Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10225 |
| ensemblid | ENSG00000153283.13 |
| hgncid | 16892 |
| symbol | CD96 |
| name | CD96 molecule |
| refseq_nuc | NM_005816.5 |
| refseq_prot | NP_005807.1 |
| ensembl_nuc | ENST00000352690.9 |
| ensembl_prot | ENSP00000342040.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 111542197 |
| end | 111652372 |
| strand | + |
| ver | v1.2 |
| region | chr3:111542197-111652372 |
| region5000 | chr3:111537197-111657372 |
| regionname0 | CD96_chr3_111542197_111652372 |
| regionname5000 | CD96_chr3_111537197_111657372 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 569 | 271 | 71 | 51 | 101 | 14 | 32 | 80 | CD96_chr3_111537197_111657372 | CD96 | MEKKW others(564): Show |
chr3 | 111537197 | 111657372 |
| a0002 | 0/0 | 569 | 21 | 1 | 1 | 17 | 0 | 2 | 12 | CD96_chr3_111537197_111657372 | CD96 | MEKKW others(564): Show |
chr3 | 111537197 | 111657372 |
| a0003 | 0/0 | 569 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | MEKKW others(564): Show |
chr3 | 111537197 | 111657372 |
| a0004 | 0/0 | 569 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | MEKKW others(564): Show |
chr3 | 111537197 | 111657372 |
| a0005 | 0/0 | 569 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | MEKKW others(564): Show |
chr3 | 111537197 | 111657372 |
| a0006 | 0/0 | 569 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | MEKKW others(564): Show |
chr3 | 111537197 | 111657372 |
| a0007 | 0/0 | 569 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | MEKKW others(564): Show |
chr3 | 111537197 | 111657372 |
| a0008 | 0/0 | 569 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | MEKKW others(564): Show |
chr3 | 111537197 | 111657372 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1707 | 255 | 63 | 48 | 100 | 12 | 32 | CD96_chr3_111537197_111657372 | CD96 | ATGGA others(1702): Show |
chr3 | 111537197 | 111657372 | ||
| a0001c0003 | 0/0 | 1707 | 4 | 3 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | ATGGA others(1702): Show |
chr3 | 111537197 | 111657372 | ||
| a0001c0004 | 0/1 | 1707 | 4 | 0 | 1 | 0 | 2 | 0 | CD96_chr3_111537197_111657372 | CD96 | ATGGA others(1702): Show |
chr3 | 111537197 | 111657372 | ||
| a0001c0005 | 1/0 | 1707 | 4 | 3 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | ATGGA others(1702): Show |
chr3 | 111537197 | 111657372 | ||
| a0001c0011 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | ATGGA others(1702): Show |
chr3 | 111537197 | 111657372 | ||
| a0001c0012 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | ATGGA others(1702): Show |
chr3 | 111537197 | 111657372 | ||
| a0001c0014 | 0/0 | 1707 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | ATGGA others(1702): Show |
chr3 | 111537197 | 111657372 | ||
| a0001c0015 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | ATGGA others(1702): Show |
chr3 | 111537197 | 111657372 | ||
| a0002c0002 | 0/0 | 1707 | 21 | 1 | 1 | 17 | 0 | 2 | CD96_chr3_111537197_111657372 | CD96 | ATGGA others(1702): Show |
chr3 | 111537197 | 111657372 | ||
| a0003c0006 | 0/0 | 1707 | 3 | 3 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | ATGGA others(1702): Show |
chr3 | 111537197 | 111657372 | ||
| a0004c0010 | 0/0 | 1707 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | ATGGA others(1702): Show |
chr3 | 111537197 | 111657372 | ||
| a0005c0007 | 0/0 | 1707 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | ATGGA others(1702): Show |
chr3 | 111537197 | 111657372 | ||
| a0006c0008 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | ATGGA others(1702): Show |
chr3 | 111537197 | 111657372 | ||
| a0007c0009 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | ATGGA others(1702): Show |
chr3 | 111537197 | 111657372 | ||
| a0008c0013 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | ATGGA others(1702): Show |
chr3 | 111537197 | 111657372 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4328 | 140 | 16 | 29 | 67 | 8 | 20 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0002 | 0/0 | 4327 | 37 | 9 | 3 | 19 | 0 | 6 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4322): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0003 | 0/0 | 4328 | 17 | 14 | 0 | 2 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0004 | 0/0 | 4327 | 14 | 1 | 7 | 2 | 1 | 3 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4322): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0005 | 0/0 | 4327 | 11 | 9 | 2 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4322): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0006 | 0/0 | 4328 | 5 | 2 | 1 | 1 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0007 | 0/0 | 4328 | 6 | 0 | 4 | 0 | 2 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0008 | 0/0 | 4328 | 2 | 1 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0009 | 0/0 | 4328 | 4 | 3 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0010 | 0/0 | 4328 | 4 | 0 | 0 | 4 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0011 | 0/0 | 4328 | 2 | 2 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0012 | 0/0 | 4328 | 2 | 0 | 0 | 2 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0013 | 0/0 | 4328 | 2 | 2 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0014 | 0/0 | 4328 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0015 | 0/0 | 4328 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0016 | 0/0 | 4328 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0017 | 0/0 | 4328 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0018 | 0/0 | 4328 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0019 | 0/0 | 4328 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0020 | 0/0 | 4327 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4322): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0021 | 0/0 | 4328 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0001t0022 | 0/0 | 4328 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0003t0001 | 0/0 | 4328 | 4 | 3 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0004t0008 | 0/0 | 4328 | 3 | 0 | 1 | 0 | 2 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0004t0024 | 0/1 | 4331 | 1 | 0 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4326): Show |
chr3 | 111537197 | 111657372 |
| a0001c0005t0006 | 1/0 | 4328 | 4 | 3 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0011t0023 | 0/0 | 4327 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4322): Show |
chr3 | 111537197 | 111657372 |
| a0001c0012t0006 | 0/0 | 4328 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0014t0001 | 0/0 | 4328 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0001c0015t0001 | 0/0 | 4328 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0002c0002t0001 | 0/0 | 4328 | 10 | 0 | 0 | 9 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0002c0002t0002 | 0/0 | 4327 | 10 | 1 | 1 | 8 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4322): Show |
chr3 | 111537197 | 111657372 |
| a0002c0002t0006 | 0/0 | 4328 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0003c0006t0003 | 0/0 | 4328 | 2 | 2 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0003c0006t0005 | 0/0 | 4327 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4322): Show |
chr3 | 111537197 | 111657372 |
| a0004c0010t0008 | 0/0 | 4328 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0005c0007t0002 | 0/0 | 4327 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4322): Show |
chr3 | 111537197 | 111657372 |
| a0006c0008t0001 | 0/0 | 4328 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0007c0009t0001 | 0/0 | 4328 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| a0008c0013t0001 | 0/0 | 4328 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | AATTG others(4323): Show |
chr3 | 111537197 | 111657372 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0006g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0007g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0007g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0007g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0007g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0008g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0009g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0010g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0010g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0010g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0010g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0011g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0011g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0012g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0013g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0013g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0014g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0015g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0016g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0017g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0018g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0019g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0020g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0021g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0001t0022g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0004t0008g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0004t0008g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0004t0008g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0004t0024g0096 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0005t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0005t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0005t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0005t0006g0150 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0011t0023g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0012t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0014t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0001c0015t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0002c0002t0006g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0003c0006t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0003c0006t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0003c0006t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0004c0010t0008g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0005c0007t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0006c0008t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0007c0009t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| a0008c0013t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0008 | g0237 | EUR | GBR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0284 | EUR | GBR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | GBR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00140 | hp2 | a0001 | c0001 | t0007 | g0011 | EUR | GBR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | FIN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00280 | hp2 | a0001 | c0004 | t0008 | g0236 | EUR | FIN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00323 | hp1 | a0001 | c0001 | t0007 | g0262 | EUR | FIN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0253 | EUR | FIN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00733 | hp1 | a0001 | c0001 | t0007 | g0011 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0142 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01071 | hp1 | a0001 | c0001 | t0008 | g0185 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0198 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0192 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01081 | hp2 | a0001 | c0004 | t0008 | g0235 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0155 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0073 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0263 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01192 | hp2 | a0001 | c0001 | t0009 | g0051 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0072 | AMR | PUR | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01255 | hp1 | a0001 | c0014 | t0001 | g0095 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01255 | hp2 | a0004 | c0010 | t0008 | g0220 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0152 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0154 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0268 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0160 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01361 | hp2 | a0001 | c0001 | t0007 | g0141 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | IBS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | IBS | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0025 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01978 | hp1 | a0005 | c0007 | t0002 | g0023 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0147 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02055 | hp1 | a0001 | c0001 | t0013 | g0067 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02074 | hp1 | a0001 | c0001 | t0012 | g0010 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02080 | hp1 | a0001 | c0001 | t0012 | g0010 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02165 | hp1 | a0001 | c0001 | t0010 | g0021 | EAS | CDX | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | CDX | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02257 | hp1 | a0001 | c0001 | t0022 | g0017 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02280 | hp2 | a0003 | c0006 | t0003 | g0163 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0162 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0281 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0194 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02622 | hp1 | a0001 | c0005 | t0006 | g0062 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0196 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0052 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0183 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0144 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0042 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02818 | hp2 | a0001 | c0001 | t0021 | g0063 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02895 | hp2 | a0001 | c0011 | t0023 | g0038 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0190 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0202 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0191 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03041 | hp2 | a0006 | c0008 | t0001 | g0036 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03139 | hp1 | a0003 | c0006 | t0003 | g0165 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0186 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0064 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0188 | AFR | ESN | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03209 | hp1 | a0001 | c0001 | t0020 | g0044 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03209 | hp2 | a0001 | c0012 | t0006 | g0066 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03225 | hp1 | a0003 | c0006 | t0005 | g0164 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03453 | hp1 | a0001 | c0001 | t0014 | g0061 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03453 | hp2 | a0001 | c0001 | t0013 | g0069 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03486 | hp2 | a0001 | c0005 | t0006 | g0148 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0075 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0151 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03669 | hp2 | a0002 | c0002 | t0006 | g0029 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | BEB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | STU | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0228 | SAS | STU | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0034 | SAS | BEB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG04228 | hp1 | a0001 | c0001 | t0018 | g0131 | SAS | STU | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | STU | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0071 | AFR | YRI | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0053 | AFR | YRI | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18939 | hp2 | a0001 | c0015 | t0001 | g0117 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18953 | hp1 | a0001 | c0001 | t0010 | g0005 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18961 | hp1 | a0001 | c0001 | t0017 | g0102 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18967 | hp1 | a0001 | c0001 | t0006 | g0199 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18971 | hp1 | a0001 | c0001 | t0015 | g0252 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19002 | hp2 | a0007 | c0009 | t0001 | g0241 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0128 | AFR | LWK | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0189 | AFR | LWK | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19058 | hp2 | a0008 | c0013 | t0001 | g0274 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19060 | hp2 | a0001 | c0001 | t0016 | g0087 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19077 | hp1 | a0001 | c0001 | t0010 | g0048 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19088 | hp1 | a0001 | c0001 | t0010 | g0100 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | YRI | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA19240 | hp2 | a0001 | c0005 | t0006 | g0149 | AFR | YRI | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0157 | EUR | TSI | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0285 | EUR | TSI | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA20805 | hp1 | a0001 | c0001 | t0019 | g0112 | EUR | TSI | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | TSI | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0161 | SAS | GIH | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | GIH | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0049 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG02559 | hp2 | a0001 | c0001 | t0011 | g0277 | AFR | ACB | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0170 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | MSL | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | USA | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | USA | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | LWK | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | LWK | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| homoSapiens | chm13v2 | a0001 | c0004 | t0024 | g0096 | REF | REF | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| homoSapiens | grch38p0 | a0001 | c0005 | t0006 | g0150 | REF | REF | CD96_chr3_111537197_111657372 | CD96 | chr3 | 111537197 | 111657372 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:111567528 | G | C | 3 | a0002 a0005 a0006 |
23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
missense_variant | MODERATE | c.424G>C | p.Ala142Pro | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/14 | 476/4328 | 424/1710 | 142/569 | chr3 | 111567528 | |||
| chr3:111579061 | A | C | 2 | a0003 a0006 |
4 | HG02280.hp2 HG03041.hp2 HG03139.hp1 others(1): Show |
missense_variant | MODERATE | c.578A>C | p.Gln193Pro | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/14 | 630/4328 | 578/1710 | 193/569 | chr3 | 111579061 | |||
| chr3:111600797 | G | A | 1 | a0007 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.970G>A | p.Val324Ile | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/14 | 1022/4328 | 970/1710 | 324/569 | chr3 | 111600797 | |||
| chr3:111623777 | A | T | 1 | a0008 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.1204A>T | p.Thr402Ser | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 9/14 | 1256/4328 | 1204/1710 | 402/569 | chr3 | 111623777 | |||
| chr3:111637205 | G | A | 1 | a0005 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.1331G>A | p.Arg444Gln | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/14 | 1383/4328 | 1331/1710 | 444/569 | chr3 | 111637205 | |||
| chr3:111638124 | C | A | 1 | a0004 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1433C>A | p.Thr478Lys | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/14 | 1485/4328 | 1433/1710 | 478/569 | chr3 | 111638124 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:111579152 | C | T | 1 | a0001c0015 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.669C>T | p.Phe223Phe | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/14 | 721/4328 | 669/1710 | 223/569 | chr3 | 111579152 | |||
| chr3:111600793 | A | G | 1 | a0001c0014 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.966A>G | p.Thr322Thr | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/14 | 1018/4328 | 966/1710 | 322/569 | chr3 | 111600793 | |||
| chr3:111637236 | G | C | 13 | a0001c0001 a0001c0003 a0001c0004 others(10): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
synonymous_variant | LOW | c.1362G>C | p.Pro454Pro | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/14 | 1414/4328 | 1362/1710 | 454/569 | chr3 | 111637236 | |||
| chr3:111637245 | A | G | 1 | a0001c0004 | 3 | HG00099.hp1 HG00280.hp2 HG01081.hp2 |
synonymous_variant | LOW | c.1371A>G | p.Ala457Ala | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/14 | 1423/4328 | 1371/1710 | 457/569 | chr3 | 111637245 | |||
| chr3:111638083 | T | C | 1 | a0001c0012 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1392T>C | p.Asn464Asn | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/14 | 1444/4328 | 1392/1710 | 464/569 | chr3 | 111638083 | |||
| chr3:111647649 | T | C | 1 | a0001c0011 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.1584T>C | p.Cys528Cys | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/14 | 1636/4328 | 1584/1710 | 528/569 | chr3 | 111647649 | |||
| chr3:111649767 | C | T | 1 | a0001c0003 | 4 | HG01081.hp1 HG02717.hp2 HG02896.hp1 others(1): Show |
synonymous_variant | LOW | c.1671C>T | p.Asn557Asn | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1723/4328 | 1671/1710 | 557/569 | chr3 | 111649767 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:111649966 | C | T | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(12): Show |
91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*160C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 160 | chr3 | 111649966 | ||||||
| chr3:111650241 | C | T | 3 | a0001c0001t0008 a0001c0004t0008 a0004c0010t0008 |
6 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*435C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 435 | chr3 | 111650241 | ||||||
| chr3:111650337 | A | G | 1 | a0001c0001t0007 | 6 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*531A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 531 | chr3 | 111650337 | ||||||
| chr3:111650423 | A | T | 1 | a0001c0001t0013 | 2 | HG02055.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*617A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 617 | chr3 | 111650423 | ||||||
| chr3:111650626 | A | G | 32 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(29): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*820A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 820 | chr3 | 111650626 | ||||||
| chr3:111650730 | A | C | 1 | a0001c0011t0023 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*924A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 924 | chr3 | 111650730 | ||||||
| chr3:111650922 | C | A | 1 | a0001c0001t0012 | 2 | HG02074.hp1 HG02080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1116C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1116 | chr3 | 111650922 | ||||||
| chr3:111651136 | T | G | 1 | a0001c0001t0014 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1330T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1330 | chr3 | 111651136 | ||||||
| chr3:111651329 | G | A | 1 | a0001c0001t0015 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1523G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1523 | chr3 | 111651329 | ||||||
| chr3:111651345 | G | T | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(13): Show |
93 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1539G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1539 | chr3 | 111651345 | ||||||
| chr3:111651359 | C | T | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(32): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*1553C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1553 | chr3 | 111651359 | ||||||
| chr3:111651609 | G | A | 2 | a0001c0001t0012 a0001c0001t0015 |
3 | HG02074.hp1 HG02080.hp1 NA18971.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1803G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1803 | chr3 | 111651609 | ||||||
| chr3:111651621 | G | A | 2 | a0001c0001t0010 a0001c0001t0020 |
5 | HG02165.hp1 HG03209.hp1 NA18953.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1815G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1815 | chr3 | 111651621 | ||||||
| chr3:111651679 | G | A | 2 | a0001c0001t0011 a0001c0001t0021 |
3 | HG02559.hp2 HG02818.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1873G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 1873 | chr3 | 111651679 | ||||||
| chr3:111651883 | CA | C | 8 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(5): Show |
76 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*2093delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2093 | INFO_REALIGN_3_PRIME | chr3 | 111651883 | |||||
| chr3:111651896 | A | AAAAAGAA others(14): Show |
1 | a0001c0001t0003 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2093_*2094insAGAA others(17): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2094 | INFO_REALIGN_3_PRIME | chr3 | 111651896 | |||||
| chr3:111651896 | A | AAAAAGAA others(18): Show |
1 | a0001c0001t0003 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2093_*2094insAGAA others(21): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2094 | INFO_REALIGN_3_PRIME | chr3 | 111651896 | |||||
| chr3:111651896 | A | AAAAAGAA others(34): Show |
1 | a0001c0001t0003 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2093_*2094insAGAA others(37): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2094 | INFO_REALIGN_3_PRIME | chr3 | 111651896 | |||||
| chr3:111652017 | A | G | 1 | a0001c0001t0019 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2211A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2211 | chr3 | 111652017 | ||||||
| chr3:111652075 | G | T | 1 | a0001c0001t0018 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2269G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2269 | chr3 | 111652075 | ||||||
| chr3:111652093 | A | C | 1 | a0001c0001t0017 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2287A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2287 | chr3 | 111652093 | ||||||
| chr3:111652186 | C | T | 2 | a0001c0001t0005 a0003c0006t0005 |
12 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2380C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2380 | chr3 | 111652186 | ||||||
| chr3:111652284 | C | T | 1 | a0001c0001t0016 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2478C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2478 | chr3 | 111652284 | ||||||
| chr3:111652298 | A | G | 1 | a0001c0001t0022 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2492A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 14/14 | 2492 | chr3 | 111652298 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:111542326 | T | C | 7 | a0001c0001t0001g0014 a0001c0001t0002g0016 a0001c0001t0003g0003 others(4): Show |
8 | HG02257.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+17T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111542326 | |||||||
| chr3:111542357 | C | T | 1 | a0001c0001t0002g0286 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.61+48C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111542357 | |||||||
| chr3:111542395 | G | GCTGCTGA others(12): Show |
116 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0174 others(113): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.61+87_61+105dupCTG others(16): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 111542395 | ||||||
| chr3:111542584 | T | C | 181 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(178): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.61+275T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111542584 | |||||||
| chr3:111542670 | A | G | 6 | a0001c0001t0002g0074 a0001c0001t0003g0076 a0001c0001t0005g0072 others(3): Show |
6 | HG01106.hp1 HG01243.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+361A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111542670 | |||||||
| chr3:111542918 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.61+609G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111542918 | |||||||
| chr3:111542974 | C | T | 185 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(182): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.61+665C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111542974 | |||||||
| chr3:111542980 | T | G | 29 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0172 others(26): Show |
31 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.61+671T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111542980 | |||||||
| chr3:111542983 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(53): Show |
62 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.61+674G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111542983 | |||||||
| chr3:111543049 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.61+740G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543049 | |||||||
| chr3:111543364 | C | T | 5 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(2): Show |
5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+1055C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543364 | |||||||
| chr3:111543365 | A | G | 185 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(182): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.61+1056A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543365 | |||||||
| chr3:111543456 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | HG01361.hp1 HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.61+1147G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543456 | |||||||
| chr3:111543532 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.61+1223G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543532 | |||||||
| chr3:111543644 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0008g0128 |
2 | HG01496.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.61+1335G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543644 | |||||||
| chr3:111543746 | AC | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0005g0041 others(1): Show |
4 | HG02895.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-1295delC | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 111543746 | ||||||
| chr3:111543757 | T | C | 1 | a0001c0001t0009g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.62-1289T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543757 | |||||||
| chr3:111543815 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(238): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.62-1231T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543815 | |||||||
| chr3:111543907 | A | G | 185 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(182): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.62-1139A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543907 | |||||||
| chr3:111543910 | T | G | 1 | a0001c0001t0001g0178 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.62-1136T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543910 | |||||||
| chr3:111543991 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.62-1055C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111543991 | |||||||
| chr3:111544016 | G | C | 1 | a0001c0001t0004g0179 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.62-1030G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544016 | |||||||
| chr3:111544073 | G | T | 181 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0035 others(178): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.62-973G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544073 | |||||||
| chr3:111544089 | A | G | 3 | a0001c0001t0005g0064 a0001c0001t0021g0063 a0001c0005t0006g0062 |
3 | HG02622.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.62-957A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544089 | |||||||
| chr3:111544095 | T | G | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.62-951T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544095 | |||||||
| chr3:111544233 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.62-813C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544233 | |||||||
| chr3:111544434 | C | T | 3 | a0001c0001t0005g0064 a0001c0001t0021g0063 a0001c0005t0006g0062 |
3 | HG02622.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.62-612C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544434 | |||||||
| chr3:111544557 | T | A | 181 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0035 others(178): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.62-489T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544557 | |||||||
| chr3:111544566 | C | A | 3 | a0001c0001t0002g0043 a0001c0001t0002g0065 a0001c0001t0020g0044 |
3 | HG02717.hp1 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.62-480C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544566 | |||||||
| chr3:111544578 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0005g0041 others(1): Show |
4 | HG02895.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-468T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544578 | |||||||
| chr3:111544622 | C | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0124 others(2): Show |
8 | HG02027.hp1 HG02074.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-424C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544622 | |||||||
| chr3:111544648 | TTATATTC others(3): Show |
T | 1 | a0001c0001t0001g0284 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.62-396_62-387delAT others(8): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 111544648 | ||||||
| chr3:111544663 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0002g0065 |
2 | HG02886.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.62-383G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544663 | |||||||
| chr3:111544695 | C | T | 92 | a0001c0001t0001g0012 a0001c0001t0001g0174 a0001c0001t0001g0175 others(89): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.62-351C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544695 | |||||||
| chr3:111544708 | G | A | 94 | a0001c0001t0001g0012 a0001c0001t0001g0174 a0001c0001t0001g0175 others(91): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.62-338G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544708 | |||||||
| chr3:111544763 | C | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG02132.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.62-283C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544763 | |||||||
| chr3:111544835 | A | G | 181 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0035 others(178): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.62-211A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544835 | |||||||
| chr3:111544869 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.62-177T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544869 | |||||||
| chr3:111544881 | T | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.62-165T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544881 | |||||||
| chr3:111544972 | G | C | 1 | a0001c0001t0006g0071 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.62-74G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544972 | |||||||
| chr3:111544979 | G | A | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.62-67G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544979 | |||||||
| chr3:111544995 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.62-51G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 1/13 | chr3 | 111544995 | |||||||
| chr3:111545665 | T | G | 181 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0035 others(178): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.418+263T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111545665 | |||||||
| chr3:111545798 | G | A | 33 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0039 others(30): Show |
35 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.418+396G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111545798 | |||||||
| chr3:111545999 | TA | T | 91 | a0001c0001t0001g0012 a0001c0001t0001g0174 a0001c0001t0001g0175 others(88): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.418+608delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111545999 | ||||||
| chr3:111546191 | A | T | 1 | a0001c0001t0001g0012 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.418+789A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111546191 | |||||||
| chr3:111546338 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.418+936T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111546338 | |||||||
| chr3:111546419 | C | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.418+1017C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111546419 | |||||||
| chr3:111546419 | C | T | 159 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0035 others(156): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.418+1017C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111546419 | |||||||
| chr3:111546579 | T | C | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+1177T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111546579 | |||||||
| chr3:111546698 | G | A | 2 | a0001c0001t0002g0043 a0001c0001t0020g0044 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.418+1296G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111546698 | |||||||
| chr3:111546706 | C | T | 15 | a0001c0001t0001g0047 a0001c0001t0001g0054 a0001c0001t0001g0058 others(12): Show |
15 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.418+1304C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111546706 | |||||||
| chr3:111546919 | T | TAC | 18 | a0001c0001t0001g0078 a0001c0001t0001g0132 a0001c0001t0001g0136 others(15): Show |
18 | HG00621.hp1 HG00738.hp1 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.418+1544_418+1545d others(4): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | ||||||
| chr3:111546919 | T | TACAC | 5 | a0001c0001t0001g0045 a0001c0001t0003g0068 a0001c0001t0005g0041 others(2): Show |
5 | HG02055.hp1 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+1542_418+1545d others(6): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | ||||||
| chr3:111546919 | T | TACACAC | 4 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0076 others(1): Show |
4 | HG02055.hp2 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.418+1540_418+1545d others(8): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | ||||||
| chr3:111546919 | T | TACACACA others(1): Show |
16 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0054 others(13): Show |
16 | HG01192.hp2 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.418+1538_418+1545d others(10): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | ||||||
| chr3:111546919 | T | TACACACA others(3): Show |
5 | a0001c0001t0001g0035 a0001c0001t0003g0050 a0001c0001t0006g0071 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+1536_418+1545d others(12): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | ||||||
| chr3:111546919 | T | TACACACA others(5): Show |
24 | a0001c0001t0001g0014 a0001c0001t0001g0172 a0001c0001t0002g0016 others(21): Show |
26 | HG00408.hp2 HG01952.hp2 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.418+1534_418+1545d others(14): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | ||||||
| chr3:111546919 | T | TACACACA others(7): Show |
9 | a0001c0001t0001g0012 a0001c0001t0002g0074 a0001c0001t0005g0049 others(6): Show |
10 | HG00544.hp1 HG00544.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.418+1532_418+1545d others(16): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | ||||||
| chr3:111546919 | T | TACACACA others(9): Show |
7 | a0001c0001t0001g0177 a0001c0001t0001g0278 a0001c0001t0001g0279 others(4): Show |
7 | HG01106.hp1 HG01243.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.418+1530_418+1545d others(18): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | ||||||
| chr3:111546919 | T | TACACACA others(11): Show |
21 | a0001c0001t0001g0176 a0001c0001t0001g0204 a0001c0001t0001g0205 others(18): Show |
22 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.418+1528_418+1545d others(20): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | ||||||
| chr3:111546919 | T | TACACACA others(13): Show |
16 | a0001c0001t0001g0203 a0001c0001t0001g0249 a0001c0001t0001g0250 others(13): Show |
16 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(13): Show |
intron_variant | MODIFIER | c.418+1526_418+1545d others(22): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | ||||||
| chr3:111546919 | T | TACACACA others(15): Show |
34 | a0001c0001t0001g0047 a0001c0001t0001g0174 a0001c0001t0001g0175 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.418+1524_418+1545d others(24): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | ||||||
| chr3:111546919 | T | TACACACA others(17): Show |
8 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(5): Show |
9 | HG02027.hp2 HG02074.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.418+1522_418+1545d others(26): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | ||||||
| chr3:111546919 | T | TACACACA others(19): Show |
3 | a0001c0001t0001g0210 a0001c0001t0001g0212 a0001c0001t0003g0211 |
3 | HG00438.hp2 HG01256.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.418+1520_418+1545d others(28): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | ||||||
| chr3:111546919 | T | TACACACA others(21): Show |
1 | a0001c0001t0003g0209 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.418+1518_418+1545d others(30): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | ||||||
| chr3:111546919 | T | TACACACA others(23): Show |
2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG01074.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.418+1545_418+1546i others(32): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | ||||||
| chr3:111546919 | T | TTACACAC others(12): Show |
1 | a0001c0001t0001g0283 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.418+1517_418+1518i others(21): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111546919 | |||||||
| chr3:111546919 | TACAC | T | 3 | a0001c0001t0002g0043 a0001c0001t0002g0065 a0001c0001t0020g0044 |
3 | HG02717.hp1 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.418+1542_418+1545d others(6): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111546919 | ||||||
| chr3:111547114 | C | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(57): Show |
67 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.418+1712C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547114 | |||||||
| chr3:111547139 | T | C | 1 | a0001c0001t0007g0262 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.418+1737T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547139 | |||||||
| chr3:111547309 | T | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0249 |
2 | HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.418+1907T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547309 | |||||||
| chr3:111547416 | GT | G | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+2022delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111547416 | ||||||
| chr3:111547465 | C | T | 2 | a0001c0001t0001g0035 a0006c0008t0001g0036 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.418+2063C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547465 | |||||||
| chr3:111547518 | T | C | 3 | a0001c0001t0009g0051 a0001c0001t0009g0052 a0001c0001t0009g0053 |
3 | HG01192.hp2 HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.418+2116T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547518 | |||||||
| chr3:111547701 | T | C | 11 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0002g0055 others(8): Show |
11 | HG01192.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.418+2299T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547701 | |||||||
| chr3:111547715 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0005g0041 others(1): Show |
4 | HG02895.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.418+2313G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547715 | |||||||
| chr3:111547729 | C | T | 21 | a0001c0001t0001g0047 a0001c0001t0001g0054 a0001c0001t0001g0058 others(18): Show |
21 | HG01106.hp1 HG01192.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.418+2327C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547729 | |||||||
| chr3:111547763 | G | A | 5 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(2): Show |
5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+2361G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547763 | |||||||
| chr3:111547966 | T | C | 33 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0039 others(30): Show |
35 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.418+2564T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111547966 | |||||||
| chr3:111548368 | T | A | 1 | a0001c0001t0001g0079 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.418+2966T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548368 | |||||||
| chr3:111548640 | T | C | 1 | a0001c0001t0006g0183 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.418+3238T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548640 | |||||||
| chr3:111548656 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.418+3254G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548656 | |||||||
| chr3:111548717 | C | T | 180 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0035 others(177): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.418+3315C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548717 | |||||||
| chr3:111548848 | C | T | 3 | a0001c0001t0001g0284 a0001c0001t0002g0247 a0001c0001t0002g0248 |
3 | HG00099.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.418+3446C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548848 | |||||||
| chr3:111548894 | G | C | 1 | a0001c0001t0003g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.418+3492G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548894 | |||||||
| chr3:111548898 | T | C | 33 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0039 others(30): Show |
35 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.418+3496T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548898 | |||||||
| chr3:111548934 | G | A | 3 | a0001c0001t0005g0064 a0001c0001t0021g0063 a0001c0005t0006g0062 |
3 | HG02622.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.418+3532G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548934 | |||||||
| chr3:111548961 | G | A | 18 | a0001c0001t0001g0047 a0001c0001t0001g0054 a0001c0001t0001g0058 others(15): Show |
18 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.418+3559G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548961 | |||||||
| chr3:111548983 | G | T | 1 | a0001c0001t0003g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.418+3581G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111548983 | |||||||
| chr3:111549121 | C | T | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+3719C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111549121 | |||||||
| chr3:111549364 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.418+3962C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111549364 | |||||||
| chr3:111549499 | C | G | 1 | a0001c0001t0003g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.418+4097C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111549499 | |||||||
| chr3:111549500 | A | G | 93 | a0001c0001t0001g0012 a0001c0001t0001g0174 a0001c0001t0001g0175 others(90): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.418+4098A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111549500 | |||||||
| chr3:111549507 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.418+4105G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111549507 | |||||||
| chr3:111550039 | C | T | 5 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(2): Show |
5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+4637C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111550039 | |||||||
| chr3:111550389 | G | A | 93 | a0001c0001t0001g0012 a0001c0001t0001g0174 a0001c0001t0001g0175 others(90): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.418+4987G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111550389 | |||||||
| chr3:111550483 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.418+5081G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111550483 | |||||||
| chr3:111550533 | G | A | 1 | a0001c0001t0007g0263 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.418+5131G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111550533 | |||||||
| chr3:111550702 | C | G | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+5300C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111550702 | |||||||
| chr3:111550872 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.418+5470G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111550872 | |||||||
| chr3:111550942 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.418+5540G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111550942 | |||||||
| chr3:111551173 | A | G | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+5771A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111551173 | |||||||
| chr3:111551181 | A | G | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+5779A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111551181 | |||||||
| chr3:111551297 | G | T | 3 | a0001c0001t0002g0074 a0001c0001t0005g0072 a0001c0001t0005g0073 |
3 | HG01106.hp1 HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.418+5895G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111551297 | |||||||
| chr3:111551400 | A | T | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+5998A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111551400 | |||||||
| chr3:111551410 | A | G | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.418+6008A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111551410 | |||||||
| chr3:111551419 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0005g0041 others(1): Show |
4 | HG02895.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.418+6017C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111551419 | |||||||
| chr3:111551483 | C | A | 1 | a0004c0010t0008g0220 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.418+6081C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111551483 | |||||||
| chr3:111551879 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.418+6477C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111551879 | |||||||
| chr3:111552145 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.418+6743T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552145 | |||||||
| chr3:111552164 | G | C | 1 | a0004c0010t0008g0220 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.418+6762G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552164 | |||||||
| chr3:111552249 | T | C | 2 | a0001c0001t0010g0021 a0002c0002t0002g0019 |
2 | HG00544.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.418+6847T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552249 | |||||||
| chr3:111552274 | G | T | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+6872G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552274 | |||||||
| chr3:111552281 | T | A | 2 | a0001c0001t0002g0043 a0001c0001t0020g0044 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.418+6879T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552281 | |||||||
| chr3:111552467 | C | T | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(257): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.418+7065C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552467 | |||||||
| chr3:111552555 | G | C | 2 | a0001c0001t0005g0072 a0001c0001t0005g0073 |
2 | HG01106.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.418+7153G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552555 | |||||||
| chr3:111552604 | T | TAAAAAGC others(323): Show |
2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.418+7218_418+7219i others(332): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111552604 | ||||||
| chr3:111552604 | T | TAAAAAGC others(324): Show |
2 | a0001c0001t0005g0041 a0001c0011t0023g0038 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.418+7218_418+7219i others(333): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111552604 | ||||||
| chr3:111552637 | G | A | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+7235G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552637 | |||||||
| chr3:111552774 | T | G | 1 | a0001c0003t0001g0022 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.418+7372T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111552774 | |||||||
| chr3:111553072 | A | T | 1 | a0001c0001t0005g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.418+7670A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553072 | |||||||
| chr3:111553083 | TA | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0121 others(4): Show |
7 | HG01106.hp1 HG01243.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.418+7689delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111553083 | ||||||
| chr3:111553158 | G | GATA | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(239): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.418+7758_418+7759i others(5): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111553158 | ||||||
| chr3:111553171 | G | GT | 10 | a0001c0001t0001g0014 a0001c0001t0002g0016 a0001c0001t0003g0003 others(7): Show |
11 | HG02257.hp1 HG02559.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.418+7780dupT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111553171 | ||||||
| chr3:111553171 | GT | G | 23 | a0001c0001t0001g0047 a0001c0001t0001g0054 a0001c0001t0001g0058 others(20): Show |
23 | HG01106.hp1 HG01192.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.418+7780delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111553171 | ||||||
| chr3:111553207 | T | C | 1 | a0001c0003t0001g0022 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.418+7805T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553207 | |||||||
| chr3:111553239 | T | C | 3 | a0001c0001t0002g0074 a0001c0001t0005g0072 a0001c0001t0005g0073 |
3 | HG01106.hp1 HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.418+7837T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553239 | |||||||
| chr3:111553253 | T | C | 4 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0007g0141 others(1): Show |
4 | HG00735.hp1 HG01361.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.418+7851T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553253 | |||||||
| chr3:111553254 | A | G | 4 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(1): Show |
4 | HG02055.hp1 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.418+7852A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553254 | |||||||
| chr3:111553413 | A | C | 182 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0035 others(179): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.418+8011A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553413 | |||||||
| chr3:111553434 | CT | C | 177 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0035 others(174): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.418+8047delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111553434 | ||||||
| chr3:111553436 | T | G | 1 | a0001c0001t0001g0058 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.418+8034T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553436 | |||||||
| chr3:111553437 | T | G | 17 | a0001c0001t0001g0047 a0001c0001t0001g0054 a0001c0001t0002g0055 others(14): Show |
17 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.418+8035T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553437 | |||||||
| chr3:111553946 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0008g0185 |
2 | HG00639.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.418+8544G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111553946 | |||||||
| chr3:111554024 | G | T | 19 | a0001c0001t0001g0132 a0001c0001t0001g0136 a0001c0001t0001g0166 others(16): Show |
19 | HG02145.hp1 HG02486.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.418+8622G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554024 | |||||||
| chr3:111554091 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.418+8689C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554091 | |||||||
| chr3:111554211 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.418+8809T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554211 | |||||||
| chr3:111554300 | C | G | 1 | a0001c0001t0014g0061 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.418+8898C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554300 | |||||||
| chr3:111554329 | A | G | 2 | a0001c0001t0002g0043 a0001c0001t0020g0044 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.418+8927A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554329 | |||||||
| chr3:111554403 | T | A | 2 | a0001c0001t0002g0145 a0001c0001t0003g0146 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.418+9001T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554403 | |||||||
| chr3:111554456 | T | G | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | NA18969.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.418+9054T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554456 | |||||||
| chr3:111554479 | G | T | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+9077G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554479 | |||||||
| chr3:111554629 | A | C | 7 | a0001c0001t0001g0014 a0001c0001t0002g0016 a0001c0001t0003g0003 others(4): Show |
8 | HG02257.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.418+9227A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554629 | |||||||
| chr3:111554659 | G | T | 2 | a0002c0002t0001g0032 a0002c0002t0001g0033 |
2 | NA18959.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.418+9257G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554659 | |||||||
| chr3:111554685 | T | G | 182 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0035 others(179): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.418+9283T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554685 | |||||||
| chr3:111554753 | T | C | 93 | a0001c0001t0001g0012 a0001c0001t0001g0174 a0001c0001t0001g0175 others(90): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.418+9351T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554753 | |||||||
| chr3:111554992 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.418+9590A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111554992 | |||||||
| chr3:111555081 | G | A | 29 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0172 others(26): Show |
31 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.418+9679G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555081 | |||||||
| chr3:111555118 | T | C | 10 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0002g0004 others(7): Show |
11 | HG00609.hp2 NA18945.hp1 NA18969.hp2 others(8): Show |
intron_variant | MODIFIER | c.418+9716T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555118 | |||||||
| chr3:111555220 | A | G | 41 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0039 others(38): Show |
43 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.418+9818A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555220 | |||||||
| chr3:111555303 | C | T | 21 | a0001c0001t0001g0047 a0001c0001t0001g0054 a0001c0001t0001g0058 others(18): Show |
21 | HG01106.hp1 HG01192.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.418+9901C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555303 | |||||||
| chr3:111555385 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.418+9983A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555385 | |||||||
| chr3:111555418 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.418+10016C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555418 | |||||||
| chr3:111555442 | A | G | 1 | a0002c0002t0001g0033 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.418+10040A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555442 | |||||||
| chr3:111555681 | G | T | 1 | a0001c0001t0001g0276 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.418+10279G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555681 | |||||||
| chr3:111555758 | G | T | 93 | a0001c0001t0001g0012 a0001c0001t0001g0174 a0001c0001t0001g0175 others(90): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.418+10356G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111555758 | |||||||
| chr3:111556013 | G | A | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+10611G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556013 | |||||||
| chr3:111556075 | C | T | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+10673C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556075 | |||||||
| chr3:111556206 | CT | C | 27 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0178 others(24): Show |
27 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.418+10814delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111556206 | ||||||
| chr3:111556216 | T | A | 5 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(2): Show |
5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+10814T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556216 | |||||||
| chr3:111556225 | T | C | 1 | a0001c0001t0002g0089 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.418+10823T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556225 | |||||||
| chr3:111556247 | A | G | 5 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.418+10845A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556247 | |||||||
| chr3:111556296 | C | T | 23 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(20): Show |
23 | HG00621.hp2 HG00639.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.418+10894C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556296 | |||||||
| chr3:111556301 | C | G | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+10899C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556301 | |||||||
| chr3:111556431 | A | T | 1 | a0001c0012t0006g0066 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.418+11029A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556431 | |||||||
| chr3:111556451 | G | C | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.418+11049G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556451 | |||||||
| chr3:111556473 | C | T | 33 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0039 others(30): Show |
35 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.419-11050C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556473 | |||||||
| chr3:111556490 | A | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(268): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.419-11033A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556490 | |||||||
| chr3:111556560 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.419-10963T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556560 | |||||||
| chr3:111556565 | C | T | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-10958C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556565 | |||||||
| chr3:111556577 | T | G | 11 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0001g0195 others(8): Show |
11 | HG01081.hp1 HG02572.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.419-10946T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556577 | |||||||
| chr3:111556646 | A | G | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-10877A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556646 | |||||||
| chr3:111556698 | A | G | 1 | a0001c0001t0020g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.419-10825A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556698 | |||||||
| chr3:111556737 | C | G | 24 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(21): Show |
24 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.419-10786C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556737 | |||||||
| chr3:111556746 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.419-10777T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556746 | |||||||
| chr3:111556783 | G | C | 6 | a0001c0001t0001g0132 a0001c0001t0002g0007 a0001c0001t0002g0130 others(3): Show |
6 | HG02735.hp2 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-10740G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556783 | |||||||
| chr3:111556812 | G | C | 2 | a0001c0001t0003g0059 a0001c0001t0003g0060 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.419-10711G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556812 | |||||||
| chr3:111556892 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(238): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.419-10631T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556892 | |||||||
| chr3:111556951 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.419-10572G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556951 | |||||||
| chr3:111556989 | A | T | 182 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0035 others(179): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.419-10534A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111556989 | |||||||
| chr3:111557031 | C | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(74): Show |
84 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.419-10492C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557031 | |||||||
| chr3:111557034 | A | C | 19 | a0001c0001t0001g0047 a0001c0001t0001g0054 a0001c0001t0001g0058 others(16): Show |
19 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.419-10489A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557034 | |||||||
| chr3:111557160 | G | C | 1 | a0001c0001t0004g0147 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.419-10363G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557160 | |||||||
| chr3:111557188 | G | T | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-10335G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557188 | |||||||
| chr3:111557192 | A | G | 1 | a0001c0003t0001g0022 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.419-10331A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557192 | |||||||
| chr3:111557215 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.419-10308T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557215 | |||||||
| chr3:111557222 | C | T | 65 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0039 others(62): Show |
67 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.419-10301C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557222 | |||||||
| chr3:111557225 | C | G | 2 | a0001c0001t0001g0259 a0001c0001t0002g0260 |
2 | HG00438.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.419-10298C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557225 | |||||||
| chr3:111557233 | G | T | 6 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0259 others(3): Show |
6 | HG00438.hp1 HG02895.hp2 NA19030.hp2 others(3): Show |
intron_variant | MODIFIER | c.419-10290G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557233 | |||||||
| chr3:111557262 | A | G | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-10261A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557262 | |||||||
| chr3:111557397 | G | A | 33 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0039 others(30): Show |
35 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.419-10126G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557397 | |||||||
| chr3:111557429 | G | A | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-10094G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557429 | |||||||
| chr3:111557447 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.419-10076A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557447 | |||||||
| chr3:111557473 | C | G | 2 | a0001c0001t0001g0047 a0001c0001t0010g0048 |
2 | HG02258.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.419-10050C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557473 | |||||||
| chr3:111557487 | C | G | 1 | a0002c0002t0001g0031 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.419-10036C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557487 | |||||||
| chr3:111557518 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.419-10005G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557518 | |||||||
| chr3:111557523 | C | T | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.419-10000C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557523 | |||||||
| chr3:111557528 | T | A | 1 | a0001c0001t0005g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.419-9995T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557528 | |||||||
| chr3:111557599 | G | T | 5 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(2): Show |
5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-9924G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557599 | |||||||
| chr3:111557625 | G | A | 5 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(2): Show |
5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-9898G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557625 | |||||||
| chr3:111557666 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.419-9857T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557666 | |||||||
| chr3:111557669 | G | C | 2 | a0001c0001t0001g0127 a0001c0001t0008g0128 |
2 | HG01496.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.419-9854G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557669 | |||||||
| chr3:111557681 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.419-9842C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557681 | |||||||
| chr3:111557682 | G | A | 3 | a0001c0001t0005g0064 a0001c0001t0021g0063 a0001c0005t0006g0062 |
3 | HG02622.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.419-9841G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557682 | |||||||
| chr3:111557686 | C | T | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-9837C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557686 | |||||||
| chr3:111557751 | T | A | 1 | a0003c0006t0003g0163 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.419-9772T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557751 | |||||||
| chr3:111557922 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0010g0048 |
2 | HG02258.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.419-9601A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557922 | |||||||
| chr3:111557936 | G | T | 5 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(2): Show |
5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-9587G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111557936 | |||||||
| chr3:111558106 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.419-9417G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558106 | |||||||
| chr3:111558132 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.419-9391T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558132 | |||||||
| chr3:111558170 | C | T | 3 | a0001c0001t0005g0064 a0001c0001t0021g0063 a0001c0005t0006g0062 |
3 | HG02622.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.419-9353C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558170 | |||||||
| chr3:111558314 | G | A | 5 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(2): Show |
5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-9209G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558314 | |||||||
| chr3:111558376 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.419-9147G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558376 | |||||||
| chr3:111558390 | G | T | 25 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0178 others(22): Show |
25 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.419-9133G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558390 | |||||||
| chr3:111558417 | G | T | 93 | a0001c0001t0001g0012 a0001c0001t0001g0174 a0001c0001t0001g0175 others(90): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.419-9106G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558417 | |||||||
| chr3:111558441 | T | C | 5 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(2): Show |
5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-9082T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558441 | |||||||
| chr3:111558443 | T | C | 5 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(2): Show |
5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-9080T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558443 | |||||||
| chr3:111558519 | G | A | 11 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0002g0055 others(8): Show |
11 | HG01192.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.419-9004G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558519 | |||||||
| chr3:111558656 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.419-8867G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558656 | |||||||
| chr3:111558691 | G | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(56): Show |
66 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.419-8832G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558691 | |||||||
| chr3:111558705 | A | G | 5 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0278 others(2): Show |
5 | HG01952.hp1 HG01978.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-8818A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558705 | |||||||
| chr3:111558737 | G | T | 1 | a0001c0001t0008g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.419-8786G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558737 | |||||||
| chr3:111558816 | G | A | 1 | a0001c0001t0003g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.419-8707G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558816 | |||||||
| chr3:111558873 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0005g0041 others(1): Show |
4 | HG02895.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.419-8650C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558873 | |||||||
| chr3:111558910 | G | T | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.419-8613G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558910 | |||||||
| chr3:111558971 | C | A | 1 | a0001c0001t0001g0264 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.419-8552C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111558971 | |||||||
| chr3:111559045 | G | C | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.419-8478G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559045 | |||||||
| chr3:111559271 | G | C | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.419-8252G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559271 | |||||||
| chr3:111559383 | A | G | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-8140A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559383 | |||||||
| chr3:111559458 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.419-8065G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559458 | |||||||
| chr3:111559553 | T | C | 1 | a0001c0001t0008g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.419-7970T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559553 | |||||||
| chr3:111559568 | A | T | 9 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0197 others(6): Show |
9 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.419-7955A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559568 | |||||||
| chr3:111559618 | T | G | 1 | a0001c0001t0001g0090 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.419-7905T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559618 | |||||||
| chr3:111559628 | C | G | 1 | a0001c0001t0001g0120 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.419-7895C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559628 | |||||||
| chr3:111559638 | A | C | 13 | a0001c0001t0001g0153 a0001c0001t0001g0158 a0001c0001t0001g0159 others(10): Show |
13 | HG01071.hp2 HG01099.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.419-7885A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559638 | |||||||
| chr3:111559725 | T | C | 7 | a0001c0001t0001g0014 a0001c0001t0002g0016 a0001c0001t0003g0003 others(4): Show |
8 | HG02257.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-7798T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559725 | |||||||
| chr3:111559728 | G | T | 183 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0035 others(180): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.419-7795G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559728 | |||||||
| chr3:111559780 | G | A | 7 | a0001c0001t0001g0014 a0001c0001t0002g0016 a0001c0001t0003g0003 others(4): Show |
8 | HG02257.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-7743G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559780 | |||||||
| chr3:111559833 | G | T | 7 | a0001c0001t0001g0014 a0001c0001t0002g0016 a0001c0001t0003g0003 others(4): Show |
8 | HG02257.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-7690G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559833 | |||||||
| chr3:111559929 | T | C | 7 | a0001c0001t0001g0014 a0001c0001t0002g0016 a0001c0001t0003g0003 others(4): Show |
8 | HG02257.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-7594T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559929 | |||||||
| chr3:111559982 | T | G | 5 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(2): Show |
5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-7541T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111559982 | |||||||
| chr3:111560082 | T | C | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-7441T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560082 | |||||||
| chr3:111560109 | C | T | 93 | a0001c0001t0001g0012 a0001c0001t0001g0174 a0001c0001t0001g0175 others(90): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.419-7414C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560109 | |||||||
| chr3:111560192 | A | C | 5 | a0001c0001t0001g0222 a0001c0001t0001g0239 a0001c0001t0001g0240 others(2): Show |
5 | NA18950.hp1 NA18952.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-7331A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560192 | |||||||
| chr3:111560203 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.419-7320T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560203 | |||||||
| chr3:111560222 | G | T | 3 | a0001c0001t0002g0043 a0001c0001t0020g0044 a0004c0010t0008g0220 |
3 | HG01255.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.419-7301G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560222 | |||||||
| chr3:111560448 | A | T | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-7075A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560448 | |||||||
| chr3:111560578 | A | G | 23 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(20): Show |
23 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.419-6945A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560578 | |||||||
| chr3:111560578 | A | T | 1 | a0001c0003t0001g0144 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.419-6945A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560578 | |||||||
| chr3:111560604 | G | A | 2 | a0001c0001t0003g0209 a0001c0001t0003g0211 |
2 | HG00438.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.419-6919G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560604 | |||||||
| chr3:111560681 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.419-6842T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560681 | |||||||
| chr3:111560701 | C | A | 1 | a0001c0001t0001g0223 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.419-6822C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560701 | |||||||
| chr3:111560741 | T | G | 1 | a0001c0001t0001g0224 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.419-6782T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560741 | |||||||
| chr3:111560747 | C | T | 2 | a0001c0001t0001g0118 a0001c0015t0001g0117 |
2 | NA18939.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.419-6776C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560747 | |||||||
| chr3:111560942 | G | A | 3 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0003g0046 |
3 | HG02486.hp2 HG02683.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.419-6581G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560942 | |||||||
| chr3:111560997 | A | G | 5 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(2): Show |
5 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-6526A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111560997 | |||||||
| chr3:111561001 | T | C | 56 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0039 others(53): Show |
58 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.419-6522T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561001 | |||||||
| chr3:111561035 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.419-6488C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561035 | |||||||
| chr3:111561045 | G | A | 9 | a0001c0001t0002g0145 a0001c0001t0003g0146 a0001c0001t0004g0142 others(6): Show |
9 | HG00735.hp1 HG01361.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.419-6478G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561045 | |||||||
| chr3:111561046 | G | GT | 21 | a0001c0001t0001g0047 a0001c0001t0001g0054 a0001c0001t0001g0058 others(18): Show |
21 | HG01106.hp1 HG01192.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.419-6473dupT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111561046 | ||||||
| chr3:111561060 | C | G | 14 | a0001c0001t0001g0132 a0001c0001t0001g0136 a0001c0001t0002g0007 others(11): Show |
14 | HG02523.hp2 HG02735.hp2 HG03491.hp1 others(11): Show |
intron_variant | MODIFIER | c.419-6463C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561060 | |||||||
| chr3:111561079 | T | A | 1 | a0001c0001t0001g0203 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.419-6444T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561079 | |||||||
| chr3:111561081 | T | C | 21 | a0001c0001t0001g0047 a0001c0001t0001g0054 a0001c0001t0001g0058 others(18): Show |
21 | HG01106.hp1 HG01192.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.419-6442T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561081 | |||||||
| chr3:111561082 | G | A | 2 | a0001c0001t0002g0043 a0001c0001t0020g0044 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.419-6441G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561082 | |||||||
| chr3:111561114 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.419-6409A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561114 | |||||||
| chr3:111561135 | T | C | 1 | a0001c0001t0001g0267 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.419-6388T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561135 | |||||||
| chr3:111561164 | G | A | 2 | a0001c0001t0002g0247 a0001c0001t0002g0248 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.419-6359G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561164 | |||||||
| chr3:111561189 | G | A | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-6334G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561189 | |||||||
| chr3:111561195 | T | G | 3 | a0001c0001t0005g0064 a0001c0001t0021g0063 a0001c0005t0006g0062 |
3 | HG02622.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.419-6328T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561195 | |||||||
| chr3:111561196 | T | C | 3 | a0001c0001t0005g0064 a0001c0001t0021g0063 a0001c0005t0006g0062 |
3 | HG02622.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.419-6327T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561196 | |||||||
| chr3:111561241 | G | A | 7 | a0001c0001t0001g0014 a0001c0001t0002g0016 a0001c0001t0003g0003 others(4): Show |
8 | HG02257.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-6282G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561241 | |||||||
| chr3:111561259 | T | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0250 |
2 | HG01167.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.419-6264T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561259 | |||||||
| chr3:111561282 | G | A | 1 | a0001c0001t0007g0141 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.419-6241G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561282 | |||||||
| chr3:111561315 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.419-6208C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561315 | |||||||
| chr3:111561347 | C | T | 33 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0039 others(30): Show |
35 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.419-6176C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561347 | |||||||
| chr3:111561350 | T | C | 1 | a0002c0002t0001g0032 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.419-6173T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561350 | |||||||
| chr3:111561352 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.419-6171G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561352 | |||||||
| chr3:111561374 | C | A | 2 | a0001c0001t0002g0037 a0001c0001t0003g0046 |
2 | HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.419-6149C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561374 | |||||||
| chr3:111561386 | C | T | 1 | a0002c0002t0001g0031 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.419-6137C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561386 | |||||||
| chr3:111561389 | T | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(57): Show |
67 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.419-6134T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561389 | |||||||
| chr3:111561462 | C | T | 1 | a0001c0003t0001g0022 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.419-6061C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561462 | |||||||
| chr3:111561466 | C | T | 3 | a0001c0001t0005g0064 a0001c0001t0021g0063 a0001c0005t0006g0062 |
3 | HG02622.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.419-6057C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561466 | |||||||
| chr3:111561468 | T | G | 100 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0092 others(97): Show |
103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.419-6055T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561468 | |||||||
| chr3:111561480 | A | G | 1 | a0006c0008t0001g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.419-6043A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561480 | |||||||
| chr3:111561495 | C | G | 1 | a0001c0001t0001g0116 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.419-6028C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561495 | |||||||
| chr3:111561496 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.419-6027G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561496 | |||||||
| chr3:111561529 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.419-5994G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561529 | |||||||
| chr3:111561563 | G | C | 11 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0204 others(8): Show |
11 | HG00099.hp2 HG01952.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.419-5960G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561563 | |||||||
| chr3:111561564 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0005g0041 others(1): Show |
4 | HG02895.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.419-5959G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561564 | |||||||
| chr3:111561575 | T | G | 1 | a0001c0001t0002g0080 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.419-5948T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561575 | |||||||
| chr3:111561581 | T | C | 2 | a0001c0001t0001g0284 a0001c0001t0005g0186 |
2 | HG00099.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.419-5942T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561581 | |||||||
| chr3:111561623 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.419-5900A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561623 | |||||||
| chr3:111561648 | A | C | 4 | a0001c0001t0002g0043 a0001c0001t0002g0065 a0001c0001t0020g0044 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.419-5875A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561648 | |||||||
| chr3:111561664 | TTGTC | T | 4 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(1): Show |
4 | HG02055.hp1 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.419-5855_419-5852d others(6): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111561664 | ||||||
| chr3:111561720 | G | A | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-5803G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561720 | |||||||
| chr3:111561743 | C | G | 33 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0039 others(30): Show |
35 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.419-5780C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561743 | |||||||
| chr3:111561744 | G | C | 1 | a0001c0001t0001g0093 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.419-5779G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561744 | |||||||
| chr3:111561744 | G | T | 1 | a0001c0001t0013g0069 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.419-5779G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561744 | |||||||
| chr3:111561752 | C | T | 33 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0039 others(30): Show |
35 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.419-5771C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561752 | |||||||
| chr3:111561753 | G | A | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.419-5770G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561753 | |||||||
| chr3:111561761 | T | C | 2 | a0002c0002t0001g0032 a0002c0002t0001g0033 |
2 | NA18959.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.419-5762T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561761 | |||||||
| chr3:111561772 | G | T | 1 | a0001c0001t0003g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.419-5751G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561772 | |||||||
| chr3:111561862 | T | C | 32 | a0001c0001t0001g0047 a0001c0001t0001g0054 a0001c0001t0001g0058 others(29): Show |
32 | HG01071.hp2 HG01099.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.419-5661T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561862 | |||||||
| chr3:111561865 | C | T | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-5658C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561865 | |||||||
| chr3:111561871 | C | T | 2 | a0001c0001t0002g0043 a0001c0001t0020g0044 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.419-5652C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561871 | |||||||
| chr3:111561930 | G | A | 4 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(1): Show |
4 | HG02055.hp1 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.419-5593G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561930 | |||||||
| chr3:111561951 | G | A | 1 | a0001c0001t0002g0225 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.419-5572G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561951 | |||||||
| chr3:111561964 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.419-5559C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561964 | |||||||
| chr3:111561984 | G | A | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-5539G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111561984 | |||||||
| chr3:111562003 | C | T | 1 | a0001c0001t0003g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.419-5520C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562003 | |||||||
| chr3:111562080 | G | A | 2 | a0001c0001t0001g0035 a0006c0008t0001g0036 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.419-5443G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562080 | |||||||
| chr3:111562234 | C | A | 2 | a0001c0001t0002g0043 a0001c0001t0020g0044 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.419-5289C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562234 | |||||||
| chr3:111562302 | C | T | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-5221C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562302 | |||||||
| chr3:111562329 | C | T | 19 | a0001c0001t0001g0178 a0001c0001t0001g0187 a0001c0001t0001g0193 others(16): Show |
19 | HG00738.hp1 HG01074.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.419-5194C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562329 | |||||||
| chr3:111562535 | C | CA | 191 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0035 others(188): Show |
196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.419-4988_419-4987i others(3): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562535 | |||||||
| chr3:111562600 | C | A | 1 | a0001c0001t0001g0250 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.419-4923C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562600 | |||||||
| chr3:111562678 | C | A | 1 | a0001c0001t0002g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.419-4845C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562678 | |||||||
| chr3:111562711 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.419-4812A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562711 | |||||||
| chr3:111562759 | C | G | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-4764C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562759 | |||||||
| chr3:111562842 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.419-4681A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111562842 | |||||||
| chr3:111563017 | C | T | 95 | a0001c0001t0001g0012 a0001c0001t0001g0172 a0001c0001t0001g0174 others(92): Show |
98 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.419-4506C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563017 | |||||||
| chr3:111563039 | G | T | 11 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0001g0195 others(8): Show |
11 | HG01081.hp1 HG02572.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.419-4484G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563039 | |||||||
| chr3:111563175 | C | T | 1 | a0001c0001t0004g0162 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.419-4348C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563175 | |||||||
| chr3:111563184 | A | C | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-4339A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563184 | |||||||
| chr3:111563187 | C | A | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.419-4336C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563187 | |||||||
| chr3:111563212 | A | C | 2 | a0001c0001t0001g0184 a0001c0001t0008g0185 |
2 | HG00639.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.419-4311A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563212 | |||||||
| chr3:111563512 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.419-4011C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563512 | |||||||
| chr3:111563572 | C | T | 1 | a0001c0001t0005g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.419-3951C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563572 | |||||||
| chr3:111563582 | ATTG | A | 4 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(1): Show |
4 | HG02055.hp1 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.419-3932_419-3930d others(5): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111563582 | ||||||
| chr3:111563717 | A | G | 39 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0039 others(36): Show |
41 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.419-3806A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563717 | |||||||
| chr3:111563841 | T | C | 1 | a0002c0002t0002g0173 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.419-3682T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563841 | |||||||
| chr3:111563872 | G | A | 1 | a0001c0001t0002g0119 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.419-3651G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563872 | |||||||
| chr3:111563896 | T | C | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-3627T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563896 | |||||||
| chr3:111563982 | C | T | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-3541C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111563982 | |||||||
| chr3:111564023 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0005g0041 others(1): Show |
4 | HG02895.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.419-3500G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564023 | |||||||
| chr3:111564150 | C | G | 2 | a0001c0001t0002g0037 a0001c0001t0003g0046 |
2 | HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.419-3373C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564150 | |||||||
| chr3:111564150 | C | T | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.419-3373C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564150 | |||||||
| chr3:111564208 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.419-3315T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564208 | |||||||
| chr3:111564226 | T | C | 2 | a0001c0005t0006g0148 a0001c0005t0006g0149 |
2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.419-3297T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564226 | |||||||
| chr3:111564284 | C | A | 2 | a0001c0001t0001g0175 a0001c0001t0004g0151 |
2 | HG03654.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.419-3239C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564284 | |||||||
| chr3:111564468 | TA | T | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-3050delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 111564468 | ||||||
| chr3:111564503 | C | T | 21 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.419-3020C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564503 | |||||||
| chr3:111564535 | A | G | 1 | a0001c0001t0010g0021 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.419-2988A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564535 | |||||||
| chr3:111564594 | G | C | 19 | a0001c0001t0001g0178 a0001c0001t0001g0187 a0001c0001t0001g0193 others(16): Show |
19 | HG00738.hp1 HG01074.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.419-2929G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564594 | |||||||
| chr3:111564682 | T | A | 7 | a0001c0001t0001g0269 a0001c0001t0001g0285 a0001c0001t0007g0011 others(4): Show |
8 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-2841T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564682 | |||||||
| chr3:111564708 | G | A | 7 | a0001c0001t0001g0269 a0001c0001t0001g0285 a0001c0001t0007g0011 others(4): Show |
8 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-2815G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564708 | |||||||
| chr3:111564881 | G | A | 1 | a0006c0008t0001g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.419-2642G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111564881 | |||||||
| chr3:111565077 | G | A | 2 | a0001c0001t0004g0142 a0001c0001t0004g0143 |
2 | HG00735.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.419-2446G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565077 | |||||||
| chr3:111565264 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.419-2259C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565264 | |||||||
| chr3:111565565 | G | A | 7 | a0001c0001t0001g0178 a0001c0001t0001g0197 a0001c0001t0001g0200 others(4): Show |
7 | HG00738.hp1 HG01074.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.419-1958G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565565 | |||||||
| chr3:111565565 | G | T | 2 | a0001c0001t0002g0043 a0001c0001t0020g0044 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.419-1958G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565565 | |||||||
| chr3:111565614 | G | T | 22 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0030 others(19): Show |
23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.419-1909G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565614 | |||||||
| chr3:111565648 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.419-1875T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565648 | |||||||
| chr3:111565714 | T | G | 22 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0030 others(19): Show |
23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.419-1809T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565714 | |||||||
| chr3:111565898 | T | C | 22 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0030 others(19): Show |
23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.419-1625T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565898 | |||||||
| chr3:111565999 | A | G | 2 | a0001c0003t0001g0022 a0001c0003t0001g0144 |
2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.419-1524A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111565999 | |||||||
| chr3:111566017 | T | A | 91 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0172 others(88): Show |
93 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.419-1506T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566017 | |||||||
| chr3:111566039 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.419-1484T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566039 | |||||||
| chr3:111566167 | C | T | 22 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0030 others(19): Show |
23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.419-1356C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566167 | |||||||
| chr3:111566168 | G | A | 3 | a0001c0001t0001g0094 a0001c0011t0023g0038 a0001c0014t0001g0095 |
3 | HG01255.hp1 HG01358.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.419-1355G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566168 | |||||||
| chr3:111566204 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.419-1319T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566204 | |||||||
| chr3:111566247 | T | G | 10 | a0001c0001t0001g0153 a0001c0001t0001g0158 a0001c0001t0001g0159 others(7): Show |
10 | HG01071.hp2 HG01099.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.419-1276T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566247 | |||||||
| chr3:111566287 | G | A | 22 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0030 others(19): Show |
23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.419-1236G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566287 | |||||||
| chr3:111566672 | A | T | 22 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0030 others(19): Show |
23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.419-851A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566672 | |||||||
| chr3:111566970 | T | A | 22 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0030 others(19): Show |
23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.419-553T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566970 | |||||||
| chr3:111566976 | C | A | 7 | a0001c0001t0001g0269 a0001c0001t0001g0285 a0001c0001t0007g0011 others(4): Show |
8 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-547C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111566976 | |||||||
| chr3:111567029 | C | T | 53 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0153 others(50): Show |
53 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.419-494C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111567029 | |||||||
| chr3:111567030 | G | T | 1 | a0001c0001t0003g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.419-493G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111567030 | |||||||
| chr3:111567272 | C | G | 184 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0035 others(181): Show |
188 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.419-251C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 2/13 | chr3 | 111567272 | |||||||
| chr3:111567912 | G | A | 22 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0030 others(19): Show |
23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.543+265G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111567912 | |||||||
| chr3:111568042 | T | G | 21 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0030 others(18): Show |
22 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.543+395T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111568042 | |||||||
| chr3:111568378 | C | T | 22 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0030 others(19): Show |
23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.543+731C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111568378 | |||||||
| chr3:111568401 | A | C | 22 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0030 others(19): Show |
23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.543+754A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111568401 | |||||||
| chr3:111568715 | G | T | 2 | a0001c0001t0002g0247 a0001c0001t0002g0248 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.543+1068G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111568715 | |||||||
| chr3:111568724 | C | T | 5 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0040 others(2): Show |
5 | HG02572.hp2 HG02895.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+1077C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111568724 | |||||||
| chr3:111568733 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.543+1086C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111568733 | |||||||
| chr3:111569022 | T | C | 1 | a0001c0001t0002g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.543+1375T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111569022 | |||||||
| chr3:111569215 | T | C | 2 | a0001c0001t0004g0142 a0001c0001t0004g0143 |
2 | HG00735.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.543+1568T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111569215 | |||||||
| chr3:111569352 | C | T | 22 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0030 others(19): Show |
23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.543+1705C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111569352 | |||||||
| chr3:111569607 | C | T | 1 | a0001c0001t0003g0070 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.543+1960C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111569607 | |||||||
| chr3:111569666 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.543+2019C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111569666 | |||||||
| chr3:111569692 | C | T | 50 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0115 others(47): Show |
50 | HG00738.hp1 HG01071.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.543+2045C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111569692 | |||||||
| chr3:111569745 | G | A | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.543+2098G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111569745 | |||||||
| chr3:111569849 | A | AC | 7 | a0001c0001t0001g0159 a0001c0001t0001g0231 a0001c0001t0001g0261 others(4): Show |
7 | HG00621.hp2 HG02145.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+2207dupC | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 111569849 | ||||||
| chr3:111569989 | T | A | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.543+2342T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111569989 | |||||||
| chr3:111570034 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.543+2387C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570034 | |||||||
| chr3:111570388 | G | A | 3 | a0001c0001t0005g0049 a0001c0001t0005g0072 a0001c0001t0005g0073 |
3 | HG01106.hp1 HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.543+2741G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570388 | |||||||
| chr3:111570473 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.543+2826G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570473 | |||||||
| chr3:111570490 | G | A | 22 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0030 others(19): Show |
23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.543+2843G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570490 | |||||||
| chr3:111570641 | G | A | 2 | a0001c0001t0002g0043 a0001c0001t0020g0044 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.543+2994G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570641 | |||||||
| chr3:111570713 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.543+3066A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570713 | |||||||
| chr3:111570850 | G | A | 1 | a0001c0001t0003g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.543+3203G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570850 | |||||||
| chr3:111570946 | T | C | 29 | a0001c0001t0002g0016 a0001c0001t0002g0037 a0001c0001t0003g0003 others(26): Show |
31 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.543+3299T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570946 | |||||||
| chr3:111570980 | A | G | 183 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0045 others(180): Show |
187 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.543+3333A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111570980 | |||||||
| chr3:111571141 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(53): Show |
63 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.543+3494C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571141 | |||||||
| chr3:111571201 | T | G | 3 | a0001c0001t0001g0259 a0001c0001t0002g0260 a0001c0001t0014g0061 |
3 | HG00438.hp1 HG03453.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.543+3554T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571201 | |||||||
| chr3:111571220 | GT | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(217): Show |
230 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.543+3585delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 111571220 | ||||||
| chr3:111571221 | T | G | 1 | a0002c0002t0006g0029 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.543+3574T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571221 | |||||||
| chr3:111571231 | T | G | 1 | a0001c0001t0002g0037 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.543+3584T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571231 | |||||||
| chr3:111571260 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.543+3613C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571260 | |||||||
| chr3:111571284 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.543+3637T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571284 | |||||||
| chr3:111571292 | A | C | 1 | a0001c0001t0002g0037 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.543+3645A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571292 | |||||||
| chr3:111571304 | A | T | 1 | a0001c0001t0002g0086 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.543+3657A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571304 | |||||||
| chr3:111571375 | A | G | 1 | a0001c0001t0002g0016 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.543+3728A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571375 | |||||||
| chr3:111571565 | G | T | 5 | a0001c0001t0002g0016 a0001c0001t0003g0003 a0001c0001t0003g0013 others(2): Show |
6 | HG02809.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+3918G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111571565 | |||||||
| chr3:111572194 | A | C | 1 | a0001c0001t0002g0086 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.543+4547A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572194 | |||||||
| chr3:111572197 | T | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0120 others(3): Show |
9 | HG02027.hp1 HG02074.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.543+4550T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572197 | |||||||
| chr3:111572235 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.543+4588A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572235 | |||||||
| chr3:111572256 | A | G | 1 | a0002c0002t0002g0019 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.543+4609A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572256 | |||||||
| chr3:111572285 | C | T | 2 | a0001c0001t0001g0187 a0001c0001t0021g0063 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.543+4638C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572285 | |||||||
| chr3:111572491 | A | T | 1 | a0002c0002t0002g0171 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.543+4844A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572491 | |||||||
| chr3:111572492 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.543+4845T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572492 | |||||||
| chr3:111572499 | G | T | 1 | a0001c0001t0002g0074 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.543+4852G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572499 | |||||||
| chr3:111572582 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.543+4935A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572582 | |||||||
| chr3:111572617 | A | C | 1 | a0001c0001t0008g0185 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.543+4970A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572617 | |||||||
| chr3:111572848 | C | T | 159 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0045 others(156): Show |
162 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.543+5201C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572848 | |||||||
| chr3:111572924 | C | T | 1 | a0001c0001t0002g0140 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.543+5277C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572924 | |||||||
| chr3:111572952 | C | T | 1 | a0002c0002t0002g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.543+5305C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572952 | |||||||
| chr3:111572966 | A | G | 1 | a0001c0001t0014g0061 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.543+5319A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111572966 | |||||||
| chr3:111573056 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.543+5409G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111573056 | |||||||
| chr3:111573099 | C | T | 161 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0045 others(158): Show |
164 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.543+5452C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111573099 | |||||||
| chr3:111573254 | A | G | 1 | a0001c0001t0020g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.543+5607A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111573254 | |||||||
| chr3:111573369 | A | T | 1 | a0001c0001t0001g0258 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.544-5658A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111573369 | |||||||
| chr3:111573398 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0004g0157 |
2 | HG02738.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.544-5629C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111573398 | |||||||
| chr3:111573746 | T | A | 1 | a0001c0001t0002g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.544-5281T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111573746 | |||||||
| chr3:111573930 | G | T | 2 | a0001c0001t0001g0216 a0001c0001t0016g0087 |
2 | NA18951.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.544-5097G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111573930 | |||||||
| chr3:111573936 | A | G | 1 | a0001c0001t0008g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.544-5091A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111573936 | |||||||
| chr3:111574015 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.544-5012T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574015 | |||||||
| chr3:111574032 | G | A | 6 | a0001c0001t0001g0127 a0001c0001t0001g0234 a0001c0001t0008g0128 others(3): Show |
6 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-4995G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574032 | |||||||
| chr3:111574196 | G | A | 1 | a0001c0001t0002g0286 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.544-4831G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574196 | |||||||
| chr3:111574228 | C | T | 10 | a0001c0001t0001g0058 a0001c0001t0002g0055 a0001c0001t0002g0056 others(7): Show |
10 | HG01192.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-4799C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574228 | |||||||
| chr3:111574243 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.544-4784G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574243 | |||||||
| chr3:111574348 | A | G | 3 | a0001c0001t0005g0049 a0001c0001t0005g0072 a0001c0001t0005g0073 |
3 | HG01106.hp1 HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.544-4679A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574348 | |||||||
| chr3:111574763 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.544-4264T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574763 | |||||||
| chr3:111574776 | A | C | 52 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0115 others(49): Show |
52 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.544-4251A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574776 | |||||||
| chr3:111574778 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.544-4249G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574778 | |||||||
| chr3:111574788 | A | AT | 55 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0115 others(52): Show |
55 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.544-4227dupT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 111574788 | ||||||
| chr3:111574830 | C | T | 2 | a0001c0001t0002g0037 a0001c0001t0014g0061 |
2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.544-4197C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574830 | |||||||
| chr3:111574922 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.544-4105C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111574922 | |||||||
| chr3:111574951 | CT | C | 160 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0045 others(157): Show |
163 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.544-4062delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 111574951 | ||||||
| chr3:111575013 | T | G | 1 | a0001c0001t0004g0142 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.544-4014T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111575013 | |||||||
| chr3:111575050 | T | G | 1 | a0001c0001t0001g0180 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.544-3977T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111575050 | |||||||
| chr3:111575154 | G | A | 1 | a0005c0007t0002g0023 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.544-3873G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111575154 | |||||||
| chr3:111575192 | G | C | 6 | a0001c0001t0002g0016 a0001c0001t0003g0003 a0001c0001t0003g0013 others(3): Show |
7 | HG02809.hp1 HG02818.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.544-3835G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111575192 | |||||||
| chr3:111575520 | A | G | 21 | a0001c0001t0001g0054 a0001c0001t0001g0132 a0001c0001t0001g0136 others(18): Show |
21 | HG02145.hp1 HG02486.hp2 HG02523.hp2 others(18): Show |
intron_variant | MODIFIER | c.544-3507A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111575520 | |||||||
| chr3:111575527 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(249): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.544-3500C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111575527 | |||||||
| chr3:111575969 | T | C | 1 | a0001c0001t0002g0088 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.544-3058T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111575969 | |||||||
| chr3:111575972 | A | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(279): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.544-3055A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111575972 | |||||||
| chr3:111576400 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.544-2627T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111576400 | |||||||
| chr3:111576446 | G | T | 2 | a0001c0003t0001g0022 a0001c0003t0001g0144 |
2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.544-2581G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111576446 | |||||||
| chr3:111576478 | A | G | 1 | a0001c0001t0001g0283 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.544-2549A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111576478 | |||||||
| chr3:111576495 | C | A | 1 | a0001c0001t0001g0172 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.544-2532C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111576495 | |||||||
| chr3:111576974 | C | T | 1 | a0002c0002t0002g0173 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.544-2053C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111576974 | |||||||
| chr3:111577000 | A | G | 1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.544-2027A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111577000 | |||||||
| chr3:111577341 | G | T | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.544-1686G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111577341 | |||||||
| chr3:111577348 | G | A | 1 | a0002c0002t0002g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.544-1679G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111577348 | |||||||
| chr3:111577907 | C | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(43): Show |
52 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.544-1120C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111577907 | |||||||
| chr3:111578116 | C | G | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.544-911C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578116 | |||||||
| chr3:111578177 | G | A | 2 | a0001c0001t0003g0003 a0001c0001t0003g0018 |
3 | HG02809.hp1 HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.544-850G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578177 | |||||||
| chr3:111578267 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(223): Show |
237 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.544-760A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578267 | |||||||
| chr3:111578288 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0002g0037 |
2 | HG03098.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.544-739C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578288 | |||||||
| chr3:111578302 | G | A | 7 | a0001c0001t0001g0269 a0001c0001t0001g0285 a0001c0001t0007g0011 others(4): Show |
8 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-725G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578302 | |||||||
| chr3:111578449 | T | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(223): Show |
237 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.544-578T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578449 | |||||||
| chr3:111578493 | C | T | 1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.544-534C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578493 | |||||||
| chr3:111578680 | G | A | 3 | a0001c0001t0002g0016 a0001c0001t0002g0074 a0001c0001t0005g0064 |
3 | HG02896.hp2 HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.544-347G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578680 | |||||||
| chr3:111578870 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.544-157A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 3/13 | chr3 | 111578870 | |||||||
| chr3:111579298 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(45): Show |
54 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.751+64A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111579298 | |||||||
| chr3:111579447 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.751+213C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111579447 | |||||||
| chr3:111579698 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.751+464T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111579698 | |||||||
| chr3:111579795 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.751+561T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111579795 | |||||||
| chr3:111579921 | A | G | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.751+687A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111579921 | |||||||
| chr3:111580175 | G | A | 2 | a0002c0002t0001g0034 a0002c0002t0002g0024 |
2 | HG04184.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.751+941G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111580175 | |||||||
| chr3:111580229 | A | G | 6 | a0001c0001t0001g0184 a0001c0001t0001g0203 a0001c0001t0001g0207 others(3): Show |
6 | HG00639.hp2 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.751+995A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111580229 | |||||||
| chr3:111580315 | A | G | 1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.751+1081A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111580315 | |||||||
| chr3:111580327 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.751+1093T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111580327 | |||||||
| chr3:111580460 | CAATT | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(210): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.751+1232_751+1235d others(6): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 111580460 | ||||||
| chr3:111580639 | A | C | 1 | a0001c0001t0003g0068 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.751+1405A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111580639 | |||||||
| chr3:111580673 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.751+1439C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111580673 | |||||||
| chr3:111580764 | G | A | 1 | a0001c0001t0010g0048 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.751+1530G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111580764 | |||||||
| chr3:111580821 | T | G | 6 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0009g0042 others(3): Show |
6 | HG01192.hp2 HG02055.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.751+1587T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111580821 | |||||||
| chr3:111581036 | C | A | 1 | a0001c0001t0012g0010 | 2 | HG02074.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.751+1802C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581036 | |||||||
| chr3:111581060 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.751+1826T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581060 | |||||||
| chr3:111581066 | T | C | 1 | a0001c0001t0002g0134 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.751+1832T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581066 | |||||||
| chr3:111581168 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.751+1934C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581168 | |||||||
| chr3:111581618 | G | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(45): Show |
54 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.751+2384G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581618 | |||||||
| chr3:111581648 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.751+2414C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581648 | |||||||
| chr3:111581741 | T | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0120 others(3): Show |
9 | HG02027.hp1 HG02074.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.751+2507T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581741 | |||||||
| chr3:111581775 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.751+2541G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581775 | |||||||
| chr3:111581850 | C | T | 6 | a0001c0001t0001g0054 a0001c0001t0001g0166 a0001c0001t0001g0167 others(3): Show |
6 | HG02145.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.751+2616C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581850 | |||||||
| chr3:111581928 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(195): Show |
208 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.751+2694G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581928 | |||||||
| chr3:111581975 | C | CATAGGTT others(19): Show |
1 | a0001c0001t0001g0111 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.751+2743_751+2768d others(28): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 111581975 | ||||||
| chr3:111581984 | A | G | 15 | a0001c0001t0001g0222 a0001c0001t0001g0231 a0001c0001t0001g0239 others(12): Show |
15 | HG00280.hp1 HG01496.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.751+2750A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111581984 | |||||||
| chr3:111582309 | T | C | 1 | a0001c0001t0002g0016 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.752-3014T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111582309 | |||||||
| chr3:111582398 | G | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0120 others(3): Show |
9 | HG02027.hp1 HG02074.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.752-2925G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111582398 | |||||||
| chr3:111582611 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.752-2712G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111582611 | |||||||
| chr3:111582966 | T | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(236): Show |
251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.752-2357T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111582966 | |||||||
| chr3:111582996 | A | C | 1 | a0001c0001t0002g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.752-2327A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111582996 | |||||||
| chr3:111583045 | A | C | 6 | a0001c0001t0002g0043 a0001c0001t0002g0145 a0001c0001t0003g0050 others(3): Show |
6 | HG02109.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.752-2278A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583045 | |||||||
| chr3:111583064 | C | T | 6 | a0001c0001t0002g0043 a0001c0001t0002g0145 a0001c0001t0003g0050 others(3): Show |
6 | HG02109.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.752-2259C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583064 | |||||||
| chr3:111583129 | T | C | 2 | a0001c0001t0002g0016 a0001c0001t0002g0074 |
2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.752-2194T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583129 | |||||||
| chr3:111583292 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(236): Show |
251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.752-2031T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583292 | |||||||
| chr3:111583381 | G | A | 13 | a0001c0001t0002g0065 a0001c0001t0002g0085 a0002c0002t0001g0027 others(10): Show |
14 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.752-1942G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583381 | |||||||
| chr3:111583459 | C | T | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.752-1864C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583459 | |||||||
| chr3:111583637 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0002g0016 a0001c0001t0002g0074 |
3 | HG02896.hp2 HG02970.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.752-1686C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583637 | |||||||
| chr3:111583769 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.752-1554G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583769 | |||||||
| chr3:111583848 | G | C | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.752-1475G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583848 | |||||||
| chr3:111583874 | G | A | 2 | a0001c0001t0010g0048 a0001c0001t0010g0100 |
2 | NA19077.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.752-1449G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583874 | |||||||
| chr3:111583944 | G | A | 19 | a0001c0001t0001g0047 a0001c0001t0001g0153 a0001c0001t0001g0159 others(16): Show |
19 | HG01071.hp2 HG01099.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.752-1379G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583944 | |||||||
| chr3:111583959 | T | C | 2 | a0001c0003t0001g0022 a0001c0003t0001g0144 |
2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.752-1364T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583959 | |||||||
| chr3:111583965 | C | A | 1 | a0001c0001t0001g0012 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.752-1358C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583965 | |||||||
| chr3:111583975 | G | T | 141 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0081 others(138): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.752-1348G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111583975 | |||||||
| chr3:111584063 | G | T | 2 | a0001c0001t0002g0016 a0001c0001t0002g0074 |
2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.752-1260G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584063 | |||||||
| chr3:111584064 | C | G | 2 | a0001c0001t0002g0016 a0001c0001t0002g0074 |
2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.752-1259C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584064 | |||||||
| chr3:111584078 | C | G | 1 | a0001c0001t0003g0194 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.752-1245C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584078 | |||||||
| chr3:111584387 | C | T | 11 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0040 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.752-936C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584387 | |||||||
| chr3:111584430 | G | A | 11 | a0001c0001t0001g0127 a0001c0001t0001g0234 a0001c0001t0003g0003 others(8): Show |
12 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.752-893G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584430 | |||||||
| chr3:111584473 | G | C | 6 | a0001c0001t0001g0127 a0001c0001t0001g0234 a0001c0001t0008g0128 others(3): Show |
6 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.752-850G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584473 | |||||||
| chr3:111584538 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.752-785T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584538 | |||||||
| chr3:111584547 | C | G | 1 | a0002c0002t0002g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.752-776C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584547 | |||||||
| chr3:111584631 | G | A | 17 | a0001c0001t0001g0047 a0001c0001t0001g0153 a0001c0001t0001g0159 others(14): Show |
17 | HG01071.hp2 HG01099.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.752-692G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584631 | |||||||
| chr3:111584644 | C | T | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.752-679C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584644 | |||||||
| chr3:111584645 | G | A | 1 | a0002c0002t0002g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.752-678G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584645 | |||||||
| chr3:111584647 | G | A | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(259): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.752-676G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584647 | |||||||
| chr3:111584741 | G | A | 8 | a0001c0001t0001g0127 a0001c0001t0001g0221 a0001c0001t0001g0234 others(5): Show |
8 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.752-582G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584741 | |||||||
| chr3:111584820 | A | G | 1 | a0001c0001t0002g0139 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.752-503A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584820 | |||||||
| chr3:111584966 | C | G | 1 | a0001c0001t0001g0006 | 2 | NA19004.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.752-357C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584966 | |||||||
| chr3:111584994 | T | G | 14 | a0001c0001t0002g0037 a0001c0001t0002g0065 a0001c0001t0002g0085 others(11): Show |
15 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.752-329T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111584994 | |||||||
| chr3:111585116 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.752-207A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111585116 | |||||||
| chr3:111585228 | A | G | 2 | a0001c0001t0001g0213 a0001c0001t0001g0215 |
2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.752-95A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 4/13 | chr3 | 111585228 | |||||||
| chr3:111585479 | G | A | 1 | a0001c0001t0012g0010 | 2 | HG02074.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.807+101G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111585479 | |||||||
| chr3:111585613 | G | GA | 7 | a0001c0001t0001g0127 a0001c0001t0001g0234 a0001c0001t0003g0046 others(4): Show |
7 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(4): Show |
intron_variant | MODIFIER | c.807+244dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111585613 | ||||||
| chr3:111585642 | C | T | 2 | a0001c0003t0001g0022 a0001c0003t0001g0144 |
2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.807+264C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111585642 | |||||||
| chr3:111585650 | T | C | 11 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0040 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.807+272T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111585650 | |||||||
| chr3:111585748 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.807+370G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111585748 | |||||||
| chr3:111585787 | T | C | 102 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0081 others(99): Show |
105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.807+409T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111585787 | |||||||
| chr3:111585967 | C | T | 1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.807+589C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111585967 | |||||||
| chr3:111586003 | C | T | 4 | a0001c0001t0001g0132 a0001c0001t0002g0007 a0001c0001t0003g0007 others(1): Show |
4 | HG03491.hp1 HG03492.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.807+625C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111586003 | |||||||
| chr3:111586030 | A | G | 1 | a0006c0008t0001g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.807+652A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111586030 | |||||||
| chr3:111586307 | G | T | 1 | a0001c0001t0001g0242 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.807+929G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111586307 | |||||||
| chr3:111586620 | G | A | 25 | a0001c0001t0001g0014 a0001c0001t0001g0132 a0001c0001t0002g0007 others(22): Show |
25 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.807+1242G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111586620 | |||||||
| chr3:111586735 | C | G | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0007c0009t0001g0241 |
3 | HG02132.hp1 NA18999.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.807+1357C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111586735 | |||||||
| chr3:111586780 | C | G | 2 | a0001c0001t0002g0043 a0001c0001t0020g0044 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.807+1402C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111586780 | |||||||
| chr3:111586818 | A | G | 1 | a0001c0001t0005g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.807+1440A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111586818 | |||||||
| chr3:111587009 | C | T | 11 | a0001c0001t0001g0127 a0001c0001t0001g0234 a0001c0001t0003g0003 others(8): Show |
12 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.807+1631C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587009 | |||||||
| chr3:111587033 | T | G | 3 | a0001c0001t0005g0049 a0001c0001t0005g0072 a0001c0001t0005g0073 |
3 | HG01106.hp1 HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.807+1655T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587033 | |||||||
| chr3:111587065 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.807+1687G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587065 | |||||||
| chr3:111587100 | C | T | 1 | a0001c0001t0016g0087 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.807+1722C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587100 | |||||||
| chr3:111587167 | A | T | 1 | a0001c0001t0002g0225 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.807+1789A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587167 | |||||||
| chr3:111587499 | G | A | 1 | a0001c0001t0022g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.807+2121G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587499 | |||||||
| chr3:111587513 | G | A | 25 | a0001c0001t0001g0014 a0001c0001t0001g0132 a0001c0001t0002g0007 others(22): Show |
25 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.807+2135G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587513 | |||||||
| chr3:111587540 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.807+2162T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587540 | |||||||
| chr3:111587635 | G | C | 25 | a0001c0001t0001g0014 a0001c0001t0001g0132 a0001c0001t0002g0007 others(22): Show |
25 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.807+2257G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587635 | |||||||
| chr3:111587657 | C | T | 7 | a0001c0001t0001g0127 a0001c0001t0001g0234 a0001c0001t0003g0046 others(4): Show |
7 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(4): Show |
intron_variant | MODIFIER | c.807+2279C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587657 | |||||||
| chr3:111587658 | G | A | 3 | a0002c0002t0001g0027 a0002c0002t0002g0025 a0002c0002t0002g0026 |
3 | HG01952.hp2 NA19058.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.807+2280G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587658 | |||||||
| chr3:111587689 | G | A | 1 | a0001c0001t0002g0119 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.807+2311G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587689 | |||||||
| chr3:111587694 | C | T | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(250): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.807+2316C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587694 | |||||||
| chr3:111587695 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.807+2317C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587695 | |||||||
| chr3:111587713 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.807+2335G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587713 | |||||||
| chr3:111587853 | C | G | 3 | a0001c0001t0002g0145 a0001c0001t0003g0050 a0001c0001t0003g0146 |
3 | HG02109.hp2 HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.807+2475C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587853 | |||||||
| chr3:111587993 | C | A | 4 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0015 others(1): Show |
5 | HG02809.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.807+2615C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111587993 | |||||||
| chr3:111588199 | A | G | 94 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0081 others(91): Show |
96 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.807+2821A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588199 | |||||||
| chr3:111588378 | G | A | 3 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 |
3 | HG02922.hp1 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.807+3000G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588378 | |||||||
| chr3:111588432 | C | G | 101 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0081 others(98): Show |
104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.807+3054C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588432 | |||||||
| chr3:111588471 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.807+3093G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588471 | |||||||
| chr3:111588509 | C | G | 19 | a0001c0001t0001g0127 a0001c0001t0001g0234 a0001c0001t0003g0003 others(16): Show |
20 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.807+3131C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588509 | |||||||
| chr3:111588814 | A | T | 1 | a0001c0001t0022g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.807+3436A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588814 | |||||||
| chr3:111588931 | G | C | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.807+3553G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588931 | |||||||
| chr3:111588953 | T | C | 1 | a0002c0002t0002g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.807+3575T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588953 | |||||||
| chr3:111588954 | CT | C | 7 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0251 others(4): Show |
7 | HG00733.hp2 HG00735.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.807+3591delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111588954 | ||||||
| chr3:111588954 | CTT | C | 41 | a0001c0001t0001g0014 a0001c0001t0001g0132 a0001c0001t0002g0007 others(38): Show |
42 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.807+3590_807+3591d others(4): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111588954 | ||||||
| chr3:111588957 | T | G | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.807+3579T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111588957 | |||||||
| chr3:111589151 | C | T | 1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.807+3773C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589151 | |||||||
| chr3:111589172 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(258): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.807+3794A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589172 | |||||||
| chr3:111589193 | G | A | 12 | a0001c0001t0001g0127 a0001c0001t0001g0234 a0001c0001t0003g0003 others(9): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.807+3815G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589193 | |||||||
| chr3:111589196 | C | T | 6 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
6 | HG02257.hp2 HG02572.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.807+3818C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589196 | |||||||
| chr3:111589250 | T | A | 25 | a0001c0001t0001g0014 a0001c0001t0001g0132 a0001c0001t0002g0007 others(22): Show |
25 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.807+3872T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589250 | |||||||
| chr3:111589552 | G | C | 5 | a0001c0001t0001g0054 a0001c0001t0001g0166 a0001c0001t0001g0167 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.807+4174G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589552 | |||||||
| chr3:111589721 | A | G | 12 | a0001c0001t0001g0127 a0001c0001t0001g0234 a0001c0001t0003g0003 others(9): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.807+4343A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589721 | |||||||
| chr3:111589887 | A | T | 28 | a0001c0001t0001g0047 a0001c0001t0001g0111 a0001c0001t0001g0153 others(25): Show |
29 | HG00438.hp2 HG00609.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.807+4509A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589887 | |||||||
| chr3:111589897 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.807+4519C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589897 | |||||||
| chr3:111589903 | C | T | 23 | a0001c0001t0001g0014 a0001c0001t0001g0132 a0001c0001t0002g0007 others(20): Show |
23 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.807+4525C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589903 | |||||||
| chr3:111589937 | A | T | 1 | a0001c0001t0001g0242 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.807+4559A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111589937 | |||||||
| chr3:111590132 | C | T | 1 | a0001c0001t0006g0199 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.807+4754C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590132 | |||||||
| chr3:111590249 | C | T | 1 | a0006c0008t0001g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.807+4871C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590249 | |||||||
| chr3:111590377 | A | G | 95 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0081 others(92): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.807+4999A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590377 | |||||||
| chr3:111590543 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.807+5165C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590543 | |||||||
| chr3:111590683 | T | A | 1 | a0001c0001t0001g0091 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.807+5305T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590683 | |||||||
| chr3:111590825 | G | C | 17 | a0001c0001t0001g0132 a0001c0001t0002g0007 a0001c0001t0002g0089 others(14): Show |
17 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.807+5447G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590825 | |||||||
| chr3:111590832 | A | C | 41 | a0001c0001t0001g0014 a0001c0001t0001g0132 a0001c0001t0002g0007 others(38): Show |
42 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.807+5454A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590832 | |||||||
| chr3:111590909 | C | T | 1 | a0001c0001t0003g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.807+5531C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590909 | |||||||
| chr3:111590938 | C | T | 22 | a0001c0001t0001g0014 a0001c0001t0001g0132 a0001c0001t0002g0007 others(19): Show |
22 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.807+5560C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111590938 | |||||||
| chr3:111591021 | C | T | 22 | a0001c0001t0001g0014 a0001c0001t0001g0132 a0001c0001t0002g0007 others(19): Show |
22 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.807+5643C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111591021 | |||||||
| chr3:111591022 | A | T | 14 | a0001c0001t0002g0037 a0001c0001t0002g0065 a0001c0001t0002g0085 others(11): Show |
15 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.807+5644A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111591022 | |||||||
| chr3:111591098 | G | A | 1 | a0001c0001t0014g0061 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.807+5720G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111591098 | |||||||
| chr3:111591150 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.807+5772G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111591150 | |||||||
| chr3:111591189 | G | A | 1 | a0007c0009t0001g0241 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.807+5811G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111591189 | |||||||
| chr3:111591368 | T | TC | 18 | a0001c0001t0001g0250 a0001c0001t0002g0037 a0001c0001t0002g0145 others(15): Show |
19 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.807+5991dupC | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111591368 | ||||||
| chr3:111591370 | T | C | 108 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0081 others(105): Show |
111 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.807+5992T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111591370 | |||||||
| chr3:111591371 | T | A | 18 | a0001c0001t0001g0250 a0001c0001t0002g0037 a0001c0001t0002g0145 others(15): Show |
19 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.807+5993T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111591371 | |||||||
| chr3:111591371 | T | TA | 13 | a0001c0001t0002g0089 a0001c0001t0002g0137 a0001c0001t0003g0003 others(10): Show |
14 | HG02055.hp1 HG02647.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.807+6017dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111591371 | ||||||
| chr3:111591371 | T | TAA | 93 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0045 others(90): Show |
96 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.807+6016_807+6017d others(4): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111591371 | ||||||
| chr3:111591371 | T | TAAA | 14 | a0001c0001t0001g0113 a0001c0001t0001g0222 a0001c0001t0001g0231 others(11): Show |
14 | HG00280.hp1 HG01496.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.807+6015_807+6017d others(5): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111591371 | ||||||
| chr3:111591371 | TA | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(48): Show |
57 | HG00609.hp1 HG00621.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.807+6017delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111591371 | ||||||
| chr3:111591371 | TAA | T | 34 | a0001c0001t0001g0047 a0001c0001t0001g0054 a0001c0001t0001g0098 others(31): Show |
35 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.807+6016_807+6017d others(4): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111591371 | ||||||
| chr3:111591939 | C | A | 1 | a0001c0001t0007g0268 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.808-6181C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111591939 | |||||||
| chr3:111592141 | A | C | 7 | a0001c0001t0001g0127 a0001c0001t0001g0234 a0001c0001t0003g0046 others(4): Show |
7 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(4): Show |
intron_variant | MODIFIER | c.808-5979A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111592141 | |||||||
| chr3:111592328 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.808-5792A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111592328 | |||||||
| chr3:111592567 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.808-5553A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111592567 | |||||||
| chr3:111592573 | GTC | G | 13 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0040 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.808-5541_808-5540d others(4): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111592573 | ||||||
| chr3:111592610 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0004g0151 |
2 | HG03654.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.808-5510A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111592610 | |||||||
| chr3:111592980 | A | G | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.808-5140A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111592980 | |||||||
| chr3:111593296 | T | C | 1 | a0001c0001t0004g0160 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.808-4824T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111593296 | |||||||
| chr3:111593331 | A | G | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.808-4789A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111593331 | |||||||
| chr3:111593339 | G | A | 3 | a0001c0003t0001g0022 a0001c0003t0001g0144 a0003c0006t0005g0164 |
3 | HG02717.hp2 HG02896.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.808-4781G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111593339 | |||||||
| chr3:111593458 | T | C | 15 | a0001c0001t0001g0132 a0001c0001t0002g0007 a0001c0001t0002g0089 others(12): Show |
15 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.808-4662T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111593458 | |||||||
| chr3:111593497 | C | G | 1 | a0001c0001t0004g0147 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.808-4623C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111593497 | |||||||
| chr3:111593598 | A | G | 4 | a0001c0001t0002g0145 a0001c0001t0003g0050 a0001c0001t0003g0146 others(1): Show |
4 | HG02109.hp2 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.808-4522A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111593598 | |||||||
| chr3:111593966 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.808-4154C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111593966 | |||||||
| chr3:111594118 | A | T | 14 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0040 others(11): Show |
14 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.808-4002A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111594118 | |||||||
| chr3:111594233 | G | A | 1 | a0002c0002t0002g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.808-3887G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111594233 | |||||||
| chr3:111594495 | C | A | 1 | a0001c0001t0001g0200 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.808-3625C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111594495 | |||||||
| chr3:111594572 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.808-3548C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111594572 | |||||||
| chr3:111594610 | T | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(218): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.808-3510T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111594610 | |||||||
| chr3:111594682 | G | A | 1 | a0001c0001t0003g0015 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.808-3438G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111594682 | |||||||
| chr3:111594695 | G | C | 1 | a0001c0004t0008g0235 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.808-3425G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111594695 | |||||||
| chr3:111595007 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(253): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.808-3113C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111595007 | |||||||
| chr3:111595281 | G | A | 15 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0040 others(12): Show |
15 | HG02145.hp1 HG02257.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.808-2839G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111595281 | |||||||
| chr3:111595490 | C | T | 1 | a0002c0002t0002g0024 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.808-2630C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111595490 | |||||||
| chr3:111595524 | C | G | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.808-2596C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111595524 | |||||||
| chr3:111595662 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.808-2458A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111595662 | |||||||
| chr3:111595794 | G | C | 1 | a0001c0001t0010g0100 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.808-2326G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111595794 | |||||||
| chr3:111596151 | G | A | 1 | a0001c0001t0016g0087 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.808-1969G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111596151 | |||||||
| chr3:111596161 | C | CA | 93 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0081 others(90): Show |
96 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.808-1952dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111596161 | ||||||
| chr3:111596219 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1901G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111596219 | |||||||
| chr3:111596268 | G | GA | 4 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0101 others(1): Show |
6 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.808-1844dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111596268 | ||||||
| chr3:111596350 | A | C | 1 | a0001c0001t0022g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.808-1770A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111596350 | |||||||
| chr3:111596463 | G | A | 2 | a0001c0001t0011g0170 a0001c0001t0011g0277 |
2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.808-1657G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111596463 | |||||||
| chr3:111596615 | A | C | 1 | a0001c0001t0001g0098 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.808-1505A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111596615 | |||||||
| chr3:111596793 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1327T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111596793 | |||||||
| chr3:111596958 | A | G | 11 | a0001c0001t0001g0222 a0001c0001t0001g0231 a0001c0001t0001g0239 others(8): Show |
11 | HG01496.hp2 HG02132.hp1 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.808-1162A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111596958 | |||||||
| chr3:111597517 | G | A | 16 | a0001c0001t0001g0234 a0001c0001t0003g0003 a0001c0001t0003g0013 others(13): Show |
17 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.808-603G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111597517 | |||||||
| chr3:111597571 | C | T | 3 | a0001c0001t0003g0146 a0001c0001t0014g0061 a0001c0001t0020g0044 |
3 | HG02559.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.808-549C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111597571 | |||||||
| chr3:111597651 | G | A | 7 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0238 others(4): Show |
7 | HG02083.hp1 HG02523.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.808-469G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111597651 | |||||||
| chr3:111597804 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.808-316T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111597804 | |||||||
| chr3:111597954 | G | A | 5 | a0001c0001t0001g0221 a0001c0001t0001g0245 a0001c0001t0001g0253 others(2): Show |
5 | HG00099.hp2 HG00323.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.808-166G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | chr3 | 111597954 | |||||||
| chr3:111598039 | C | CTTATG | 93 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0039 others(90): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.808-77_808-76insGT others(3): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 111598039 | ||||||
| chr3:111598401 | A | G | 1 | a0001c0001t0004g0179 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.898+191A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111598401 | |||||||
| chr3:111598424 | A | G | 1 | a0002c0002t0002g0019 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.898+214A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111598424 | |||||||
| chr3:111598863 | G | C | 5 | a0001c0001t0001g0054 a0001c0001t0001g0166 a0001c0001t0001g0167 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.898+653G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111598863 | |||||||
| chr3:111598923 | A | G | 1 | a0001c0001t0007g0263 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.898+713A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111598923 | |||||||
| chr3:111598957 | T | TTTTTA | 18 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0039 others(15): Show |
18 | HG02145.hp1 HG02486.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.898+772_898+776dup others(5): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr3 | 111598957 | ||||||
| chr3:111598957 | T | TTTTTATT others(3): Show |
1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.898+767_898+776dup others(10): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr3 | 111598957 | ||||||
| chr3:111599009 | C | G | 1 | a0001c0001t0001g0238 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.898+799C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599009 | |||||||
| chr3:111599125 | C | T | 5 | a0001c0001t0007g0011 a0001c0001t0007g0141 a0001c0001t0007g0262 others(2): Show |
6 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(3): Show |
intron_variant | MODIFIER | c.898+915C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599125 | |||||||
| chr3:111599158 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(53): Show |
62 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.898+948C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599158 | |||||||
| chr3:111599333 | T | C | 1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.898+1123T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599333 | |||||||
| chr3:111599373 | A | T | 1 | a0001c0001t0003g0194 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.898+1163A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599373 | |||||||
| chr3:111599445 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.898+1235C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599445 | |||||||
| chr3:111599479 | G | A | 2 | a0001c0001t0006g0071 a0001c0001t0006g0075 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.899-1247G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599479 | |||||||
| chr3:111599486 | G | A | 17 | a0001c0001t0001g0234 a0001c0001t0003g0003 a0001c0001t0003g0013 others(14): Show |
18 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.899-1240G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599486 | |||||||
| chr3:111599546 | C | G | 2 | a0001c0001t0006g0071 a0001c0001t0006g0075 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.899-1180C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599546 | |||||||
| chr3:111599677 | C | T | 89 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0081 others(86): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.899-1049C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599677 | |||||||
| chr3:111599678 | G | A | 1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.899-1048G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599678 | |||||||
| chr3:111599865 | T | G | 7 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0005g0041 others(4): Show |
7 | HG01192.hp2 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.899-861T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111599865 | |||||||
| chr3:111600074 | C | T | 1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.899-652C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111600074 | |||||||
| chr3:111600093 | G | A | 3 | a0001c0001t0003g0146 a0001c0001t0014g0061 a0001c0001t0020g0044 |
3 | HG02559.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.899-633G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111600093 | |||||||
| chr3:111600186 | C | T | 8 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0015 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.899-540C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111600186 | |||||||
| chr3:111600515 | C | A | 1 | a0001c0001t0002g0037 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.899-211C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111600515 | |||||||
| chr3:111600517 | C | G | 3 | a0001c0001t0002g0156 a0001c0001t0002g0247 a0001c0001t0002g0248 |
3 | HG01168.hp2 HG01169.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.899-209C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111600517 | |||||||
| chr3:111600631 | A | G | 1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.899-95A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 6/13 | chr3 | 111600631 | |||||||
| chr3:111601055 | A | G | 3 | a0001c0001t0003g0146 a0001c0001t0014g0061 a0001c0001t0020g0044 |
3 | HG02559.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1087+141A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111601055 | |||||||
| chr3:111601232 | T | A | 1 | a0001c0001t0002g0086 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1087+318T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111601232 | |||||||
| chr3:111601256 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1087+342A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111601256 | |||||||
| chr3:111601397 | G | A | 2 | a0001c0001t0003g0209 a0001c0001t0003g0211 |
2 | HG00438.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1087+483G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111601397 | |||||||
| chr3:111601486 | T | C | 1 | a0006c0008t0001g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1087+572T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111601486 | |||||||
| chr3:111601487 | C | T | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1087+573C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111601487 | |||||||
| chr3:111601532 | A | G | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1087+618A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111601532 | |||||||
| chr3:111602418 | A | G | 1 | a0006c0008t0001g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1087+1504A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111602418 | |||||||
| chr3:111602504 | C | A | 1 | a0001c0001t0002g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1087+1590C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111602504 | |||||||
| chr3:111602531 | T | G | 12 | a0001c0001t0002g0057 a0001c0001t0002g0089 a0001c0001t0002g0130 others(9): Show |
12 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1087+1617T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111602531 | |||||||
| chr3:111602572 | C | T | 2 | a0001c0001t0006g0071 a0001c0001t0006g0075 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1087+1658C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111602572 | |||||||
| chr3:111602593 | A | C | 1 | a0001c0001t0001g0125 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1087+1679A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111602593 | |||||||
| chr3:111602689 | A | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0251 |
2 | HG01258.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1087+1775A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111602689 | |||||||
| chr3:111602732 | T | C | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1087+1818T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111602732 | |||||||
| chr3:111602742 | G | A | 7 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0015 others(4): Show |
8 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1087+1828G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111602742 | |||||||
| chr3:111603135 | A | G | 27 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0080 others(24): Show |
29 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.1087+2221A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111603135 | |||||||
| chr3:111603444 | C | CA | 9 | a0001c0001t0001g0045 a0001c0001t0001g0115 a0001c0001t0001g0126 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.1087+2545dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr3 | 111603444 | ||||||
| chr3:111603444 | CA | C | 21 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0039 others(18): Show |
22 | HG01081.hp1 HG02109.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1087+2545delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr3 | 111603444 | ||||||
| chr3:111603567 | A | G | 14 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0015 others(11): Show |
15 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1087+2653A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111603567 | |||||||
| chr3:111603597 | A | T | 6 | a0001c0001t0008g0128 a0001c0001t0008g0185 a0001c0004t0008g0235 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1087+2683A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111603597 | |||||||
| chr3:111603861 | C | G | 1 | a0001c0001t0001g0259 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1088-2839C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111603861 | |||||||
| chr3:111603887 | C | T | 8 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0015 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1088-2813C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111603887 | |||||||
| chr3:111603973 | A | T | 3 | a0001c0001t0002g0089 a0001c0001t0002g0130 a0001c0001t0002g0133 |
3 | HG02735.hp2 HG03710.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1088-2727A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111603973 | |||||||
| chr3:111604007 | A | G | 87 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(84): Show |
90 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1088-2693A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604007 | |||||||
| chr3:111604157 | G | A | 4 | a0001c0001t0001g0111 a0001c0001t0001g0230 a0001c0001t0001g0246 others(1): Show |
4 | HG02015.hp2 HG02080.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.1088-2543G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604157 | |||||||
| chr3:111604172 | C | T | 15 | a0001c0001t0001g0047 a0001c0001t0004g0142 a0001c0001t0004g0143 others(12): Show |
15 | HG00735.hp1 HG01099.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1088-2528C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604172 | |||||||
| chr3:111604206 | A | G | 14 | a0001c0001t0002g0037 a0001c0001t0002g0057 a0001c0001t0002g0089 others(11): Show |
14 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1088-2494A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604206 | |||||||
| chr3:111604257 | C | T | 1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1088-2443C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604257 | |||||||
| chr3:111604264 | A | T | 90 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0081 others(87): Show |
93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1088-2436A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604264 | |||||||
| chr3:111604588 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0018g0131 |
2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1088-2112C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604588 | |||||||
| chr3:111604602 | A | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG01358.hp2 HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1088-2098A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604602 | |||||||
| chr3:111604887 | A | AG | 37 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(34): Show |
39 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1088-1810dupG | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr3 | 111604887 | ||||||
| chr3:111604887 | A | G | 1 | a0001c0001t0002g0086 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1088-1813A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604887 | |||||||
| chr3:111604893 | A | G | 10 | a0001c0001t0005g0041 a0001c0001t0005g0049 a0001c0001t0005g0072 others(7): Show |
10 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1088-1807A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604893 | |||||||
| chr3:111604900 | G | T | 3 | a0001c0001t0009g0051 a0001c0001t0009g0052 a0001c0001t0009g0053 |
3 | HG01192.hp2 HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1088-1800G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604900 | |||||||
| chr3:111604963 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1088-1737A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111604963 | |||||||
| chr3:111605379 | G | A | 5 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088-1321G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111605379 | |||||||
| chr3:111605582 | C | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0251 |
2 | HG01258.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1088-1118C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111605582 | |||||||
| chr3:111605618 | C | A | 6 | a0001c0001t0008g0128 a0001c0001t0008g0185 a0001c0004t0008g0235 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1088-1082C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111605618 | |||||||
| chr3:111605618 | C | T | 1 | a0001c0001t0005g0281 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1088-1082C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111605618 | |||||||
| chr3:111605942 | A | G | 3 | a0001c0001t0001g0218 a0001c0001t0001g0261 a0002c0002t0001g0275 |
3 | HG00621.hp2 NA18953.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1088-758A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111605942 | |||||||
| chr3:111606007 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0206 |
3 | HG02698.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1088-693C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111606007 | |||||||
| chr3:111606124 | C | T | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1088-576C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111606124 | |||||||
| chr3:111606129 | G | A | 5 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0103 others(2): Show |
5 | NA18952.hp2 NA18961.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1088-571G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111606129 | |||||||
| chr3:111606333 | A | T | 1 | a0001c0001t0002g0086 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1088-367A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111606333 | |||||||
| chr3:111606628 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1088-72A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 7/13 | chr3 | 111606628 | |||||||
| chr3:111607548 | C | T | 1 | a0001c0001t0003g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1180+756C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111607548 | |||||||
| chr3:111607691 | G | A | 90 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0081 others(87): Show |
93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1180+899G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111607691 | |||||||
| chr3:111607875 | T | C | 83 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(80): Show |
86 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1180+1083T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111607875 | |||||||
| chr3:111607876 | G | A | 2 | a0003c0006t0003g0163 a0003c0006t0003g0165 |
2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1180+1084G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111607876 | |||||||
| chr3:111608009 | A | G | 3 | a0001c0001t0003g0146 a0001c0001t0014g0061 a0001c0001t0020g0044 |
3 | HG02559.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1180+1217A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111608009 | |||||||
| chr3:111608106 | T | TTGGCTGA others(39): Show |
14 | a0001c0001t0002g0037 a0001c0001t0002g0057 a0001c0001t0002g0089 others(11): Show |
14 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1180+1355_1180+135 others(50): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111608106 | ||||||
| chr3:111608139 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1180+1347T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111608139 | |||||||
| chr3:111608484 | T | G | 1 | a0001c0001t0009g0051 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1180+1692T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111608484 | |||||||
| chr3:111608514 | G | C | 7 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0015 others(4): Show |
8 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180+1722G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111608514 | |||||||
| chr3:111608652 | A | G | 10 | a0001c0001t0005g0041 a0001c0001t0005g0049 a0001c0001t0005g0072 others(7): Show |
10 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1180+1860A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111608652 | |||||||
| chr3:111609063 | C | T | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1180+2271C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111609063 | |||||||
| chr3:111609205 | G | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0101 others(1): Show |
6 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180+2413G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111609205 | |||||||
| chr3:111609213 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1180+2421G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111609213 | |||||||
| chr3:111609273 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1180+2481G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111609273 | |||||||
| chr3:111609554 | T | C | 1 | a0001c0001t0008g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1180+2762T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111609554 | |||||||
| chr3:111609591 | A | C | 1 | a0001c0001t0001g0058 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1180+2799A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111609591 | |||||||
| chr3:111609711 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1180+2919A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111609711 | |||||||
| chr3:111609751 | G | A | 6 | a0001c0001t0008g0128 a0001c0001t0008g0185 a0001c0004t0008g0235 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1180+2959G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111609751 | |||||||
| chr3:111610077 | C | T | 1 | a0001c0001t0014g0061 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1180+3285C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610077 | |||||||
| chr3:111610085 | A | G | 8 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0015 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1180+3293A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610085 | |||||||
| chr3:111610188 | T | G | 1 | a0002c0002t0002g0020 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1180+3396T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610188 | |||||||
| chr3:111610247 | T | A | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1180+3455T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610247 | |||||||
| chr3:111610283 | T | C | 1 | a0001c0001t0004g0151 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1180+3491T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610283 | |||||||
| chr3:111610387 | G | A | 5 | a0001c0001t0001g0054 a0001c0001t0001g0166 a0001c0001t0001g0167 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180+3595G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610387 | |||||||
| chr3:111610877 | C | T | 1 | a0001c0001t0003g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1180+4085C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610877 | |||||||
| chr3:111610935 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1180+4143G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610935 | |||||||
| chr3:111610952 | G | C | 15 | a0001c0001t0001g0047 a0001c0001t0004g0142 a0001c0001t0004g0143 others(12): Show |
15 | HG00735.hp1 HG01099.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1180+4160G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111610952 | |||||||
| chr3:111611164 | T | C | 1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1180+4372T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611164 | |||||||
| chr3:111611214 | G | T | 83 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(80): Show |
86 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1180+4422G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611214 | |||||||
| chr3:111611289 | A | G | 6 | a0001c0001t0008g0128 a0001c0001t0008g0185 a0001c0004t0008g0235 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1180+4497A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611289 | |||||||
| chr3:111611407 | G | T | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1180+4615G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611407 | |||||||
| chr3:111611551 | A | G | 1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1180+4759A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611551 | |||||||
| chr3:111611629 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1180+4837A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611629 | |||||||
| chr3:111611718 | G | A | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1180+4926G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611718 | |||||||
| chr3:111611856 | G | T | 1 | a0001c0014t0001g0095 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1180+5064G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611856 | |||||||
| chr3:111611879 | T | G | 2 | a0001c0001t0002g0055 a0001c0001t0002g0056 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1180+5087T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111611879 | |||||||
| chr3:111612075 | C | T | 87 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(84): Show |
90 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1180+5283C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111612075 | |||||||
| chr3:111612107 | A | G | 36 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(33): Show |
38 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.1180+5315A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111612107 | |||||||
| chr3:111612628 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1180+5836G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111612628 | |||||||
| chr3:111612999 | T | C | 1 | a0001c0015t0001g0117 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1180+6207T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111612999 | |||||||
| chr3:111613436 | G | A | 10 | a0001c0001t0005g0041 a0001c0001t0005g0049 a0001c0001t0005g0072 others(7): Show |
10 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1180+6644G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111613436 | |||||||
| chr3:111613514 | A | G | 10 | a0001c0001t0005g0041 a0001c0001t0005g0049 a0001c0001t0005g0072 others(7): Show |
10 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1180+6722A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111613514 | |||||||
| chr3:111613546 | G | C | 83 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(80): Show |
86 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1180+6754G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111613546 | |||||||
| chr3:111613610 | A | T | 2 | a0001c0001t0002g0247 a0001c0001t0002g0248 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1180+6818A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111613610 | |||||||
| chr3:111613717 | C | T | 8 | a0001c0001t0004g0147 a0001c0001t0004g0151 a0001c0001t0004g0152 others(5): Show |
8 | HG01099.hp1 HG01256.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180+6925C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111613717 | |||||||
| chr3:111613956 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1180+7164A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111613956 | |||||||
| chr3:111614186 | A | G | 1 | a0001c0001t0005g0202 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1180+7394A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111614186 | |||||||
| chr3:111614414 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1180+7622G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111614414 | |||||||
| chr3:111614441 | T | C | 5 | a0001c0001t0001g0054 a0001c0001t0001g0166 a0001c0001t0001g0167 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180+7649T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111614441 | |||||||
| chr3:111614551 | G | C | 1 | a0001c0001t0001g0094 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1180+7759G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111614551 | |||||||
| chr3:111614707 | G | A | 6 | a0001c0001t0006g0183 a0001c0001t0006g0198 a0001c0001t0006g0199 others(3): Show |
6 | HG01074.hp1 HG02559.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180+7915G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111614707 | |||||||
| chr3:111614733 | T | G | 1 | a0001c0001t0005g0072 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1180+7941T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111614733 | |||||||
| chr3:111614905 | C | G | 1 | a0006c0008t0001g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1180+8113C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111614905 | |||||||
| chr3:111615008 | C | A | 1 | a0001c0001t0003g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1180+8216C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111615008 | |||||||
| chr3:111615070 | G | A | 3 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0002c0002t0002g0196 |
3 | HG02258.hp2 HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1180+8278G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111615070 | |||||||
| chr3:111615117 | C | T | 1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1180+8325C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111615117 | |||||||
| chr3:111615177 | G | A | 14 | a0001c0001t0002g0037 a0001c0001t0002g0057 a0001c0001t0002g0089 others(11): Show |
14 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1180+8385G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111615177 | |||||||
| chr3:111615267 | C | T | 10 | a0001c0001t0005g0041 a0001c0001t0005g0049 a0001c0001t0005g0072 others(7): Show |
10 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1180+8475C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111615267 | |||||||
| chr3:111615381 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1181-8373C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111615381 | |||||||
| chr3:111615741 | G | A | 6 | a0001c0001t0008g0128 a0001c0001t0008g0185 a0001c0004t0008g0235 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1181-8013G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111615741 | |||||||
| chr3:111615809 | C | G | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1181-7945C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111615809 | |||||||
| chr3:111616112 | C | A | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7642C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616112 | |||||||
| chr3:111616114 | C | A | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7640C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616114 | |||||||
| chr3:111616116 | T | A | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7638T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616116 | |||||||
| chr3:111616117 | T | A | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7637T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616117 | |||||||
| chr3:111616118 | T | A | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7636T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616118 | |||||||
| chr3:111616122 | C | A | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7632C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616122 | |||||||
| chr3:111616124 | C | A | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7630C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616124 | |||||||
| chr3:111616125 | C | A | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7629C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616125 | |||||||
| chr3:111616128 | C | A | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7626C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616128 | |||||||
| chr3:111616144 | T | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7610T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616144 | |||||||
| chr3:111616155 | C | T | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7599C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616155 | |||||||
| chr3:111616159 | C | A | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7595C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616159 | |||||||
| chr3:111616160 | A | AT | 17 | a0001c0001t0005g0041 a0001c0001t0005g0049 a0001c0001t0005g0072 others(14): Show |
17 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1181-7593dupT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111616160 | ||||||
| chr3:111616175 | C | T | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7579C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616175 | |||||||
| chr3:111616185 | C | A | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7569C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616185 | |||||||
| chr3:111616194 | T | A | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7560T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616194 | |||||||
| chr3:111616206 | T | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7548T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616206 | |||||||
| chr3:111616209 | A | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7545A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616209 | |||||||
| chr3:111616212 | G | T | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7542G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616212 | |||||||
| chr3:111616213 | A | G | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7541A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616213 | |||||||
| chr3:111616223 | A | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7531A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616223 | |||||||
| chr3:111616224 | T | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7530T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616224 | |||||||
| chr3:111616226 | A | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7528A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616226 | |||||||
| chr3:111616229 | T | TCCCCCCC others(36): Show |
1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7525_1181-752 others(47): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616229 | |||||||
| chr3:111616231 | G | A | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7523G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616231 | |||||||
| chr3:111616242 | A | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7512A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616242 | |||||||
| chr3:111616244 | A | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7510A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616244 | |||||||
| chr3:111616246 | A | G | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7508A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616246 | |||||||
| chr3:111616256 | A | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7498A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616256 | |||||||
| chr3:111616256 | A | G | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-7498A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616256 | |||||||
| chr3:111616257 | T | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7497T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616257 | |||||||
| chr3:111616258 | A | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7496A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616258 | |||||||
| chr3:111616271 | T | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7483T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616271 | |||||||
| chr3:111616272 | C | A | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7482C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616272 | |||||||
| chr3:111616273 | A | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7481A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616273 | |||||||
| chr3:111616278 | A | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7476A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616278 | |||||||
| chr3:111616283 | T | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7471T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616283 | |||||||
| chr3:111616284 | T | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7470T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616284 | |||||||
| chr3:111616285 | T | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7469T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616285 | |||||||
| chr3:111616289 | A | C | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7465A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616289 | |||||||
| chr3:111616290 | T | A | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7464T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616290 | |||||||
| chr3:111616324 | T | A | 1 | a0001c0001t0018g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1181-7430T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616324 | |||||||
| chr3:111616499 | T | C | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-7255T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616499 | |||||||
| chr3:111616511 | A | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(64): Show |
73 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1181-7243A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616511 | |||||||
| chr3:111616631 | A | G | 28 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0080 others(25): Show |
30 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.1181-7123A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616631 | |||||||
| chr3:111616656 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1181-7098G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616656 | |||||||
| chr3:111616711 | G | A | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1181-7043G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616711 | |||||||
| chr3:111616751 | G | A | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1181-7003G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616751 | |||||||
| chr3:111616809 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1181-6945C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111616809 | |||||||
| chr3:111617205 | G | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-6549G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111617205 | |||||||
| chr3:111617323 | A | G | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-6431A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111617323 | |||||||
| chr3:111617460 | G | A | 4 | a0001c0001t0009g0042 a0001c0001t0009g0051 a0001c0001t0009g0052 others(1): Show |
4 | HG01192.hp2 HG02630.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181-6294G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111617460 | |||||||
| chr3:111617571 | A | G | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-6183A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111617571 | |||||||
| chr3:111617605 | T | A | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1181-6149T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111617605 | |||||||
| chr3:111617885 | T | C | 1 | a0001c0001t0002g0135 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1181-5869T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111617885 | |||||||
| chr3:111617900 | G | A | 8 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0015 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1181-5854G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111617900 | |||||||
| chr3:111618074 | T | C | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-5680T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618074 | |||||||
| chr3:111618121 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1181-5633C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618121 | |||||||
| chr3:111618160 | G | A | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1181-5594G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618160 | |||||||
| chr3:111618196 | C | T | 1 | a0001c0001t0006g0199 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1181-5558C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618196 | |||||||
| chr3:111618311 | T | C | 89 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(86): Show |
92 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1181-5443T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618311 | |||||||
| chr3:111618319 | C | G | 1 | a0001c0001t0003g0146 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1181-5435C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618319 | |||||||
| chr3:111618322 | G | A | 2 | a0001c0001t0002g0037 a0001c0011t0023g0038 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1181-5432G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618322 | |||||||
| chr3:111618429 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1181-5325C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618429 | |||||||
| chr3:111618444 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1181-5310G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618444 | |||||||
| chr3:111618461 | T | C | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-5293T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618461 | |||||||
| chr3:111618581 | T | C | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1181-5173T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618581 | |||||||
| chr3:111618581 | TC | T | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-5172delC | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618581 | |||||||
| chr3:111618582 | C | CT | 50 | a0001c0001t0001g0167 a0001c0001t0001g0276 a0001c0001t0002g0004 others(47): Show |
51 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.1181-5152dupT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111618582 | ||||||
| chr3:111618582 | CT | C | 35 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0126 others(32): Show |
36 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1181-5152delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111618582 | ||||||
| chr3:111618645 | C | A | 1 | a0006c0008t0001g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1181-5109C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618645 | |||||||
| chr3:111618817 | C | T | 52 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(49): Show |
54 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1181-4937C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618817 | |||||||
| chr3:111618851 | A | G | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-4903A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618851 | |||||||
| chr3:111618863 | G | A | 2 | a0001c0001t0004g0142 a0001c0001t0004g0143 |
2 | HG00735.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1181-4891G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111618863 | |||||||
| chr3:111619262 | GT | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(268): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1181-4483delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111619262 | ||||||
| chr3:111619322 | G | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(58): Show |
67 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1181-4432G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619322 | |||||||
| chr3:111619465 | G | A | 5 | a0001c0001t0007g0011 a0001c0001t0007g0141 a0001c0001t0007g0262 others(2): Show |
6 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(3): Show |
intron_variant | MODIFIER | c.1181-4289G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619465 | |||||||
| chr3:111619486 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(273): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1181-4268T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619486 | |||||||
| chr3:111619489 | A | G | 89 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(86): Show |
92 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1181-4265A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619489 | |||||||
| chr3:111619629 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1181-4125T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619629 | |||||||
| chr3:111619647 | A | C | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-4107A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619647 | |||||||
| chr3:111619665 | T | C | 2 | a0001c0001t0003g0076 a0001c0001t0021g0063 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1181-4089T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619665 | |||||||
| chr3:111619731 | TA | T | 11 | a0001c0001t0005g0041 a0001c0001t0005g0049 a0001c0001t0005g0072 others(8): Show |
11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1181-4019delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111619731 | ||||||
| chr3:111619880 | A | G | 1 | a0002c0002t0002g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1181-3874A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619880 | |||||||
| chr3:111619939 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1181-3815G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111619939 | |||||||
| chr3:111620139 | TC | T | 6 | a0001c0001t0008g0128 a0001c0001t0008g0185 a0001c0004t0008g0235 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1181-3612delC | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111620139 | ||||||
| chr3:111620272 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1181-3482G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111620272 | |||||||
| chr3:111620342 | C | CA | 8 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0015 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1181-3404dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111620342 | ||||||
| chr3:111620352 | G | A | 1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1181-3402G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111620352 | |||||||
| chr3:111620660 | G | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0249 |
2 | HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1181-3094G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111620660 | |||||||
| chr3:111620661 | A | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0249 |
2 | HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1181-3093A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111620661 | |||||||
| chr3:111620662 | G | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0249 |
2 | HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1181-3092G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111620662 | |||||||
| chr3:111620846 | C | T | 2 | a0001c0001t0011g0170 a0001c0001t0011g0277 |
2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1181-2908C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111620846 | |||||||
| chr3:111620960 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1181-2794A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111620960 | |||||||
| chr3:111620978 | A | G | 1 | a0001c0001t0009g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1181-2776A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111620978 | |||||||
| chr3:111621119 | T | G | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-2635T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111621119 | |||||||
| chr3:111621509 | GA | G | 6 | a0001c0001t0008g0128 a0001c0001t0008g0185 a0001c0004t0008g0235 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1181-2243delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111621509 | ||||||
| chr3:111621575 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1181-2179G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111621575 | |||||||
| chr3:111621753 | C | T | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-2001C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111621753 | |||||||
| chr3:111622119 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1181-1635C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622119 | |||||||
| chr3:111622129 | A | G | 28 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0080 others(25): Show |
30 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.1181-1625A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622129 | |||||||
| chr3:111622156 | G | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-1598G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622156 | |||||||
| chr3:111622202 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1181-1552G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622202 | |||||||
| chr3:111622410 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1181-1344A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622410 | |||||||
| chr3:111622425 | T | C | 1 | a0001c0001t0001g0280 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1181-1329T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622425 | |||||||
| chr3:111622441 | G | A | 1 | a0002c0002t0006g0029 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1181-1313G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622441 | |||||||
| chr3:111622459 | T | C | 1 | a0001c0001t0020g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1181-1295T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622459 | |||||||
| chr3:111622543 | C | A | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1181-1211C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622543 | |||||||
| chr3:111622606 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1181-1148A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622606 | |||||||
| chr3:111622781 | ATAAC | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-970_1181-967d others(6): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 111622781 | ||||||
| chr3:111622917 | G | T | 6 | a0001c0001t0008g0128 a0001c0001t0008g0185 a0001c0004t0008g0235 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1181-837G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622917 | |||||||
| chr3:111622938 | G | A | 1 | a0001c0001t0006g0071 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1181-816G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111622938 | |||||||
| chr3:111623144 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1181-610T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111623144 | |||||||
| chr3:111623181 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1181-573C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111623181 | |||||||
| chr3:111623294 | T | C | 8 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0015 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1181-460T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111623294 | |||||||
| chr3:111623348 | A | G | 2 | a0001c0001t0002g0037 a0001c0011t0023g0038 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1181-406A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111623348 | |||||||
| chr3:111623460 | G | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1181-294G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111623460 | |||||||
| chr3:111623707 | C | T | 1 | a0002c0002t0002g0026 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1181-47C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111623707 | |||||||
| chr3:111623733 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1181-21G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 8/13 | chr3 | 111623733 | |||||||
| chr3:111623952 | G | A | 3 | a0001c0001t0010g0021 a0001c0001t0010g0048 a0001c0001t0010g0100 |
3 | HG02165.hp1 NA19077.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1249+130G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 9/13 | chr3 | 111623952 | |||||||
| chr3:111623958 | G | T | 1 | a0001c0001t0001g0224 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1249+136G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 9/13 | chr3 | 111623958 | |||||||
| chr3:111624056 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1249+234G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 9/13 | chr3 | 111624056 | |||||||
| chr3:111624187 | G | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1250-146G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 9/13 | chr3 | 111624187 | |||||||
| chr3:111624222 | C | T | 47 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(44): Show |
49 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1250-111C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 9/13 | chr3 | 111624222 | |||||||
| chr3:111624446 | G | T | 1 | a0001c0001t0019g0112 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1321+42G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624446 | |||||||
| chr3:111624472 | C | T | 11 | a0001c0001t0005g0041 a0001c0001t0005g0049 a0001c0001t0005g0072 others(8): Show |
11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1321+68C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624472 | |||||||
| chr3:111624522 | A | G | 1 | a0001c0001t0019g0112 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1321+118A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624522 | |||||||
| chr3:111624729 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1321+325C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624729 | |||||||
| chr3:111624733 | TGAGCAAT others(6): Show |
T | 2 | a0001c0001t0002g0037 a0001c0011t0023g0038 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1321+330_1321+342d others(15): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624733 | |||||||
| chr3:111624753 | C | A | 1 | a0001c0001t0004g0179 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1321+349C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624753 | |||||||
| chr3:111624837 | G | C | 4 | a0001c0001t0001g0079 a0001c0001t0001g0103 a0001c0001t0001g0116 others(1): Show |
4 | NA18952.hp2 NA18961.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1321+433G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624837 | |||||||
| chr3:111624853 | T | G | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+449T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624853 | |||||||
| chr3:111624899 | A | G | 1 | a0001c0001t0019g0112 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1321+495A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624899 | |||||||
| chr3:111624909 | A | G | 88 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(85): Show |
91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1321+505A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111624909 | |||||||
| chr3:111625072 | T | C | 88 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(85): Show |
91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1321+668T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111625072 | |||||||
| chr3:111625084 | C | T | 1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1321+680C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111625084 | |||||||
| chr3:111625167 | C | T | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+763C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111625167 | |||||||
| chr3:111625414 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1321+1010C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111625414 | |||||||
| chr3:111625425 | A | G | 11 | a0001c0001t0005g0041 a0001c0001t0005g0049 a0001c0001t0005g0072 others(8): Show |
11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1321+1021A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111625425 | |||||||
| chr3:111625426 | T | C | 2 | a0001c0001t0002g0037 a0001c0011t0023g0038 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1321+1022T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111625426 | |||||||
| chr3:111625573 | GA | G | 4 | a0001c0001t0001g0193 a0001c0001t0003g0046 a0001c0001t0003g0059 others(1): Show |
4 | HG02055.hp2 HG02451.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1321+1177delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 111625573 | ||||||
| chr3:111625606 | A | C | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+1202A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111625606 | |||||||
| chr3:111626042 | G | A | 11 | a0001c0001t0005g0041 a0001c0001t0005g0049 a0001c0001t0005g0072 others(8): Show |
11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1321+1638G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626042 | |||||||
| chr3:111626161 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1321+1757C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626161 | |||||||
| chr3:111626168 | G | T | 11 | a0001c0001t0005g0041 a0001c0001t0005g0049 a0001c0001t0005g0072 others(8): Show |
11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1321+1764G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626168 | |||||||
| chr3:111626185 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(63): Show |
72 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1321+1781C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626185 | |||||||
| chr3:111626194 | G | A | 11 | a0001c0001t0005g0041 a0001c0001t0005g0049 a0001c0001t0005g0072 others(8): Show |
11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1321+1790G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626194 | |||||||
| chr3:111626206 | C | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+1802C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626206 | |||||||
| chr3:111626306 | C | CA | 124 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0039 others(121): Show |
128 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1321+1924dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 111626306 | ||||||
| chr3:111626306 | C | CAA | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(91): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.1321+1923_1321+192 others(6): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 111626306 | ||||||
| chr3:111626353 | C | A | 1 | a0001c0001t0002g0080 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1321+1949C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626353 | |||||||
| chr3:111626514 | T | A | 3 | a0001c0001t0002g0137 a0001c0001t0002g0138 a0001c0001t0002g0140 |
3 | NA18975.hp2 NA18981.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1321+2110T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626514 | |||||||
| chr3:111626516 | C | T | 1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1321+2112C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626516 | |||||||
| chr3:111626525 | T | G | 1 | a0002c0002t0002g0020 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1321+2121T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626525 | |||||||
| chr3:111626718 | A | T | 7 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0003g0146 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1321+2314A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626718 | |||||||
| chr3:111626782 | C | T | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1321+2378C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626782 | |||||||
| chr3:111626959 | G | A | 15 | a0001c0001t0001g0047 a0001c0001t0004g0142 a0001c0001t0004g0143 others(12): Show |
15 | HG00735.hp1 HG01099.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1321+2555G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111626959 | |||||||
| chr3:111627150 | G | A | 88 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(85): Show |
91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1321+2746G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627150 | |||||||
| chr3:111627236 | T | C | 1 | a0001c0001t0001g0012 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1321+2832T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627236 | |||||||
| chr3:111627398 | C | T | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+2994C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627398 | |||||||
| chr3:111627459 | C | A | 5 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1321+3055C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627459 | |||||||
| chr3:111627470 | C | T | 88 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0081 others(85): Show |
91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1321+3066C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627470 | |||||||
| chr3:111627913 | A | G | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+3509A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627913 | |||||||
| chr3:111627936 | G | A | 7 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0003g0146 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1321+3532G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627936 | |||||||
| chr3:111627961 | A | G | 1 | a0001c0001t0006g0071 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1321+3557A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627961 | |||||||
| chr3:111627994 | G | A | 8 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0015 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1321+3590G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111627994 | |||||||
| chr3:111628070 | T | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+3666T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111628070 | |||||||
| chr3:111628344 | T | C | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+3940T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111628344 | |||||||
| chr3:111628363 | A | G | 1 | a0001c0001t0004g0155 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1321+3959A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111628363 | |||||||
| chr3:111628710 | G | A | 6 | a0001c0001t0008g0128 a0001c0001t0008g0185 a0001c0004t0008g0235 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1321+4306G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111628710 | |||||||
| chr3:111628830 | C | T | 81 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(78): Show |
84 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.1321+4426C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111628830 | |||||||
| chr3:111628995 | G | C | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1321+4591G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111628995 | |||||||
| chr3:111629044 | T | A | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(271): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1321+4640T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111629044 | |||||||
| chr3:111629172 | T | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(271): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1321+4768T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111629172 | |||||||
| chr3:111629689 | T | A | 1 | a0001c0001t0004g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1321+5285T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111629689 | |||||||
| chr3:111629695 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1321+5291A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111629695 | |||||||
| chr3:111629786 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1321+5382A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111629786 | |||||||
| chr3:111629845 | C | A | 1 | a0001c0001t0002g0016 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1321+5441C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111629845 | |||||||
| chr3:111629968 | A | G | 1 | a0001c0001t0020g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1321+5564A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111629968 | |||||||
| chr3:111630059 | T | C | 1 | a0001c0011t0023g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1321+5655T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630059 | |||||||
| chr3:111630235 | A | G | 4 | a0001c0001t0001g0079 a0001c0001t0001g0103 a0001c0001t0001g0116 others(1): Show |
4 | NA18952.hp2 NA18961.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1321+5831A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630235 | |||||||
| chr3:111630247 | A | G | 7 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0003g0146 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1321+5843A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630247 | |||||||
| chr3:111630288 | G | A | 8 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0015 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1321+5884G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630288 | |||||||
| chr3:111630354 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1321+5950C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630354 | |||||||
| chr3:111630359 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1321+5955G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630359 | |||||||
| chr3:111630480 | G | A | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1321+6076G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630480 | |||||||
| chr3:111630547 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1321+6143A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630547 | |||||||
| chr3:111630674 | C | A | 1 | a0001c0001t0001g0215 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1321+6270C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111630674 | |||||||
| chr3:111631266 | A | AG | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-5930_1322-592 others(5): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111631266 | |||||||
| chr3:111631276 | C | T | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1322-5920C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111631276 | |||||||
| chr3:111631333 | G | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-5863G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111631333 | |||||||
| chr3:111631341 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1322-5855A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111631341 | |||||||
| chr3:111631630 | G | GA | 7 | a0001c0001t0001g0091 a0001c0001t0003g0046 a0001c0001t0005g0188 others(4): Show |
7 | HG01081.hp1 HG02896.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1322-5554dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 111631630 | ||||||
| chr3:111631630 | GA | G | 53 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(50): Show |
55 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1322-5554delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 111631630 | ||||||
| chr3:111631676 | C | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-5520C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111631676 | |||||||
| chr3:111631804 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1322-5392A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111631804 | |||||||
| chr3:111632177 | A | G | 50 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(47): Show |
52 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1322-5019A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111632177 | |||||||
| chr3:111632191 | G | T | 1 | a0001c0001t0012g0010 | 2 | HG02074.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1322-5005G>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111632191 | |||||||
| chr3:111632648 | A | G | 1 | a0001c0001t0009g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1322-4548A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111632648 | |||||||
| chr3:111632699 | G | A | 1 | a0001c0001t0006g0183 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1322-4497G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111632699 | |||||||
| chr3:111632967 | A | G | 2 | a0001c0001t0002g0037 a0001c0011t0023g0038 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1322-4229A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111632967 | |||||||
| chr3:111633145 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1322-4051A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111633145 | |||||||
| chr3:111633398 | G | A | 1 | a0001c0001t0003g0076 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1322-3798G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111633398 | |||||||
| chr3:111633417 | C | A | 6 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0003g0146 others(3): Show |
6 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1322-3779C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111633417 | |||||||
| chr3:111633502 | T | C | 1 | a0001c0005t0006g0148 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1322-3694T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111633502 | |||||||
| chr3:111633558 | T | A | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1322-3638T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111633558 | |||||||
| chr3:111633602 | G | C | 1 | a0001c0011t0023g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1322-3594G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111633602 | |||||||
| chr3:111633751 | C | A | 1 | a0001c0001t0002g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1322-3445C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111633751 | |||||||
| chr3:111634221 | A | C | 1 | a0006c0008t0001g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1322-2975A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634221 | |||||||
| chr3:111634357 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1322-2839C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634357 | |||||||
| chr3:111634382 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1322-2814G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634382 | |||||||
| chr3:111634473 | C | G | 1 | a0001c0001t0003g0146 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1322-2723C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634473 | |||||||
| chr3:111634558 | G | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-2638G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634558 | |||||||
| chr3:111634625 | G | A | 86 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0081 others(83): Show |
89 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1322-2571G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634625 | |||||||
| chr3:111634632 | C | T | 2 | a0001c0001t0003g0076 a0001c0001t0021g0063 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1322-2564C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634632 | |||||||
| chr3:111634635 | G | A | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1322-2561G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634635 | |||||||
| chr3:111634658 | A | G | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-2538A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634658 | |||||||
| chr3:111634725 | C | T | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-2471C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634725 | |||||||
| chr3:111634729 | T | C | 1 | a0001c0001t0005g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1322-2467T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634729 | |||||||
| chr3:111634754 | G | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-2442G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634754 | |||||||
| chr3:111634852 | G | A | 48 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(45): Show |
50 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1322-2344G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634852 | |||||||
| chr3:111634895 | C | CA | 12 | a0001c0001t0002g0074 a0001c0001t0005g0041 a0001c0001t0005g0049 others(9): Show |
12 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1322-2288dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 111634895 | ||||||
| chr3:111634895 | CA | C | 15 | a0001c0001t0001g0047 a0001c0001t0004g0142 a0001c0001t0004g0143 others(12): Show |
15 | HG00735.hp1 HG01099.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1322-2288delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 111634895 | ||||||
| chr3:111634972 | G | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-2224G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111634972 | |||||||
| chr3:111635002 | C | T | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1322-2194C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635002 | |||||||
| chr3:111635339 | T | C | 1 | a0002c0002t0006g0029 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1322-1857T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635339 | |||||||
| chr3:111635403 | T | G | 7 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0015 others(4): Show |
8 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1322-1793T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635403 | |||||||
| chr3:111635404 | A | T | 1 | a0001c0001t0020g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1322-1792A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635404 | |||||||
| chr3:111635617 | A | C | 11 | a0001c0001t0005g0041 a0001c0001t0005g0049 a0001c0001t0005g0072 others(8): Show |
11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1322-1579A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635617 | |||||||
| chr3:111635769 | G | A | 7 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0003g0146 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1322-1427G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635769 | |||||||
| chr3:111635788 | T | C | 6 | a0001c0001t0008g0128 a0001c0001t0008g0185 a0001c0004t0008g0235 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1322-1408T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635788 | |||||||
| chr3:111635933 | G | A | 1 | a0001c0001t0006g0198 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1322-1263G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635933 | |||||||
| chr3:111635986 | C | G | 3 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0002c0002t0002g0196 |
3 | HG02258.hp2 HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1322-1210C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111635986 | |||||||
| chr3:111636109 | C | T | 1 | a0002c0002t0001g0031 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1322-1087C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111636109 | |||||||
| chr3:111636206 | C | T | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1322-990C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111636206 | |||||||
| chr3:111636392 | C | A | 50 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(47): Show |
52 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1322-804C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111636392 | |||||||
| chr3:111636394 | T | C | 1 | a0001c0001t0022g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1322-802T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111636394 | |||||||
| chr3:111636574 | A | C | 2 | a0001c0001t0006g0071 a0001c0001t0006g0075 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1322-622A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | chr3 | 111636574 | |||||||
| chr3:111636874 | A | AT | 8 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0015 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1322-312dupT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 111636874 | ||||||
| chr3:111637431 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0120 others(2): Show |
8 | HG02027.hp1 HG02074.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1387+170A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | chr3 | 111637431 | |||||||
| chr3:111637444 | C | T | 1 | a0001c0001t0014g0061 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1387+183C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | chr3 | 111637444 | |||||||
| chr3:111637527 | A | G | 4 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387+266A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | chr3 | 111637527 | |||||||
| chr3:111637576 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1387+315T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | chr3 | 111637576 | |||||||
| chr3:111637577 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(267): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.1387+316T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | chr3 | 111637577 | |||||||
| chr3:111637733 | C | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0213 a0001c0001t0001g0215 |
3 | HG02027.hp2 HG02523.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1388-346C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | chr3 | 111637733 | |||||||
| chr3:111637768 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1388-311A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | chr3 | 111637768 | |||||||
| chr3:111637795 | CT | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(263): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1388-270delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 111637795 | ||||||
| chr3:111637848 | AT | A | 8 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0015 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1388-222delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 111637848 | ||||||
| chr3:111637864 | C | A | 88 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(85): Show |
91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1388-215C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 11/13 | chr3 | 111637864 | |||||||
| chr3:111638491 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1477+323G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111638491 | |||||||
| chr3:111638528 | C | G | 3 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0002c0002t0002g0196 |
3 | HG02258.hp2 HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1477+360C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111638528 | |||||||
| chr3:111638623 | T | G | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1477+455T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111638623 | |||||||
| chr3:111638660 | A | G | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1477+492A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111638660 | |||||||
| chr3:111638862 | T | C | 8 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0015 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1477+694T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111638862 | |||||||
| chr3:111638901 | CA | C | 7 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0003g0146 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1477+738delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111638901 | ||||||
| chr3:111638913 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1477+745T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111638913 | |||||||
| chr3:111638997 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1477+829C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111638997 | |||||||
| chr3:111639029 | G | C | 8 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0015 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1477+861G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111639029 | |||||||
| chr3:111639283 | G | A | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1477+1115G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111639283 | |||||||
| chr3:111639618 | A | T | 1 | a0001c0001t0005g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1477+1450A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111639618 | |||||||
| chr3:111639815 | GACAACCT others(6): Show |
G | 3 | a0001c0001t0001g0118 a0002c0002t0001g0032 a0002c0002t0001g0033 |
3 | NA18959.hp2 NA18974.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1477+1648_1477+166 others(17): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111639815 | |||||||
| chr3:111639935 | G | A | 4 | a0001c0005t0006g0062 a0001c0005t0006g0148 a0001c0005t0006g0149 others(1): Show |
4 | HG02622.hp1 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1477+1767G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111639935 | |||||||
| chr3:111639995 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0251 |
2 | HG01258.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1477+1827G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111639995 | |||||||
| chr3:111640097 | C | G | 1 | a0001c0001t0001g0259 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1477+1929C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640097 | |||||||
| chr3:111640166 | T | C | 1 | a0001c0004t0008g0236 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1477+1998T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640166 | |||||||
| chr3:111640185 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1477+2017A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640185 | |||||||
| chr3:111640264 | C | G | 11 | a0001c0001t0005g0041 a0001c0001t0005g0049 a0001c0001t0005g0072 others(8): Show |
11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1477+2096C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640264 | |||||||
| chr3:111640486 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+2318A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640486 | |||||||
| chr3:111640501 | C | G | 1 | a0001c0001t0004g0160 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1477+2333C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640501 | |||||||
| chr3:111640521 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0114 |
2 | HG00609.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1477+2353G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640521 | |||||||
| chr3:111640588 | C | A | 1 | a0002c0002t0001g0032 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1477+2420C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640588 | |||||||
| chr3:111640633 | A | G | 47 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(44): Show |
49 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1477+2465A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640633 | |||||||
| chr3:111640817 | G | C | 5 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1477+2649G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640817 | |||||||
| chr3:111640854 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1477+2686A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111640854 | |||||||
| chr3:111641469 | C | T | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1477+3301C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111641469 | |||||||
| chr3:111641846 | C | A | 2 | a0001c0001t0004g0142 a0001c0001t0004g0143 |
2 | HG00735.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1477+3678C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111641846 | |||||||
| chr3:111642011 | A | G | 50 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(47): Show |
52 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1477+3843A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642011 | |||||||
| chr3:111642195 | A | G | 1 | a0001c0001t0004g0155 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1477+4027A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642195 | |||||||
| chr3:111642427 | C | A | 1 | a0001c0001t0002g0043 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1477+4259C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642427 | |||||||
| chr3:111642469 | C | T | 1 | a0004c0010t0008g0220 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1477+4301C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642469 | |||||||
| chr3:111642561 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1477+4393C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642561 | |||||||
| chr3:111642584 | G | A | 7 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0003g0146 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1477+4416G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642584 | |||||||
| chr3:111642607 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1477+4439G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642607 | |||||||
| chr3:111642611 | C | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1477+4443C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642611 | |||||||
| chr3:111642636 | G | A | 1 | a0002c0002t0001g0034 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1477+4468G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642636 | |||||||
| chr3:111642665 | G | A | 4 | a0001c0001t0001g0257 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
4 | NA18944.hp1 NA18948.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1477+4497G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642665 | |||||||
| chr3:111642722 | G | A | 5 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1477+4554G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642722 | |||||||
| chr3:111642812 | A | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(62): Show |
71 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.1477+4644A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642812 | |||||||
| chr3:111642816 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1477+4648T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111642816 | |||||||
| chr3:111642927 | A | AT | 88 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(85): Show |
91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1478-4615dupT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111642927 | ||||||
| chr3:111643070 | T | TA | 13 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0001g0239 others(10): Show |
13 | HG00323.hp1 HG01261.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1478-4453dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111643070 | ||||||
| chr3:111643070 | TA | T | 9 | a0001c0001t0001g0039 a0001c0001t0001g0125 a0001c0001t0001g0174 others(6): Show |
9 | HG01074.hp2 HG01167.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1478-4453delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111643070 | ||||||
| chr3:111643084 | A | C | 1 | a0001c0001t0001g0178 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1478-4459A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643084 | |||||||
| chr3:111643188 | C | T | 5 | a0001c0001t0007g0011 a0001c0001t0007g0141 a0001c0001t0007g0262 others(2): Show |
6 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(3): Show |
intron_variant | MODIFIER | c.1478-4355C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643188 | |||||||
| chr3:111643218 | T | A | 2 | a0001c0001t0002g0037 a0001c0011t0023g0038 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1478-4325T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643218 | |||||||
| chr3:111643255 | A | G | 1 | a0001c0001t0004g0161 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1478-4288A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643255 | |||||||
| chr3:111643268 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1478-4275A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643268 | |||||||
| chr3:111643293 | T | G | 1 | a0001c0001t0004g0228 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1478-4250T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643293 | |||||||
| chr3:111643298 | C | T | 1 | a0001c0001t0022g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1478-4245C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643298 | |||||||
| chr3:111643381 | T | C | 6 | a0001c0001t0008g0128 a0001c0001t0008g0185 a0001c0004t0008g0235 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1478-4162T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643381 | |||||||
| chr3:111643634 | C | T | 1 | a0001c0001t0021g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1478-3909C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643634 | |||||||
| chr3:111643639 | A | G | 1 | a0001c0001t0005g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1478-3904A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643639 | |||||||
| chr3:111643735 | C | CA | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(162): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1478-3791dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111643735 | ||||||
| chr3:111643735 | C | CAA | 27 | a0001c0001t0001g0047 a0001c0001t0001g0175 a0001c0001t0001g0254 others(24): Show |
28 | HG00735.hp1 HG01099.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1478-3792_1478-379 others(6): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111643735 | ||||||
| chr3:111643735 | CA | C | 49 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(46): Show |
51 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.1478-3791delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111643735 | ||||||
| chr3:111643931 | A | C | 6 | a0001c0001t0008g0128 a0001c0001t0008g0185 a0001c0004t0008g0235 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1478-3612A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643931 | |||||||
| chr3:111643961 | T | G | 58 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(55): Show |
61 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.1478-3582T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111643961 | |||||||
| chr3:111644172 | T | C | 5 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1478-3371T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111644172 | |||||||
| chr3:111644267 | A | G | 12 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0039 others(9): Show |
12 | HG01081.hp1 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1478-3276A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111644267 | |||||||
| chr3:111644463 | C | A | 88 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(85): Show |
91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1478-3080C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111644463 | |||||||
| chr3:111644555 | G | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1478-2988G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111644555 | |||||||
| chr3:111644605 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1478-2938A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111644605 | |||||||
| chr3:111644652 | ACT | A | 6 | a0001c0001t0008g0128 a0001c0001t0008g0185 a0001c0004t0008g0235 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1478-2889_1478-288 others(6): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111644652 | ||||||
| chr3:111644775 | A | C | 6 | a0001c0001t0008g0128 a0001c0001t0008g0185 a0001c0004t0008g0235 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1478-2768A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111644775 | |||||||
| chr3:111644891 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(72): Show |
81 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1478-2652G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111644891 | |||||||
| chr3:111645119 | C | T | 1 | a0006c0008t0001g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1478-2424C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645119 | |||||||
| chr3:111645120 | A | G | 2 | a0001c0001t0002g0037 a0001c0011t0023g0038 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1478-2423A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645120 | |||||||
| chr3:111645122 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1478-2421C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645122 | |||||||
| chr3:111645151 | T | C | 7 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0003g0146 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1478-2392T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645151 | |||||||
| chr3:111645156 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1478-2387A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645156 | |||||||
| chr3:111645189 | C | A | 78 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(75): Show |
81 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1478-2354C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645189 | |||||||
| chr3:111645210 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1478-2333C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645210 | |||||||
| chr3:111645350 | A | G | 11 | a0001c0001t0005g0041 a0001c0001t0005g0049 a0001c0001t0005g0072 others(8): Show |
11 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1478-2193A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645350 | |||||||
| chr3:111645388 | C | T | 2 | a0001c0001t0003g0076 a0001c0001t0021g0063 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1478-2155C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645388 | |||||||
| chr3:111645436 | T | A | 88 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(85): Show |
91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1478-2107T>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645436 | |||||||
| chr3:111645572 | C | G | 7 | a0001c0001t0004g0147 a0001c0001t0004g0152 a0001c0001t0004g0154 others(4): Show |
7 | HG01099.hp1 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1478-1971C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645572 | |||||||
| chr3:111645812 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1478-1731G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645812 | |||||||
| chr3:111645824 | C | A | 7 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0003g0146 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1478-1719C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645824 | |||||||
| chr3:111645849 | A | G | 1 | a0002c0002t0002g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1478-1694A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645849 | |||||||
| chr3:111645921 | A | T | 1 | a0001c0001t0001g0105 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1478-1622A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111645921 | |||||||
| chr3:111646097 | C | A | 1 | a0001c0001t0001g0177 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1478-1446C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111646097 | |||||||
| chr3:111646158 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1478-1385T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111646158 | |||||||
| chr3:111646321 | A | G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(75): Show |
81 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1478-1222A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111646321 | |||||||
| chr3:111646370 | C | T | 3 | a0001c0001t0005g0049 a0001c0001t0005g0072 a0001c0001t0005g0073 |
3 | HG01106.hp1 HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1478-1173C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111646370 | |||||||
| chr3:111646540 | TA | T | 46 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(43): Show |
48 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.1478-990delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111646540 | ||||||
| chr3:111646829 | A | G | 6 | a0001c0001t0008g0128 a0001c0001t0008g0185 a0001c0004t0008g0235 others(3): Show |
6 | HG00099.hp1 HG00280.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1478-714A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111646829 | |||||||
| chr3:111646882 | A | G | 88 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(85): Show |
91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1478-661A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111646882 | |||||||
| chr3:111647038 | A | G | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1478-505A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111647038 | |||||||
| chr3:111647088 | T | TA | 9 | a0001c0001t0001g0158 a0001c0001t0001g0231 a0001c0001t0002g0057 others(6): Show |
9 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1478-434dupA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111647088 | ||||||
| chr3:111647088 | TA | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(110): Show |
120 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1478-434delA | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111647088 | ||||||
| chr3:111647088 | TAA | T | 6 | a0001c0001t0001g0054 a0001c0001t0001g0091 a0001c0001t0001g0126 others(3): Show |
6 | HG02165.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1478-435_1478-434d others(4): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 111647088 | ||||||
| chr3:111647100 | A | C | 1 | a0001c0001t0002g0043 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1478-443A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111647100 | |||||||
| chr3:111647188 | C | G | 9 | a0001c0001t0001g0113 a0001c0001t0001g0158 a0001c0001t0001g0214 others(6): Show |
9 | HG00741.hp2 HG01258.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.1478-355C>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111647188 | |||||||
| chr3:111647207 | A | G | 5 | a0001c0001t0001g0105 a0001c0001t0001g0118 a0001c0015t0001g0117 others(2): Show |
5 | NA18939.hp2 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1478-336A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111647207 | |||||||
| chr3:111647226 | A | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0212 |
2 | HG01106.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1478-317A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111647226 | |||||||
| chr3:111647319 | T | C | 1 | a0001c0001t0003g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-224T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111647319 | |||||||
| chr3:111647473 | A | C | 1 | a0001c0011t0023g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1478-70A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 12/13 | chr3 | 111647473 | |||||||
| chr3:111647709 | A | G | 1 | a0005c0007t0002g0023 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1601+43A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111647709 | |||||||
| chr3:111647757 | T | C | 1 | a0001c0001t0004g0142 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1601+91T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111647757 | |||||||
| chr3:111647961 | A | C | 14 | a0001c0001t0001g0047 a0001c0001t0004g0142 a0001c0001t0004g0143 others(11): Show |
14 | HG00735.hp1 HG01099.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.1601+295A>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111647961 | |||||||
| chr3:111648092 | CT | C | 81 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(78): Show |
84 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.1601+433delT | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr3 | 111648092 | ||||||
| chr3:111648243 | C | A | 1 | a0001c0001t0002g0145 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1601+577C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648243 | |||||||
| chr3:111648302 | C | T | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1601+636C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648302 | |||||||
| chr3:111648350 | A | T | 12 | a0001c0001t0005g0041 a0001c0001t0005g0049 a0001c0001t0005g0064 others(9): Show |
12 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1601+684A>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648350 | |||||||
| chr3:111648374 | A | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(279): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1601+708A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648374 | |||||||
| chr3:111648384 | C | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1601+718C>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648384 | |||||||
| chr3:111648485 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1601+819A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648485 | |||||||
| chr3:111648672 | C | T | 88 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0016 others(85): Show |
91 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1601+1006C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648672 | |||||||
| chr3:111648692 | G | A | 1 | a0001c0003t0001g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1602-1006G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648692 | |||||||
| chr3:111648723 | G | C | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1602-975G>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648723 | |||||||
| chr3:111648729 | ATC | A | 4 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0013g0067 others(1): Show |
4 | HG02055.hp1 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602-963_1602-962d others(4): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr3 | 111648729 | ||||||
| chr3:111648803 | G | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1602-895G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648803 | |||||||
| chr3:111648937 | G | A | 1 | a0001c0001t0002g0138 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1602-761G>A | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648937 | |||||||
| chr3:111648987 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1602-711C>T | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111648987 | |||||||
| chr3:111649130 | T | C | 1 | a0002c0002t0001g0275 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1602-568T>C | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111649130 | |||||||
| chr3:111649467 | A | G | 1 | a0001c0001t0002g0043 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1602-231A>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111649467 | |||||||
| chr3:111649571 | ACTGGGAG others(7): Show |
A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0107 |
5 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602-124_1602-111d others(16): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr3 | 111649571 | ||||||
| chr3:111649572 | CTGGGAGA others(5): Show |
C | 1 | a0001c0001t0001g0101 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1602-124_1602-113d others(14): Show |
CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr3 | 111649572 | ||||||
| chr3:111649604 | T | G | 3 | a0001c0001t0003g0046 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG02055.hp2 HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1602-94T>G | CD96 | ENSG00000153283.13 | transcript | ENST00000352690.9 | protein_coding | 13/13 | chr3 | 111649604 |