Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23471 |
| ensemblid | ENSG00000067167.8 |
| hgncid | 20568 |
| symbol | TRAM1 |
| name | translocation associated membrane protein 1 |
| refseq_nuc | NM_014294.6 |
| refseq_prot | NP_055109.1 |
| ensembl_nuc | ENST00000262213.7 |
| ensembl_prot | ENSP00000262213.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 70573218 |
| end | 70608416 |
| strand | - |
| ver | v1.2 |
| region | chr8:70573218-70608416 |
| region5000 | chr8:70568218-70613416 |
| regionname0 | TRAM1_chr8_70573218_70608416 |
| regionname5000 | TRAM1_chr8_70568218_70613416 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 374 | 321 | 80 | 62 | 131 | 12 | 34 | 109 | TRAM1_chr8_70568218_70613416 | TRAM1 | MAIRK others(369): Show |
chr8 | 70568218 | 70613416 |
| a0002 | 0/0 | 374 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | MAIRK others(369): Show |
chr8 | 70568218 | 70613416 |
| a0003 | 0/0 | 374 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | MAIRK others(369): Show |
chr8 | 70568218 | 70613416 |
| a0004 | 0/0 | 374 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | MAIRK others(369): Show |
chr8 | 70568218 | 70613416 |
| a0005 | 0/0 | 374 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | MAIRK others(369): Show |
chr8 | 70568218 | 70613416 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1122 | 318 | 80 | 62 | 128 | 12 | 34 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGGC others(1117): Show |
chr8 | 70568218 | 70613416 | ||
| a0001c0003 | 0/0 | 1122 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGGC others(1117): Show |
chr8 | 70568218 | 70613416 | ||
| a0001c0007 | 0/0 | 1122 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGGC others(1117): Show |
chr8 | 70568218 | 70613416 | ||
| a0001c0008 | 0/0 | 1122 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGGC others(1117): Show |
chr8 | 70568218 | 70613416 | ||
| a0002c0002 | 0/0 | 1122 | 6 | 6 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGGC others(1117): Show |
chr8 | 70568218 | 70613416 | ||
| a0003c0006 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGGC others(1117): Show |
chr8 | 70568218 | 70613416 | ||
| a0004c0004 | 0/0 | 1122 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGGC others(1117): Show |
chr8 | 70568218 | 70613416 | ||
| a0005c0005 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGGC others(1117): Show |
chr8 | 70568218 | 70613416 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3057 | 183 | 40 | 29 | 85 | 8 | 20 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0001c0001t0002 | 1/0 | 3056 | 56 | 5 | 14 | 32 | 1 | 3 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3051): Show |
chr8 | 70568218 | 70613416 |
| a0001c0001t0003 | 0/0 | 3057 | 45 | 26 | 7 | 6 | 0 | 6 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0001c0001t0004 | 0/0 | 3058 | 9 | 0 | 2 | 3 | 0 | 4 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3053): Show |
chr8 | 70568218 | 70613416 |
| a0001c0001t0005 | 0/0 | 3057 | 7 | 1 | 4 | 0 | 2 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0001c0001t0006 | 0/0 | 3057 | 3 | 1 | 1 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0001c0001t0007 | 0/0 | 3055 | 3 | 2 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3050): Show |
chr8 | 70568218 | 70613416 |
| a0001c0001t0008 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0001c0001t0009 | 0/0 | 3059 | 2 | 1 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3054): Show |
chr8 | 70568218 | 70613416 |
| a0001c0001t0010 | 0/0 | 3057 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0001c0001t0011 | 0/0 | 3058 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3053): Show |
chr8 | 70568218 | 70613416 |
| a0001c0001t0012 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0001c0001t0013 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0001c0001t0014 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0001c0001t0015 | 0/0 | 3059 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3054): Show |
chr8 | 70568218 | 70613416 |
| a0001c0001t0016 | 0/0 | 3057 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0001c0001t0017 | 0/0 | 3057 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0001c0003t0001 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0001c0007t0001 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0001c0008t0001 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0002c0002t0003 | 0/0 | 3057 | 4 | 4 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0002c0002t0008 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0002c0002t0011 | 0/0 | 3058 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3053): Show |
chr8 | 70568218 | 70613416 |
| a0003c0006t0008 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0004c0004t0001 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| a0005c0005t0001 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | ATGCT others(3052): Show |
chr8 | 70568218 | 70613416 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0003 | 0/0 | 9 | 4 | 2 | 2 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 2 | 0 | 2 | 2 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0019 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0207 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0001 | 0/0 | 12 | 0 | 2 | 9 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0004 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0011 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0017 | 1/0 | 3 | 0 | 1 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0005 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0005g0007 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0006g0022 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0007g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0009g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0009g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0010g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0010g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0011g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0012g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0013g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0014g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0015g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0016g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0001t0017g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0007t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0001c0008t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0002c0002t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0002c0002t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0002c0002t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0002c0002t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0002c0002t0008g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0002c0002t0011g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0003c0006t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0004c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| a0005c0005t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0017 | EUR | GBR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | GBR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0022 | EUR | GBR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0081 | EUR | FIN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00609 | hp2 | a0001 | c0008 | t0001 | g0209 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0195 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0022 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01106 | hp2 | a0001 | c0001 | t0009 | g0196 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0038 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01167 | hp2 | a0001 | c0001 | t0016 | g0181 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0082 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01192 | hp1 | a0001 | c0001 | t0011 | g0220 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | PUR | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0215 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | IBS | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0183 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0212 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0184 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0188 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0193 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0213 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0175 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03139 | hp1 | a0003 | c0006 | t0008 | g0176 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0077 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03209 | hp1 | a0002 | c0002 | t0003 | g0203 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0189 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03453 | hp2 | a0002 | c0002 | t0003 | g0202 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03516 | hp1 | a0002 | c0002 | t0011 | g0221 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0205 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0216 | SAS | BEB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0214 | SAS | BEB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0197 | SAS | BEB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03942 | hp1 | a0001 | c0001 | t0015 | g0122 | SAS | BEB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0218 | SAS | BEB | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | STU | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0198 | SAS | STU | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | STU | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18522 | hp1 | a0002 | c0002 | t0003 | g0177 | AFR | YRI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18522 | hp2 | a0001 | c0001 | t0014 | g0078 | AFR | YRI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | YRI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18962 | hp1 | a0004 | c0004 | t0001 | g0061 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA18999 | hp2 | a0001 | c0001 | t0012 | g0060 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | LWK | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | LWK | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | LWK | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19054 | hp1 | a0001 | c0003 | t0001 | g0089 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19066 | hp2 | a0001 | c0001 | t0013 | g0129 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19068 | hp1 | a0001 | c0007 | t0001 | g0167 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | YRI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | ASW | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ASW | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0007 | EUR | TSI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | TSI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG01123 | hp2 | a0001 | c0001 | t0017 | g0210 | AMR | CLM | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | USA | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| HG06807 | hp2 | a0002 | c0002 | t0008 | g0178 | AFR | USA | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | USA | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA20300 | hp2 | a0002 | c0002 | t0003 | g0204 | AFR | USA | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA21309 | hp1 | a0005 | c0005 | t0001 | g0174 | AFR | LWK | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0207 | REF | REF | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0017 | REF | REF | TRAM1_chr8_70568218_70613416 | TRAM1 | chr8 | 70568218 | 70613416 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:70574975 | T | C | 1 | a0003 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.1082A>G | p.Asn361Ser | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1299/3056 | 1082/1125 | 361/374 | chr8 | 70574975 | |||
| chr8:70583738 | A | T | 1 | a0005 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.802T>A | p.Ser268Thr | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 9/11 | 1019/3056 | 802/1125 | 268/374 | chr8 | 70583738 | |||
| chr8:70596265 | C | T | 1 | a0004 | 1 | NA18962.hp1 | missense_variant&splice_region_variant | MODERATE | c.483G>A | p.Met161Ile | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/11 | 700/3056 | 483/1125 | 161/374 | chr8 | 70596265 | |||
| chr8:70596318 | T | C | 1 | a0002 | 6 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
missense_variant | MODERATE | c.430A>G | p.Asn144Asp | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/11 | 647/3056 | 430/1125 | 144/374 | chr8 | 70596318 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:70583314 | G | A | 1 | a0001c0007 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.901C>T | p.Leu301Leu | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/11 | 1118/3056 | 901/1125 | 301/374 | chr8 | 70583314 | |||
| chr8:70597940 | C | T | 1 | a0001c0003 | 1 | NA19054.hp1 | synonymous_variant | LOW | c.381G>A | p.Ala127Ala | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/11 | 598/3056 | 381/1125 | 127/374 | chr8 | 70597940 | |||
| chr8:70608101 | G | A | 1 | a0001c0008 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.99C>T | p.Val33Val | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/11 | 316/3056 | 99/1125 | 33/374 | chr8 | 70608101 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:70573247 | T | C | 3 | a0001c0001t0008 a0002c0002t0008 a0003c0006t0008 |
3 | HG02970.hp2 HG03139.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1685A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1685 | chr8 | 70573247 | ||||||
| chr8:70573283 | C | A | 1 | a0001c0001t0010 | 2 | HG02647.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1649G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1649 | chr8 | 70573283 | ||||||
| chr8:70573408 | A | T | 14 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(11): Show |
209 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*1524T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1524 | chr8 | 70573408 | ||||||
| chr8:70573793 | A | G | 2 | a0001c0001t0014 a0001c0001t0016 |
2 | HG01167.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1139T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1139 | chr8 | 70573793 | ||||||
| chr8:70573850 | A | C | 14 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(11): Show |
209 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*1082T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1082 | chr8 | 70573850 | ||||||
| chr8:70573851 | G | A | 1 | a0001c0001t0005 | 7 | HG00323.hp2 HG01168.hp1 HG01175.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1081C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1081 | chr8 | 70573851 | ||||||
| chr8:70573857 | A | AAT | 2 | a0001c0001t0009 a0001c0001t0015 |
3 | HG01106.hp2 HG02572.hp1 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1073_*1074dupAT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1074 | chr8 | 70573857 | ||||||
| chr8:70573857 | AAT | A | 1 | a0001c0001t0007 | 3 | HG01109.hp1 HG02280.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1073_*1074delAT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 1073 | chr8 | 70573857 | ||||||
| chr8:70573964 | G | T | 1 | a0001c0001t0006 | 3 | HG00140.hp2 HG01071.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*968C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 968 | chr8 | 70573964 | ||||||
| chr8:70574333 | G | C | 17 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(14): Show |
212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*599C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 599 | chr8 | 70574333 | ||||||
| chr8:70574556 | T | G | 3 | a0001c0001t0008 a0002c0002t0008 a0003c0006t0008 |
3 | HG02970.hp2 HG03139.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*376A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 376 | chr8 | 70574556 | ||||||
| chr8:70574557 | T | C | 3 | a0001c0001t0008 a0002c0002t0008 a0003c0006t0008 |
3 | HG02970.hp2 HG03139.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*375A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 375 | chr8 | 70574557 | ||||||
| chr8:70574809 | C | T | 2 | a0001c0001t0013 a0001c0001t0014 |
2 | NA18522.hp2 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*123G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 11/11 | 123 | chr8 | 70574809 | ||||||
| chr8:70608218 | G | T | 1 | a0001c0001t0012 | 1 | NA18999.hp2 | 5_prime_UTR_variant | MODIFIER | c.-19C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/11 | 19 | chr8 | 70608218 | ||||||
| chr8:70608298 | G | A | 1 | a0001c0001t0017 | 1 | HG01123.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-99C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/11 | chr8 | 70608298 | |||||||
| chr8:70608373 | G | GA | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(19): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
5_prime_UTR_variant | MODIFIER | c.-175dupT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/11 | 175 | chr8 | 70608373 | ||||||
| chr8:70608373 | G | GAA | 3 | a0001c0001t0004 a0001c0001t0011 a0002c0002t0011 |
11 | HG01192.hp1 HG01261.hp2 HG01934.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-176_-175dupTT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/11 | 175 | chr8 | 70608373 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:70575159 | T | G | 4 | a0001c0001t0003g0039 a0001c0001t0003g0190 a0001c0001t0003g0191 others(1): Show |
5 | HG02055.hp2 HG02717.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1052-154A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70575159 | |||||||
| chr8:70575403 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1052-398C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70575403 | |||||||
| chr8:70575871 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1052-866C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70575871 | |||||||
| chr8:70576009 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0148 |
3 | HG02015.hp2 HG02132.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1052-1004A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576009 | |||||||
| chr8:70576025 | C | G | 8 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0001c0001t0001g0106 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1052-1020G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576025 | |||||||
| chr8:70576069 | T | TA | 14 | a0001c0001t0001g0076 a0001c0001t0001g0123 a0001c0001t0001g0130 others(11): Show |
14 | HG01167.hp2 HG01175.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1052-1065dupT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576069 | |||||||
| chr8:70576069 | TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0004g0218 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1052-1077_1052-106 others(17): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576069 | |||||||
| chr8:70576070 | AAAAAAAA others(3): Show |
A | 48 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0018 others(45): Show |
66 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.1052-1075_1052-106 others(14): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576070 | |||||||
| chr8:70576079 | AG | A | 15 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0026 others(12): Show |
17 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1052-1075delC | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576079 | |||||||
| chr8:70576080 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(84): Show |
128 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1052-1075C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576080 | |||||||
| chr8:70576102 | A | C | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1052-1097T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576102 | |||||||
| chr8:70576103 | A | C | 29 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0010 others(26): Show |
55 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1052-1098T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576103 | |||||||
| chr8:70576107 | A | C | 50 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0018 others(47): Show |
68 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.1052-1102T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576107 | |||||||
| chr8:70576445 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1052-1440G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576445 | |||||||
| chr8:70576472 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0125 a0001c0001t0001g0157 others(1): Show |
5 | HG01081.hp1 HG01106.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1052-1467C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576472 | |||||||
| chr8:70576842 | C | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(185): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1052-1837G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576842 | |||||||
| chr8:70576845 | T | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(185): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1052-1840A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576845 | |||||||
| chr8:70576850 | A | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(147): Show |
211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1052-1845T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576850 | |||||||
| chr8:70576921 | G | A | 2 | a0001c0001t0007g0038 a0001c0001t0007g0077 |
3 | HG01109.hp1 HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1052-1916C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576921 | |||||||
| chr8:70576954 | C | G | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.1052-1949G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576954 | |||||||
| chr8:70576965 | A | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(147): Show |
211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1052-1960T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576965 | |||||||
| chr8:70576980 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1052-1975G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70576980 | |||||||
| chr8:70577042 | G | A | 1 | a0001c0001t0003g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1052-2037C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577042 | |||||||
| chr8:70577092 | C | T | 5 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0008g0175 others(2): Show |
5 | HG02922.hp1 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1052-2087G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577092 | |||||||
| chr8:70577171 | C | T | 1 | a0001c0001t0003g0193 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1052-2166G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577171 | |||||||
| chr8:70577197 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1052-2192C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577197 | |||||||
| chr8:70577325 | C | T | 5 | a0001c0001t0009g0184 a0002c0002t0003g0202 a0002c0002t0003g0203 others(2): Show |
5 | HG02572.hp1 HG03209.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1052-2320G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577325 | |||||||
| chr8:70577447 | C | A | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(147): Show |
211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1052-2442G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577447 | |||||||
| chr8:70577463 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1052-2458A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577463 | |||||||
| chr8:70577672 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0028 a0001c0001t0001g0111 others(5): Show |
11 | NA18943.hp2 NA18969.hp2 NA18977.hp2 others(8): Show |
intron_variant | MODIFIER | c.1052-2667C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577672 | |||||||
| chr8:70577674 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0065 a0001c0001t0001g0067 others(1): Show |
5 | HG02965.hp2 HG03098.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1052-2669G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577674 | |||||||
| chr8:70577815 | C | T | 1 | a0001c0001t0006g0022 | 3 | HG00140.hp2 HG01071.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1052-2810G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577815 | |||||||
| chr8:70577887 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1052-2882G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577887 | |||||||
| chr8:70577929 | G | A | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1052-2924C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70577929 | |||||||
| chr8:70578211 | G | A | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.1052-3206C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70578211 | |||||||
| chr8:70578258 | A | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0150 a0001c0001t0001g0153 |
3 | NA18975.hp1 NA19055.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.1052-3253T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70578258 | |||||||
| chr8:70578304 | T | C | 26 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0039 others(23): Show |
38 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1052-3299A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70578304 | |||||||
| chr8:70578588 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1052-3583C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70578588 | |||||||
| chr8:70578867 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0004g0212 |
3 | HG01168.hp2 HG01169.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1052-3862G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70578867 | |||||||
| chr8:70578885 | A | G | 4 | a0001c0001t0003g0039 a0001c0001t0003g0190 a0001c0001t0003g0191 others(1): Show |
5 | HG02055.hp2 HG02717.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1052-3880T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70578885 | |||||||
| chr8:70579081 | T | C | 27 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0039 others(24): Show |
39 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1052-4076A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579081 | |||||||
| chr8:70579111 | G | T | 1 | a0001c0001t0012g0060 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1051+4053C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579111 | |||||||
| chr8:70579115 | T | C | 2 | a0001c0001t0001g0173 a0005c0005t0001g0174 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1051+4049A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579115 | |||||||
| chr8:70579161 | C | T | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(145): Show |
209 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.1051+4003G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579161 | |||||||
| chr8:70579258 | G | T | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1051+3906C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579258 | |||||||
| chr8:70579309 | GTATCTAA others(3): Show |
G | 1 | a0001c0001t0001g0126 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1051+3845_1051+385 others(14): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579309 | |||||||
| chr8:70579365 | T | C | 1 | a0001c0001t0003g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1051+3799A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579365 | |||||||
| chr8:70579453 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1051+3711A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579453 | |||||||
| chr8:70579760 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1051+3404G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579760 | |||||||
| chr8:70579783 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1051+3381C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579783 | |||||||
| chr8:70579877 | C | T | 4 | a0001c0001t0003g0012 a0001c0001t0003g0079 a0001c0001t0003g0182 others(1): Show |
7 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1051+3287G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579877 | |||||||
| chr8:70579923 | G | C | 2 | a0001c0001t0007g0038 a0001c0001t0007g0077 |
3 | HG01109.hp1 HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1051+3241C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579923 | |||||||
| chr8:70579956 | A | G | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1051+3208T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70579956 | |||||||
| chr8:70580118 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0201 |
7 | HG00140.hp1 HG00735.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1051+3046G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70580118 | |||||||
| chr8:70580219 | T | A | 1 | a0001c0001t0003g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1051+2945A>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70580219 | |||||||
| chr8:70580243 | A | G | 4 | a0002c0002t0003g0202 a0002c0002t0003g0203 a0002c0002t0003g0204 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051+2921T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70580243 | |||||||
| chr8:70580383 | G | A | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1051+2781C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70580383 | |||||||
| chr8:70580388 | G | A | 2 | a0001c0001t0007g0038 a0001c0001t0007g0077 |
3 | HG01109.hp1 HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1051+2776C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70580388 | |||||||
| chr8:70580487 | A | G | 1 | a0001c0001t0003g0182 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1051+2677T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70580487 | |||||||
| chr8:70580488 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1051+2676A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70580488 | |||||||
| chr8:70580862 | T | C | 2 | a0001c0001t0003g0182 a0001c0001t0003g0183 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1051+2302A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70580862 | |||||||
| chr8:70581053 | A | T | 1 | a0001c0001t0003g0183 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1051+2111T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581053 | |||||||
| chr8:70581107 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0148 a0001c0001t0001g0149 |
4 | HG02015.hp2 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1051+2057C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581107 | |||||||
| chr8:70581312 | C | T | 8 | a0001c0001t0001g0033 a0001c0001t0001g0083 a0001c0001t0001g0088 others(5): Show |
9 | HG00438.hp1 HG00609.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1051+1852G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581312 | |||||||
| chr8:70581375 | G | A | 1 | a0001c0001t0001g0029 | 2 | NA18971.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1051+1789C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581375 | |||||||
| chr8:70581549 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1051+1615A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581549 | |||||||
| chr8:70581613 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1051+1551A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581613 | |||||||
| chr8:70581687 | T | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(77): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1051+1477A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581687 | |||||||
| chr8:70581801 | T | C | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1051+1363A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581801 | |||||||
| chr8:70581879 | T | G | 26 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0039 others(23): Show |
38 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1051+1285A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70581879 | |||||||
| chr8:70582179 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1051+985T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582179 | |||||||
| chr8:70582199 | T | C | 1 | a0001c0001t0003g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1051+965A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582199 | |||||||
| chr8:70582273 | T | C | 3 | a0001c0001t0008g0175 a0002c0002t0008g0178 a0003c0006t0008g0176 |
3 | HG02970.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1051+891A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582273 | |||||||
| chr8:70582277 | C | G | 1 | a0001c0007t0001g0167 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1051+887G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582277 | |||||||
| chr8:70582289 | A | AT | 18 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0026 others(15): Show |
23 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.1051+874dupA | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582289 | |||||||
| chr8:70582289 | AT | A | 10 | a0001c0001t0001g0133 a0001c0001t0001g0140 a0001c0001t0001g0153 others(7): Show |
10 | HG01891.hp2 HG03209.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1051+874delA | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582289 | |||||||
| chr8:70582519 | GA | G | 7 | a0001c0001t0002g0047 a0001c0001t0002g0050 a0001c0001t0003g0180 others(4): Show |
9 | HG00140.hp2 HG01071.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1051+644delT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582519 | |||||||
| chr8:70582545 | G | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(131): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1051+619C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582545 | |||||||
| chr8:70582762 | T | TA | 2 | a0001c0001t0003g0012 a0001c0001t0003g0079 |
5 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1051+401dupT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582762 | |||||||
| chr8:70582782 | T | C | 1 | a0001c0001t0003g0197 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1051+382A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70582782 | |||||||
| chr8:70583073 | GAC | G | 15 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(12): Show |
17 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1051+89_1051+90del others(2): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70583073 | |||||||
| chr8:70583098 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1051+66A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70583098 | |||||||
| chr8:70583131 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1051+33G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 10/10 | chr8 | 70583131 | |||||||
| chr8:70583549 | C | T | 1 | a0001c0001t0003g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.890+101G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 9/10 | chr8 | 70583549 | |||||||
| chr8:70583612 | A | G | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.890+38T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 9/10 | chr8 | 70583612 | |||||||
| chr8:70583810 | G | A | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.747-17C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70583810 | |||||||
| chr8:70583904 | T | C | 3 | a0001c0001t0003g0012 a0001c0001t0003g0079 a0001c0001t0003g0080 |
6 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.747-111A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70583904 | |||||||
| chr8:70584120 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0084 a0001c0001t0001g0121 others(1): Show |
6 | HG00639.hp2 HG00738.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.747-327C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584120 | |||||||
| chr8:70584160 | A | G | 2 | a0001c0001t0002g0041 a0001c0001t0003g0064 |
2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.747-367T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584160 | |||||||
| chr8:70584505 | C | A | 1 | a0001c0001t0002g0023 | 2 | HG02735.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.747-712G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584505 | |||||||
| chr8:70584583 | A | T | 1 | a0001c0001t0001g0201 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.747-790T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584583 | |||||||
| chr8:70584726 | T | C | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.747-933A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584726 | |||||||
| chr8:70584756 | A | T | 1 | a0001c0001t0001g0098 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.747-963T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584756 | |||||||
| chr8:70584816 | A | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(147): Show |
211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.747-1023T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584816 | |||||||
| chr8:70584844 | G | C | 1 | a0001c0001t0003g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.747-1051C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584844 | |||||||
| chr8:70584961 | C | T | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.747-1168G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584961 | |||||||
| chr8:70584979 | C | T | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.747-1186G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584979 | |||||||
| chr8:70584984 | C | T | 1 | a0001c0001t0003g0183 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.747-1191G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70584984 | |||||||
| chr8:70585041 | C | T | 2 | a0001c0001t0002g0049 a0001c0001t0002g0056 |
2 | NA19065.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.747-1248G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585041 | |||||||
| chr8:70585046 | T | A | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.747-1253A>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585046 | |||||||
| chr8:70585141 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.747-1348G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585141 | |||||||
| chr8:70585529 | G | C | 10 | a0001c0001t0001g0026 a0001c0001t0001g0066 a0001c0001t0001g0068 others(7): Show |
11 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.746+1366C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585529 | |||||||
| chr8:70585583 | A | AAAAC | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.746+1308_746+1311d others(6): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585583 | |||||||
| chr8:70585741 | AG | A | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.746+1153delC | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585741 | |||||||
| chr8:70585749 | T | C | 2 | a0001c0001t0001g0107 a0001c0001t0014g0078 |
2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.746+1146A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585749 | |||||||
| chr8:70585782 | G | A | 2 | a0001c0001t0003g0185 a0001c0001t0003g0186 |
2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.746+1113C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585782 | |||||||
| chr8:70585822 | C | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(184): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.746+1073G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585822 | |||||||
| chr8:70585909 | C | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(184): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.746+986G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585909 | |||||||
| chr8:70585928 | T | C | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.746+967A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585928 | |||||||
| chr8:70585987 | G | A | 2 | a0001c0001t0007g0038 a0001c0001t0007g0077 |
3 | HG01109.hp1 HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.746+908C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70585987 | |||||||
| chr8:70586059 | G | A | 1 | a0001c0001t0003g0182 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.746+836C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70586059 | |||||||
| chr8:70586278 | T | TG | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(184): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.746+616dupC | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70586278 | |||||||
| chr8:70586284 | A | G | 1 | a0001c0001t0003g0197 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.746+611T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70586284 | |||||||
| chr8:70586382 | C | A | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.746+513G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70586382 | |||||||
| chr8:70586507 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.746+388G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70586507 | |||||||
| chr8:70586776 | A | T | 26 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0039 others(23): Show |
38 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.746+119T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70586776 | |||||||
| chr8:70586874 | T | C | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.746+21A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 8/10 | chr8 | 70586874 | |||||||
| chr8:70587344 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.571-168A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70587344 | |||||||
| chr8:70587377 | GA | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0142 |
5 | HG02257.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-202delT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70587377 | |||||||
| chr8:70587426 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.571-250G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70587426 | |||||||
| chr8:70587504 | A | T | 5 | a0002c0002t0003g0177 a0002c0002t0003g0202 a0002c0002t0003g0203 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-328T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70587504 | |||||||
| chr8:70587610 | A | C | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.571-434T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70587610 | |||||||
| chr8:70588014 | C | T | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(186): Show |
269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.571-838G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588014 | |||||||
| chr8:70588034 | C | G | 1 | a0001c0001t0002g0046 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.571-858G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588034 | |||||||
| chr8:70588038 | A | G | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.571-862T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588038 | |||||||
| chr8:70588066 | T | G | 2 | a0001c0001t0007g0038 a0001c0001t0007g0077 |
3 | HG01109.hp1 HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.571-890A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588066 | |||||||
| chr8:70588315 | A | C | 4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
4 | NA18969.hp2 NA18979.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-1139T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588315 | |||||||
| chr8:70588353 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.571-1177T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588353 | |||||||
| chr8:70588830 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0142 |
5 | HG02257.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-1654G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588830 | |||||||
| chr8:70588831 | G | A | 4 | a0002c0002t0003g0202 a0002c0002t0003g0203 a0002c0002t0003g0204 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-1655C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588831 | |||||||
| chr8:70588870 | C | T | 1 | a0001c0001t0003g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.571-1694G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70588870 | |||||||
| chr8:70589023 | C | T | 7 | a0001c0001t0001g0027 a0001c0001t0001g0087 a0001c0001t0001g0090 others(4): Show |
8 | NA18954.hp1 NA18957.hp1 NA18982.hp2 others(5): Show |
intron_variant | MODIFIER | c.571-1847G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70589023 | |||||||
| chr8:70589057 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0004g0218 |
2 | HG04184.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.571-1881C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70589057 | |||||||
| chr8:70589239 | A | C | 27 | a0001c0001t0001g0100 a0001c0001t0003g0005 a0001c0001t0003g0016 others(24): Show |
39 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.571-2063T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70589239 | |||||||
| chr8:70589665 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | NA18990.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.571-2489G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70589665 | |||||||
| chr8:70589710 | T | C | 16 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(13): Show |
21 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.571-2534A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70589710 | |||||||
| chr8:70589786 | C | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.571-2610G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70589786 | |||||||
| chr8:70590097 | T | C | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.571-2921A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590097 | |||||||
| chr8:70590141 | T | TA | 8 | a0001c0001t0001g0147 a0001c0001t0001g0156 a0001c0001t0002g0011 others(5): Show |
11 | HG00621.hp1 HG01192.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.571-2966dupT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590141 | |||||||
| chr8:70590141 | TA | T | 100 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0018 others(97): Show |
134 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.571-2966delT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590141 | |||||||
| chr8:70590141 | TAA | T | 7 | a0001c0001t0001g0096 a0001c0001t0014g0078 a0002c0002t0003g0177 others(4): Show |
7 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-2967_571-2966d others(4): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590141 | |||||||
| chr8:70590202 | AT | A | 18 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(15): Show |
20 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.571-3027delA | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590202 | |||||||
| chr8:70590308 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.571-3132A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590308 | |||||||
| chr8:70590333 | C | G | 1 | a0001c0001t0001g0095 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.571-3157G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590333 | |||||||
| chr8:70590340 | T | C | 15 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(12): Show |
17 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.571-3164A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590340 | |||||||
| chr8:70590363 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.571-3187G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590363 | |||||||
| chr8:70590404 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.571-3228C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590404 | |||||||
| chr8:70590577 | T | C | 5 | a0002c0002t0003g0177 a0002c0002t0003g0202 a0002c0002t0003g0203 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-3401A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590577 | |||||||
| chr8:70590632 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.571-3456C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590632 | |||||||
| chr8:70590689 | A | T | 4 | a0002c0002t0003g0202 a0002c0002t0003g0203 a0002c0002t0003g0204 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-3513T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590689 | |||||||
| chr8:70590927 | T | C | 3 | a0001c0001t0007g0038 a0001c0001t0007g0077 a0001c0001t0016g0181 |
4 | HG01109.hp1 HG01167.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+3579A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70590927 | |||||||
| chr8:70591004 | T | TAC | 9 | a0001c0001t0001g0026 a0001c0001t0001g0068 a0001c0001t0001g0069 others(6): Show |
10 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.570+3501_570+3502i others(4): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591004 | |||||||
| chr8:70591005 | A | AC | 5 | a0001c0001t0001g0025 a0001c0001t0001g0065 a0001c0001t0001g0066 others(2): Show |
6 | HG02622.hp1 HG02965.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+3500_570+3501i others(3): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591005 | |||||||
| chr8:70591007 | T | A | 16 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(13): Show |
18 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.570+3499A>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591007 | |||||||
| chr8:70591070 | A | C | 1 | a0001c0001t0003g0183 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.570+3436T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591070 | |||||||
| chr8:70591076 | C | A | 1 | a0001c0001t0003g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.570+3430G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591076 | |||||||
| chr8:70591350 | C | T | 1 | a0001c0001t0001g0020 | 3 | HG00639.hp2 HG00738.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.570+3156G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591350 | |||||||
| chr8:70591517 | A | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(149): Show |
213 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.570+2989T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591517 | |||||||
| chr8:70591726 | C | T | 4 | a0002c0002t0003g0202 a0002c0002t0003g0203 a0002c0002t0003g0204 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+2780G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591726 | |||||||
| chr8:70591727 | A | C | 1 | a0001c0001t0002g0048 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.570+2779T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591727 | |||||||
| chr8:70591916 | A | G | 2 | a0001c0001t0003g0182 a0001c0001t0003g0183 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.570+2590T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70591916 | |||||||
| chr8:70592041 | T | A | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.570+2465A>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70592041 | |||||||
| chr8:70592181 | T | C | 3 | a0001c0001t0003g0012 a0001c0001t0003g0079 a0001c0001t0003g0080 |
6 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+2325A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70592181 | |||||||
| chr8:70592237 | A | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(186): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.570+2269T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70592237 | |||||||
| chr8:70592699 | C | T | 2 | a0001c0001t0003g0012 a0001c0001t0003g0079 |
5 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+1807G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70592699 | |||||||
| chr8:70592827 | C | T | 6 | a0001c0001t0003g0012 a0001c0001t0003g0079 a0001c0001t0003g0080 others(3): Show |
9 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.570+1679G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70592827 | |||||||
| chr8:70592888 | A | G | 3 | a0001c0001t0003g0012 a0001c0001t0003g0079 a0001c0001t0003g0080 |
6 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1618T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70592888 | |||||||
| chr8:70592911 | C | T | 24 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0039 others(21): Show |
36 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.570+1595G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70592911 | |||||||
| chr8:70592985 | T | C | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.570+1521A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70592985 | |||||||
| chr8:70593407 | A | G | 4 | a0002c0002t0003g0202 a0002c0002t0003g0203 a0002c0002t0003g0204 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+1099T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70593407 | |||||||
| chr8:70593428 | C | T | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.570+1078G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70593428 | |||||||
| chr8:70593458 | A | G | 1 | a0001c0001t0003g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.570+1048T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70593458 | |||||||
| chr8:70593527 | C | A | 1 | a0001c0001t0016g0181 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.570+979G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70593527 | |||||||
| chr8:70593528 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.570+978G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70593528 | |||||||
| chr8:70593596 | T | TA | 3 | a0001c0001t0003g0012 a0001c0001t0003g0079 a0001c0001t0014g0078 |
6 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+909dupT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70593596 | |||||||
| chr8:70593596 | TA | T | 65 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0018 others(62): Show |
83 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.570+909delT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70593596 | |||||||
| chr8:70594066 | A | C | 1 | a0001c0001t0003g0195 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.570+440T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70594066 | |||||||
| chr8:70594165 | C | T | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.570+341G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70594165 | |||||||
| chr8:70594305 | G | GT | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.570+200dupA | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70594305 | |||||||
| chr8:70594305 | G | GTT | 8 | a0001c0001t0001g0028 a0001c0001t0001g0094 a0001c0001t0001g0119 others(5): Show |
13 | HG01109.hp1 HG02280.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.570+199_570+200dup others(2): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70594305 | |||||||
| chr8:70594305 | GT | G | 6 | a0001c0001t0003g0195 a0002c0002t0003g0177 a0002c0002t0003g0202 others(3): Show |
6 | HG00738.hp2 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+200delA | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70594305 | |||||||
| chr8:70594311 | T | TG | 9 | a0001c0001t0001g0033 a0001c0001t0001g0083 a0001c0001t0001g0088 others(6): Show |
10 | HG00438.hp1 HG00609.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.570+194_570+195ins others(1): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70594311 | |||||||
| chr8:70594361 | G | A | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.570+145C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70594361 | |||||||
| chr8:70594399 | G | C | 42 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0018 others(39): Show |
60 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.570+107C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 6/10 | chr8 | 70594399 | |||||||
| chr8:70594639 | T | A | 2 | a0001c0001t0003g0012 a0001c0001t0003g0079 |
5 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.486-49A>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70594639 | |||||||
| chr8:70594640 | A | T | 9 | a0001c0001t0001g0031 a0001c0001t0001g0125 a0001c0001t0001g0146 others(6): Show |
10 | HG00323.hp1 HG01081.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.486-50T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70594640 | |||||||
| chr8:70594777 | T | C | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.486-187A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70594777 | |||||||
| chr8:70595038 | G | GT | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.486-449dupA | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70595038 | |||||||
| chr8:70595038 | GT | G | 13 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(10): Show |
15 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.486-449delA | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70595038 | |||||||
| chr8:70595212 | A | T | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.486-622T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70595212 | |||||||
| chr8:70595380 | A | G | 1 | a0002c0002t0003g0202 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.486-790T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70595380 | |||||||
| chr8:70595462 | C | T | 24 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0039 others(21): Show |
36 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.485+801G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70595462 | |||||||
| chr8:70595955 | T | G | 1 | a0001c0001t0001g0143 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.485+308A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 5/10 | chr8 | 70595955 | |||||||
| chr8:70596496 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0004g0214 |
2 | HG03017.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.427-175A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596496 | |||||||
| chr8:70596670 | A | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(77): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.427-349T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596670 | |||||||
| chr8:70596677 | A | G | 1 | a0001c0001t0003g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.427-356T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596677 | |||||||
| chr8:70596700 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.427-379T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596700 | |||||||
| chr8:70596749 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.427-428G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596749 | |||||||
| chr8:70596819 | T | TA | 19 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0034 others(16): Show |
22 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.427-499dupT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596819 | |||||||
| chr8:70596819 | TA | T | 30 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0145 others(27): Show |
42 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.427-499delT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596819 | |||||||
| chr8:70596820 | A | T | 4 | a0002c0002t0003g0202 a0002c0002t0003g0203 a0002c0002t0003g0204 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.427-499T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596820 | |||||||
| chr8:70596967 | T | G | 1 | a0001c0001t0003g0197 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.427-646A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70596967 | |||||||
| chr8:70597296 | A | G | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(149): Show |
213 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.426+599T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70597296 | |||||||
| chr8:70597656 | G | A | 1 | a0001c0001t0017g0210 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.426+239C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70597656 | |||||||
| chr8:70597668 | C | CA | 82 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(79): Show |
119 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.426+226dupT | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70597668 | |||||||
| chr8:70597668 | C | CAA | 53 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0035 others(50): Show |
79 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.426+225_426+226dup others(2): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70597668 | |||||||
| chr8:70597668 | C | CAAA | 8 | a0001c0001t0001g0114 a0001c0001t0001g0123 a0001c0001t0001g0155 others(5): Show |
9 | HG01175.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.426+224_426+226dup others(3): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70597668 | |||||||
| chr8:70597853 | T | C | 4 | a0001c0001t0003g0039 a0001c0001t0003g0190 a0001c0001t0003g0191 others(1): Show |
5 | HG02055.hp2 HG02717.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.426+42A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70597853 | |||||||
| chr8:70597858 | A | G | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(186): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.426+37T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 4/10 | chr8 | 70597858 | |||||||
| chr8:70598484 | G | A | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.188-229C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70598484 | |||||||
| chr8:70598511 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.188-256T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70598511 | |||||||
| chr8:70598652 | C | A | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.188-397G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70598652 | |||||||
| chr8:70598814 | A | G | 1 | a0001c0001t0007g0038 | 2 | HG01109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.188-559T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70598814 | |||||||
| chr8:70598916 | C | T | 1 | a0001c0001t0003g0182 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.188-661G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70598916 | |||||||
| chr8:70599040 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.188-785G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70599040 | |||||||
| chr8:70599081 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.188-826C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70599081 | |||||||
| chr8:70599261 | T | C | 1 | a0001c0001t0003g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.187+758A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70599261 | |||||||
| chr8:70599321 | G | T | 1 | a0001c0001t0005g0081 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.187+698C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70599321 | |||||||
| chr8:70599502 | A | G | 3 | a0001c0001t0007g0038 a0001c0001t0007g0077 a0001c0001t0016g0181 |
4 | HG01109.hp1 HG01167.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+517T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70599502 | |||||||
| chr8:70599933 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.187+86G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 2/10 | chr8 | 70599933 | |||||||
| chr8:70600114 | A | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(128): Show |
190 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.124-32T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600114 | |||||||
| chr8:70600142 | C | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(76): Show |
120 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.124-60G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600142 | |||||||
| chr8:70600143 | G | A | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.124-61C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600143 | |||||||
| chr8:70600154 | A | G | 4 | a0002c0002t0003g0202 a0002c0002t0003g0203 a0002c0002t0003g0204 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-72T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600154 | |||||||
| chr8:70600176 | C | T | 3 | a0001c0001t0007g0038 a0001c0001t0007g0077 a0001c0001t0016g0181 |
4 | HG01109.hp1 HG01167.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-94G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600176 | |||||||
| chr8:70600429 | G | A | 1 | a0001c0001t0003g0192 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.124-347C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600429 | |||||||
| chr8:70600449 | G | C | 1 | a0001c0001t0003g0200 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.124-367C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600449 | |||||||
| chr8:70600561 | G | A | 1 | a0002c0002t0003g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.124-479C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600561 | |||||||
| chr8:70600651 | G | T | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.124-569C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600651 | |||||||
| chr8:70600666 | G | T | 1 | a0001c0001t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.124-584C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600666 | |||||||
| chr8:70600772 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.124-690A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600772 | |||||||
| chr8:70600797 | GT | G | 8 | a0001c0001t0003g0016 a0001c0001t0003g0040 a0001c0001t0003g0185 others(5): Show |
12 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-716delA | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600797 | |||||||
| chr8:70600856 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.124-774G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600856 | |||||||
| chr8:70600895 | T | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(128): Show |
190 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.124-813A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70600895 | |||||||
| chr8:70601155 | T | C | 1 | a0001c0001t0003g0183 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.124-1073A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601155 | |||||||
| chr8:70601413 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.124-1331T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601413 | |||||||
| chr8:70601546 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.124-1464G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601546 | |||||||
| chr8:70601602 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.124-1520C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601602 | |||||||
| chr8:70601619 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.124-1537C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601619 | |||||||
| chr8:70601684 | A | C | 1 | a0001c0001t0001g0030 | 2 | HG00099.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.124-1602T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601684 | |||||||
| chr8:70601806 | T | C | 24 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0039 others(21): Show |
36 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.124-1724A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601806 | |||||||
| chr8:70601834 | A | T | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(185): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.124-1752T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601834 | |||||||
| chr8:70601853 | C | A | 1 | a0001c0001t0003g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.124-1771G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601853 | |||||||
| chr8:70601957 | G | A | 2 | a0001c0001t0010g0188 a0001c0001t0010g0189 |
2 | HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.124-1875C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70601957 | |||||||
| chr8:70602024 | A | C | 1 | a0001c0001t0002g0043 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.124-1942T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602024 | |||||||
| chr8:70602068 | A | G | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(129): Show |
191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.124-1986T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602068 | |||||||
| chr8:70602115 | A | C | 24 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0039 others(21): Show |
36 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.124-2033T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602115 | |||||||
| chr8:70602259 | T | C | 1 | a0002c0002t0008g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.124-2177A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602259 | |||||||
| chr8:70602332 | C | T | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(185): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.124-2250G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602332 | |||||||
| chr8:70602379 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.124-2297T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602379 | |||||||
| chr8:70602388 | G | C | 1 | a0001c0001t0002g0057 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.124-2306C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602388 | |||||||
| chr8:70602437 | T | C | 3 | a0001c0001t0007g0038 a0001c0001t0007g0077 a0001c0001t0016g0181 |
4 | HG01109.hp1 HG01167.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-2355A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602437 | |||||||
| chr8:70602558 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.124-2476G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602558 | |||||||
| chr8:70602636 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(184): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.124-2554C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602636 | |||||||
| chr8:70602721 | C | A | 1 | a0001c0001t0001g0159 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.124-2639G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602721 | |||||||
| chr8:70602773 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.124-2691A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602773 | |||||||
| chr8:70602785 | A | G | 1 | a0001c0001t0015g0122 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.124-2703T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70602785 | |||||||
| chr8:70603020 | C | T | 9 | a0001c0001t0001g0026 a0001c0001t0001g0068 a0001c0001t0001g0069 others(6): Show |
10 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.124-2938G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603020 | |||||||
| chr8:70603040 | C | T | 4 | a0002c0002t0003g0202 a0002c0002t0003g0203 a0002c0002t0003g0204 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-2958G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603040 | |||||||
| chr8:70603242 | TTATA | T | 5 | a0001c0001t0003g0012 a0001c0001t0003g0079 a0001c0001t0003g0080 others(2): Show |
8 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-3164_124-3161d others(6): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603242 | |||||||
| chr8:70603287 | C | T | 1 | a0001c0001t0003g0182 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.124-3205G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603287 | |||||||
| chr8:70603300 | T | TTA | 10 | a0001c0001t0003g0005 a0001c0001t0003g0040 a0001c0001t0003g0197 others(7): Show |
16 | HG01106.hp2 HG01192.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.124-3220_124-3219d others(4): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603300 | |||||||
| chr8:70603303 | T | TAC | 3 | a0001c0001t0002g0009 a0001c0001t0002g0056 a0001c0001t0003g0200 |
6 | HG02451.hp2 HG02615.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-3223_124-3222d others(4): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | |||||||
| chr8:70603303 | T | TACACACA others(3): Show |
2 | a0001c0001t0001g0025 a0001c0001t0001g0065 |
3 | HG02965.hp2 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.124-3231_124-3222d others(12): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | |||||||
| chr8:70603303 | T | TATACAC | 3 | a0002c0002t0003g0202 a0002c0002t0003g0203 a0002c0002t0011g0221 |
3 | HG03209.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.124-3222_124-3221i others(8): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | |||||||
| chr8:70603303 | T | TATACACA others(1): Show |
6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(3): Show |
6 | HG00642.hp1 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-3222_124-3221i others(10): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | |||||||
| chr8:70603303 | T | TATACACA others(3): Show |
2 | a0001c0001t0001g0066 a0001c0001t0001g0072 |
2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.124-3222_124-3221i others(12): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | |||||||
| chr8:70603303 | T | TATACACA others(5): Show |
3 | a0001c0001t0001g0026 a0001c0001t0001g0073 a0001c0001t0001g0074 |
4 | HG02738.hp1 HG03098.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-3222_124-3221i others(14): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | |||||||
| chr8:70603303 | T | TATACACA others(9): Show |
1 | a0001c0001t0001g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.124-3222_124-3221i others(18): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | |||||||
| chr8:70603303 | TAC | T | 17 | a0001c0001t0001g0021 a0001c0001t0001g0118 a0001c0001t0001g0160 others(14): Show |
23 | HG02055.hp1 HG02055.hp2 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.124-3223_124-3222d others(4): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | |||||||
| chr8:70603303 | TACAC | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(74): Show |
119 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.124-3225_124-3222d others(6): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | |||||||
| chr8:70603303 | TACACAC | T | 2 | a0001c0001t0007g0038 a0001c0001t0007g0077 |
3 | HG01109.hp1 HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.124-3227_124-3222d others(8): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | |||||||
| chr8:70603303 | TACACACA others(1): Show |
T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG01071.hp2 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.124-3229_124-3222d others(10): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | |||||||
| chr8:70603303 | TACACACA others(3): Show |
T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | NA19066.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.124-3231_124-3222d others(12): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | |||||||
| chr8:70603303 | TACACACA others(5): Show |
T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0018 others(48): Show |
69 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.124-3233_124-3222d others(14): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603303 | |||||||
| chr8:70603305 | C | T | 2 | a0001c0001t0003g0183 a0001c0001t0003g0194 |
2 | HG00673.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.124-3223G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603305 | |||||||
| chr8:70603307 | C | T | 12 | a0001c0001t0001g0173 a0001c0001t0003g0012 a0001c0001t0003g0039 others(9): Show |
16 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.124-3225G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603307 | |||||||
| chr8:70603309 | C | T | 6 | a0001c0001t0003g0016 a0001c0001t0003g0185 a0001c0001t0003g0186 others(3): Show |
9 | HG01243.hp2 HG01884.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.124-3227G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603309 | |||||||
| chr8:70603312 | A | T | 1 | a0001c0001t0001g0118 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.124-3230T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603312 | |||||||
| chr8:70603450 | C | T | 1 | a0001c0001t0009g0184 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.124-3368G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603450 | |||||||
| chr8:70603494 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.124-3412G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603494 | |||||||
| chr8:70603506 | C | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | NA18990.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.124-3424G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603506 | |||||||
| chr8:70603585 | C | T | 1 | a0001c0001t0007g0077 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.124-3503G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603585 | |||||||
| chr8:70603586 | G | A | 1 | a0001c0001t0003g0183 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.124-3504C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603586 | |||||||
| chr8:70603630 | T | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | NA18990.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.124-3548A>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603630 | |||||||
| chr8:70603693 | G | T | 4 | a0002c0002t0003g0202 a0002c0002t0003g0203 a0002c0002t0003g0204 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-3611C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603693 | |||||||
| chr8:70603869 | TAGA | T | 29 | a0001c0001t0003g0005 a0001c0001t0003g0012 a0001c0001t0003g0016 others(26): Show |
44 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.124-3790_124-3788d others(5): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70603869 | |||||||
| chr8:70604000 | C | T | 2 | a0001c0001t0001g0173 a0005c0005t0001g0174 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.124-3918G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604000 | |||||||
| chr8:70604002 | C | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0165 a0001c0001t0001g0166 |
7 | HG02258.hp1 HG02886.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-3920G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604002 | |||||||
| chr8:70604058 | T | C | 1 | a0001c0007t0001g0167 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.124-3976A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604058 | |||||||
| chr8:70604239 | C | CAAT | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(187): Show |
270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.123+3837_123+3838i others(5): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604239 | |||||||
| chr8:70604285 | C | G | 1 | a0001c0001t0003g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.123+3792G>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604285 | |||||||
| chr8:70604525 | A | C | 6 | a0002c0002t0003g0177 a0002c0002t0003g0202 a0002c0002t0003g0203 others(3): Show |
6 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+3552T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604525 | |||||||
| chr8:70604576 | A | G | 2 | a0001c0001t0003g0012 a0001c0001t0003g0079 |
5 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+3501T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604576 | |||||||
| chr8:70604654 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0085 |
5 | HG00673.hp2 NA18971.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+3423T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604654 | |||||||
| chr8:70604662 | A | G | 1 | a0001c0001t0016g0181 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.123+3415T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604662 | |||||||
| chr8:70604711 | G | A | 4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
4 | NA18969.hp2 NA18979.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+3366C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604711 | |||||||
| chr8:70604784 | AAT | A | 3 | a0001c0001t0007g0038 a0001c0001t0007g0077 a0001c0001t0016g0181 |
4 | HG01109.hp1 HG01167.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+3291_123+3292d others(4): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604784 | |||||||
| chr8:70604819 | C | T | 4 | a0001c0001t0001g0173 a0001c0001t0008g0175 a0003c0006t0008g0176 others(1): Show |
4 | HG02895.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+3258G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604819 | |||||||
| chr8:70604930 | T | C | 3 | a0001c0001t0007g0038 a0001c0001t0007g0077 a0001c0001t0016g0181 |
4 | HG01109.hp1 HG01167.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+3147A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604930 | |||||||
| chr8:70604954 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.123+3123T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70604954 | |||||||
| chr8:70605066 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.123+3011T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605066 | |||||||
| chr8:70605083 | A | T | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+2994T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605083 | |||||||
| chr8:70605166 | C | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(132): Show |
195 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.123+2911G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605166 | |||||||
| chr8:70605189 | G | T | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+2888C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605189 | |||||||
| chr8:70605255 | A | T | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+2822T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605255 | |||||||
| chr8:70605325 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.123+2752G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605325 | |||||||
| chr8:70605370 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.123+2707A>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605370 | |||||||
| chr8:70605380 | C | T | 3 | a0001c0001t0005g0007 a0001c0001t0005g0081 a0001c0001t0005g0082 |
7 | HG00323.hp2 HG01168.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+2697G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605380 | |||||||
| chr8:70605598 | C | T | 1 | a0001c0001t0009g0184 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.123+2479G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605598 | |||||||
| chr8:70605628 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.123+2449C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605628 | |||||||
| chr8:70605807 | A | T | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.123+2270T>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605807 | |||||||
| chr8:70605863 | A | G | 24 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0039 others(21): Show |
36 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.123+2214T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605863 | |||||||
| chr8:70605878 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.123+2199C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605878 | |||||||
| chr8:70605922 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.123+2155C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70605922 | |||||||
| chr8:70606126 | C | A | 5 | a0001c0001t0003g0012 a0001c0001t0003g0079 a0001c0001t0003g0080 others(2): Show |
8 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.123+1951G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606126 | |||||||
| chr8:70606136 | G | A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(215): Show |
324 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.123+1941C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606136 | |||||||
| chr8:70606313 | C | T | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(129): Show |
191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.123+1764G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606313 | |||||||
| chr8:70606314 | G | T | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+1763C>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606314 | |||||||
| chr8:70606334 | G | A | 5 | a0001c0001t0003g0012 a0001c0001t0003g0079 a0001c0001t0003g0080 others(2): Show |
8 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.123+1743C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606334 | |||||||
| chr8:70606371 | T | G | 1 | a0001c0001t0002g0057 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.123+1706A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606371 | |||||||
| chr8:70606686 | C | A | 24 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0039 others(21): Show |
36 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.123+1391G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606686 | |||||||
| chr8:70606762 | A | G | 3 | a0001c0001t0003g0012 a0001c0001t0003g0079 a0001c0001t0003g0080 |
6 | HG02451.hp1 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+1315T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606762 | |||||||
| chr8:70606935 | CATCTT | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0201 |
7 | HG00140.hp1 HG00735.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.123+1137_123+1141d others(7): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70606935 | |||||||
| chr8:70607013 | T | C | 1 | a0001c0001t0002g0058 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.123+1064A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607013 | |||||||
| chr8:70607103 | C | T | 1 | a0001c0001t0014g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.123+974G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607103 | |||||||
| chr8:70607165 | A | G | 1 | a0001c0001t0007g0077 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.123+912T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607165 | |||||||
| chr8:70607180 | T | A | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+897A>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607180 | |||||||
| chr8:70607242 | T | C | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+835A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607242 | |||||||
| chr8:70607365 | T | C | 4 | a0002c0002t0003g0202 a0002c0002t0003g0203 a0002c0002t0003g0204 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+712A>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607365 | |||||||
| chr8:70607379 | G | A | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+698C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607379 | |||||||
| chr8:70607544 | G | C | 1 | a0001c0001t0003g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.123+533C>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607544 | |||||||
| chr8:70607582 | C | A | 1 | a0001c0001t0001g0206 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.123+495G>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607582 | |||||||
| chr8:70607596 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.123+481T>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607596 | |||||||
| chr8:70607671 | C | T | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+406G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607671 | |||||||
| chr8:70607689 | CCCGAG | C | 40 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0018 others(37): Show |
56 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.123+383_123+387del others(5): Show |
TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607689 | |||||||
| chr8:70607712 | G | A | 1 | a0001c0001t0002g0059 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.123+365C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607712 | |||||||
| chr8:70607729 | A | C | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0065 others(11): Show |
16 | HG00642.hp1 HG01074.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+348T>G | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607729 | |||||||
| chr8:70607789 | T | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(212): Show |
318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.123+288A>C | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607789 | |||||||
| chr8:70607882 | C | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
6 | NA18959.hp1 NA18962.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+195G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607882 | |||||||
| chr8:70607913 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.123+164C>T | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70607913 | |||||||
| chr8:70608023 | C | T | 1 | a0001c0001t0004g0211 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.123+54G>A | TRAM1 | ENSG00000067167.8 | transcript | ENST00000262213.7 | protein_coding | 1/10 | chr8 | 70608023 |