Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23554 |
| ensemblid | ENSG00000106025.9 |
| hgncid | 21641 |
| symbol | TSPAN12 |
| name | tetraspanin 12 |
| refseq_nuc | NM_012338.4 |
| refseq_prot | NP_036470.1 |
| ensembl_nuc | ENST00000222747.8 |
| ensembl_prot | ENSP00000222747.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 120787320 |
| end | 120858144 |
| strand | - |
| ver | v1.2 |
| region | chr7:120787320-120858144 |
| region5000 | chr7:120782320-120863144 |
| regionname0 | TSPAN12_chr7_120787320_120858144 |
| regionname5000 | TSPAN12_chr7_120782320_120863144 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 305 | 292 | 90 | 52 | 124 | 2 | 22 | 98 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | MARED others(300): Show |
chr7 | 120782320 | 120863144 |
| a0002 | 0/0 | 305 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | MARED others(300): Show |
chr7 | 120782320 | 120863144 |
| a0003 | 0/0 | 305 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | MARED others(300): Show |
chr7 | 120782320 | 120863144 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 915 | 254 | 72 | 41 | 121 | 1 | 18 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | ATGGC others(910): Show |
chr7 | 120782320 | 120863144 | ||
| a0001c0002 | 1/0 | 915 | 36 | 16 | 11 | 3 | 1 | 4 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | ATGGC others(910): Show |
chr7 | 120782320 | 120863144 | ||
| a0001c0003 | 0/0 | 915 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | ATGGC others(910): Show |
chr7 | 120782320 | 120863144 | ||
| a0002c0005 | 0/0 | 915 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | ATGGC others(910): Show |
chr7 | 120782320 | 120863144 | ||
| a0003c0004 | 0/0 | 915 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | ATGGC others(910): Show |
chr7 | 120782320 | 120863144 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2585 | 166 | 63 | 26 | 65 | 1 | 10 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | GCGCT others(2580): Show |
chr7 | 120782320 | 120863144 |
| a0001c0001t0002 | 0/0 | 2586 | 71 | 2 | 14 | 48 | 0 | 7 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | GCGCT others(2581): Show |
chr7 | 120782320 | 120863144 |
| a0001c0001t0003 | 0/0 | 2585 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | GCGCT others(2580): Show |
chr7 | 120782320 | 120863144 |
| a0001c0001t0005 | 0/0 | 2585 | 7 | 0 | 0 | 7 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | GCGCT others(2580): Show |
chr7 | 120782320 | 120863144 |
| a0001c0001t0006 | 0/0 | 2585 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | GCGCT others(2580): Show |
chr7 | 120782320 | 120863144 |
| a0001c0001t0007 | 0/0 | 2585 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | GCGCT others(2580): Show |
chr7 | 120782320 | 120863144 |
| a0001c0001t0009 | 0/0 | 2585 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | GCGCT others(2580): Show |
chr7 | 120782320 | 120863144 |
| a0001c0001t0010 | 0/0 | 2585 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | GCGCT others(2580): Show |
chr7 | 120782320 | 120863144 |
| a0001c0001t0011 | 0/0 | 2585 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | GCGCT others(2580): Show |
chr7 | 120782320 | 120863144 |
| a0001c0001t0012 | 0/0 | 2585 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | GCGCT others(2580): Show |
chr7 | 120782320 | 120863144 |
| a0001c0001t0013 | 0/0 | 2586 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | GCGCT others(2581): Show |
chr7 | 120782320 | 120863144 |
| a0001c0002t0003 | 1/0 | 2585 | 27 | 14 | 6 | 2 | 0 | 4 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | GCGCT others(2580): Show |
chr7 | 120782320 | 120863144 |
| a0001c0002t0004 | 0/0 | 2586 | 8 | 2 | 5 | 0 | 1 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | GCGCT others(2581): Show |
chr7 | 120782320 | 120863144 |
| a0001c0002t0008 | 0/0 | 2585 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | GCGCT others(2580): Show |
chr7 | 120782320 | 120863144 |
| a0001c0003t0002 | 0/0 | 2586 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | GCGCT others(2581): Show |
chr7 | 120782320 | 120863144 |
| a0002c0005t0001 | 0/0 | 2585 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | GCGCT others(2580): Show |
chr7 | 120782320 | 120863144 |
| a0003c0004t0001 | 0/0 | 2585 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | GCGCT others(2580): Show |
chr7 | 120782320 | 120863144 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0003 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0005 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0003g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0005g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0009g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0010g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0011g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0012g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0001t0013g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0140 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0002t0008g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0003t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0001c0003t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0002c0005t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| a0003c0004t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0104 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00733 | hp1 | a0001 | c0002 | t0003 | g0068 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0072 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0073 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00741 | hp1 | a0001 | c0002 | t0004 | g0220 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0075 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01168 | hp2 | a0002 | c0005 | t0001 | g0117 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0058 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01258 | hp2 | a0001 | c0002 | t0004 | g0216 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01433 | hp2 | a0001 | c0002 | t0004 | g0215 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0015 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01934 | hp2 | a0001 | c0002 | t0004 | g0179 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01978 | hp1 | a0001 | c0002 | t0004 | g0180 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02004 | hp2 | a0003 | c0004 | t0001 | g0127 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02015 | hp1 | a0001 | c0001 | t0013 | g0178 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0070 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02071 | hp1 | a0001 | c0002 | t0008 | g0061 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02257 | hp1 | a0001 | c0001 | t0012 | g0175 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02280 | hp2 | a0001 | c0002 | t0003 | g0064 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02630 | hp2 | a0001 | c0002 | t0003 | g0067 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0066 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0057 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02922 | hp2 | a0001 | c0002 | t0003 | g0053 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0071 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03209 | hp1 | a0001 | c0003 | t0002 | g0187 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0177 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0036 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0168 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03239 | hp2 | a0001 | c0002 | t0003 | g0069 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03490 | hp2 | a0001 | c0002 | t0003 | g0014 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03491 | hp1 | a0001 | c0002 | t0003 | g0074 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03492 | hp2 | a0001 | c0002 | t0003 | g0014 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0176 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03579 | hp2 | a0001 | c0001 | t0010 | g0079 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | STU | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | STU | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03710 | hp2 | a0001 | c0001 | t0011 | g0102 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | BEB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | BEB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | YRI | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | CHB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18906 | hp1 | a0001 | c0003 | t0002 | g0188 | AFR | YRI | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0167 | AFR | YRI | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18943 | hp2 | a0001 | c0002 | t0003 | g0062 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18954 | hp1 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18959 | hp1 | a0001 | c0002 | t0003 | g0063 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0161 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18988 | hp2 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | LWK | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19043 | hp2 | a0001 | c0002 | t0003 | g0015 | AFR | LWK | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19075 | hp2 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19084 | hp1 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19240 | hp1 | a0001 | c0002 | t0003 | g0060 | AFR | YRI | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0090 | AFR | YRI | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ASW | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ASW | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA20752 | hp1 | a0001 | c0002 | t0004 | g0196 | EUR | TSI | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02486 | hp1 | a0001 | c0002 | t0003 | g0065 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0054 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0033 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | USA | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0214 | AFR | USA | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | USA | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | USA | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| NA21309 | hp2 | a0001 | c0002 | t0004 | g0181 | AFR | LWK | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0051 | REF | REF | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0003 | g0140 | REF | REF | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:120787321 | T | A | 1 | a0001 | 1 | HG02071.hp1 | splice_region_variant | LOW | c.*1271A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 8/8 | chr7 | 120787321 | |||||||
| chr7:120787322 | A | C | 1 | a0001 | 1 | HG03579.hp2 | splice_region_variant | LOW | c.*1270T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 8/8 | chr7 | 120787322 | |||||||
| chr7:120788677 | A | G | 1 | a0002 | 1 | HG01168.hp2 | missense_variant | MODERATE | c.833T>C | p.Leu278Pro | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 8/8 | 1228/2585 | 833/918 | 278/305 | chr7 | 120788677 | |||
| chr7:120840030 | G | T | 1 | a0003 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.146C>A | p.Thr49Lys | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 3/8 | 541/2585 | 146/918 | 49/305 | chr7 | 120840030 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:120788745 | C | A | 4 | a0001c0001 a0001c0003 a0002c0005 others(1): Show |
257 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(254): Show |
synonymous_variant | LOW | c.765G>T | p.Pro255Pro | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 8/8 | 1160/2585 | 765/918 | 255/305 | chr7 | 120788745 | |||
| chr7:120815738 | C | T | 1 | a0001c0003 | 2 | HG03209.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.351G>A | p.Gln117Gln | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/8 | 746/2585 | 351/918 | 117/305 | chr7 | 120815738 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:120787349 | T | A | 1 | a0001c0001t0011 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1243A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 8/8 | 1243 | chr7 | 120787349 | ||||||
| chr7:120787453 | T | A | 1 | a0001c0001t0005 | 7 | HG00558.hp1 NA18954.hp1 NA18970.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1139A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 8/8 | 1139 | chr7 | 120787453 | ||||||
| chr7:120788150 | C | T | 1 | a0001c0001t0009 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*442G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 8/8 | 442 | chr7 | 120788150 | ||||||
| chr7:120788553 | G | A | 13 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(10): Show |
255 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*39C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 8/8 | 39 | chr7 | 120788553 | ||||||
| chr7:120857825 | G | A | 1 | a0001c0001t0012 | 1 | HG02257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-76C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/8 | 1062 | chr7 | 120857825 | ||||||
| chr7:120857880 | G | A | 1 | a0001c0001t0006 | 2 | HG03209.hp2 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-131C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/8 | 1117 | chr7 | 120857880 | ||||||
| chr7:120857905 | C | T | 1 | a0001c0001t0007 | 1 | HG02559.hp2 | 5_prime_UTR_variant | MODIFIER | c.-156G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/8 | 1142 | chr7 | 120857905 | ||||||
| chr7:120857961 | C | G | 1 | a0001c0001t0013 | 1 | HG02015.hp1 | 5_prime_UTR_variant | MODIFIER | c.-212G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/8 | 1198 | chr7 | 120857961 | ||||||
| chr7:120857999 | G | GA | 4 | a0001c0001t0002 a0001c0001t0013 a0001c0002t0004 others(1): Show |
82 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
5_prime_UTR_variant | MODIFIER | c.-251dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/8 | 1237 | chr7 | 120857999 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:120788978 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.613-81A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120788978 | |||||||
| chr7:120788983 | G | A | 3 | a0001c0002t0003g0065 a0001c0002t0003g0167 a0001c0002t0003g0168 |
3 | HG02486.hp1 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.613-86C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120788983 | |||||||
| chr7:120789519 | T | C | 3 | a0001c0001t0001g0084 a0001c0003t0002g0187 a0001c0003t0002g0188 |
3 | HG01433.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.613-622A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120789519 | |||||||
| chr7:120789753 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.613-856A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120789753 | |||||||
| chr7:120789850 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.613-953C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120789850 | |||||||
| chr7:120789989 | T | C | 6 | a0001c0001t0001g0044 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.613-1092A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120789989 | |||||||
| chr7:120790008 | C | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0041 others(11): Show |
17 | HG00558.hp2 HG02109.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.613-1111G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790008 | |||||||
| chr7:120790022 | G | A | 1 | a0001c0002t0003g0065 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.613-1125C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790022 | |||||||
| chr7:120790074 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.613-1177A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790074 | |||||||
| chr7:120790092 | G | A | 1 | a0001c0002t0003g0075 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.613-1195C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790092 | |||||||
| chr7:120790240 | G | A | 4 | a0001c0001t0001g0076 a0001c0001t0006g0176 a0001c0001t0006g0177 others(1): Show |
4 | HG03130.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-1343C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790240 | |||||||
| chr7:120790341 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.613-1444G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790341 | |||||||
| chr7:120790342 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.613-1445A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790342 | |||||||
| chr7:120790360 | T | G | 1 | a0001c0001t0002g0223 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.613-1463A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790360 | |||||||
| chr7:120790362 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.613-1465C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790362 | |||||||
| chr7:120790376 | G | T | 1 | a0001c0002t0003g0167 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.613-1479C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790376 | |||||||
| chr7:120790473 | G | C | 3 | a0001c0002t0003g0065 a0001c0002t0003g0167 a0001c0002t0003g0168 |
3 | HG02486.hp1 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.613-1576C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790473 | |||||||
| chr7:120790685 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.613-1788T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790685 | |||||||
| chr7:120790754 | C | T | 9 | a0001c0002t0003g0014 a0001c0002t0003g0054 a0001c0002t0003g0057 others(6): Show |
10 | HG01243.hp1 HG01934.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.613-1857G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790754 | |||||||
| chr7:120790981 | T | A | 2 | a0001c0002t0003g0014 a0001c0002t0003g0054 |
3 | HG02559.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.613-2084A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790981 | |||||||
| chr7:120791060 | G | A | 2 | a0001c0002t0003g0057 a0001c0002t0003g0058 |
2 | HG01243.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.613-2163C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791060 | |||||||
| chr7:120791327 | T | G | 1 | a0001c0001t0002g0219 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.613-2430A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791327 | |||||||
| chr7:120791328 | C | CA | 16 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(13): Show |
20 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.613-2432dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791328 | |||||||
| chr7:120791416 | T | C | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.613-2519A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791416 | |||||||
| chr7:120791425 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.613-2528A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791425 | |||||||
| chr7:120791453 | A | G | 4 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
4 | HG02559.hp2 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-2556T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791453 | |||||||
| chr7:120791500 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.613-2603A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791500 | |||||||
| chr7:120791561 | G | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(12): Show |
19 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.613-2664C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791561 | |||||||
| chr7:120791916 | T | C | 52 | a0001c0001t0001g0165 a0001c0001t0002g0002 a0001c0001t0002g0005 others(49): Show |
67 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.613-3019A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791916 | |||||||
| chr7:120791936 | G | C | 1 | a0001c0001t0003g0013 | 2 | HG00735.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.613-3039C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791936 | |||||||
| chr7:120792023 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.613-3126A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792023 | |||||||
| chr7:120792033 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.613-3136G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792033 | |||||||
| chr7:120792075 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.613-3178T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792075 | |||||||
| chr7:120792164 | G | A | 3 | a0001c0001t0002g0007 a0001c0001t0002g0199 a0001c0001t0002g0207 |
6 | NA18956.hp2 NA18969.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.613-3267C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792164 | |||||||
| chr7:120792344 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.613-3447G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792344 | |||||||
| chr7:120792489 | ATGAATAG others(24): Show |
A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0170 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.613-3623_613-3593d others(33): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792489 | |||||||
| chr7:120792673 | T | A | 1 | a0001c0003t0002g0188 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.613-3776A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792673 | |||||||
| chr7:120792913 | T | C | 4 | a0001c0001t0001g0059 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
4 | HG02630.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-4016A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792913 | |||||||
| chr7:120792967 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0085 |
3 | HG00558.hp2 NA18952.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.613-4070C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792967 | |||||||
| chr7:120793150 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.613-4253G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120793150 | |||||||
| chr7:120793363 | T | C | 2 | a0001c0002t0003g0070 a0001c0002t0003g0071 |
2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.613-4466A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120793363 | |||||||
| chr7:120793416 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-4519G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120793416 | |||||||
| chr7:120793699 | A | T | 1 | a0001c0002t0003g0015 | 2 | HG01496.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.613-4802T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120793699 | |||||||
| chr7:120793716 | C | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.613-4819G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120793716 | |||||||
| chr7:120793874 | C | A | 19 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0029 others(16): Show |
22 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.613-4977G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120793874 | |||||||
| chr7:120793893 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0012g0175 |
2 | HG00738.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.613-4996A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120793893 | |||||||
| chr7:120794129 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.613-5232A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120794129 | |||||||
| chr7:120794142 | G | C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-5245C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120794142 | |||||||
| chr7:120794468 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.613-5571A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120794468 | |||||||
| chr7:120794678 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.613-5781G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120794678 | |||||||
| chr7:120794699 | A | G | 52 | a0001c0001t0001g0165 a0001c0001t0002g0002 a0001c0001t0002g0005 others(49): Show |
67 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.613-5802T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120794699 | |||||||
| chr7:120794774 | A | ACAGT | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(115): Show |
148 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.613-5881_613-5878d others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120794774 | |||||||
| chr7:120794972 | T | C | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.613-6075A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120794972 | |||||||
| chr7:120795072 | T | C | 1 | a0001c0002t0004g0216 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.613-6175A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120795072 | |||||||
| chr7:120795246 | T | C | 1 | a0001c0001t0002g0209 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.613-6349A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120795246 | |||||||
| chr7:120795584 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(119): Show |
152 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.613-6687A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120795584 | |||||||
| chr7:120796003 | C | G | 2 | a0001c0001t0006g0176 a0001c0001t0006g0177 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.613-7106G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796003 | |||||||
| chr7:120796068 | CA | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(119): Show |
152 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.613-7172delT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796068 | |||||||
| chr7:120796107 | C | G | 1 | a0001c0001t0002g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.613-7210G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796107 | |||||||
| chr7:120796516 | G | A | 1 | a0002c0005t0001g0117 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.613-7619C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796516 | |||||||
| chr7:120796529 | T | C | 1 | a0001c0001t0005g0022 | 2 | NA18970.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.613-7632A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796529 | |||||||
| chr7:120796549 | G | A | 2 | a0001c0003t0002g0187 a0001c0003t0002g0188 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.613-7652C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796549 | |||||||
| chr7:120796739 | T | C | 2 | a0001c0001t0001g0172 a0001c0001t0010g0079 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.613-7842A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796739 | |||||||
| chr7:120796826 | CTCCACTT others(2): Show |
C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-7938_613-7930d others(11): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796826 | |||||||
| chr7:120796894 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.613-7997C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796894 | |||||||
| chr7:120796930 | C | T | 1 | a0001c0001t0003g0013 | 2 | HG00735.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.613-8033G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796930 | |||||||
| chr7:120796948 | G | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-8051C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796948 | |||||||
| chr7:120797016 | G | T | 1 | a0001c0001t0005g0119 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.613-8119C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797016 | |||||||
| chr7:120797088 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.613-8191G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797088 | |||||||
| chr7:120797104 | C | A | 2 | a0001c0002t0003g0053 a0001c0002t0003g0090 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.613-8207G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797104 | |||||||
| chr7:120797138 | CAG | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0080 others(2): Show |
8 | HG00558.hp2 NA18952.hp2 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.613-8243_613-8242d others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797138 | |||||||
| chr7:120797144 | C | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(218): Show |
277 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(274): Show |
intron_variant | MODIFIER | c.613-8247G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797144 | |||||||
| chr7:120797223 | A | G | 18 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0029 others(15): Show |
21 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.613-8326T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797223 | |||||||
| chr7:120797553 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
250 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(247): Show |
intron_variant | MODIFIER | c.613-8656G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797553 | |||||||
| chr7:120797611 | T | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.613-8714A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797611 | |||||||
| chr7:120797740 | C | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.612+8809G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797740 | |||||||
| chr7:120798158 | A | G | 55 | a0001c0001t0001g0165 a0001c0001t0002g0002 a0001c0001t0002g0005 others(52): Show |
70 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.612+8391T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798158 | |||||||
| chr7:120798180 | C | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0109 |
3 | HG02572.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.612+8369G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798180 | |||||||
| chr7:120798194 | G | A | 7 | a0001c0001t0002g0194 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG00438.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.612+8355C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798194 | |||||||
| chr7:120798349 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
3 | HG02145.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.612+8200C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798349 | |||||||
| chr7:120798416 | T | C | 1 | a0001c0001t0001g0016 | 2 | HG01074.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.612+8133A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798416 | |||||||
| chr7:120798507 | G | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(115): Show |
148 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.612+8042C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798507 | |||||||
| chr7:120798527 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(88): Show |
118 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.612+8022C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798527 | |||||||
| chr7:120798643 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+7906G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798643 | |||||||
| chr7:120798835 | A | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
127 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.612+7714T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798835 | |||||||
| chr7:120798851 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.612+7698G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798851 | |||||||
| chr7:120798871 | ATTCTTT | A | 10 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.612+7672_612+7677d others(8): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798871 | |||||||
| chr7:120798980 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.612+7569G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798980 | |||||||
| chr7:120798997 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.612+7552G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798997 | |||||||
| chr7:120799082 | G | A | 12 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0024 others(9): Show |
18 | HG00597.hp1 HG01975.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.612+7467C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799082 | |||||||
| chr7:120799109 | G | A | 2 | a0001c0003t0002g0187 a0001c0003t0002g0188 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.612+7440C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799109 | |||||||
| chr7:120799278 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.612+7271C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799278 | |||||||
| chr7:120799354 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.612+7195G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799354 | |||||||
| chr7:120799460 | A | C | 1 | a0001c0001t0001g0003 | 5 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.612+7089T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799460 | |||||||
| chr7:120799462 | TTACATAA others(15): Show |
T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0085 |
3 | HG00558.hp2 NA18952.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.612+7065_612+7086d others(24): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799462 | |||||||
| chr7:120799465 | C | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
251 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(248): Show |
intron_variant | MODIFIER | c.612+7084G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799465 | |||||||
| chr7:120799506 | T | TTAATTAT others(17): Show |
4 | a0001c0001t0001g0044 a0001c0001t0001g0148 a0001c0001t0002g0189 others(1): Show |
4 | HG02004.hp2 HG03927.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+7019_612+7042d others(26): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799506 | |||||||
| chr7:120799506 | T | TTAATTAT others(55): Show |
1 | a0001c0001t0002g0223 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.612+7042_612+7043i others(64): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799506 | |||||||
| chr7:120799520 | TTAATTAT others(19): Show |
T | 1 | a0001c0001t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.612+7003_612+7028d others(28): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799520 | |||||||
| chr7:120799524 | TTATATAT others(15): Show |
T | 1 | a0001c0001t0001g0027 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.612+7003_612+7024d others(24): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799524 | |||||||
| chr7:120799527 | T | A | 1 | a0001c0001t0001g0025 | 2 | HG02071.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.612+7022A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799527 | |||||||
| chr7:120799534 | TTATATAT others(5): Show |
T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.612+7003_612+7014d others(14): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799534 | |||||||
| chr7:120799546 | A | AATTATAT others(15): Show |
3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0084 |
3 | HG01433.hp1 HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.612+7002_612+7003i others(24): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799546 | |||||||
| chr7:120799570 | T | A | 39 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(36): Show |
48 | HG00558.hp2 HG00741.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.612+6979A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799570 | |||||||
| chr7:120799599 | T | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(83): Show |
111 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.612+6950A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799599 | |||||||
| chr7:120799605 | A | ATT | 4 | a0001c0001t0001g0021 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
5 | HG00621.hp1 NA18947.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.612+6942_612+6943d others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799605 | |||||||
| chr7:120799640 | C | A | 1 | a0001c0001t0001g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.612+6909G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799640 | |||||||
| chr7:120799700 | TTATTA | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+6844_612+6848d others(7): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799700 | |||||||
| chr7:120799720 | TTTA | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.612+6826_612+6828d others(5): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799720 | |||||||
| chr7:120799739 | TTA | T | 3 | a0001c0001t0006g0176 a0001c0001t0006g0177 a0001c0001t0009g0036 |
3 | HG03209.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.612+6808_612+6809d others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799739 | |||||||
| chr7:120799783 | A | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+6766T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799783 | |||||||
| chr7:120799913 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.612+6636T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799913 | |||||||
| chr7:120799914 | T | A | 1 | a0001c0002t0004g0179 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.612+6635A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799914 | |||||||
| chr7:120800190 | G | A | 10 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.612+6359C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800190 | |||||||
| chr7:120800250 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+6299C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800250 | |||||||
| chr7:120800292 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.612+6257C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800292 | |||||||
| chr7:120800653 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.612+5896C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800653 | |||||||
| chr7:120800744 | G | GTT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(58): Show |
82 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.612+5803_612+5804d others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800744 | |||||||
| chr7:120800744 | G | GTTT | 40 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0023 others(37): Show |
47 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.612+5802_612+5804d others(5): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800744 | |||||||
| chr7:120800744 | G | GTTTT | 7 | a0001c0001t0001g0028 a0001c0001t0001g0039 a0001c0001t0001g0091 others(4): Show |
8 | HG02145.hp2 HG02647.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+5801_612+5804d others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800744 | |||||||
| chr7:120800754 | G | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(119): Show |
152 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.612+5795C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800754 | |||||||
| chr7:120800844 | GTTCACCT others(21): Show |
G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+5677_612+5704d others(30): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800844 | |||||||
| chr7:120801033 | G | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.612+5516C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120801033 | |||||||
| chr7:120801123 | T | A | 1 | a0001c0001t0009g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.612+5426A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120801123 | |||||||
| chr7:120801327 | T | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+5222A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120801327 | |||||||
| chr7:120801586 | C | G | 1 | a0001c0001t0002g0007 | 4 | NA18969.hp2 NA18994.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.612+4963G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120801586 | |||||||
| chr7:120801727 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.612+4822G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120801727 | |||||||
| chr7:120801935 | A | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+4614T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120801935 | |||||||
| chr7:120802317 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0107 |
2 | HG01361.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.612+4232C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120802317 | |||||||
| chr7:120803018 | A | G | 1 | a0001c0002t0004g0216 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.612+3531T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120803018 | |||||||
| chr7:120803131 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(95): Show |
125 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.612+3418C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120803131 | |||||||
| chr7:120803256 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.612+3293G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120803256 | |||||||
| chr7:120803416 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.612+3133A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120803416 | |||||||
| chr7:120803773 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.612+2776A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120803773 | |||||||
| chr7:120804048 | T | C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+2501A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120804048 | |||||||
| chr7:120804074 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.612+2475C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120804074 | |||||||
| chr7:120804337 | T | G | 55 | a0001c0001t0001g0165 a0001c0001t0002g0002 a0001c0001t0002g0005 others(52): Show |
70 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.612+2212A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120804337 | |||||||
| chr7:120805014 | C | T | 2 | a0001c0001t0001g0055 a0002c0005t0001g0117 |
2 | HG01168.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.612+1535G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120805014 | |||||||
| chr7:120805080 | G | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(80): Show |
104 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.612+1469C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120805080 | |||||||
| chr7:120805269 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0149 |
3 | HG03490.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.612+1280A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120805269 | |||||||
| chr7:120805299 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.612+1250T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120805299 | |||||||
| chr7:120805498 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.612+1051G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120805498 | |||||||
| chr7:120805815 | C | A | 1 | a0001c0001t0001g0016 | 2 | HG01074.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.612+734G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120805815 | |||||||
| chr7:120806074 | A | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(87): Show |
117 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.612+475T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120806074 | |||||||
| chr7:120806335 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.612+214C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120806335 | |||||||
| chr7:120806538 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.612+11A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120806538 | |||||||
| chr7:120806832 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.469-140A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120806832 | |||||||
| chr7:120806855 | G | T | 1 | a0001c0002t0003g0053 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.469-163C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120806855 | |||||||
| chr7:120806871 | G | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-179C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120806871 | |||||||
| chr7:120806874 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.469-182A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120806874 | |||||||
| chr7:120806992 | T | C | 1 | a0001c0001t0002g0234 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.469-300A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120806992 | |||||||
| chr7:120807152 | A | C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.469-460T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120807152 | |||||||
| chr7:120807406 | G | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
252 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(249): Show |
intron_variant | MODIFIER | c.469-714C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120807406 | |||||||
| chr7:120807580 | C | T | 1 | a0001c0002t0003g0065 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.469-888G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120807580 | |||||||
| chr7:120807707 | T | A | 1 | a0001c0001t0002g0217 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.469-1015A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120807707 | |||||||
| chr7:120807799 | A | G | 1 | a0001c0002t0003g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.469-1107T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120807799 | |||||||
| chr7:120807816 | C | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(11): Show |
18 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.469-1124G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120807816 | |||||||
| chr7:120807884 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.469-1192A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120807884 | |||||||
| chr7:120808245 | T | C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-1553A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120808245 | |||||||
| chr7:120808325 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(95): Show |
125 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.469-1633A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120808325 | |||||||
| chr7:120808543 | T | C | 2 | a0001c0001t0002g0191 a0001c0001t0002g0193 |
2 | NA18944.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.469-1851A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120808543 | |||||||
| chr7:120808670 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+1793G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120808670 | |||||||
| chr7:120808683 | C | A | 1 | a0001c0001t0001g0150 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.468+1780G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120808683 | |||||||
| chr7:120808748 | G | A | 2 | a0001c0003t0002g0187 a0001c0003t0002g0188 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.468+1715C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120808748 | |||||||
| chr7:120808749 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0010g0079 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.468+1714T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120808749 | |||||||
| chr7:120808830 | T | A | 18 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0029 others(15): Show |
21 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.468+1633A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120808830 | |||||||
| chr7:120809003 | G | A | 1 | a0001c0001t0005g0119 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.468+1460C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809003 | |||||||
| chr7:120809037 | C | T | 3 | a0001c0001t0001g0124 a0001c0001t0001g0137 a0001c0001t0011g0102 |
3 | HG01123.hp1 HG01168.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.468+1426G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809037 | |||||||
| chr7:120809071 | T | C | 2 | a0001c0002t0003g0070 a0001c0002t0003g0071 |
2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.468+1392A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809071 | |||||||
| chr7:120809141 | T | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
3 | HG02145.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.468+1322A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809141 | |||||||
| chr7:120809149 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.468+1314C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809149 | |||||||
| chr7:120809191 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.468+1272A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809191 | |||||||
| chr7:120809396 | C | G | 1 | a0001c0001t0010g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.468+1067G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809396 | |||||||
| chr7:120809729 | G | A | 1 | a0001c0001t0002g0238 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.468+734C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809729 | |||||||
| chr7:120809756 | A | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(95): Show |
125 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.468+707T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809756 | |||||||
| chr7:120809759 | C | T | 2 | a0001c0003t0002g0187 a0001c0003t0002g0188 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.468+704G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809759 | |||||||
| chr7:120809877 | T | A | 2 | a0001c0002t0003g0070 a0001c0002t0003g0071 |
2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.468+586A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809877 | |||||||
| chr7:120810216 | G | A | 1 | a0001c0002t0008g0061 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.468+247C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120810216 | |||||||
| chr7:120810430 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.468+33G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120810430 | |||||||
| chr7:120810604 | G | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
252 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(249): Show |
intron_variant | MODIFIER | c.361-34C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810604 | |||||||
| chr7:120810624 | T | TCA | 95 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(92): Show |
126 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.361-56_361-55dupTG | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810624 | |||||||
| chr7:120810624 | T | TCACA | 16 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0049 others(13): Show |
17 | HG01123.hp1 HG01168.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.361-58_361-55dupTG others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810624 | |||||||
| chr7:120810624 | T | TCACACA | 4 | a0001c0001t0001g0021 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
5 | HG00621.hp1 NA18947.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.361-60_361-55dupTG others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810624 | |||||||
| chr7:120810624 | TCA | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0087 others(67): Show |
89 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.361-56_361-55delTG | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810624 | |||||||
| chr7:120810624 | TCACA | T | 14 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.361-58_361-55delTG others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810624 | |||||||
| chr7:120810624 | TCACACA | T | 3 | a0001c0002t0003g0063 a0001c0003t0002g0187 a0001c0003t0002g0188 |
3 | HG03209.hp1 NA18906.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.361-60_361-55delTG others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810624 | |||||||
| chr7:120810672 | G | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.361-102C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810672 | |||||||
| chr7:120810682 | C | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(113): Show |
146 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.361-112G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810682 | |||||||
| chr7:120810715 | G | A | 7 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0002t0003g0014 others(4): Show |
8 | HG01243.hp1 HG01975.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.361-145C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810715 | |||||||
| chr7:120811049 | C | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(11): Show |
18 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.361-479G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120811049 | |||||||
| chr7:120811150 | T | C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.361-580A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120811150 | |||||||
| chr7:120811578 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(95): Show |
125 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.361-1008C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120811578 | |||||||
| chr7:120811594 | C | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.361-1024G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120811594 | |||||||
| chr7:120811869 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.361-1299C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120811869 | |||||||
| chr7:120811896 | G | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(11): Show |
18 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.361-1326C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120811896 | |||||||
| chr7:120812330 | G | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.361-1760C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812330 | |||||||
| chr7:120812360 | C | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.361-1790G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812360 | |||||||
| chr7:120812416 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG02071.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.361-1846G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812416 | |||||||
| chr7:120812573 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.361-2003A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812573 | |||||||
| chr7:120812760 | C | A | 18 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0029 others(15): Show |
21 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.361-2190G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812760 | |||||||
| chr7:120812885 | C | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(11): Show |
18 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.361-2315G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812885 | |||||||
| chr7:120812887 | A | G | 1 | a0001c0001t0002g0206 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.361-2317T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812887 | |||||||
| chr7:120812894 | C | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(11): Show |
18 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.361-2324G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812894 | |||||||
| chr7:120812936 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.361-2366A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812936 | |||||||
| chr7:120813016 | A | C | 1 | a0001c0001t0002g0235 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.361-2446T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120813016 | |||||||
| chr7:120813019 | C | G | 1 | a0001c0001t0010g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.361-2449G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120813019 | |||||||
| chr7:120813197 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.360+2532A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120813197 | |||||||
| chr7:120813588 | A | C | 1 | a0001c0001t0010g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.360+2141T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120813588 | |||||||
| chr7:120813897 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.360+1832A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120813897 | |||||||
| chr7:120814057 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.360+1672C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120814057 | |||||||
| chr7:120814433 | C | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(11): Show |
18 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.360+1296G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120814433 | |||||||
| chr7:120814801 | T | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(11): Show |
18 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.360+928A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120814801 | |||||||
| chr7:120815587 | A | T | 4 | a0001c0001t0001g0076 a0001c0001t0006g0176 a0001c0001t0006g0177 others(1): Show |
4 | HG03130.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+142T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120815587 | |||||||
| chr7:120815695 | T | C | 1 | a0001c0001t0002g0226 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.360+34A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120815695 | |||||||
| chr7:120815824 | A | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.286-21T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120815824 | |||||||
| chr7:120816137 | A | G | 1 | a0001c0001t0005g0104 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.286-334T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120816137 | |||||||
| chr7:120816209 | A | G | 1 | a0001c0001t0002g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.286-406T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120816209 | |||||||
| chr7:120816252 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG02071.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.286-449T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120816252 | |||||||
| chr7:120816365 | C | CA | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(89): Show |
119 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.286-563dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120816365 | |||||||
| chr7:120816551 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.286-748C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120816551 | |||||||
| chr7:120816917 | C | T | 147 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(144): Show |
176 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.286-1114G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120816917 | |||||||
| chr7:120817127 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.286-1324C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120817127 | |||||||
| chr7:120817171 | C | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-1368G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120817171 | |||||||
| chr7:120817172 | G | A | 55 | a0001c0001t0001g0165 a0001c0001t0002g0002 a0001c0001t0002g0005 others(52): Show |
70 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.286-1369C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120817172 | |||||||
| chr7:120817236 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0085 |
3 | HG00558.hp2 NA18952.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.286-1433T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120817236 | |||||||
| chr7:120817403 | GATT | G | 144 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(141): Show |
173 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(170): Show |
intron_variant | MODIFIER | c.286-1603_286-1601d others(5): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120817403 | |||||||
| chr7:120817416 | C | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-1613G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120817416 | |||||||
| chr7:120817920 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.286-2117G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120817920 | |||||||
| chr7:120818016 | G | A | 1 | a0001c0001t0003g0013 | 2 | HG00735.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.286-2213C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120818016 | |||||||
| chr7:120818218 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG00597.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.286-2415C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120818218 | |||||||
| chr7:120818269 | AT | A | 4 | a0001c0001t0001g0076 a0001c0001t0006g0176 a0001c0001t0006g0177 others(1): Show |
4 | HG03130.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-2467delA | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120818269 | |||||||
| chr7:120818440 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.286-2637C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120818440 | |||||||
| chr7:120818671 | C | T | 1 | a0001c0001t0010g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.286-2868G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120818671 | |||||||
| chr7:120818924 | T | C | 37 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0056 others(34): Show |
40 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.286-3121A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120818924 | |||||||
| chr7:120819230 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.286-3427G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120819230 | |||||||
| chr7:120819376 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.286-3573C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120819376 | |||||||
| chr7:120819439 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.286-3636T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120819439 | |||||||
| chr7:120819477 | A | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
175 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.286-3674T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120819477 | |||||||
| chr7:120819650 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.286-3847G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120819650 | |||||||
| chr7:120819703 | T | C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-3900A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120819703 | |||||||
| chr7:120819776 | C | T | 1 | a0001c0002t0003g0074 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.286-3973G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120819776 | |||||||
| chr7:120820018 | T | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0163 |
2 | NA18969.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.286-4215A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820018 | |||||||
| chr7:120820062 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.286-4259A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820062 | |||||||
| chr7:120820177 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.286-4374A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820177 | |||||||
| chr7:120820346 | C | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
9 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.286-4543G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820346 | |||||||
| chr7:120820407 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.286-4604G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820407 | |||||||
| chr7:120820657 | C | T | 1 | a0001c0001t0002g0205 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.286-4854G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820657 | |||||||
| chr7:120820731 | G | C | 8 | a0001c0001t0002g0005 a0001c0001t0002g0184 a0001c0001t0002g0200 others(5): Show |
12 | HG01123.hp2 HG01192.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.286-4928C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820731 | |||||||
| chr7:120820876 | C | T | 57 | a0001c0001t0001g0165 a0001c0001t0002g0002 a0001c0001t0002g0005 others(54): Show |
72 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.286-5073G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820876 | |||||||
| chr7:120820939 | A | G | 37 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0056 others(34): Show |
40 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.286-5136T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820939 | |||||||
| chr7:120820976 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.286-5173A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820976 | |||||||
| chr7:120821000 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.286-5197G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120821000 | |||||||
| chr7:120821382 | A | T | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG03710.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.286-5579T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120821382 | |||||||
| chr7:120821429 | T | TA | 38 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0056 others(35): Show |
41 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.286-5627dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120821429 | |||||||
| chr7:120821429 | TA | T | 10 | a0001c0001t0001g0048 a0001c0001t0001g0139 a0001c0001t0002g0032 others(7): Show |
11 | HG02015.hp1 HG02015.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-5627delT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120821429 | |||||||
| chr7:120821490 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.286-5687C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120821490 | |||||||
| chr7:120821607 | G | T | 55 | a0001c0001t0001g0165 a0001c0001t0002g0002 a0001c0001t0002g0005 others(52): Show |
70 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.286-5804C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120821607 | |||||||
| chr7:120821682 | C | A | 1 | a0001c0001t0010g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.286-5879G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120821682 | |||||||
| chr7:120821892 | G | T | 147 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(144): Show |
176 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.286-6089C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120821892 | |||||||
| chr7:120822159 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.286-6356G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822159 | |||||||
| chr7:120822170 | T | G | 1 | a0001c0001t0002g0193 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.286-6367A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822170 | |||||||
| chr7:120822247 | T | G | 6 | a0001c0001t0001g0044 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-6444A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822247 | |||||||
| chr7:120822345 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.286-6542T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822345 | |||||||
| chr7:120822364 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.286-6561T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822364 | |||||||
| chr7:120822423 | T | C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-6620A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822423 | |||||||
| chr7:120822527 | CAAAGCAG | C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-6731_286-6725d others(9): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822527 | |||||||
| chr7:120822587 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.286-6784T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822587 | |||||||
| chr7:120822730 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0096 others(6): Show |
13 | HG00423.hp2 HG02074.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.286-6927G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822730 | |||||||
| chr7:120822901 | G | A | 55 | a0001c0001t0001g0165 a0001c0001t0002g0002 a0001c0001t0002g0005 others(52): Show |
70 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.286-7098C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822901 | |||||||
| chr7:120822955 | G | A | 2 | a0001c0003t0002g0187 a0001c0003t0002g0188 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.286-7152C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822955 | |||||||
| chr7:120823235 | C | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-7432G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120823235 | |||||||
| chr7:120823236 | T | C | 2 | a0001c0001t0001g0152 a0001c0001t0010g0079 |
2 | HG03579.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.286-7433A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120823236 | |||||||
| chr7:120823296 | GAT | G | 55 | a0001c0001t0001g0165 a0001c0001t0002g0002 a0001c0001t0002g0005 others(52): Show |
70 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.286-7495_286-7494d others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120823296 | |||||||
| chr7:120823314 | T | C | 1 | a0001c0001t0002g0205 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.286-7511A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120823314 | |||||||
| chr7:120824000 | G | A | 2 | a0001c0001t0006g0176 a0001c0001t0006g0177 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.286-8197C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824000 | |||||||
| chr7:120824012 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.286-8209C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824012 | |||||||
| chr7:120824112 | A | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-8309T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824112 | |||||||
| chr7:120824133 | G | C | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG03710.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.286-8330C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824133 | |||||||
| chr7:120824276 | C | CA | 18 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0024 others(15): Show |
24 | HG00597.hp1 HG01975.hp2 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.286-8474dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824276 | |||||||
| chr7:120824276 | C | CAA | 37 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0055 others(34): Show |
44 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.286-8475_286-8474d others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824276 | |||||||
| chr7:120824495 | C | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
175 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.286-8692G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824495 | |||||||
| chr7:120824515 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.286-8712C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824515 | |||||||
| chr7:120824552 | T | C | 2 | a0001c0003t0002g0187 a0001c0003t0002g0188 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.286-8749A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824552 | |||||||
| chr7:120824839 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.286-9036G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824839 | |||||||
| chr7:120825043 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.286-9240G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825043 | |||||||
| chr7:120825090 | C | T | 2 | a0001c0003t0002g0187 a0001c0003t0002g0188 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.286-9287G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825090 | |||||||
| chr7:120825100 | A | C | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.286-9297T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825100 | |||||||
| chr7:120825262 | G | C | 2 | a0001c0002t0004g0180 a0001c0002t0004g0181 |
2 | HG01978.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.286-9459C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825262 | |||||||
| chr7:120825276 | C | T | 2 | a0001c0002t0003g0068 a0001c0002t0003g0072 |
2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.286-9473G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825276 | |||||||
| chr7:120825505 | T | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
175 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.286-9702A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825505 | |||||||
| chr7:120825824 | G | A | 1 | a0001c0001t0002g0236 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.286-10021C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825824 | |||||||
| chr7:120825903 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.286-10100G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825903 | |||||||
| chr7:120825913 | A | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(142): Show |
174 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.286-10110T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825913 | |||||||
| chr7:120825986 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.286-10183A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825986 | |||||||
| chr7:120826005 | G | A | 10 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-10202C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120826005 | |||||||
| chr7:120826171 | A | T | 6 | a0001c0001t0001g0044 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-10368T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120826171 | |||||||
| chr7:120826426 | T | C | 57 | a0001c0001t0001g0165 a0001c0001t0002g0002 a0001c0001t0002g0005 others(54): Show |
72 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.286-10623A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120826426 | |||||||
| chr7:120826496 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.286-10693A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120826496 | |||||||
| chr7:120826548 | T | C | 1 | a0001c0001t0002g0206 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.286-10745A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120826548 | |||||||
| chr7:120826924 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.286-11121G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120826924 | |||||||
| chr7:120826955 | A | T | 147 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(144): Show |
176 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.286-11152T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120826955 | |||||||
| chr7:120826992 | A | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
175 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.286-11189T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120826992 | |||||||
| chr7:120827005 | G | A | 1 | a0001c0001t0012g0175 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.286-11202C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120827005 | |||||||
| chr7:120827122 | T | TAATAGCT others(311): Show |
1 | a0001c0001t0001g0091 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.286-11320_286-1131 others(322): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120827122 | |||||||
| chr7:120827122 | T | TAATAGCT others(312): Show |
4 | a0001c0001t0001g0044 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | HG02647.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-11320_286-1131 others(323): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120827122 | |||||||
| chr7:120827122 | T | TAATAGCT others(316): Show |
1 | a0001c0001t0001g0095 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.286-11320_286-1131 others(327): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120827122 | |||||||
| chr7:120827515 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(10): Show |
19 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.285+11262G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120827515 | |||||||
| chr7:120827871 | C | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.285+10906G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120827871 | |||||||
| chr7:120827993 | G | C | 12 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0024 others(9): Show |
18 | HG00597.hp1 HG01975.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.285+10784C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120827993 | |||||||
| chr7:120827995 | A | T | 1 | a0001c0002t0004g0214 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.285+10782T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120827995 | |||||||
| chr7:120828015 | A | G | 2 | a0001c0003t0002g0187 a0001c0003t0002g0188 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.285+10762T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828015 | |||||||
| chr7:120828158 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.285+10619T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828158 | |||||||
| chr7:120828189 | T | C | 3 | a0001c0001t0002g0007 a0001c0001t0002g0199 a0001c0001t0002g0207 |
6 | NA18956.hp2 NA18969.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+10588A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828189 | |||||||
| chr7:120828443 | C | G | 1 | a0001c0001t0002g0223 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.285+10334G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828443 | |||||||
| chr7:120828554 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.285+10223G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828554 | |||||||
| chr7:120828655 | C | CT | 64 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0041 others(61): Show |
80 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.285+10121dupA | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828655 | |||||||
| chr7:120828655 | C | CTT | 8 | a0001c0001t0001g0091 a0001c0001t0002g0189 a0001c0001t0002g0197 others(5): Show |
8 | HG02074.hp2 HG02486.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+10120_285+1012 others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828655 | |||||||
| chr7:120828655 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.285+10122G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828655 | |||||||
| chr7:120828655 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0193 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.285+10112_285+1012 others(14): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828655 | |||||||
| chr7:120828888 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.285+9889T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828888 | |||||||
| chr7:120828949 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.285+9828A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828949 | |||||||
| chr7:120829220 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.285+9557C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120829220 | |||||||
| chr7:120829266 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.285+9511G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120829266 | |||||||
| chr7:120829388 | A | AT | 4 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0130 others(1): Show |
8 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+9388dupA | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120829388 | |||||||
| chr7:120829636 | T | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
175 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.285+9141A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120829636 | |||||||
| chr7:120830006 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.285+8771G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120830006 | |||||||
| chr7:120830556 | A | T | 1 | a0001c0002t0003g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.285+8221T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120830556 | |||||||
| chr7:120830698 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0109 |
3 | HG02572.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.285+8079C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120830698 | |||||||
| chr7:120831099 | T | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+7678A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120831099 | |||||||
| chr7:120831308 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0078 |
6 | HG02109.hp2 HG02280.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.285+7469C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120831308 | |||||||
| chr7:120831327 | CAG | C | 6 | a0001c0001t0002g0032 a0001c0001t0002g0227 a0001c0001t0002g0228 others(3): Show |
7 | HG02015.hp2 NA18962.hp2 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+7448_285+7449d others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120831327 | |||||||
| chr7:120831499 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.285+7278T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120831499 | |||||||
| chr7:120831923 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.285+6854G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120831923 | |||||||
| chr7:120832004 | CAAAT | C | 36 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0056 others(33): Show |
39 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.285+6769_285+6772d others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120832004 | |||||||
| chr7:120832006 | A | C | 1 | a0003c0004t0001g0127 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.285+6771T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120832006 | |||||||
| chr7:120832402 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.285+6375G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120832402 | |||||||
| chr7:120832504 | C | T | 1 | a0001c0001t0002g0234 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.285+6273G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120832504 | |||||||
| chr7:120832590 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.285+6187C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120832590 | |||||||
| chr7:120832729 | G | A | 2 | a0001c0001t0002g0208 a0001c0001t0013g0178 |
2 | HG02015.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.285+6048C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120832729 | |||||||
| chr7:120832916 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.285+5861C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120832916 | |||||||
| chr7:120832990 | G | A | 1 | a0001c0002t0003g0075 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.285+5787C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120832990 | |||||||
| chr7:120833296 | C | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
175 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.285+5481G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120833296 | |||||||
| chr7:120833418 | A | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0087 others(5): Show |
12 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.285+5359T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120833418 | |||||||
| chr7:120833484 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.285+5293A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120833484 | |||||||
| chr7:120833537 | C | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0170 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.285+5240G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120833537 | |||||||
| chr7:120833699 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.285+5078A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120833699 | |||||||
| chr7:120834000 | G | C | 124 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(121): Show |
146 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.285+4777C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834000 | |||||||
| chr7:120834010 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.285+4767A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834010 | |||||||
| chr7:120834114 | G | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
175 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.285+4663C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834114 | |||||||
| chr7:120834128 | T | C | 1 | a0001c0001t0002g0209 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.285+4649A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834128 | |||||||
| chr7:120834132 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.285+4645C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834132 | |||||||
| chr7:120834261 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0128 |
4 | NA18962.hp1 NA18975.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+4516T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834261 | |||||||
| chr7:120834388 | G | C | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.285+4389C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834388 | |||||||
| chr7:120834481 | G | T | 2 | a0001c0001t0006g0176 a0001c0001t0006g0177 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.285+4296C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834481 | |||||||
| chr7:120834520 | A | G | 36 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0056 others(33): Show |
39 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.285+4257T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834520 | |||||||
| chr7:120834587 | T | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+4190A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834587 | |||||||
| chr7:120834633 | C | A | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.285+4144G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834633 | |||||||
| chr7:120834691 | T | C | 2 | a0001c0001t0002g0210 a0001c0001t0002g0213 |
2 | NA18968.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.285+4086A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834691 | |||||||
| chr7:120834748 | T | C | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.285+4029A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834748 | |||||||
| chr7:120834955 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.285+3822A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834955 | |||||||
| chr7:120835275 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.285+3502C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120835275 | |||||||
| chr7:120835432 | A | T | 1 | a0001c0001t0002g0230 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.285+3345T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120835432 | |||||||
| chr7:120835468 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.285+3309T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120835468 | |||||||
| chr7:120835471 | T | A | 7 | a0001c0001t0002g0194 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG00438.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+3306A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120835471 | |||||||
| chr7:120835537 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
9 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.285+3240C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120835537 | |||||||
| chr7:120835955 | C | CA | 2 | a0001c0001t0003g0013 a0001c0002t0003g0072 |
3 | HG00735.hp1 HG00735.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.285+2821dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120835955 | |||||||
| chr7:120836091 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0105 |
3 | NA18949.hp1 NA19065.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.285+2686G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836091 | |||||||
| chr7:120836102 | C | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0055 others(38): Show |
48 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.285+2675G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836102 | |||||||
| chr7:120836316 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0092 |
2 | HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.285+2461C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836316 | |||||||
| chr7:120836491 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.285+2286T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836491 | |||||||
| chr7:120836550 | T | C | 1 | a0001c0002t0003g0075 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.285+2227A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836550 | |||||||
| chr7:120836553 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.285+2224C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836553 | |||||||
| chr7:120836591 | C | T | 2 | a0001c0001t0006g0176 a0001c0001t0006g0177 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.285+2186G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836591 | |||||||
| chr7:120836771 | T | C | 97 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): Show |
118 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.285+2006A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836771 | |||||||
| chr7:120836789 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.285+1988A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836789 | |||||||
| chr7:120837008 | G | A | 1 | a0001c0002t0004g0216 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.285+1769C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837008 | |||||||
| chr7:120837152 | G | A | 2 | a0001c0002t0003g0167 a0001c0002t0003g0168 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.285+1625C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837152 | |||||||
| chr7:120837311 | A | AT | 4 | a0001c0001t0002g0201 a0001c0001t0002g0218 a0001c0002t0004g0180 others(1): Show |
4 | HG01071.hp2 HG01081.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+1465dupA | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837311 | |||||||
| chr7:120837315 | A | AT | 109 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(106): Show |
132 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.285+1461dupA | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837315 | |||||||
| chr7:120837315 | A | T | 5 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0001t0002g0218 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+1462T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837315 | |||||||
| chr7:120837318 | T | TA | 18 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(15): Show |
22 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.285+1458_285+1459i others(3): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837318 | |||||||
| chr7:120837372 | C | T | 1 | a0001c0002t0004g0179 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.285+1405G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837372 | |||||||
| chr7:120837404 | C | T | 58 | a0001c0001t0001g0165 a0001c0001t0002g0002 a0001c0001t0002g0005 others(55): Show |
73 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.285+1373G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837404 | |||||||
| chr7:120837436 | C | T | 2 | a0001c0001t0002g0200 a0001c0001t0002g0226 |
2 | HG01255.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.285+1341G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837436 | |||||||
| chr7:120837792 | T | G | 1 | a0001c0003t0002g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.285+985A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837792 | |||||||
| chr7:120837804 | G | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+973C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837804 | |||||||
| chr7:120837876 | T | C | 1 | a0001c0001t0002g0185 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.285+901A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837876 | |||||||
| chr7:120837982 | TAA | T | 9 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(6): Show |
10 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+793_285+794del others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837982 | |||||||
| chr7:120837988 | C | T | 9 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(6): Show |
10 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+789G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837988 | |||||||
| chr7:120838296 | C | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0157 |
3 | NA18612.hp1 NA19007.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.285+481G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120838296 | |||||||
| chr7:120838497 | T | G | 1 | a0001c0002t0008g0061 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.285+280A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120838497 | |||||||
| chr7:120838601 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.285+176G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120838601 | |||||||
| chr7:120839149 | T | C | 1 | a0001c0002t0004g0220 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.150-237A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 3/7 | chr7 | 120839149 | |||||||
| chr7:120839319 | T | A | 1 | a0001c0001t0002g0217 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.150-407A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 3/7 | chr7 | 120839319 | |||||||
| chr7:120839812 | T | G | 1 | a0001c0001t0001g0055 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.149+215A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 3/7 | chr7 | 120839812 | |||||||
| chr7:120839926 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.149+101A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 3/7 | chr7 | 120839926 | |||||||
| chr7:120840132 | C | T | 18 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(15): Show |
22 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.67-23G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840132 | |||||||
| chr7:120840156 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.67-47A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840156 | |||||||
| chr7:120840202 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.67-93T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840202 | |||||||
| chr7:120840221 | T | C | 2 | a0001c0001t0002g0195 a0001c0001t0002g0219 |
2 | HG00642.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.67-112A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840221 | |||||||
| chr7:120840420 | G | A | 19 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(16): Show |
23 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.67-311C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840420 | |||||||
| chr7:120840491 | C | CA | 19 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(16): Show |
23 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.67-383dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840491 | |||||||
| chr7:120840575 | T | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-466A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840575 | |||||||
| chr7:120840633 | T | C | 32 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0056 others(29): Show |
35 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.67-524A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840633 | |||||||
| chr7:120840697 | TACTCA | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
3 | HG02145.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.67-593_67-589delTG others(3): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840697 | |||||||
| chr7:120841077 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.67-968G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841077 | |||||||
| chr7:120841103 | G | A | 3 | a0001c0001t0001g0059 a0001c0002t0003g0057 a0001c0002t0003g0058 |
3 | HG01243.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.67-994C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841103 | |||||||
| chr7:120841194 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.67-1085G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841194 | |||||||
| chr7:120841232 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67-1123C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841232 | |||||||
| chr7:120841281 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.67-1172T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841281 | |||||||
| chr7:120841515 | C | T | 32 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0056 others(29): Show |
35 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.67-1406G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841515 | |||||||
| chr7:120841633 | A | ATTAAGC | 4 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0002t0003g0014 others(1): Show |
5 | HG01975.hp1 HG02559.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-1525_67-1524ins others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841633 | |||||||
| chr7:120841649 | T | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0077 others(7): Show |
13 | HG00558.hp2 HG02559.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.67-1540A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841649 | |||||||
| chr7:120841723 | A | C | 1 | a0001c0001t0001g0018 | 2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.67-1614T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841723 | |||||||
| chr7:120841764 | C | T | 147 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(144): Show |
176 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.67-1655G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841764 | |||||||
| chr7:120842033 | G | T | 9 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(6): Show |
10 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-1924C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842033 | |||||||
| chr7:120842053 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.67-1944T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842053 | |||||||
| chr7:120842448 | TA | T | 9 | a0001c0001t0001g0050 a0001c0001t0001g0122 a0001c0001t0001g0123 others(6): Show |
9 | HG00738.hp2 HG01081.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.67-2340delT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842448 | |||||||
| chr7:120842448 | TAA | T | 132 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(129): Show |
156 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.67-2341_67-2340del others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842448 | |||||||
| chr7:120842448 | TAAA | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0081 a0001c0001t0002g0185 others(3): Show |
7 | HG01074.hp2 HG01192.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-2342_67-2340del others(3): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842448 | |||||||
| chr7:120842610 | T | A | 4 | a0001c0001t0001g0076 a0001c0001t0006g0176 a0001c0001t0006g0177 others(1): Show |
4 | HG03130.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-2501A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842610 | |||||||
| chr7:120842624 | G | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-2515C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842624 | |||||||
| chr7:120842831 | A | G | 1 | a0001c0001t0011g0102 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.67-2722T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842831 | |||||||
| chr7:120842881 | A | T | 2 | a0001c0001t0006g0176 a0001c0001t0006g0177 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.67-2772T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842881 | |||||||
| chr7:120842904 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.67-2795G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842904 | |||||||
| chr7:120842905 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0105 others(1): Show |
6 | HG01975.hp2 NA18949.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.67-2796C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842905 | |||||||
| chr7:120843041 | C | T | 63 | a0001c0001t0001g0165 a0001c0001t0002g0002 a0001c0001t0002g0005 others(60): Show |
78 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.67-2932G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843041 | |||||||
| chr7:120843117 | A | T | 1 | a0001c0001t0010g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.67-3008T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843117 | |||||||
| chr7:120843124 | G | A | 93 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(90): Show |
112 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.67-3015C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843124 | |||||||
| chr7:120843205 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67-3096T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843205 | |||||||
| chr7:120843282 | T | C | 147 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(144): Show |
176 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.67-3173A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843282 | |||||||
| chr7:120843445 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.67-3336T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843445 | |||||||
| chr7:120843476 | G | A | 1 | a0001c0001t0002g0194 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.67-3367C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843476 | |||||||
| chr7:120843486 | C | T | 1 | a0001c0001t0001g0018 | 2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.67-3377G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843486 | |||||||
| chr7:120843667 | T | A | 93 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(90): Show |
112 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.67-3558A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843667 | |||||||
| chr7:120843707 | G | C | 4 | a0001c0001t0001g0076 a0001c0001t0006g0176 a0001c0001t0006g0177 others(1): Show |
4 | HG03130.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-3598C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843707 | |||||||
| chr7:120843804 | G | A | 5 | a0001c0002t0003g0015 a0001c0002t0003g0053 a0001c0002t0003g0064 others(2): Show |
6 | HG01496.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.67-3695C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843804 | |||||||
| chr7:120843843 | A | G | 57 | a0001c0001t0001g0165 a0001c0001t0002g0002 a0001c0001t0002g0005 others(54): Show |
72 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.67-3734T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843843 | |||||||
| chr7:120843855 | G | A | 1 | a0001c0002t0003g0014 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.67-3746C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843855 | |||||||
| chr7:120843999 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.67-3890G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843999 | |||||||
| chr7:120844028 | C | G | 3 | a0001c0001t0001g0101 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG00597.hp2 NA19057.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.67-3919G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120844028 | |||||||
| chr7:120844336 | C | T | 1 | a0001c0001t0002g0197 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.67-4227G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120844336 | |||||||
| chr7:120844343 | C | T | 1 | a0001c0002t0003g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.67-4234G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120844343 | |||||||
| chr7:120844418 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67-4309C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120844418 | |||||||
| chr7:120844565 | T | G | 1 | a0001c0002t0004g0220 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.67-4456A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120844565 | |||||||
| chr7:120844628 | C | T | 6 | a0001c0001t0002g0032 a0001c0001t0002g0227 a0001c0001t0002g0228 others(3): Show |
7 | HG02015.hp2 NA18962.hp2 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-4519G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120844628 | |||||||
| chr7:120844629 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.67-4520C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120844629 | |||||||
| chr7:120845241 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.67-5132C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120845241 | |||||||
| chr7:120845373 | C | T | 32 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0056 others(29): Show |
35 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.67-5264G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120845373 | |||||||
| chr7:120845497 | A | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.67-5388T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120845497 | |||||||
| chr7:120845711 | G | T | 1 | a0001c0001t0001g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.67-5602C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120845711 | |||||||
| chr7:120845768 | G | C | 1 | a0001c0001t0002g0222 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.67-5659C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120845768 | |||||||
| chr7:120845826 | T | C | 1 | a0001c0001t0009g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.67-5717A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120845826 | |||||||
| chr7:120845936 | T | C | 147 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(144): Show |
176 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.67-5827A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120845936 | |||||||
| chr7:120846006 | A | C | 1 | a0001c0001t0006g0176 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.67-5897T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120846006 | |||||||
| chr7:120846112 | G | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.67-6003C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120846112 | |||||||
| chr7:120846114 | G | C | 9 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(6): Show |
10 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-6005C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120846114 | |||||||
| chr7:120846459 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.67-6350A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120846459 | |||||||
| chr7:120846516 | CA | C | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.67-6408delT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120846516 | |||||||
| chr7:120846695 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.67-6586G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120846695 | |||||||
| chr7:120846743 | T | C | 147 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(144): Show |
176 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.67-6634A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120846743 | |||||||
| chr7:120846843 | G | A | 1 | a0001c0002t0004g0179 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.67-6734C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120846843 | |||||||
| chr7:120847131 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0105 |
5 | NA18949.hp1 NA18971.hp2 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-7022G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847131 | |||||||
| chr7:120847233 | C | CA | 12 | a0001c0001t0001g0085 a0001c0001t0001g0164 a0001c0001t0001g0165 others(9): Show |
14 | HG00621.hp2 HG01981.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.67-7125dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847233 | |||||||
| chr7:120847233 | C | CAA | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.67-7126_67-7125dup others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847233 | |||||||
| chr7:120847233 | CA | C | 40 | a0001c0001t0001g0044 a0001c0001t0001g0050 a0001c0001t0001g0055 others(37): Show |
43 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.67-7125delT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847233 | |||||||
| chr7:120847244 | A | C | 6 | a0001c0001t0005g0022 a0001c0001t0005g0104 a0001c0001t0005g0110 others(3): Show |
7 | HG00558.hp1 NA18954.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-7135T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847244 | |||||||
| chr7:120847246 | AAC | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0170 others(1): Show |
9 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.67-7139_67-7138del others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847246 | |||||||
| chr7:120847247 | AC | A | 25 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0037 others(22): Show |
31 | HG00558.hp2 HG00642.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.67-7139delG | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847247 | |||||||
| chr7:120847248 | C | A | 75 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0029 others(72): Show |
89 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.67-7139G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847248 | |||||||
| chr7:120847530 | T | C | 1 | a0001c0003t0002g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67-7421A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847530 | |||||||
| chr7:120847808 | T | C | 64 | a0001c0001t0001g0165 a0001c0001t0002g0002 a0001c0001t0002g0005 others(61): Show |
79 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.67-7699A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847808 | |||||||
| chr7:120847875 | C | T | 1 | a0001c0002t0008g0061 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.67-7766G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847875 | |||||||
| chr7:120847966 | G | A | 1 | a0001c0002t0003g0074 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.67-7857C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847966 | |||||||
| chr7:120848015 | C | T | 1 | a0001c0001t0002g0228 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.67-7906G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848015 | |||||||
| chr7:120848027 | C | T | 2 | a0001c0003t0002g0187 a0001c0003t0002g0188 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.67-7918G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848027 | |||||||
| chr7:120848169 | T | A | 1 | a0001c0001t0001g0159 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.67-8060A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848169 | |||||||
| chr7:120848196 | C | G | 1 | a0002c0005t0001g0117 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.67-8087G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848196 | |||||||
| chr7:120848297 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.67-8188T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848297 | |||||||
| chr7:120848506 | TG | T | 4 | a0001c0002t0003g0015 a0001c0002t0003g0053 a0001c0002t0003g0064 others(1): Show |
5 | HG01496.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+8191delC | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848506 | |||||||
| chr7:120848550 | A | T | 1 | a0001c0001t0001g0160 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.66+8148T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848550 | |||||||
| chr7:120848580 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.66+8118T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848580 | |||||||
| chr7:120848715 | A | C | 1 | a0001c0002t0003g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.66+7983T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848715 | |||||||
| chr7:120848723 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.66+7975C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848723 | |||||||
| chr7:120848787 | T | C | 5 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
5 | HG02559.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+7911A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848787 | |||||||
| chr7:120848857 | A | C | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.66+7841T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848857 | |||||||
| chr7:120849082 | G | A | 1 | a0001c0002t0003g0075 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.66+7616C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120849082 | |||||||
| chr7:120849385 | G | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+7313C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120849385 | |||||||
| chr7:120849409 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.66+7289A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120849409 | |||||||
| chr7:120849601 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.66+7097T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120849601 | |||||||
| chr7:120849657 | C | T | 32 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0056 others(29): Show |
35 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.66+7041G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120849657 | |||||||
| chr7:120849950 | C | T | 1 | a0001c0002t0003g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.66+6748G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120849950 | |||||||
| chr7:120850009 | TGA | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0100 a0001c0001t0001g0111 others(3): Show |
7 | HG00621.hp1 HG02083.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+6687_66+6688del others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120850009 | |||||||
| chr7:120850464 | C | T | 1 | a0001c0001t0005g0110 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.66+6234G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120850464 | |||||||
| chr7:120850549 | T | C | 2 | a0001c0001t0002g0225 a0001c0001t0002g0231 |
2 | HG02074.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.66+6149A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120850549 | |||||||
| chr7:120850753 | G | A | 64 | a0001c0001t0001g0165 a0001c0001t0002g0002 a0001c0001t0002g0005 others(61): Show |
79 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.66+5945C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120850753 | |||||||
| chr7:120850874 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.66+5824C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120850874 | |||||||
| chr7:120850979 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0109 |
3 | HG02572.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.66+5719G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120850979 | |||||||
| chr7:120850985 | C | T | 1 | a0001c0001t0012g0175 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.66+5713G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120850985 | |||||||
| chr7:120851060 | T | C | 64 | a0001c0001t0001g0165 a0001c0001t0002g0002 a0001c0001t0002g0005 others(61): Show |
79 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.66+5638A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120851060 | |||||||
| chr7:120851232 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.66+5466C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120851232 | |||||||
| chr7:120851398 | G | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0046 others(4): Show |
9 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+5300C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120851398 | |||||||
| chr7:120851570 | A | G | 1 | a0001c0002t0003g0064 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.66+5128T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120851570 | |||||||
| chr7:120851905 | T | C | 17 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0029 others(14): Show |
20 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.66+4793A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120851905 | |||||||
| chr7:120851928 | T | G | 149 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(146): Show |
178 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.66+4770A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120851928 | |||||||
| chr7:120852020 | G | T | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.66+4678C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852020 | |||||||
| chr7:120852023 | G | A | 1 | a0001c0001t0002g0236 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.66+4675C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852023 | |||||||
| chr7:120852069 | T | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+4629A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852069 | |||||||
| chr7:120852191 | T | A | 16 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0037 others(13): Show |
19 | HG00558.hp2 HG01433.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.66+4507A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852191 | |||||||
| chr7:120852452 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0109 |
3 | HG02572.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.66+4246G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852452 | |||||||
| chr7:120852516 | A | T | 1 | a0001c0002t0004g0196 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.66+4182T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852516 | |||||||
| chr7:120852517 | T | C | 1 | a0001c0002t0003g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.66+4181A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852517 | |||||||
| chr7:120852610 | G | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+4088C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852610 | |||||||
| chr7:120852644 | T | C | 4 | a0001c0002t0003g0062 a0001c0002t0003g0063 a0001c0002t0004g0179 others(1): Show |
4 | HG01934.hp2 HG02071.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+4054A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852644 | |||||||
| chr7:120852728 | T | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
9 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+3970A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852728 | |||||||
| chr7:120852837 | G | C | 1 | a0001c0001t0001g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.66+3861C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852837 | |||||||
| chr7:120852855 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+3843T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852855 | |||||||
| chr7:120852998 | C | T | 2 | a0001c0001t0002g0032 a0001c0001t0002g0227 |
3 | NA18962.hp2 NA19081.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.66+3700G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852998 | |||||||
| chr7:120853007 | C | A | 1 | a0001c0001t0002g0226 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.66+3691G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853007 | |||||||
| chr7:120853090 | A | AT | 116 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(113): Show |
140 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.66+3607dupA | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853090 | |||||||
| chr7:120853090 | A | ATT | 33 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0055 others(30): Show |
37 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.66+3606_66+3607dup others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853090 | |||||||
| chr7:120853217 | C | T | 1 | a0001c0001t0005g0104 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.66+3481G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853217 | |||||||
| chr7:120853242 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0092 |
2 | HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.66+3456G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853242 | |||||||
| chr7:120853316 | T | A | 96 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(93): Show |
117 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.66+3382A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853316 | |||||||
| chr7:120853362 | C | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
9 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+3336G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853362 | |||||||
| chr7:120853371 | T | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.66+3327A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853371 | |||||||
| chr7:120853449 | C | A | 1 | a0001c0001t0005g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.66+3249G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853449 | |||||||
| chr7:120853471 | G | GAT | 15 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(12): Show |
21 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.66+3225_66+3226dup others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853471 | |||||||
| chr7:120853471 | G | GATAGAT | 2 | a0001c0002t0003g0015 a0001c0002t0003g0067 |
3 | HG01496.hp2 HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.66+3226_66+3227ins others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853471 | |||||||
| chr7:120853471 | G | GATAT | 4 | a0001c0001t0001g0043 a0001c0001t0001g0091 a0001c0001t0001g0173 others(1): Show |
4 | HG02886.hp1 HG02976.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+3223_66+3226dup others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853471 | |||||||
| chr7:120853471 | G | GATATAT | 12 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0041 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.66+3221_66+3226dup others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853471 | |||||||
| chr7:120853471 | G | GATATATA others(1): Show |
14 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0055 others(11): Show |
15 | HG01243.hp1 HG01934.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.66+3219_66+3226dup others(8): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853471 | |||||||
| chr7:120853471 | G | GATATATA others(3): Show |
1 | a0001c0001t0003g0013 | 2 | HG00735.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.66+3217_66+3226dup others(10): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853471 | |||||||
| chr7:120853471 | G | GATATATA others(5): Show |
1 | a0001c0002t0003g0053 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.66+3215_66+3226dup others(12): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853471 | |||||||
| chr7:120853471 | GAT | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0162 a0001c0001t0001g0170 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+3225_66+3226del others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853471 | |||||||
| chr7:120853493 | T | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(19): Show |
26 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.66+3205A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853493 | |||||||
| chr7:120853493 | T | TAC | 5 | a0001c0001t0001g0049 a0001c0001t0001g0076 a0001c0001t0001g0077 others(2): Show |
5 | HG02818.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+3203_66+3204dup others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853493 | |||||||
| chr7:120853493 | T | TACAC | 7 | a0001c0001t0002g0032 a0001c0001t0002g0227 a0001c0001t0002g0228 others(4): Show |
8 | HG02015.hp2 NA18962.hp2 NA18998.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+3201_66+3204dup others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853493 | |||||||
| chr7:120853493 | T | TATAC | 56 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(53): Show |
72 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.66+3204_66+3205ins others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853493 | |||||||
| chr7:120853493 | T | TATATAC | 17 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0002g0192 others(14): Show |
17 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.66+3204_66+3205ins others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853493 | |||||||
| chr7:120853505 | T | C | 3 | a0001c0001t0001g0165 a0001c0001t0002g0232 a0001c0001t0002g0233 |
3 | NA18977.hp2 NA18989.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.66+3193A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853505 | |||||||
| chr7:120853533 | T | C | 1 | a0001c0001t0002g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.66+3165A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853533 | |||||||
| chr7:120853572 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.66+3126G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853572 | |||||||
| chr7:120853769 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.66+2929C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853769 | |||||||
| chr7:120853862 | G | A | 3 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0002g0236 |
3 | NA18971.hp1 NA19063.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.66+2836C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853862 | |||||||
| chr7:120853872 | C | CA | 60 | a0001c0001t0001g0035 a0001c0001t0001g0165 a0001c0001t0002g0002 others(57): Show |
75 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.66+2825dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853872 | |||||||
| chr7:120853884 | A | G | 32 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0056 others(29): Show |
35 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.66+2814T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853884 | |||||||
| chr7:120854189 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.66+2509A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120854189 | |||||||
| chr7:120854357 | C | A | 88 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(85): Show |
107 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.66+2341G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120854357 | |||||||
| chr7:120854805 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.66+1893T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120854805 | |||||||
| chr7:120855006 | A | G | 1 | a0001c0001t0009g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.66+1692T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120855006 | |||||||
| chr7:120855363 | G | A | 1 | a0001c0001t0002g0237 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.66+1335C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120855363 | |||||||
| chr7:120855523 | G | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(146): Show |
178 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.66+1175C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120855523 | |||||||
| chr7:120855771 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.66+927T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120855771 | |||||||
| chr7:120855891 | A | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0045 others(5): Show |
10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.66+807T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120855891 | |||||||
| chr7:120855967 | T | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+731A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120855967 | |||||||
| chr7:120856330 | A | G | 9 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(6): Show |
10 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+368T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120856330 | |||||||
| chr7:120856612 | AGCCATGC others(6): Show |
A | 1 | a0001c0001t0002g0238 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.66+73_66+85delCAAA others(9): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120856612 | |||||||
| chr7:120856626 | G | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+72C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120856626 | |||||||
| chr7:120856917 | C | T | 9 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(6): Show |
10 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-70-84G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120856917 | |||||||
| chr7:120857219 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-70-386T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857219 | |||||||
| chr7:120857371 | C | CGGGGCG | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG02145.hp2 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-71+443_-71+448dup others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857371 | |||||||
| chr7:120857396 | A | G | 148 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(145): Show |
177 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(174): Show |
intron_variant | MODIFIER | c.-71+424T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857396 | |||||||
| chr7:120857397 | G | A | 62 | a0001c0001t0001g0165 a0001c0001t0002g0002 a0001c0001t0002g0005 others(59): Show |
77 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.-71+423C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857397 | |||||||
| chr7:120857397 | G | GGGCGGGG others(5): Show |
1 | a0001c0001t0002g0184 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-71+422_-71+423ins others(12): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857397 | |||||||
| chr7:120857513 | G | A | 3 | a0001c0001t0001g0166 a0001c0002t0003g0167 a0001c0002t0003g0168 |
3 | HG02970.hp2 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-71+307C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857513 | |||||||
| chr7:120857586 | G | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG02630.hp1 HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-71+234C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857586 | |||||||
| chr7:120857588 | C | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-71+232G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857588 | |||||||
| chr7:120857592 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-71+228C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857592 | |||||||
| chr7:120857652 | G | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0173 |
3 | HG02486.hp2 HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-71+168C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857652 | |||||||
| chr7:120857707 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-71+113C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857707 |