 621/1384 | chr17 | 42690744 | |||
| chr17:42690830 | C | T | 1 | a0001c0022 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.1947C>T | p.Ile649Ile | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 13/24 | 2246/5537 | 1947/4155 | 649/1384 | chr17 | 42690830 | |||
| chr17:42691507 | C | A | 1 | a0001c0016 | 1 | HG00140.hp1 | synonymous_variant | LOW | c.2340C>A | p.Gly780Gly | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 15/24 | 2639/5537 | 2340/4155 | 780/1384 | chr17 | 42691507 | |||
| chr17:42693523 | A | G | 3 | a0001c0010 a0001c0021 a0002c0007 |
3 | HG03130.hp1 HG03209.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.2979A>G | p.Pro993Pro | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/24 | 3278/5537 | 2979/4155 | 993/1384 | chr17 | 42693523 | |||
| chr17:42695564 | C | T | 1 | a0001c0020 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.3036C>T | p.Asn1012Asn | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 19/24 | 3335/5537 | 3036/4155 | 1012/1384 | chr17 | 42695564 | |||
| chr17:42697328 | T | C | 1 | a0001c0018 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.3529T>C | p.Leu1177Leu | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 21/24 | 3828/5537 | 3529/4155 | 1177/1384 | chr17 | 42697328 | |||
| chr17:42697555 | G | A | 4 | a0001c0005 a0001c0009 a0001c0011 others(1): Show |
10 | HG02132.hp1 HG02145.hp1 HG03704.hp1 others(7): Show |
splice_region_variant&synonymous_variant | LOW | c.3570G>A | p.Glu1190Glu | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 22/24 | 3869/5537 | 3570/4155 | 1190/1384 | chr17 | 42697555 | |||
| chr17:42697922 | T | C | 1 | a0001c0019 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.3834T>C | p.Asp1278Asp | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/24 | 4133/5537 | 3834/4155 | 1278/1384 | chr17 | 42697922 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:42682609 | G | A | 1 | a0001c0001t0005 | 1 | NA19066.hp1 | 5_prime_UTR_variant | MODIFIER | c.-221G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 1/24 | 221 | chr17 | 42682609 | ||||||
| chr17:42682613 | G | C | 17 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(14): Show |
170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
5_prime_UTR_variant | MODIFIER | c.-217G>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 1/24 | 217 | chr17 | 42682613 | ||||||
| chr17:42682641 | A | G | 1 | a0001c0001t0004 | 4 | HG02809.hp1 HG02818.hp2 HG06807.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-189A>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 1/24 | 189 | chr17 | 42682641 | ||||||
| chr17:42699036 | C | G | 1 | a0002c0014t0010 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*126C>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 24/24 | 126 | chr17 | 42699036 | ||||||
| chr17:42699042 | C | A | 1 | a0001c0001t0006 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*132C>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 24/24 | 132 | chr17 | 42699042 | ||||||
| chr17:42699706 | A | G | 1 | a0001c0001t0009 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*796A>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 24/24 | 796 | chr17 | 42699706 | ||||||
| chr17:42699720 | T | C | 1 | a0001c0001t0007 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*810T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 24/24 | 810 | chr17 | 42699720 | ||||||
| chr17:42699767 | C | T | 3 | a0001c0001t0003 a0001c0002t0003 a0001c0026t0008 |
5 | HG01099.hp2 HG01192.hp2 HG01257.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*857C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 24/24 | 857 | chr17 | 42699767 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:42683086 | G | C | 1 | a0001c0002t0001g0046 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.67+190G>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 1/23 | chr17 | 42683086 | |||||||
| chr17:42683212 | A | T | 15 | a0001c0002t0001g0190 a0001c0002t0001g0191 a0001c0011t0001g0192 others(12): Show |
21 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.67+316A>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 1/23 | chr17 | 42683212 | |||||||
| chr17:42683251 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.67+355T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 1/23 | chr17 | 42683251 | |||||||
| chr17:42683275 | T | G | 1 | a0008c0025t0002g0048 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.67+379T>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 1/23 | chr17 | 42683275 | |||||||
| chr17:42683298 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.67+402G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 1/23 | chr17 | 42683298 | |||||||
| chr17:42683303 | G | T | 1 | a0008c0025t0002g0048 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.67+407G>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 1/23 | chr17 | 42683303 | |||||||
| chr17:42683329 | G | A | 1 | a0001c0001t0007g0050 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.67+433G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 1/23 | chr17 | 42683329 | |||||||
| chr17:42683382 | G | A | 1 | a0001c0002t0001g0051 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.68-439G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 1/23 | chr17 | 42683382 | |||||||
| chr17:42683433 | A | C | 112 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(109): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.68-388A>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 1/23 | chr17 | 42683433 | |||||||
| chr17:42683478 | T | C | 1 | a0001c0002t0001g0052 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.68-343T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 1/23 | chr17 | 42683478 | |||||||
| chr17:42683596 | A | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0034 others(1): Show |
13 | HG00735.hp2 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.68-225A>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 1/23 | chr17 | 42683596 | |||||||
| chr17:42683631 | T | C | 121 | a0001c0001t0001g0055 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.68-190T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 1/23 | chr17 | 42683631 | |||||||
| chr17:42683801 | A | AT | 121 | a0001c0001t0001g0055 a0001c0001t0002g0003 a0001c0001t0002g0004 others(118): Show |
181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.68-20_68-19insT | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 1/23 | chr17 | 42683801 | |||||||
| chr17:42683973 | T | A | 1 | a0008c0025t0002g0048 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.169+51T>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 2/23 | chr17 | 42683973 | |||||||
| chr17:42684244 | A | C | 10 | a0001c0001t0002g0044 a0001c0001t0002g0178 a0001c0001t0002g0179 others(7): Show |
11 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.363+15A>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 3/23 | chr17 | 42684244 | |||||||
| chr17:42684248 | C | CG | 3 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0002t0001g0061 |
3 | NA18956.hp2 NA18988.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.363+21dupG | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr17 | 42684248 | ||||||
| chr17:42684428 | C | A | 1 | a0007c0012t0001g0062 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.363+199C>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 3/23 | chr17 | 42684428 | |||||||
| chr17:42684434 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0034 others(1): Show |
13 | HG00735.hp2 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.363+205A>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 3/23 | chr17 | 42684434 | |||||||
| chr17:42684464 | G | A | 1 | a0001c0005t0002g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.363+235G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 3/23 | chr17 | 42684464 | |||||||
| chr17:42684536 | C | A | 1 | a0008c0025t0002g0048 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.363+307C>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 3/23 | chr17 | 42684536 | |||||||
| chr17:42684548 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.363+319G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 3/23 | chr17 | 42684548 | |||||||
| chr17:42684787 | G | T | 3 | a0001c0002t0001g0022 a0001c0002t0001g0061 a0001c0002t0001g0108 |
5 | HG00558.hp2 NA18941.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-204G>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 3/23 | chr17 | 42684787 | |||||||
| chr17:42684864 | G | A | 10 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(7): Show |
12 | HG01175.hp1 HG02132.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.364-127G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 3/23 | chr17 | 42684864 | |||||||
| chr17:42684902 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.364-89G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 3/23 | chr17 | 42684902 | |||||||
| chr17:42684957 | A | G | 154 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0034 others(151): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.364-34A>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 3/23 | chr17 | 42684957 | |||||||
| chr17:42685501 | A | G | 3 | a0001c0001t0004g0029 a0001c0001t0004g0059 a0001c0001t0004g0060 |
4 | HG02809.hp1 HG02818.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.715+81A>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 5/23 | chr17 | 42685501 | |||||||
| chr17:42685742 | ATGAAATA others(17): Show |
A | 1 | a0007c0012t0001g0062 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.716-214_716-191del others(24): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 5/23 | chr17 | 42685742 | |||||||
| chr17:42685758 | T | C | 1 | a0001c0002t0001g0001 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.716-199T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 5/23 | chr17 | 42685758 | |||||||
| chr17:42685825 | T | C | 1 | a0001c0018t0002g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.716-132T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 5/23 | chr17 | 42685825 | |||||||
| chr17:42685829 | T | C | 1 | a0001c0002t0001g0063 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.716-128T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 5/23 | chr17 | 42685829 | |||||||
| chr17:42685847 | C | T | 1 | a0001c0023t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.716-110C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 5/23 | chr17 | 42685847 | |||||||
| chr17:42686369 | C | T | 1 | a0001c0001t0003g0057 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.900+228C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | chr17 | 42686369 | |||||||
| chr17:42686377 | T | TA | 5 | a0001c0001t0001g0055 a0001c0001t0003g0057 a0001c0004t0001g0056 others(2): Show |
5 | HG00323.hp2 HG01361.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+243dupA | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686377 | ||||||
| chr17:42686383 | A | T | 1 | a0002c0003t0001g0197 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.900+242A>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | chr17 | 42686383 | |||||||
| chr17:42686384 | A | T | 2 | a0002c0003t0001g0196 a0002c0003t0001g0197 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.900+243A>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | chr17 | 42686384 | |||||||
| chr17:42686385 | T | A | 125 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0034 others(122): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.900+244T>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | chr17 | 42686385 | |||||||
| chr17:42686386 | T | A | 102 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(99): Show |
160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.900+245T>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | chr17 | 42686386 | |||||||
| chr17:42686387 | T | A | 1 | a0001c0001t0002g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.900+246T>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | chr17 | 42686387 | |||||||
| chr17:42686469 | G | GT | 21 | a0001c0002t0001g0002 a0001c0002t0001g0061 a0001c0002t0001g0063 others(18): Show |
42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.900+352dupT | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686469 | ||||||
| chr17:42686469 | G | GTT | 7 | a0001c0001t0004g0060 a0001c0002t0001g0032 a0001c0002t0001g0091 others(4): Show |
8 | HG02523.hp2 HG02809.hp1 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.900+351_900+352dup others(2): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686469 | ||||||
| chr17:42686469 | G | GTTTTT | 13 | a0001c0001t0002g0047 a0001c0001t0002g0114 a0001c0001t0002g0115 others(10): Show |
15 | HG00597.hp1 HG01175.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.900+348_900+352dup others(5): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686469 | ||||||
| chr17:42686469 | G | GTTTTTT | 12 | a0001c0001t0002g0024 a0001c0001t0002g0036 a0001c0001t0002g0037 others(9): Show |
16 | HG02132.hp1 HG02486.hp2 HG03490.hp1 others(13): Show |
intron_variant | MODIFIER | c.900+347_900+352dup others(6): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686469 | ||||||
| chr17:42686469 | G | GTTTTTTT | 16 | a0001c0001t0002g0006 a0001c0001t0002g0025 a0001c0001t0002g0038 others(13): Show |
24 | HG01167.hp1 HG01192.hp2 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.900+346_900+352dup others(7): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686469 | ||||||
| chr17:42686469 | G | GTTTTTTT others(1): Show |
18 | a0001c0001t0001g0055 a0001c0001t0002g0003 a0001c0001t0002g0026 others(15): Show |
32 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.900+345_900+352dup others(8): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686469 | ||||||
| chr17:42686469 | G | GTTTTTTT others(2): Show |
15 | a0001c0001t0002g0018 a0001c0001t0002g0042 a0001c0001t0002g0043 others(12): Show |
18 | HG00423.hp2 HG00642.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.900+344_900+352dup others(9): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686469 | ||||||
| chr17:42686469 | G | GTTTTTTT others(3): Show |
9 | a0001c0001t0002g0027 a0001c0001t0002g0113 a0001c0001t0002g0172 others(6): Show |
9 | HG00099.hp1 HG00140.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.900+343_900+352dup others(10): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686469 | ||||||
| chr17:42686469 | G | GTTTTTTT others(4): Show |
2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.900+342_900+352dup others(11): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686469 | ||||||
| chr17:42686469 | G | GTTTTTTT others(5): Show |
2 | a0001c0001t0002g0175 a0001c0001t0002g0183 |
2 | HG02723.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.900+341_900+352dup others(12): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686469 | ||||||
| chr17:42686469 | G | GTTTTTTT others(6): Show |
1 | a0001c0001t0002g0184 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.900+340_900+352dup others(13): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686469 | ||||||
| chr17:42686469 | G | GTTTTTTT others(9): Show |
1 | a0001c0021t0002g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.900+337_900+352dup others(16): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686469 | ||||||
| chr17:42686469 | G | GTTTTTTT others(10): Show |
1 | a0001c0001t0002g0186 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.900+336_900+352dup others(17): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686469 | ||||||
| chr17:42686475 | T | TTTTGTTT others(1): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0109 |
11 | HG00735.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.900+337_900+338ins others(8): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686475 | ||||||
| chr17:42686475 | T | TTTTTTG | 5 | a0001c0001t0002g0049 a0001c0001t0002g0133 a0001c0001t0002g0134 others(2): Show |
9 | HG00741.hp2 HG01109.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.900+339_900+340ins others(6): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686475 | ||||||
| chr17:42686476 | T | TTTTTG | 13 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0009 others(10): Show |
36 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.900+339_900+340ins others(5): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686476 | ||||||
| chr17:42686478 | T | G | 1 | a0001c0001t0002g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.900+337T>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | chr17 | 42686478 | |||||||
| chr17:42686479 | T | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0109 others(1): Show |
12 | HG00735.hp2 HG01243.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.900+338T>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | chr17 | 42686479 | |||||||
| chr17:42686479 | T | TTGTTG | 11 | a0001c0002t0001g0008 a0001c0002t0001g0097 a0001c0002t0001g0098 others(8): Show |
15 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.900+339_900+340ins others(5): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686479 | ||||||
| chr17:42686479 | T | TTTGTTG | 18 | a0001c0001t0004g0059 a0001c0002t0001g0033 a0001c0002t0001g0104 others(15): Show |
25 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.900+340_900+341ins others(6): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 42686479 | ||||||
| chr17:42686480 | T | G | 1 | a0001c0001t0003g0057 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.900+339T>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | chr17 | 42686480 | |||||||
| chr17:42686481 | T | G | 1 | a0001c0020t0001g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.900+340T>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | chr17 | 42686481 | |||||||
| chr17:42686483 | T | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0109 others(30): Show |
52 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.900+342T>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | chr17 | 42686483 | |||||||
| chr17:42686487 | T | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0109 others(30): Show |
52 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.900+346T>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | chr17 | 42686487 | |||||||
| chr17:42686606 | T | A | 1 | a0001c0001t0002g0156 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.901-297T>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | chr17 | 42686606 | |||||||
| chr17:42686649 | C | G | 5 | a0001c0001t0004g0059 a0002c0003t0001g0011 a0002c0003t0001g0187 others(2): Show |
9 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.901-254C>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | chr17 | 42686649 | |||||||
| chr17:42686735 | C | G | 29 | a0001c0001t0002g0044 a0001c0001t0002g0124 a0001c0001t0002g0178 others(26): Show |
33 | HG01109.hp2 HG01361.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.901-168C>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | chr17 | 42686735 | |||||||
| chr17:42686811 | T | C | 31 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0109 others(28): Show |
43 | HG00735.hp2 HG01109.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.901-92T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | chr17 | 42686811 | |||||||
| chr17:42687094 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1044+48G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 7/23 | chr17 | 42687094 | |||||||
| chr17:42687158 | C | G | 1 | a0001c0002t0001g0033 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1044+112C>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 7/23 | chr17 | 42687158 | |||||||
| chr17:42687158 | C | T | 2 | a0001c0001t0002g0025 a0001c0001t0002g0041 |
5 | HG02280.hp1 HG03098.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044+112C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 7/23 | chr17 | 42687158 | |||||||
| chr17:42687199 | C | T | 1 | a0001c0010t0001g0103 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1044+153C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 7/23 | chr17 | 42687199 | |||||||
| chr17:42687405 | G | C | 1 | a0001c0001t0002g0175 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1045-315G>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 7/23 | chr17 | 42687405 | |||||||
| chr17:42687452 | G | A | 1 | a0001c0010t0001g0103 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1045-268G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 7/23 | chr17 | 42687452 | |||||||
| chr17:42687526 | G | A | 1 | a0001c0001t0002g0136 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1045-194G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 7/23 | chr17 | 42687526 | |||||||
| chr17:42688052 | G | A | 4 | a0001c0004t0001g0056 a0001c0004t0002g0010 a0001c0004t0002g0054 others(1): Show |
8 | HG01109.hp1 HG01361.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1306+71G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 8/23 | chr17 | 42688052 | |||||||
| chr17:42688115 | G | A | 2 | a0001c0002t0001g0190 a0001c0002t0001g0191 |
2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1306+134G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 8/23 | chr17 | 42688115 | |||||||
| chr17:42688116 | G | C | 1 | a0001c0002t0001g0108 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1306+135G>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 8/23 | chr17 | 42688116 | |||||||
| chr17:42688243 | T | C | 2 | a0001c0002t0003g0031 a0001c0002t0003g0078 |
3 | HG01099.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1307-219T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 8/23 | chr17 | 42688243 | |||||||
| chr17:42688322 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1307-140C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 8/23 | chr17 | 42688322 | |||||||
| chr17:42688332 | G | A | 6 | a0001c0001t0002g0181 a0001c0001t0002g0183 a0001c0001t0002g0184 others(3): Show |
6 | HG02723.hp1 HG02970.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1307-130G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 8/23 | chr17 | 42688332 | |||||||
| chr17:42688408 | T | C | 1 | a0001c0001t0002g0049 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1307-54T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 8/23 | chr17 | 42688408 | |||||||
| chr17:42688740 | G | T | 2 | a0001c0001t0002g0040 a0003c0015t0002g0040 |
2 | HG02027.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.1456+129G>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 9/23 | chr17 | 42688740 | |||||||
| chr17:42688801 | C | T | 2 | a0001c0001t0002g0037 a0001c0001t0006g0163 |
3 | HG03654.hp1 HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1457-75C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 9/23 | chr17 | 42688801 | |||||||
| chr17:42689052 | C | T | 2 | a0001c0001t0002g0038 a0001c0001t0002g0155 |
3 | HG01167.hp1 HG01952.hp1 HG04184.hp2 |
splice_region_variant&intron_variant | LOW | c.1628+5C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 10/23 | chr17 | 42689052 | |||||||
| chr17:42689192 | T | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0034 others(13): Show |
32 | HG00735.hp2 HG01109.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.1628+145T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 10/23 | chr17 | 42689192 | |||||||
| chr17:42689349 | C | T | 3 | a0001c0001t0002g0044 a0001c0001t0002g0178 a0001c0001t0002g0179 |
4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1629-172C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 10/23 | chr17 | 42689349 | |||||||
| chr17:42689379 | C | T | 107 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(104): Show |
163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1629-142C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 10/23 | chr17 | 42689379 | |||||||
| chr17:42689468 | C | A | 1 | a0001c0023t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1629-53C>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 10/23 | chr17 | 42689468 | |||||||
| chr17:42689668 | G | T | 1 | a0001c0023t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1735+41G>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 11/23 | chr17 | 42689668 | |||||||
| chr17:42689800 | G | A | 10 | a0001c0001t0002g0044 a0001c0001t0002g0178 a0001c0001t0002g0179 others(7): Show |
15 | HG01109.hp1 HG01361.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.1735+173G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 11/23 | chr17 | 42689800 | |||||||
| chr17:42689888 | A | G | 137 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0034 others(134): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1736-200A>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 11/23 | chr17 | 42689888 | |||||||
| chr17:42690066 | G | A | 123 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0034 others(120): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.1736-22G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 11/23 | chr17 | 42690066 | |||||||
| chr17:42690423 | T | C | 9 | a0001c0001t0002g0044 a0001c0001t0002g0178 a0001c0001t0002g0179 others(6): Show |
14 | HG01109.hp1 HG01361.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1855+216T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 12/23 | chr17 | 42690423 | |||||||
| chr17:42690523 | C | CA | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(79): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1856-197dupA | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr17 | 42690523 | ||||||
| chr17:42690523 | C | CAA | 28 | a0001c0001t0002g0037 a0001c0001t0002g0040 a0001c0001t0002g0047 others(25): Show |
29 | HG00423.hp2 HG00597.hp1 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.1856-198_1856-197d others(4): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr17 | 42690523 | ||||||
| chr17:42690663 | G | A | 5 | a0001c0001t0002g0181 a0001c0001t0002g0184 a0001c0001t0002g0186 others(2): Show |
5 | HG02970.hp1 HG03130.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1856-76G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 12/23 | chr17 | 42690663 | |||||||
| chr17:42690678 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1856-61C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 12/23 | chr17 | 42690678 | |||||||
| chr17:42691033 | G | C | 2 | a0001c0001t0002g0137 a0001c0001t0002g0143 |
2 | NA18993.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2059+91G>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 13/23 | chr17 | 42691033 | |||||||
| chr17:42691374 | G | T | 4 | a0001c0004t0001g0056 a0001c0004t0002g0010 a0001c0004t0002g0054 others(1): Show |
8 | HG01109.hp1 HG01361.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.2217-10G>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 14/23 | chr17 | 42691374 | |||||||
| chr17:42691692 | C | T | 1 | a0001c0023t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2345-114C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 15/23 | chr17 | 42691692 | |||||||
| chr17:42692067 | G | A | 1 | a0001c0002t0001g0069 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2530+76G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 16/23 | chr17 | 42692067 | |||||||
| chr17:42692245 | C | T | 3 | a0001c0001t0004g0029 a0001c0001t0004g0059 a0001c0001t0004g0060 |
4 | HG02809.hp1 HG02818.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2530+254C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 16/23 | chr17 | 42692245 | |||||||
| chr17:42692328 | G | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0034 others(5): Show |
20 | HG00735.hp2 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.2531-171G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 16/23 | chr17 | 42692328 | |||||||
| chr17:42692849 | T | C | 1 | a0004c0008t0001g0193 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2752+129T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 17/23 | chr17 | 42692849 | |||||||
| chr17:42692958 | C | CT | 14 | a0001c0002t0001g0104 a0002c0003t0001g0011 a0002c0003t0001g0028 others(11): Show |
20 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.2752+254dupT | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr17 | 42692958 | ||||||
| chr17:42692958 | CT | C | 6 | a0001c0001t0002g0150 a0001c0001t0002g0152 a0001c0001t0002g0179 others(3): Show |
6 | HG02735.hp2 HG02965.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.2752+254delT | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr17 | 42692958 | ||||||
| chr17:42692980 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2752+260G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 17/23 | chr17 | 42692980 | |||||||
| chr17:42693051 | G | GGTTCAAG others(12): Show |
1 | a0001c0023t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2753-245_2753-227d others(21): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr17 | 42693051 | ||||||
| chr17:42693105 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2753-192C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 17/23 | chr17 | 42693105 | |||||||
| chr17:42693160 | C | G | 1 | a0001c0002t0001g0046 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2753-137C>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 17/23 | chr17 | 42693160 | |||||||
| chr17:42693195 | G | A | 1 | a0001c0023t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2753-102G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 17/23 | chr17 | 42693195 | |||||||
| chr17:42693254 | T | C | 1 | a0001c0002t0001g0098 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2753-43T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 17/23 | chr17 | 42693254 | |||||||
| chr17:42693633 | G | A | 1 | a0001c0023t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2992+97G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/23 | chr17 | 42693633 | |||||||
| chr17:42694077 | T | C | 3 | a0001c0001t0002g0037 a0001c0001t0006g0163 a0001c0002t0001g0076 |
4 | HG03017.hp2 HG03654.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.2992+541T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/23 | chr17 | 42694077 | |||||||
| chr17:42694113 | A | C | 126 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(123): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.2992+577A>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/23 | chr17 | 42694113 | |||||||
| chr17:42694148 | C | T | 1 | a0001c0002t0003g0078 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2992+612C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/23 | chr17 | 42694148 | |||||||
| chr17:42694149 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2992+613G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/23 | chr17 | 42694149 | |||||||
| chr17:42694176 | C | CT | 5 | a0001c0001t0002g0124 a0001c0001t0002g0170 a0001c0002t0001g0008 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2992+652dupT | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr17 | 42694176 | ||||||
| chr17:42694277 | T | C | 4 | a0001c0001t0003g0057 a0001c0001t0004g0029 a0001c0001t0004g0059 others(1): Show |
5 | HG02809.hp1 HG02818.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2992+741T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/23 | chr17 | 42694277 | |||||||
| chr17:42694416 | C | T | 1 | a0001c0001t0001g0015 | 4 | HG02559.hp1 HG02976.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2992+880C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/23 | chr17 | 42694416 | |||||||
| chr17:42694450 | A | G | 1 | a0001c0023t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2992+914A>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/23 | chr17 | 42694450 | |||||||
| chr17:42694464 | G | A | 3 | a0001c0001t0002g0044 a0001c0001t0002g0178 a0001c0001t0002g0179 |
4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2992+928G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/23 | chr17 | 42694464 | |||||||
| chr17:42694585 | G | A | 1 | a0001c0023t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2993-936G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/23 | chr17 | 42694585 | |||||||
| chr17:42694596 | C | T | 1 | a0001c0001t0002g0130 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2993-925C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/23 | chr17 | 42694596 | |||||||
| chr17:42694631 | C | CA | 106 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(103): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.2993-877dupA | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr17 | 42694631 | ||||||
| chr17:42694691 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2993-830G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/23 | chr17 | 42694691 | |||||||
| chr17:42694844 | T | C | 1 | a0001c0001t0003g0057 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2993-677T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/23 | chr17 | 42694844 | |||||||
| chr17:42694896 | C | T | 103 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(100): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.2993-625C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/23 | chr17 | 42694896 | |||||||
| chr17:42695309 | T | C | 1 | a0001c0001t0002g0138 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2993-212T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 18/23 | chr17 | 42695309 | |||||||
| chr17:42696197 | G | A | 1 | a0001c0002t0001g0099 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3474+45G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 20/23 | chr17 | 42696197 | |||||||
| chr17:42696324 | AT | A | 182 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0034 others(179): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.3474+188delT | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 42696324 | ||||||
| chr17:42696324 | ATT | A | 9 | a0001c0001t0002g0042 a0001c0001t0002g0127 a0001c0001t0002g0144 others(6): Show |
9 | HG01517.hp1 NA18943.hp2 NA18977.hp1 others(6): Show |
intron_variant | MODIFIER | c.3474+187_3474+188d others(4): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 42696324 | ||||||
| chr17:42696357 | C | T | 1 | a0002c0003t0001g0107 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3474+205C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 20/23 | chr17 | 42696357 | |||||||
| chr17:42696412 | C | T | 3 | a0001c0001t0004g0029 a0001c0001t0004g0059 a0001c0001t0004g0060 |
4 | HG02809.hp1 HG02818.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3474+260C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 20/23 | chr17 | 42696412 | |||||||
| chr17:42696416 | C | T | 2 | a0002c0003t0001g0106 a0002c0003t0001g0107 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3474+264C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 20/23 | chr17 | 42696416 | |||||||
| chr17:42696438 | CT | C | 6 | a0001c0001t0003g0057 a0001c0001t0004g0029 a0001c0001t0004g0059 others(3): Show |
7 | HG02055.hp1 HG02809.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3474+287delT | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 20/23 | chr17 | 42696438 | |||||||
| chr17:42696473 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3474+321G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 20/23 | chr17 | 42696473 | |||||||
| chr17:42696543 | G | A | 2 | a0002c0003t0001g0106 a0002c0003t0001g0107 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3474+391G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 20/23 | chr17 | 42696543 | |||||||
| chr17:42696579 | T | C | 1 | a0001c0002t0001g0080 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3474+427T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 20/23 | chr17 | 42696579 | |||||||
| chr17:42696743 | T | G | 1 | a0001c0001t0002g0127 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3475-531T>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 20/23 | chr17 | 42696743 | |||||||
| chr17:42696750 | G | A | 4 | a0001c0001t0003g0057 a0001c0001t0004g0029 a0001c0001t0004g0059 others(1): Show |
5 | HG02809.hp1 HG02818.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3475-524G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 20/23 | chr17 | 42696750 | |||||||
| chr17:42696818 | G | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0002g0025 others(3): Show |
15 | HG00735.hp2 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.3475-456G>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 20/23 | chr17 | 42696818 | |||||||
| chr17:42697155 | T | C | 2 | a0001c0001t0002g0044 a0001c0001t0002g0179 |
3 | HG02622.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3475-119T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 20/23 | chr17 | 42697155 | |||||||
| chr17:42697387 | G | A | 1 | a0001c0020t0001g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3568+20G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 21/23 | chr17 | 42697387 | |||||||
| chr17:42697824 | A | G | 142 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0034 others(139): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.3814+25A>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 22/23 | chr17 | 42697824 | |||||||
| chr17:42697841 | C | T | 1 | a0001c0001t0002g0157 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3814+42C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 22/23 | chr17 | 42697841 | |||||||
| chr17:42697862 | A | G | 1 | a0002c0003t0001g0107 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3815-41A>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 22/23 | chr17 | 42697862 | |||||||
| chr17:42697990 | C | T | 3 | a0001c0002t0001g0014 a0001c0002t0001g0086 a0001c0002t0001g0094 |
6 | HG00544.hp1 HG00673.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.3862+40C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | chr17 | 42697990 | |||||||
| chr17:42698114 | G | C | 1 | a0001c0001t0002g0049 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3862+164G>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | chr17 | 42698114 | |||||||
| chr17:42698376 | C | T | 1 | a0001c0023t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3863-242C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | chr17 | 42698376 | |||||||
| chr17:42698394 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3863-224T>C | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | chr17 | 42698394 | |||||||
| chr17:42698398 | C | T | 1 | a0001c0002t0001g0033 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.3863-220C>T | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | chr17 | 42698398 | |||||||
| chr17:42698399 | G | A | 4 | a0001c0001t0001g0109 a0001c0002t0001g0071 a0001c0002t0001g0190 others(1): Show |
4 | HG01123.hp2 HG02630.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3863-219G>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | chr17 | 42698399 | |||||||
| chr17:42698445 | A | ATG | 30 | a0001c0001t0002g0005 a0001c0001t0002g0037 a0001c0001t0002g0047 others(27): Show |
40 | HG00544.hp2 HG00597.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.3863-138_3863-137d others(4): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 42698445 | ||||||
| chr17:42698445 | A | ATGTG | 7 | a0001c0001t0002g0140 a0001c0001t0002g0184 a0001c0001t0002g0186 others(4): Show |
7 | HG02155.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3863-140_3863-137d others(6): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 42698445 | ||||||
| chr17:42698445 | ATG | A | 14 | a0001c0001t0002g0036 a0001c0001t0002g0049 a0001c0001t0002g0128 others(11): Show |
17 | HG01071.hp2 HG02132.hp1 HG02273.hp1 others(14): Show |
intron_variant | MODIFIER | c.3863-138_3863-137d others(4): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 42698445 | ||||||
| chr17:42698445 | ATGTG | A | 6 | a0001c0001t0002g0044 a0001c0001t0002g0178 a0001c0001t0002g0179 others(3): Show |
9 | HG01106.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.3863-140_3863-137d others(6): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 42698445 | ||||||
| chr17:42698445 | ATGTGTG | A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0034 others(11): Show |
27 | HG00735.hp2 HG01891.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.3863-142_3863-137d others(8): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 42698445 | ||||||
| chr17:42698534 | C | CGT | 30 | a0001c0001t0001g0015 a0001c0001t0002g0004 a0001c0001t0002g0017 others(27): Show |
51 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.3863-51_3863-50dup others(2): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 42698534 | ||||||
| chr17:42698534 | C | CGTGT | 12 | a0001c0001t0002g0124 a0001c0001t0002g0129 a0001c0001t0002g0174 others(9): Show |
16 | HG01884.hp2 HG02080.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.3863-53_3863-50dup others(4): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 42698534 | ||||||
| chr17:42698534 | CGT | C | 7 | a0001c0001t0003g0057 a0001c0001t0004g0029 a0001c0001t0004g0059 others(4): Show |
8 | HG02809.hp1 HG02818.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.3863-51_3863-50del others(2): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 42698534 | ||||||
| chr17:42698534 | CGTGT | C | 14 | a0001c0001t0001g0109 a0001c0001t0002g0039 a0001c0001t0002g0169 others(11): Show |
18 | HG00673.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.3863-53_3863-50del others(4): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 42698534 | ||||||
| chr17:42698534 | CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0002g0161 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3863-59_3863-50del others(10): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 42698534 | ||||||
| chr17:42698569 | A | G | 1 | a0001c0002t0001g0073 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3863-49A>G | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | chr17 | 42698569 | |||||||
| chr17:42698596 | T | A | 2 | a0001c0002t0001g0072 a0001c0002t0001g0092 |
2 | NA19005.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.3863-22T>A | CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | chr17 | 42698596 |