Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10915 |
| ensemblid | ENSG00000113649.14 |
| hgncid | 15630 |
| symbol | TCERG1 |
| name | transcription elongation regulator 1 |
| refseq_nuc | NM_001382548.1 |
| refseq_prot | NP_001369477.1 |
| ensembl_nuc | ENST00000679501.2 |
| ensembl_prot | ENSP00000505217.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 146447333 |
| end | 146511961 |
| strand | + |
| ver | v1.2 |
| region | chr5:146447333-146511961 |
| region5000 | chr5:146442333-146516961 |
| regionname0 | TCERG1_chr5_146447333_146511961 |
| regionname5000 | TCERG1_chr5_146442333_146516961 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1115 | 298 | 76 | 49 | 131 | 8 | 32 | 107 | TCERG1_chr5_146442333_146516961 | TCERG1 | MAERG others(1110): Show |
chr5 | 146442333 | 146516961 |
| a0002 | 0/0 | 1111 | 7 | 3 | 4 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | MAERG others(1106): Show |
chr5 | 146442333 | 146516961 |
| a0003 | 0/0 | 1109 | 5 | 1 | 1 | 1 | 2 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | MAERG others(1104): Show |
chr5 | 146442333 | 146516961 |
| a0004 | 0/0 | 1113 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | MAERG others(1108): Show |
chr5 | 146442333 | 146516961 |
| a0005 | 0/0 | 1117 | 3 | 2 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | MAERG others(1112): Show |
chr5 | 146442333 | 146516961 |
| a0006 | 0/0 | 1115 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | MAERG others(1110): Show |
chr5 | 146442333 | 146516961 |
| a0007 | 0/0 | 1119 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | MAERG others(1114): Show |
chr5 | 146442333 | 146516961 |
| a0008 | 0/0 | 1115 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | MAERG others(1110): Show |
chr5 | 146442333 | 146516961 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3345 | 263 | 59 | 41 | 129 | 7 | 26 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3340): Show |
chr5 | 146442333 | 146516961 | ||
| a0001c0002 | 0/0 | 3345 | 14 | 4 | 5 | 0 | 0 | 5 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3340): Show |
chr5 | 146442333 | 146516961 | ||
| a0001c0003 | 0/0 | 3345 | 10 | 10 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3340): Show |
chr5 | 146442333 | 146516961 | ||
| a0001c0004 | 1/0 | 3345 | 6 | 1 | 3 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3340): Show |
chr5 | 146442333 | 146516961 | ||
| a0001c0008 | 0/0 | 3345 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3340): Show |
chr5 | 146442333 | 146516961 | ||
| a0001c0015 | 0/0 | 3345 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3340): Show |
chr5 | 146442333 | 146516961 | ||
| a0001c0016 | 0/0 | 3345 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3340): Show |
chr5 | 146442333 | 146516961 | ||
| a0001c0018 | 0/0 | 3345 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3340): Show |
chr5 | 146442333 | 146516961 | ||
| a0002c0005 | 0/0 | 3333 | 4 | 0 | 4 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3328): Show |
chr5 | 146442333 | 146516961 | ||
| a0002c0007 | 0/0 | 3333 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3328): Show |
chr5 | 146442333 | 146516961 | ||
| a0002c0020 | 0/0 | 3333 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3328): Show |
chr5 | 146442333 | 146516961 | ||
| a0003c0006 | 0/0 | 3327 | 3 | 0 | 1 | 0 | 2 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3322): Show |
chr5 | 146442333 | 146516961 | ||
| a0003c0013 | 0/0 | 3327 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3322): Show |
chr5 | 146442333 | 146516961 | ||
| a0003c0019 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3322): Show |
chr5 | 146442333 | 146516961 | ||
| a0004c0011 | 0/0 | 3339 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3334): Show |
chr5 | 146442333 | 146516961 | ||
| a0004c0014 | 0/0 | 3339 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3334): Show |
chr5 | 146442333 | 146516961 | ||
| a0005c0010 | 0/0 | 3351 | 2 | 1 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3346): Show |
chr5 | 146442333 | 146516961 | ||
| a0005c0021 | 0/0 | 3351 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3346): Show |
chr5 | 146442333 | 146516961 | ||
| a0006c0009 | 0/0 | 3345 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3340): Show |
chr5 | 146442333 | 146516961 | ||
| a0007c0017 | 0/0 | 3357 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3352): Show |
chr5 | 146442333 | 146516961 | ||
| a0008c0012 | 0/0 | 3345 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | ATGGC others(3340): Show |
chr5 | 146442333 | 146516961 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4688 | 140 | 30 | 24 | 67 | 2 | 17 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4683): Show |
chr5 | 146442333 | 146516961 |
| a0001c0001t0002 | 0/1 | 4688 | 90 | 1 | 14 | 61 | 4 | 9 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4683): Show |
chr5 | 146442333 | 146516961 |
| a0001c0001t0003 | 0/0 | 4688 | 7 | 6 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4683): Show |
chr5 | 146442333 | 146516961 |
| a0001c0001t0004 | 0/0 | 4684 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4679): Show |
chr5 | 146442333 | 146516961 |
| a0001c0001t0005 | 0/0 | 4685 | 10 | 9 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4680): Show |
chr5 | 146442333 | 146516961 |
| a0001c0001t0006 | 0/0 | 4685 | 4 | 4 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4680): Show |
chr5 | 146442333 | 146516961 |
| a0001c0001t0007 | 0/0 | 4685 | 3 | 3 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4680): Show |
chr5 | 146442333 | 146516961 |
| a0001c0001t0008 | 0/0 | 4687 | 3 | 2 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4682): Show |
chr5 | 146442333 | 146516961 |
| a0001c0001t0010 | 0/0 | 4688 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4683): Show |
chr5 | 146442333 | 146516961 |
| a0001c0001t0012 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4683): Show |
chr5 | 146442333 | 146516961 |
| a0001c0001t0013 | 0/0 | 4688 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4683): Show |
chr5 | 146442333 | 146516961 |
| a0001c0002t0003 | 0/0 | 4688 | 14 | 4 | 5 | 0 | 0 | 5 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4683): Show |
chr5 | 146442333 | 146516961 |
| a0001c0003t0001 | 0/0 | 4688 | 9 | 9 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4683): Show |
chr5 | 146442333 | 146516961 |
| a0001c0003t0011 | 0/0 | 4688 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4683): Show |
chr5 | 146442333 | 146516961 |
| a0001c0004t0004 | 1/0 | 4684 | 6 | 1 | 3 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4679): Show |
chr5 | 146442333 | 146516961 |
| a0001c0008t0009 | 0/0 | 4688 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4683): Show |
chr5 | 146442333 | 146516961 |
| a0001c0015t0002 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4683): Show |
chr5 | 146442333 | 146516961 |
| a0001c0016t0001 | 0/0 | 4688 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4683): Show |
chr5 | 146442333 | 146516961 |
| a0001c0018t0002 | 0/0 | 4688 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4683): Show |
chr5 | 146442333 | 146516961 |
| a0002c0005t0004 | 0/0 | 4672 | 4 | 0 | 4 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4667): Show |
chr5 | 146442333 | 146516961 |
| a0002c0007t0001 | 0/0 | 4676 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4671): Show |
chr5 | 146442333 | 146516961 |
| a0002c0020t0001 | 0/0 | 4676 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4671): Show |
chr5 | 146442333 | 146516961 |
| a0003c0006t0001 | 0/0 | 4670 | 3 | 0 | 1 | 0 | 2 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4665): Show |
chr5 | 146442333 | 146516961 |
| a0003c0013t0002 | 0/0 | 4670 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4665): Show |
chr5 | 146442333 | 146516961 |
| a0003c0019t0001 | 0/0 | 4670 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4665): Show |
chr5 | 146442333 | 146516961 |
| a0004c0011t0004 | 0/0 | 4678 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4673): Show |
chr5 | 146442333 | 146516961 |
| a0004c0014t0004 | 0/0 | 4678 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4673): Show |
chr5 | 146442333 | 146516961 |
| a0005c0010t0001 | 0/0 | 4694 | 2 | 1 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4689): Show |
chr5 | 146442333 | 146516961 |
| a0005c0021t0001 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4689): Show |
chr5 | 146442333 | 146516961 |
| a0006c0009t0004 | 0/0 | 4684 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4679): Show |
chr5 | 146442333 | 146516961 |
| a0007c0017t0002 | 0/0 | 4700 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4695): Show |
chr5 | 146442333 | 146516961 |
| a0008c0012t0001 | 0/0 | 4688 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | GAACG others(4683): Show |
chr5 | 146442333 | 146516961 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 1 | 2 | 3 | 0 | 3 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0002 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0012 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0005g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0007g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0008g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0010g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0012g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0001t0013g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0002t0003g0005 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0002t0003g0009 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0002t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0002t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0002t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0002t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0002t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0002t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0003t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0003t0011g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0004t0004g0021 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0004t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0004t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0004t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0004t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0008t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0008t0009g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0015t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0016t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0001c0018t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0002c0005t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0002c0005t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0002c0005t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0002c0005t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0002c0007t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0002c0007t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0002c0020t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0003c0006t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0003c0006t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0003c0006t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0003c0013t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0003c0019t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0004c0011t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0004c0011t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0004c0014t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0005c0010t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0005c0010t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0005c0021t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0006c0009t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0006c0009t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0007c0017t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| a0008c0012t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0016 | t0001 | g0137 | EUR | GBR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG00099 | hp2 | a0007 | c0017 | t0002 | g0036 | EUR | GBR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | GBR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG00140 | hp2 | a0001 | c0001 | t0013 | g0204 | EUR | GBR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | CHS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG00733 | hp1 | a0002 | c0005 | t0004 | g0190 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG00733 | hp2 | a0003 | c0006 | t0001 | g0172 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01069 | hp1 | a0002 | c0005 | t0004 | g0194 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01071 | hp2 | a0002 | c0005 | t0004 | g0189 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0200 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0241 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01261 | hp1 | a0001 | c0004 | t0004 | g0252 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0005 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01346 | hp1 | a0001 | c0004 | t0004 | g0251 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01358 | hp2 | a0001 | c0004 | t0004 | g0250 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01361 | hp1 | a0002 | c0005 | t0004 | g0191 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0244 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01496 | hp2 | a0004 | c0014 | t0004 | g0186 | AMR | CLM | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | IBS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0110 | EUR | IBS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01516 | hp1 | a0003 | c0006 | t0001 | g0134 | EUR | IBS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01517 | hp1 | a0003 | c0006 | t0001 | g0133 | EUR | IBS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0198 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0255 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01943 | hp1 | a0001 | c0001 | t0008 | g0274 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0245 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0242 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG01981 | hp2 | a0008 | c0012 | t0001 | g0182 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02027 | hp2 | a0001 | c0015 | t0002 | g0105 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02055 | hp1 | a0001 | c0008 | t0009 | g0239 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02074 | hp1 | a0001 | c0001 | t0012 | g0263 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02145 | hp1 | a0001 | c0002 | t0003 | g0114 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0253 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02258 | hp1 | a0001 | c0003 | t0011 | g0177 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PEL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0185 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02572 | hp2 | a0002 | c0007 | t0001 | g0165 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0180 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0235 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02647 | hp2 | a0005 | c0021 | t0001 | g0202 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0195 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0027 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0026 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02896 | hp1 | a0002 | c0007 | t0001 | g0158 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02896 | hp2 | a0004 | c0011 | t0004 | g0193 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02922 | hp1 | a0001 | c0008 | t0009 | g0240 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0173 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02965 | hp2 | a0006 | c0009 | t0004 | g0187 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0257 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0175 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03098 | hp1 | a0002 | c0020 | t0001 | g0174 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0196 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0179 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03209 | hp1 | a0005 | c0010 | t0001 | g0237 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03453 | hp1 | a0001 | c0004 | t0004 | g0021 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03491 | hp2 | a0001 | c0002 | t0003 | g0246 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03516 | hp2 | a0004 | c0011 | t0004 | g0192 | AFR | ESN | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0178 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03579 | hp2 | a0003 | c0019 | t0001 | g0236 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | BEB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | BEB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG04199 | hp2 | a0001 | c0004 | t0004 | g0249 | SAS | STU | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | STU | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | STU | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18522 | hp2 | a0006 | c0009 | t0004 | g0188 | AFR | YRI | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19000 | hp1 | a0003 | c0013 | t0002 | g0050 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19001 | hp1 | a0001 | c0018 | t0002 | g0067 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19030 | hp2 | a0001 | c0002 | t0003 | g0005 | AFR | LWK | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | LWK | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0176 | AFR | LWK | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | YRI | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | ASW | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0113 | AFR | ASW | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0275 | EUR | TSI | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA20752 | hp2 | a0005 | c0010 | t0001 | g0148 | EUR | TSI | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA20905 | hp1 | a0001 | c0002 | t0003 | g0005 | SAS | GIH | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | GIH | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0199 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0197 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0243 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | ACB | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0256 | AFR | MSL | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0005 | AFR | USA | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | USA | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | USA | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0038 | REF | REF | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| homoSapiens | grch38p0 | a0001 | c0004 | t0004 | g0021 | REF | REF | TCERG1_chr5_146442333_146516961 | TCERG1 | chr5 | 146442333 | 146516961 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:146457274 | G | A | 1 | a0008 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.377G>A | p.Gly126Asp | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/23 | 394/4684 | 377/3348 | 126/1115 | chr5 | 146457274 | |||
| chr5:146459051 | AGCTCAGG others(11): Show |
A | 1 | a0003 | 1 | NA19000.hp1 | disruptive_inframe_deletion | MODERATE | c.621_638delTCAGGCTC others(10): Show |
p.Gln208_Ala213del | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/23 | 638/4684 | 621/3348 | 207/1115 | INFO_REALIGN_3_PRIME | chr5 | 146459051 | ||
| chr5:146459072 | T | TCAGGCC | 1 | a0005 | 3 | HG02647.hp2 HG03209.hp1 NA20752.hp2 |
disruptive_inframe_insertion | MODERATE | c.660_665dupGGCCCA | p.Gln222_Ala223insAl others(4): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/23 | 683/4684 | 666/3348 | 222/1115 | INFO_REALIGN_3_PRIME | chr5 | 146459072 | ||
| chr5:146459072 | T | TCAGGCCC others(5): Show |
1 | a0007 | 1 | HG00099.hp2 | disruptive_inframe_insertion | MODERATE | c.654_665dupGGCCCAGG others(4): Show |
p.Gln222_Ala223insAl others(10): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/23 | 683/4684 | 666/3348 | 222/1115 | INFO_REALIGN_3_PRIME | chr5 | 146459072 | ||
| chr5:146459072 | TCAGGCC | T | 1 | a0004 | 3 | HG01496.hp2 HG02896.hp2 HG03516.hp2 |
disruptive_inframe_deletion | MODERATE | c.660_665delGGCCCA | p.Ala221_Gln222del | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/23 | 677/4684 | 660/3348 | 220/1115 | INFO_REALIGN_3_PRIME | chr5 | 146459072 | ||
| chr5:146459072 | TCAGGCCC others(5): Show |
T | 1 | a0002 | 7 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(4): Show |
disruptive_inframe_deletion | MODERATE | c.654_665delGGCCCAGG others(4): Show |
p.Ala219_Gln222del | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/23 | 671/4684 | 654/3348 | 218/1115 | INFO_REALIGN_3_PRIME | chr5 | 146459072 | ||
| chr5:146459072 | TCAGGCCC others(11): Show |
T | 1 | a0003 | 4 | HG00733.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
disruptive_inframe_deletion | MODERATE | c.648_665delGGCCCAGG others(10): Show |
p.Ala217_Gln222del | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/23 | 665/4684 | 648/3348 | 216/1115 | INFO_REALIGN_3_PRIME | chr5 | 146459072 | ||
| chr5:146459281 | C | T | 1 | a0006 | 2 | HG02965.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.836C>T | p.Pro279Leu | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/23 | 853/4684 | 836/3348 | 279/1115 | chr5 | 146459281 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:146447391 | C | T | 4 | a0001c0003 a0002c0020 a0003c0019 others(1): Show |
13 | HG02258.hp1 HG02451.hp1 HG02615.hp1 others(10): Show |
synonymous_variant | LOW | c.42C>T | p.Phe14Phe | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/23 | 59/4684 | 42/3348 | 14/1115 | chr5 | 146447391 | |||
| chr5:146455062 | C | T | 2 | a0002c0005 a0004c0011 |
6 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
synonymous_variant | LOW | c.66C>T | p.Ala22Ala | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/23 | 83/4684 | 66/3348 | 22/1115 | chr5 | 146455062 | |||
| chr5:146459048 | A | G | 1 | a0001c0018 | 1 | NA19001.hp1 | synonymous_variant | LOW | c.603A>G | p.Ala201Ala | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/23 | 620/4684 | 603/3348 | 201/1115 | chr5 | 146459048 | |||
| chr5:146463675 | G | A | 1 | a0001c0015 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.1017G>A | p.Thr339Thr | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/23 | 1034/4684 | 1017/3348 | 339/1115 | chr5 | 146463675 | |||
| chr5:146492961 | C | G | 1 | a0001c0008 | 2 | HG02055.hp1 HG02922.hp1 |
synonymous_variant | LOW | c.2205C>G | p.Arg735Arg | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/23 | 2222/4684 | 2205/3348 | 735/1115 | chr5 | 146492961 | |||
| chr5:146503380 | A | G | 1 | a0001c0016 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.2439A>G | p.Lys813Lys | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 18/23 | 2456/4684 | 2439/3348 | 813/1115 | chr5 | 146503380 | |||
| chr5:146507890 | G | A | 1 | a0001c0002 | 14 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(11): Show |
synonymous_variant | LOW | c.2979G>A | p.Thr993Thr | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 21/23 | 2996/4684 | 2979/3348 | 993/1115 | chr5 | 146507890 | |||
| chr5:146510465 | A | G | 20 | a0001c0001 a0001c0002 a0001c0003 others(17): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
synonymous_variant | LOW | c.3171A>G | p.Ser1057Ser | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 3188/4684 | 3171/3348 | 1057/1115 | chr5 | 146510465 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:146510665 | G | A | 3 | a0001c0001t0003 a0001c0002t0003 a0001c0008t0009 |
23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*23G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 23 | chr5 | 146510665 | ||||||
| chr5:146510714 | A | G | 1 | a0001c0001t0013 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*72A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 72 | chr5 | 146510714 | ||||||
| chr5:146510892 | C | T | 5 | a0001c0001t0002 a0001c0015t0002 a0001c0018t0002 others(2): Show |
93 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*250C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 250 | chr5 | 146510892 | ||||||
| chr5:146511063 | C | T | 1 | a0001c0001t0012 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*421C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 421 | chr5 | 146511063 | ||||||
| chr5:146511219 | CTTG | C | 1 | a0001c0001t0006 | 4 | HG02559.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*583_*585delGTT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 583 | INFO_REALIGN_3_PRIME | chr5 | 146511219 | |||||
| chr5:146511559 | C | T | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(21): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*917C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 917 | chr5 | 146511559 | ||||||
| chr5:146511569 | A | AAAG | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(21): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*928_*930dupAAG | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 931 | INFO_REALIGN_3_PRIME | chr5 | 146511569 | |||||
| chr5:146511641 | T | C | 1 | a0001c0001t0010 | 2 | HG02809.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*999T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 999 | chr5 | 146511641 | ||||||
| chr5:146511646 | A | G | 1 | a0001c0003t0011 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1004A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 1004 | chr5 | 146511646 | ||||||
| chr5:146511862 | T | G | 1 | a0001c0008t0009 | 2 | HG02055.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1220T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 1220 | chr5 | 146511862 | ||||||
| chr5:146511880 | G | A | 1 | a0001c0001t0005 | 10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1238G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 1238 | chr5 | 146511880 | ||||||
| chr5:146511884 | T | TA | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(22): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*1251dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 23/23 | 1252 | INFO_REALIGN_3_PRIME | chr5 | 146511884 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:146447522 | C | T | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.59+114C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146447522 | |||||||
| chr5:146447633 | G | T | 4 | a0001c0001t0003g0255 a0001c0001t0003g0256 a0001c0001t0003g0257 others(1): Show |
4 | HG01934.hp1 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+225G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146447633 | |||||||
| chr5:146447658 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.59+250C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146447658 | |||||||
| chr5:146447730 | G | T | 1 | a0001c0001t0007g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.59+322G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146447730 | |||||||
| chr5:146447818 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(266): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.59+410T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146447818 | |||||||
| chr5:146447983 | T | C | 4 | a0001c0001t0006g0022 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
4 | HG02559.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+575T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146447983 | |||||||
| chr5:146447996 | C | G | 1 | a0001c0001t0002g0247 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.59+588C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146447996 | |||||||
| chr5:146448048 | C | G | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG02257.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.59+640C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146448048 | |||||||
| chr5:146448122 | CAGAGGGG others(7): Show |
C | 8 | a0001c0002t0003g0005 a0001c0002t0003g0009 a0001c0002t0003g0241 others(5): Show |
13 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.59+715_59+728delAG others(12): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146448122 | |||||||
| chr5:146448328 | CT | C | 14 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(11): Show |
14 | HG00738.hp2 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.59+927delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146448328 | ||||||
| chr5:146448506 | C | T | 3 | a0001c0001t0003g0256 a0001c0001t0003g0257 a0001c0001t0003g0258 |
3 | HG02970.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.59+1098C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146448506 | |||||||
| chr5:146448670 | A | G | 2 | a0001c0008t0009g0239 a0001c0008t0009g0240 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.59+1262A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146448670 | |||||||
| chr5:146448887 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.59+1479A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146448887 | |||||||
| chr5:146448971 | A | G | 1 | a0005c0010t0001g0237 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.59+1563A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146448971 | |||||||
| chr5:146449035 | G | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(81): Show |
98 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.59+1627G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146449035 | |||||||
| chr5:146449390 | A | G | 1 | a0003c0019t0001g0236 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.59+1982A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146449390 | |||||||
| chr5:146449576 | C | T | 1 | a0001c0001t0004g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.59+2168C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146449576 | |||||||
| chr5:146449640 | A | T | 7 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(4): Show |
7 | NA18950.hp1 NA18960.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.59+2232A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146449640 | |||||||
| chr5:146449711 | G | A | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.59+2303G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146449711 | |||||||
| chr5:146449946 | A | AT | 154 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(151): Show |
170 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.59+2539dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146449946 | ||||||
| chr5:146450192 | T | A | 1 | a0001c0001t0008g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.59+2784T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146450192 | |||||||
| chr5:146450310 | T | C | 1 | a0001c0001t0004g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.59+2902T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146450310 | |||||||
| chr5:146450401 | G | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.59+2993G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146450401 | |||||||
| chr5:146450495 | T | A | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.59+3087T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146450495 | |||||||
| chr5:146450563 | G | A | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.59+3155G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146450563 | |||||||
| chr5:146450653 | A | G | 1 | a0001c0001t0013g0204 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.59+3245A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146450653 | |||||||
| chr5:146450712 | C | T | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.59+3304C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146450712 | |||||||
| chr5:146450798 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.59+3390T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146450798 | |||||||
| chr5:146451009 | C | T | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.59+3601C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451009 | |||||||
| chr5:146451094 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.59+3686A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451094 | |||||||
| chr5:146451196 | T | C | 18 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(15): Show |
23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.59+3788T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451196 | |||||||
| chr5:146451201 | A | G | 145 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(142): Show |
161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.59+3793A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451201 | |||||||
| chr5:146451308 | G | A | 152 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(149): Show |
168 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(165): Show |
intron_variant | MODIFIER | c.60-3748G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451308 | |||||||
| chr5:146451319 | C | CT | 140 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0030 others(137): Show |
161 | HG00140.hp1 HG00621.hp1 HG00673.hp2 others(158): Show |
intron_variant | MODIFIER | c.60-3721dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146451319 | ||||||
| chr5:146451319 | C | CTT | 22 | a0001c0001t0001g0010 a0001c0001t0001g0260 a0001c0001t0001g0261 others(19): Show |
24 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(21): Show |
intron_variant | MODIFIER | c.60-3722_60-3721dup others(2): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146451319 | ||||||
| chr5:146451411 | C | T | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.60-3645C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451411 | |||||||
| chr5:146451483 | C | T | 1 | a0001c0001t0004g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.60-3573C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451483 | |||||||
| chr5:146451618 | G | A | 4 | a0001c0001t0006g0022 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
4 | HG02559.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.60-3438G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451618 | |||||||
| chr5:146451635 | C | A | 9 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(6): Show |
9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.60-3421C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451635 | |||||||
| chr5:146451692 | A | C | 1 | a0001c0001t0002g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3364A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451692 | |||||||
| chr5:146451693 | ATATACTT others(326): Show |
A | 1 | a0001c0001t0002g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3362_60-3030del | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451693 | |||||||
| chr5:146451736 | T | A | 260 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(257): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.60-3320T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451736 | |||||||
| chr5:146451737 | A | T | 260 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(257): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.60-3319A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451737 | |||||||
| chr5:146451738 | T | A | 260 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(257): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.60-3318T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451738 | |||||||
| chr5:146451773 | G | GT | 76 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0260 others(73): Show |
90 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.60-3269dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146451773 | ||||||
| chr5:146451773 | G | GTTTTTTT others(348): Show |
1 | a0001c0001t0002g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.60-3269_60-3268ins others(355): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146451773 | ||||||
| chr5:146451790 | T | A | 1 | a0001c0001t0001g0232 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.60-3266T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451790 | |||||||
| chr5:146451852 | A | G | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.60-3204A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451852 | |||||||
| chr5:146451856 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.60-3200C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451856 | |||||||
| chr5:146451927 | A | G | 10 | a0001c0001t0007g0020 a0001c0002t0003g0005 a0001c0002t0003g0009 others(7): Show |
16 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.60-3129A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146451927 | |||||||
| chr5:146452029 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3027C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452029 | |||||||
| chr5:146452033 | C | A | 1 | a0001c0001t0002g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3023C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452033 | |||||||
| chr5:146452034 | C | A | 1 | a0001c0001t0002g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3022C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452034 | |||||||
| chr5:146452035 | A | G | 1 | a0001c0001t0007g0020 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.60-3021A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452035 | |||||||
| chr5:146452036 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3020C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452036 | |||||||
| chr5:146452039 | C | G | 1 | a0001c0001t0002g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3017C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452039 | |||||||
| chr5:146452040 | T | A | 1 | a0001c0001t0002g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3016T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452040 | |||||||
| chr5:146452041 | G | C | 1 | a0001c0001t0003g0255 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.60-3015G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452041 | |||||||
| chr5:146452042 | C | A | 1 | a0001c0001t0002g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3014C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452042 | |||||||
| chr5:146452047 | C | A | 1 | a0001c0001t0002g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3009C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452047 | |||||||
| chr5:146452049 | A | T | 1 | a0001c0001t0002g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3007A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452049 | |||||||
| chr5:146452050 | A | G | 1 | a0001c0001t0002g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3006A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452050 | |||||||
| chr5:146452051 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.60-3005G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452051 | |||||||
| chr5:146452085 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.60-2971G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452085 | |||||||
| chr5:146452090 | A | C | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.60-2966A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452090 | |||||||
| chr5:146452145 | G | T | 1 | a0001c0001t0007g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.60-2911G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452145 | |||||||
| chr5:146452180 | G | A | 1 | a0001c0001t0008g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.60-2876G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452180 | |||||||
| chr5:146452302 | G | GT | 123 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(120): Show |
137 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.60-2748dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146452302 | ||||||
| chr5:146452422 | A | C | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.60-2634A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452422 | |||||||
| chr5:146452704 | T | C | 145 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(142): Show |
161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.60-2352T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452704 | |||||||
| chr5:146452810 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.60-2246T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452810 | |||||||
| chr5:146452840 | C | T | 1 | a0001c0001t0004g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.60-2216C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452840 | |||||||
| chr5:146452870 | C | T | 145 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(142): Show |
161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.60-2186C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452870 | |||||||
| chr5:146452964 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.60-2092A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146452964 | |||||||
| chr5:146453133 | C | G | 1 | a0001c0001t0001g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.60-1923C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453133 | |||||||
| chr5:146453308 | A | G | 124 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(121): Show |
138 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.60-1748A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453308 | |||||||
| chr5:146453323 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(83): Show |
105 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.60-1733G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453323 | |||||||
| chr5:146453419 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.60-1637T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453419 | |||||||
| chr5:146453442 | G | C | 1 | a0001c0001t0001g0260 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.60-1614G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453442 | |||||||
| chr5:146453483 | G | T | 10 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(7): Show |
10 | HG01934.hp1 HG02055.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.60-1573G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453483 | |||||||
| chr5:146453536 | A | C | 1 | a0001c0001t0002g0111 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.60-1520A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453536 | |||||||
| chr5:146453758 | C | T | 8 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0195 others(5): Show |
10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.60-1298C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453758 | |||||||
| chr5:146453772 | TA | T | 7 | a0001c0001t0001g0234 a0001c0001t0002g0110 a0001c0001t0010g0026 others(4): Show |
7 | HG01069.hp1 HG01515.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.60-1267delA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146453772 | ||||||
| chr5:146453797 | G | C | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.60-1259G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453797 | |||||||
| chr5:146453840 | C | G | 1 | a0001c0001t0007g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.60-1216C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453840 | |||||||
| chr5:146453864 | C | T | 143 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(140): Show |
159 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.60-1192C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453864 | |||||||
| chr5:146453872 | T | C | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.60-1184T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453872 | |||||||
| chr5:146453890 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02080.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.60-1166C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453890 | |||||||
| chr5:146453915 | C | T | 1 | a0001c0001t0008g0274 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.60-1141C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453915 | |||||||
| chr5:146453924 | G | A | 1 | a0001c0001t0004g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.60-1132G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453924 | |||||||
| chr5:146453981 | C | T | 1 | a0001c0001t0003g0255 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.60-1075C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146453981 | |||||||
| chr5:146454037 | CA | C | 110 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0075 others(107): Show |
126 | HG00099.hp2 HG00140.hp1 HG00673.hp2 others(123): Show |
intron_variant | MODIFIER | c.60-995delA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146454037 | ||||||
| chr5:146454037 | CAA | C | 13 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
13 | HG00738.hp2 HG01891.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.60-996_60-995delAA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146454037 | ||||||
| chr5:146454037 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG00741.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.60-1004_60-995delA others(9): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146454037 | ||||||
| chr5:146454037 | CAAAAAAA others(4): Show |
C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(81): Show |
103 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.60-1005_60-995delA others(10): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146454037 | ||||||
| chr5:146454207 | A | AAAAAG | 140 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(137): Show |
156 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(153): Show |
intron_variant | MODIFIER | c.60-835_60-831dupAG others(3): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146454207 | ||||||
| chr5:146454261 | T | C | 1 | a0001c0001t0006g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.60-795T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454261 | |||||||
| chr5:146454274 | A | C | 85 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(82): Show |
99 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.60-782A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454274 | |||||||
| chr5:146454416 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.60-640T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454416 | |||||||
| chr5:146454474 | C | CT | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.60-579dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146454474 | ||||||
| chr5:146454569 | G | GT | 21 | a0001c0001t0001g0010 a0001c0001t0001g0223 a0001c0001t0001g0224 others(18): Show |
23 | HG01943.hp1 HG02015.hp2 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.60-476dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146454569 | ||||||
| chr5:146454590 | G | T | 1 | a0001c0001t0002g0109 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.60-466G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454590 | |||||||
| chr5:146454641 | A | G | 1 | a0001c0001t0007g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.60-415A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454641 | |||||||
| chr5:146454693 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.60-363G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454693 | |||||||
| chr5:146454702 | A | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.60-354A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454702 | |||||||
| chr5:146454718 | C | T | 1 | a0008c0012t0001g0182 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.60-338C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454718 | |||||||
| chr5:146454725 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.60-331A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454725 | |||||||
| chr5:146454736 | T | TA | 3 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 |
3 | HG02809.hp2 HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.60-319dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | 146454736 | ||||||
| chr5:146454738 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02083.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.60-318C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454738 | |||||||
| chr5:146454804 | T | G | 162 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(159): Show |
183 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(180): Show |
intron_variant | MODIFIER | c.60-252T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454804 | |||||||
| chr5:146454919 | G | A | 8 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0195 others(5): Show |
10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.60-137G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454919 | |||||||
| chr5:146454953 | T | G | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0005c0010t0001g0237 |
3 | HG02451.hp2 HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.60-103T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454953 | |||||||
| chr5:146454966 | C | T | 143 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(140): Show |
159 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.60-90C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 1/22 | chr5 | 146454966 | |||||||
| chr5:146455392 | G | T | 1 | a0001c0001t0001g0273 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.285+111G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146455392 | |||||||
| chr5:146455529 | C | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.285+248C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146455529 | |||||||
| chr5:146455544 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.285+263G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146455544 | |||||||
| chr5:146455546 | G | C | 1 | a0001c0001t0002g0040 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.285+265G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146455546 | |||||||
| chr5:146455687 | C | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.285+406C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146455687 | |||||||
| chr5:146455782 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | NA18943.hp2 NA18994.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.285+501G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146455782 | |||||||
| chr5:146455848 | T | A | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.285+567T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146455848 | |||||||
| chr5:146455872 | G | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG02080.hp1 HG02132.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.285+591G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146455872 | |||||||
| chr5:146456082 | G | T | 8 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0195 others(5): Show |
10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.285+801G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146456082 | |||||||
| chr5:146456316 | A | G | 1 | a0001c0001t0006g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286-867A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146456316 | |||||||
| chr5:146456461 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.286-722G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146456461 | |||||||
| chr5:146456468 | T | C | 1 | a0001c0002t0003g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.286-715T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146456468 | |||||||
| chr5:146456849 | T | C | 1 | a0003c0019t0001g0236 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.286-334T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146456849 | |||||||
| chr5:146457031 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.286-152G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146457031 | |||||||
| chr5:146457099 | A | T | 49 | a0001c0001t0001g0208 a0001c0001t0002g0002 a0001c0001t0002g0003 others(46): Show |
58 | HG00621.hp1 HG00673.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.286-84A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146457099 | |||||||
| chr5:146457116 | T | C | 2 | a0001c0001t0002g0077 a0001c0001t0002g0078 |
2 | HG02040.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.286-67T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146457116 | |||||||
| chr5:146457171 | G | A | 1 | a0001c0001t0007g0020 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.286-12G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 2/22 | chr5 | 146457171 | |||||||
| chr5:146457471 | G | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG01099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.438+136G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146457471 | |||||||
| chr5:146457606 | C | T | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.438+271C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146457606 | |||||||
| chr5:146457622 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.438+287G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146457622 | |||||||
| chr5:146457630 | C | T | 3 | a0001c0001t0003g0256 a0001c0001t0003g0257 a0001c0001t0003g0258 |
3 | HG02970.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.438+295C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146457630 | |||||||
| chr5:146457664 | C | T | 1 | a0001c0001t0005g0199 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.438+329C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146457664 | |||||||
| chr5:146457759 | T | G | 2 | a0001c0001t0002g0041 a0001c0001t0002g0053 |
2 | NA18965.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.438+424T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146457759 | |||||||
| chr5:146458011 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.438+676G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458011 | |||||||
| chr5:146458125 | A | G | 85 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(82): Show |
99 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.439-759A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458125 | |||||||
| chr5:146458169 | T | C | 124 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(121): Show |
138 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.439-715T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458169 | |||||||
| chr5:146458197 | A | G | 1 | a0001c0001t0007g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.439-687A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458197 | |||||||
| chr5:146458269 | C | T | 1 | a0001c0001t0004g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.439-615C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458269 | |||||||
| chr5:146458321 | C | T | 1 | a0005c0010t0001g0237 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.439-563C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458321 | |||||||
| chr5:146458467 | C | T | 1 | a0001c0001t0007g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.439-417C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458467 | |||||||
| chr5:146458494 | A | G | 1 | a0001c0001t0007g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.439-390A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458494 | |||||||
| chr5:146458512 | A | G | 154 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(151): Show |
170 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.439-372A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458512 | |||||||
| chr5:146458529 | G | C | 2 | a0002c0005t0004g0189 a0002c0005t0004g0194 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.439-355G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458529 | |||||||
| chr5:146458538 | T | A | 1 | a0001c0001t0001g0227 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.439-346T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458538 | |||||||
| chr5:146458604 | C | T | 9 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(6): Show |
9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.439-280C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458604 | |||||||
| chr5:146458710 | T | C | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.439-174T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458710 | |||||||
| chr5:146458738 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.439-146C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458738 | |||||||
| chr5:146458813 | A | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.439-71A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458813 | |||||||
| chr5:146458877 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(71): Show |
92 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(89): Show |
splice_region_variant&intron_variant | LOW | c.439-7G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 3/22 | chr5 | 146458877 | |||||||
| chr5:146459347 | A | T | 1 | a0003c0006t0001g0172 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.892+10A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459347 | |||||||
| chr5:146459352 | G | A | 3 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0003g0205 |
3 | HG02809.hp2 NA18981.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.892+15G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459352 | |||||||
| chr5:146459518 | G | T | 8 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0195 others(5): Show |
10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.892+181G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459518 | |||||||
| chr5:146459600 | C | T | 84 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(81): Show |
98 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.892+263C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459600 | |||||||
| chr5:146459689 | G | A | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.892+352G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459689 | |||||||
| chr5:146459778 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.892+441A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459778 | |||||||
| chr5:146459926 | G | A | 1 | a0001c0001t0007g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.892+589G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459926 | |||||||
| chr5:146459945 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.892+608T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459945 | |||||||
| chr5:146459988 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.892+651G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146459988 | |||||||
| chr5:146460103 | T | G | 1 | a0001c0001t0002g0080 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.892+766T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460103 | |||||||
| chr5:146460236 | A | G | 10 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(7): Show |
10 | HG01934.hp1 HG02055.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.892+899A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460236 | |||||||
| chr5:146460318 | G | A | 1 | a0001c0001t0005g0199 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.892+981G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460318 | |||||||
| chr5:146460334 | T | C | 2 | a0001c0003t0001g0173 a0002c0020t0001g0174 |
2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.892+997T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460334 | |||||||
| chr5:146460424 | T | C | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02056.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.892+1087T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460424 | |||||||
| chr5:146460426 | A | ATT | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(84): Show |
106 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.892+1095_892+1096d others(4): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 146460426 | ||||||
| chr5:146460450 | T | G | 3 | a0001c0001t0003g0256 a0001c0001t0003g0257 a0001c0001t0003g0258 |
3 | HG02970.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.892+1113T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460450 | |||||||
| chr5:146460584 | A | G | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.892+1247A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460584 | |||||||
| chr5:146460603 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0118 a0001c0001t0001g0125 others(7): Show |
13 | HG00621.hp2 HG00673.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.892+1266G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460603 | |||||||
| chr5:146460611 | G | C | 9 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(6): Show |
9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.892+1274G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460611 | |||||||
| chr5:146460747 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.892+1410G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460747 | |||||||
| chr5:146460954 | G | A | 87 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(84): Show |
101 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.892+1617G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146460954 | |||||||
| chr5:146461214 | AAATAT | A | 9 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(6): Show |
9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.892+1884_892+1888d others(7): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 146461214 | ||||||
| chr5:146461265 | T | G | 3 | a0004c0014t0004g0186 a0006c0009t0004g0187 a0006c0009t0004g0188 |
3 | HG01496.hp2 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.892+1928T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146461265 | |||||||
| chr5:146461315 | T | C | 145 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(142): Show |
161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.892+1978T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146461315 | |||||||
| chr5:146461537 | C | T | 2 | a0006c0009t0004g0187 a0006c0009t0004g0188 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.893-2014C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146461537 | |||||||
| chr5:146461658 | A | C | 1 | a0001c0001t0002g0170 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.893-1893A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146461658 | |||||||
| chr5:146461671 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.893-1880A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146461671 | |||||||
| chr5:146461897 | C | T | 1 | a0001c0001t0005g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.893-1654C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146461897 | |||||||
| chr5:146461903 | G | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(237): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.893-1648G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146461903 | |||||||
| chr5:146461959 | T | A | 1 | a0001c0001t0001g0208 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.893-1592T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146461959 | |||||||
| chr5:146462716 | A | G | 2 | a0001c0001t0001g0222 a0001c0001t0002g0108 |
2 | NA18993.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.893-835A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146462716 | |||||||
| chr5:146462906 | A | G | 26 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(23): Show |
33 | HG01167.hp1 HG01256.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.893-645A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146462906 | |||||||
| chr5:146462922 | T | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(266): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.893-629T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146462922 | |||||||
| chr5:146463121 | T | G | 1 | a0001c0001t0001g0226 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.893-430T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 4/22 | chr5 | 146463121 | |||||||
| chr5:146463870 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1135+77C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146463870 | |||||||
| chr5:146464017 | A | G | 1 | a0001c0001t0002g0053 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1135+224A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464017 | |||||||
| chr5:146464065 | A | G | 3 | a0001c0001t0002g0037 a0001c0001t0002g0106 a0001c0015t0002g0105 |
3 | HG02027.hp2 NA18942.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1135+272A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464065 | |||||||
| chr5:146464127 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1135+334C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464127 | |||||||
| chr5:146464226 | G | A | 2 | a0001c0001t0002g0054 a0001c0001t0002g0055 |
2 | NA18981.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1135+433G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464226 | |||||||
| chr5:146464269 | A | G | 1 | a0001c0001t0004g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1135+476A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464269 | |||||||
| chr5:146464300 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | NA19060.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1135+507G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464300 | |||||||
| chr5:146464391 | T | C | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.1135+598T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464391 | |||||||
| chr5:146464558 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG03654.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1135+765C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464558 | |||||||
| chr5:146464757 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1135+964C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464757 | |||||||
| chr5:146464785 | A | T | 1 | a0001c0001t0004g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1135+992A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464785 | |||||||
| chr5:146464791 | C | G | 143 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(140): Show |
159 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.1135+998C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464791 | |||||||
| chr5:146464812 | T | A | 1 | a0001c0002t0003g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1135+1019T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464812 | |||||||
| chr5:146464955 | T | A | 1 | a0001c0001t0001g0203 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1135+1162T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146464955 | |||||||
| chr5:146465038 | A | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1135+1245A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465038 | |||||||
| chr5:146465054 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(2): Show |
6 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135+1261A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465054 | |||||||
| chr5:146465351 | T | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(61): Show |
78 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1135+1558T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465351 | |||||||
| chr5:146465737 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1135+1944A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465737 | |||||||
| chr5:146465760 | G | T | 8 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0195 others(5): Show |
10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1135+1967G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465760 | |||||||
| chr5:146465801 | G | A | 1 | a0001c0001t0007g0020 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1135+2008G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465801 | |||||||
| chr5:146465884 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1135+2091C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465884 | |||||||
| chr5:146465888 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1135+2095C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465888 | |||||||
| chr5:146465961 | A | G | 154 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(151): Show |
170 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.1135+2168A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146465961 | |||||||
| chr5:146466020 | C | CA | 12 | a0001c0001t0001g0234 a0001c0001t0001g0254 a0001c0001t0002g0074 others(9): Show |
13 | HG01099.hp2 HG01884.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1135+2245dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 146466020 | ||||||
| chr5:146466020 | C | CAA | 103 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0075 others(100): Show |
117 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.1135+2244_1135+224 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 146466020 | ||||||
| chr5:146466020 | C | CAAA | 9 | a0001c0001t0001g0043 a0001c0001t0001g0233 a0001c0001t0002g0053 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1135+2243_1135+224 others(7): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 146466020 | ||||||
| chr5:146466020 | CA | C | 8 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(5): Show |
8 | HG01167.hp1 HG01257.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1135+2245delA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 146466020 | ||||||
| chr5:146466039 | G | A | 2 | a0002c0005t0004g0190 a0002c0005t0004g0191 |
2 | HG00733.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1135+2246G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466039 | |||||||
| chr5:146466332 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(83): Show |
105 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.1136-2009G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466332 | |||||||
| chr5:146466405 | AG | A | 6 | a0002c0005t0004g0189 a0002c0005t0004g0190 a0002c0005t0004g0191 others(3): Show |
6 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1136-1931delG | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 146466405 | ||||||
| chr5:146466445 | G | A | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | NA19085.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1136-1896G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466445 | |||||||
| chr5:146466462 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1136-1879A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466462 | |||||||
| chr5:146466549 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1136-1792A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466549 | |||||||
| chr5:146466592 | G | T | 1 | a0001c0008t0009g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1136-1749G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466592 | |||||||
| chr5:146466597 | C | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0264 a0001c0001t0001g0265 others(5): Show |
10 | HG02074.hp1 NA18939.hp2 NA18940.hp1 others(7): Show |
intron_variant | MODIFIER | c.1136-1744C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466597 | |||||||
| chr5:146466726 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1136-1615T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466726 | |||||||
| chr5:146466806 | A | G | 1 | a0001c0001t0002g0073 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1136-1535A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466806 | |||||||
| chr5:146466969 | G | A | 143 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(140): Show |
159 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.1136-1372G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146466969 | |||||||
| chr5:146467005 | A | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1136-1336A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146467005 | |||||||
| chr5:146467189 | T | A | 1 | a0001c0001t0002g0073 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1136-1152T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146467189 | |||||||
| chr5:146467373 | A | G | 3 | a0001c0001t0005g0018 a0001c0001t0005g0197 a0001c0001t0005g0200 |
4 | HG01167.hp1 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136-968A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146467373 | |||||||
| chr5:146467456 | C | T | 121 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(118): Show |
135 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.1136-885C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146467456 | |||||||
| chr5:146467465 | G | C | 151 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(148): Show |
167 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(164): Show |
intron_variant | MODIFIER | c.1136-876G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146467465 | |||||||
| chr5:146467776 | T | C | 1 | a0003c0019t0001g0236 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1136-565T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146467776 | |||||||
| chr5:146468023 | A | C | 1 | a0001c0001t0003g0256 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1136-318A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146468023 | |||||||
| chr5:146468090 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1136-251T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 5/22 | chr5 | 146468090 | |||||||
| chr5:146468840 | T | C | 1 | a0001c0001t0006g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1198+437T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 6/22 | chr5 | 146468840 | |||||||
| chr5:146468880 | CT | C | 6 | a0001c0001t0003g0256 a0001c0001t0003g0257 a0001c0001t0003g0258 others(3): Show |
6 | HG02486.hp1 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1198+488delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr5 | 146468880 | ||||||
| chr5:146469174 | A | T | 23 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(20): Show |
23 | HG01257.hp2 HG01258.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1199-370A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 6/22 | chr5 | 146469174 | |||||||
| chr5:146469403 | C | A | 1 | a0001c0001t0007g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1199-141C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 6/22 | chr5 | 146469403 | |||||||
| chr5:146469863 | A | G | 163 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(160): Show |
184 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.1399+119A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 7/22 | chr5 | 146469863 | |||||||
| chr5:146469965 | T | A | 1 | a0001c0001t0002g0111 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1399+221T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 7/22 | chr5 | 146469965 | |||||||
| chr5:146469966 | G | A | 145 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(142): Show |
161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1399+222G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 7/22 | chr5 | 146469966 | |||||||
| chr5:146470326 | C | G | 1 | a0001c0001t0004g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1400-310C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 7/22 | chr5 | 146470326 | |||||||
| chr5:146470506 | A | ATAT | 145 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(142): Show |
161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1400-129_1400-127d others(5): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr5 | 146470506 | ||||||
| chr5:146470765 | T | C | 145 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(142): Show |
161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1512+17T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 8/22 | chr5 | 146470765 | |||||||
| chr5:146470896 | G | GT | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(83): Show |
105 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.1512+154dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr5 | 146470896 | ||||||
| chr5:146471203 | C | T | 1 | a0003c0013t0002g0050 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1513-285C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 8/22 | chr5 | 146471203 | |||||||
| chr5:146471267 | C | T | 18 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(15): Show |
23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1513-221C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 8/22 | chr5 | 146471267 | |||||||
| chr5:146471600 | A | AT | 10 | a0001c0001t0001g0130 a0001c0001t0001g0154 a0001c0001t0004g0113 others(7): Show |
10 | HG01496.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1601+40dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146471600 | ||||||
| chr5:146471600 | AT | A | 142 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(139): Show |
158 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(155): Show |
intron_variant | MODIFIER | c.1601+40delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146471600 | ||||||
| chr5:146471621 | C | T | 9 | a0001c0002t0003g0005 a0001c0002t0003g0009 a0001c0002t0003g0114 others(6): Show |
14 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1601+45C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146471621 | |||||||
| chr5:146471747 | C | T | 3 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 |
3 | HG02809.hp2 HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1601+171C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146471747 | |||||||
| chr5:146471750 | C | T | 1 | a0001c0001t0010g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1601+174C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146471750 | |||||||
| chr5:146471839 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1601+263C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146471839 | |||||||
| chr5:146471843 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1601+267C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146471843 | |||||||
| chr5:146471887 | G | A | 3 | a0001c0003t0001g0178 a0001c0003t0001g0179 a0001c0003t0001g0185 |
3 | HG02451.hp1 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1601+311G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146471887 | |||||||
| chr5:146471892 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG01099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1601+316C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146471892 | |||||||
| chr5:146472170 | A | G | 1 | a0001c0001t0002g0103 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1601+594A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472170 | |||||||
| chr5:146472181 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1601+605C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472181 | |||||||
| chr5:146472216 | T | C | 1 | a0001c0001t0002g0056 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1601+640T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472216 | |||||||
| chr5:146472334 | C | T | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1601+758C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472334 | |||||||
| chr5:146472374 | T | C | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1601+798T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472374 | |||||||
| chr5:146472387 | T | G | 1 | a0001c0001t0002g0057 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1601+811T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472387 | |||||||
| chr5:146472467 | G | A | 1 | a0001c0001t0008g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1601+891G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472467 | |||||||
| chr5:146472536 | C | T | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1601+960C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472536 | |||||||
| chr5:146472537 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1601+961G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472537 | |||||||
| chr5:146472548 | A | G | 4 | a0002c0005t0004g0189 a0002c0005t0004g0190 a0002c0005t0004g0191 others(1): Show |
4 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1601+972A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472548 | |||||||
| chr5:146472560 | G | A | 9 | a0001c0002t0003g0005 a0001c0002t0003g0009 a0001c0002t0003g0114 others(6): Show |
14 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1601+984G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472560 | |||||||
| chr5:146472701 | T | TCGTGTGT others(13): Show |
1 | a0001c0001t0002g0045 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1601+1125_1601+112 others(24): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472701 | |||||||
| chr5:146472701 | T | TGTGTGTG others(12): Show |
1 | a0001c0001t0002g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1601+1125_1601+112 others(23): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472701 | |||||||
| chr5:146472701 | T | TTG | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(83): Show |
104 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.1601+1151_1601+115 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | ||||||
| chr5:146472701 | T | TTGTG | 11 | a0001c0001t0001g0007 a0001c0001t0001g0132 a0001c0001t0001g0155 others(8): Show |
13 | HG00733.hp2 HG01516.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.1601+1149_1601+115 others(8): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | ||||||
| chr5:146472701 | T | TTGTGTGT others(3): Show |
7 | a0001c0001t0001g0034 a0001c0001t0008g0274 a0001c0002t0003g0005 others(4): Show |
12 | HG01261.hp2 HG01361.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1601+1143_1601+115 others(14): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | ||||||
| chr5:146472701 | T | TTGTGTGT others(5): Show |
6 | a0001c0001t0001g0035 a0001c0001t0001g0218 a0001c0001t0001g0219 others(3): Show |
6 | HG01257.hp2 HG01258.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1601+1141_1601+115 others(16): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | ||||||
| chr5:146472701 | T | TTGTGTGT others(7): Show |
28 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(25): Show |
29 | HG00738.hp2 HG01358.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1601+1139_1601+115 others(18): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | ||||||
| chr5:146472701 | T | TTGTGTGT others(9): Show |
10 | a0001c0001t0001g0043 a0001c0001t0001g0221 a0001c0001t0001g0227 others(7): Show |
10 | HG01256.hp2 HG02083.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1601+1137_1601+115 others(20): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | ||||||
| chr5:146472701 | T | TTGTGTGT others(11): Show |
11 | a0001c0001t0001g0010 a0001c0001t0001g0044 a0001c0001t0001g0075 others(8): Show |
15 | HG00140.hp1 HG01167.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1601+1135_1601+115 others(22): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | ||||||
| chr5:146472701 | T | TTGTGTGT others(13): Show |
50 | a0001c0001t0001g0224 a0001c0001t0001g0276 a0001c0001t0002g0002 others(47): Show |
60 | HG00099.hp2 HG00621.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1601+1133_1601+115 others(24): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | ||||||
| chr5:146472701 | T | TTGTGTGT others(15): Show |
21 | a0001c0001t0001g0076 a0001c0001t0001g0262 a0001c0001t0001g0269 others(18): Show |
22 | HG00673.hp2 HG02015.hp1 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.1601+1131_1601+115 others(26): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | ||||||
| chr5:146472701 | T | TTGTGTGT others(17): Show |
6 | a0001c0001t0001g0259 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
6 | HG00735.hp1 HG01952.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1601+1129_1601+115 others(28): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | ||||||
| chr5:146472701 | T | TTGTGTGT others(19): Show |
4 | a0001c0001t0001g0261 a0001c0001t0001g0270 a0001c0001t0002g0084 others(1): Show |
4 | HG02027.hp2 HG02132.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1601+1127_1601+115 others(30): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | ||||||
| chr5:146472701 | T | TTGTGTGT others(21): Show |
2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1601+1152_1601+115 others(32): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | ||||||
| chr5:146472701 | T | TTGTGTGT others(23): Show |
3 | a0001c0001t0001g0260 a0001c0001t0002g0058 a0001c0001t0002g0072 |
3 | NA18943.hp1 NA19057.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1601+1152_1601+115 others(34): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472701 | ||||||
| chr5:146472727 | G | GTGTGTGT others(20): Show |
1 | a0001c0001t0001g0271 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1601+1152_1601+115 others(31): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146472727 | ||||||
| chr5:146472728 | T | TGTGTGTG others(16): Show |
1 | a0001c0001t0001g0223 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1601+1152_1601+115 others(27): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472728 | |||||||
| chr5:146472752 | C | T | 123 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(120): Show |
137 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.1601+1176C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472752 | |||||||
| chr5:146472799 | C | T | 1 | a0001c0004t0004g0252 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1601+1223C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472799 | |||||||
| chr5:146472842 | T | G | 1 | a0001c0001t0007g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1601+1266T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146472842 | |||||||
| chr5:146473061 | AGGAAG | A | 6 | a0002c0005t0004g0189 a0002c0005t0004g0190 a0002c0005t0004g0191 others(3): Show |
6 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1601+1487_1601+149 others(9): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146473061 | ||||||
| chr5:146473069 | A | G | 1 | a0001c0001t0007g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1601+1493A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473069 | |||||||
| chr5:146473114 | A | G | 8 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0195 others(5): Show |
10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1601+1538A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473114 | |||||||
| chr5:146473137 | G | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1601+1561G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473137 | |||||||
| chr5:146473187 | T | C | 1 | a0002c0007t0001g0158 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1601+1611T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473187 | |||||||
| chr5:146473351 | T | C | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1601+1775T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473351 | |||||||
| chr5:146473442 | A | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1601+1866A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473442 | |||||||
| chr5:146473539 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1601+1963T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473539 | |||||||
| chr5:146473573 | C | T | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.1601+1997C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473573 | |||||||
| chr5:146473577 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1601+2001G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473577 | |||||||
| chr5:146473681 | A | T | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1601+2105A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473681 | |||||||
| chr5:146473683 | G | A | 1 | a0001c0001t0004g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1601+2107G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473683 | |||||||
| chr5:146473701 | G | A | 1 | a0004c0011t0004g0192 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1601+2125G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473701 | |||||||
| chr5:146473866 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1601+2290G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473866 | |||||||
| chr5:146473904 | C | T | 1 | a0001c0003t0011g0177 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1601+2328C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473904 | |||||||
| chr5:146473918 | A | G | 1 | a0001c0001t0005g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1601+2342A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473918 | |||||||
| chr5:146473930 | A | G | 18 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(15): Show |
23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1601+2354A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473930 | |||||||
| chr5:146473958 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(84): Show |
106 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.1601+2382A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146473958 | |||||||
| chr5:146474020 | TGGCTATA others(25): Show |
T | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1601+2458_1601+248 others(36): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146474020 | ||||||
| chr5:146474035 | T | C | 1 | a0002c0007t0001g0158 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1601+2459T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474035 | |||||||
| chr5:146474170 | G | A | 1 | a0001c0001t0002g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1601+2594G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474170 | |||||||
| chr5:146474378 | T | C | 1 | a0001c0001t0002g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1601+2802T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474378 | |||||||
| chr5:146474407 | C | G | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1601+2831C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474407 | |||||||
| chr5:146474419 | A | G | 1 | a0001c0001t0003g0207 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1601+2843A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474419 | |||||||
| chr5:146474553 | A | G | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1601+2977A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474553 | |||||||
| chr5:146474609 | A | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1601+3033A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474609 | |||||||
| chr5:146474645 | G | A | 1 | a0001c0001t0002g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1601+3069G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474645 | |||||||
| chr5:146474646 | A | G | 1 | a0001c0001t0002g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1601+3070A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474646 | |||||||
| chr5:146474658 | C | A | 1 | a0001c0001t0002g0052 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1601+3082C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474658 | |||||||
| chr5:146474732 | G | A | 3 | a0001c0002t0003g0005 a0001c0002t0003g0243 a0001c0002t0003g0244 |
6 | HG01261.hp2 HG01361.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1601+3156G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474732 | |||||||
| chr5:146474743 | A | G | 1 | a0001c0004t0004g0252 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1601+3167A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474743 | |||||||
| chr5:146474868 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1601+3292A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474868 | |||||||
| chr5:146474983 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1601+3407T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146474983 | |||||||
| chr5:146475053 | G | A | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1602-3440G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475053 | |||||||
| chr5:146475074 | A | G | 9 | a0001c0002t0003g0005 a0001c0002t0003g0009 a0001c0002t0003g0114 others(6): Show |
14 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1602-3419A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475074 | |||||||
| chr5:146475082 | C | T | 2 | a0002c0007t0001g0158 a0002c0007t0001g0165 |
2 | HG02572.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1602-3411C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475082 | |||||||
| chr5:146475342 | G | C | 1 | a0001c0001t0002g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1602-3151G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475342 | |||||||
| chr5:146475440 | T | C | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1602-3053T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475440 | |||||||
| chr5:146475485 | A | G | 1 | a0001c0001t0002g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1602-3008A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475485 | |||||||
| chr5:146475494 | T | C | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1602-2999T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475494 | |||||||
| chr5:146475570 | TGATTAAA others(10): Show |
T | 1 | a0001c0001t0001g0181 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1602-2905_1602-288 others(21): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146475570 | ||||||
| chr5:146475668 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1602-2825G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475668 | |||||||
| chr5:146475725 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(245): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1602-2768T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475725 | |||||||
| chr5:146475771 | T | G | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1602-2722T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475771 | |||||||
| chr5:146475781 | G | C | 36 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(33): Show |
36 | HG00738.hp2 HG01257.hp2 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.1602-2712G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475781 | |||||||
| chr5:146475919 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1602-2574A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146475919 | |||||||
| chr5:146476283 | T | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1602-2210T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146476283 | |||||||
| chr5:146476285 | G | A | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.1602-2208G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146476285 | |||||||
| chr5:146476444 | T | C | 1 | a0001c0001t0002g0111 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1602-2049T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146476444 | |||||||
| chr5:146476552 | T | TA | 12 | a0001c0001t0001g0154 a0001c0003t0001g0016 a0001c0003t0001g0173 others(9): Show |
13 | HG02258.hp1 HG02451.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1602-1933dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146476552 | ||||||
| chr5:146476685 | A | G | 8 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0195 others(5): Show |
10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1602-1808A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146476685 | |||||||
| chr5:146476739 | G | A | 123 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(120): Show |
137 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.1602-1754G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146476739 | |||||||
| chr5:146476760 | C | T | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1602-1733C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146476760 | |||||||
| chr5:146476912 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1602-1581C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146476912 | |||||||
| chr5:146476997 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1602-1496C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146476997 | |||||||
| chr5:146477034 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(267): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1602-1459T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477034 | |||||||
| chr5:146477090 | G | A | 1 | a0001c0001t0004g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1602-1403G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477090 | |||||||
| chr5:146477436 | A | G | 3 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0248 |
3 | NA19002.hp1 NA19074.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1602-1057A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477436 | |||||||
| chr5:146477443 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1602-1050A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477443 | |||||||
| chr5:146477464 | C | T | 1 | a0001c0001t0003g0256 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1602-1029C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477464 | |||||||
| chr5:146477557 | A | G | 3 | a0001c0001t0005g0018 a0001c0001t0005g0197 a0001c0001t0005g0200 |
4 | HG01167.hp1 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602-936A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477557 | |||||||
| chr5:146477586 | GT | G | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1602-897delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146477586 | ||||||
| chr5:146477603 | A | C | 79 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0006 others(76): Show |
92 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.1602-890A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477603 | |||||||
| chr5:146477692 | C | CT | 120 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0035 others(117): Show |
141 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.1602-778dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146477692 | ||||||
| chr5:146477692 | C | CTT | 32 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(29): Show |
32 | HG00738.hp2 HG01175.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.1602-779_1602-778d others(4): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146477692 | ||||||
| chr5:146477692 | CT | C | 6 | a0001c0001t0001g0120 a0001c0001t0001g0136 a0001c0001t0001g0169 others(3): Show |
7 | HG02258.hp1 HG02622.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602-778delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 146477692 | ||||||
| chr5:146477718 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1602-775G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477718 | |||||||
| chr5:146477734 | A | T | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(8): Show |
11 | HG00738.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1602-759A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477734 | |||||||
| chr5:146477840 | C | T | 1 | a0001c0001t0007g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1602-653C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477840 | |||||||
| chr5:146477992 | C | T | 84 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(81): Show |
98 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.1602-501C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146477992 | |||||||
| chr5:146478069 | A | G | 3 | a0001c0001t0003g0256 a0001c0001t0003g0257 a0001c0001t0003g0258 |
3 | HG02970.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1602-424A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146478069 | |||||||
| chr5:146478239 | G | A | 2 | a0001c0001t0002g0066 a0001c0001t0002g0073 |
2 | HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1602-254G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146478239 | |||||||
| chr5:146478241 | A | T | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.1602-252A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146478241 | |||||||
| chr5:146478388 | G | A | 1 | a0005c0010t0001g0237 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1602-105G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146478388 | |||||||
| chr5:146478447 | A | G | 5 | a0001c0001t0001g0115 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
5 | HG01069.hp2 HG01257.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602-46A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146478447 | |||||||
| chr5:146478481 | A | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1602-12A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 9/22 | chr5 | 146478481 | |||||||
| chr5:146478809 | G | C | 1 | a0001c0001t0007g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1762+156G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146478809 | |||||||
| chr5:146478862 | G | T | 9 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(6): Show |
9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1762+209G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146478862 | |||||||
| chr5:146478917 | G | A | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.1762+264G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146478917 | |||||||
| chr5:146478967 | G | A | 153 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(150): Show |
169 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(166): Show |
intron_variant | MODIFIER | c.1762+314G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146478967 | |||||||
| chr5:146479225 | G | A | 1 | a0001c0001t0007g0020 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1762+572G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479225 | |||||||
| chr5:146479257 | G | T | 1 | a0001c0001t0003g0207 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1763-598G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479257 | |||||||
| chr5:146479328 | TTA | T | 9 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(6): Show |
9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1763-524_1763-523d others(4): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr5 | 146479328 | ||||||
| chr5:146479387 | A | T | 1 | a0001c0002t0003g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1763-468A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479387 | |||||||
| chr5:146479423 | C | G | 1 | a0001c0001t0001g0260 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1763-432C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479423 | |||||||
| chr5:146479453 | T | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0110 |
5 | HG01256.hp1 HG01258.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1763-402T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479453 | |||||||
| chr5:146479456 | G | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0110 |
5 | HG01256.hp1 HG01258.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1763-399G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479456 | |||||||
| chr5:146479477 | A | G | 1 | a0001c0002t0003g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1763-378A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479477 | |||||||
| chr5:146479528 | G | A | 1 | a0001c0001t0003g0205 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1763-327G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479528 | |||||||
| chr5:146479655 | A | C | 84 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(81): Show |
98 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.1763-200A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 10/22 | chr5 | 146479655 | |||||||
| chr5:146480200 | G | A | 143 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(140): Show |
159 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.1886+106G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480200 | |||||||
| chr5:146480226 | A | G | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1886+132A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480226 | |||||||
| chr5:146480309 | T | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1886+215T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480309 | |||||||
| chr5:146480414 | C | A | 2 | a0001c0008t0009g0239 a0001c0008t0009g0240 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1886+320C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480414 | |||||||
| chr5:146480532 | C | T | 1 | a0001c0001t0002g0098 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1886+438C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480532 | |||||||
| chr5:146480549 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1886+455G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480549 | |||||||
| chr5:146480559 | C | G | 1 | a0003c0019t0001g0236 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1886+465C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480559 | |||||||
| chr5:146480573 | A | T | 1 | a0001c0001t0001g0149 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1886+479A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480573 | |||||||
| chr5:146480584 | T | C | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1886+490T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480584 | |||||||
| chr5:146480617 | T | A | 1 | a0001c0001t0004g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1886+523T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480617 | |||||||
| chr5:146480627 | G | T | 1 | a0001c0001t0003g0255 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1887-523G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480627 | |||||||
| chr5:146480630 | G | A | 123 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(120): Show |
137 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.1887-520G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480630 | |||||||
| chr5:146480710 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1887-440A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480710 | |||||||
| chr5:146480837 | A | G | 1 | a0001c0001t0002g0106 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1887-313A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480837 | |||||||
| chr5:146480880 | G | A | 79 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0006 others(76): Show |
92 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.1887-270G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480880 | |||||||
| chr5:146480925 | A | G | 1 | a0001c0001t0002g0049 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1887-225A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480925 | |||||||
| chr5:146480967 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1887-183C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480967 | |||||||
| chr5:146480967 | CT | C | 24 | a0001c0001t0001g0126 a0001c0001t0001g0147 a0001c0001t0002g0100 others(21): Show |
29 | HG01069.hp1 HG01256.hp2 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.1887-174delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 146480967 | ||||||
| chr5:146480975 | T | A | 2 | a0001c0001t0002g0054 a0001c0001t0007g0020 |
3 | HG02622.hp1 NA18981.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1887-175T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480975 | |||||||
| chr5:146480975 | T | TA | 3 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0012g0263 |
3 | HG02074.hp1 HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1887-175_1887-174i others(3): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480975 | |||||||
| chr5:146480976 | T | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(241): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.1887-174T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 12/22 | chr5 | 146480976 | |||||||
| chr5:146481356 | C | CT | 18 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(15): Show |
23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1937+157dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 146481356 | ||||||
| chr5:146481868 | C | G | 1 | a0001c0001t0002g0071 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1937+668C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | chr5 | 146481868 | |||||||
| chr5:146482126 | T | C | 1 | a0001c0001t0002g0046 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1938-466T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | chr5 | 146482126 | |||||||
| chr5:146482174 | A | G | 2 | a0002c0007t0001g0158 a0002c0007t0001g0165 |
2 | HG02572.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1938-418A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | chr5 | 146482174 | |||||||
| chr5:146482281 | CT | C | 85 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(82): Show |
99 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1938-299delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 146482281 | ||||||
| chr5:146482293 | T | A | 3 | a0004c0014t0004g0186 a0006c0009t0004g0187 a0006c0009t0004g0188 |
3 | HG01496.hp2 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1938-299T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | chr5 | 146482293 | |||||||
| chr5:146482304 | G | T | 1 | a0001c0001t0001g0261 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1938-288G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | chr5 | 146482304 | |||||||
| chr5:146482346 | C | T | 84 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(81): Show |
98 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.1938-246C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | chr5 | 146482346 | |||||||
| chr5:146482377 | T | A | 123 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(120): Show |
137 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.1938-215T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | chr5 | 146482377 | |||||||
| chr5:146482420 | A | G | 1 | a0001c0001t0005g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1938-172A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 13/22 | chr5 | 146482420 | |||||||
| chr5:146482900 | A | G | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.2073+173A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 14/22 | chr5 | 146482900 | |||||||
| chr5:146483116 | C | T | 1 | a0001c0001t0007g0020 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2073+389C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 14/22 | chr5 | 146483116 | |||||||
| chr5:146483117 | A | C | 1 | a0001c0001t0007g0020 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2073+390A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 14/22 | chr5 | 146483117 | |||||||
| chr5:146483211 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2074-329C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 14/22 | chr5 | 146483211 | |||||||
| chr5:146483660 | T | TATATCTC others(4): Show |
18 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(15): Show |
23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.2163+32_2163+42dup others(11): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146483660 | ||||||
| chr5:146483695 | G | A | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2163+66G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146483695 | |||||||
| chr5:146483839 | T | G | 1 | a0001c0001t0001g0215 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2163+210T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146483839 | |||||||
| chr5:146483919 | A | G | 4 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(1): Show |
4 | NA18950.hp1 NA18978.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.2163+290A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146483919 | |||||||
| chr5:146484030 | C | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(81): Show |
98 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.2163+401C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146484030 | |||||||
| chr5:146484030 | C | T | 18 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(15): Show |
23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.2163+401C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146484030 | |||||||
| chr5:146484514 | A | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG01099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2163+885A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146484514 | |||||||
| chr5:146484520 | A | G | 1 | a0001c0001t0002g0086 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2163+891A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146484520 | |||||||
| chr5:146484581 | G | GTA | 84 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(81): Show |
98 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.2163+954_2163+955d others(4): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146484581 | ||||||
| chr5:146484659 | A | T | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2163+1030A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146484659 | |||||||
| chr5:146484753 | T | G | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.2163+1124T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146484753 | |||||||
| chr5:146484900 | C | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0146 |
3 | HG00738.hp1 HG01071.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.2163+1271C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146484900 | |||||||
| chr5:146484960 | G | A | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.2163+1331G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146484960 | |||||||
| chr5:146485020 | T | C | 4 | a0002c0005t0004g0189 a0002c0005t0004g0190 a0002c0005t0004g0191 others(1): Show |
4 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2163+1391T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146485020 | |||||||
| chr5:146485077 | T | G | 2 | a0001c0001t0005g0018 a0001c0001t0005g0200 |
3 | HG01167.hp1 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2163+1448T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146485077 | |||||||
| chr5:146485508 | T | C | 8 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0195 others(5): Show |
10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2163+1879T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146485508 | |||||||
| chr5:146485534 | G | A | 1 | a0001c0001t0004g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2163+1905G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146485534 | |||||||
| chr5:146485549 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2163+1920C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146485549 | |||||||
| chr5:146485569 | A | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2163+1940A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146485569 | |||||||
| chr5:146485701 | C | T | 153 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(150): Show |
169 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(166): Show |
intron_variant | MODIFIER | c.2163+2072C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146485701 | |||||||
| chr5:146485898 | C | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(267): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.2163+2269C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146485898 | |||||||
| chr5:146486089 | C | CT | 31 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(28): Show |
35 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2163+2460_2163+246 others(5): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486089 | |||||||
| chr5:146486090 | G | T | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.2163+2461G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486090 | |||||||
| chr5:146486092 | T | C | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2163+2463T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486092 | |||||||
| chr5:146486162 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(70): Show |
91 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.2163+2533C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486162 | |||||||
| chr5:146486229 | C | T | 2 | a0002c0007t0001g0158 a0002c0007t0001g0165 |
2 | HG02572.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2163+2600C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486229 | |||||||
| chr5:146486279 | C | G | 1 | a0005c0010t0001g0237 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2163+2650C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486279 | |||||||
| chr5:146486504 | G | T | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.2163+2875G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486504 | |||||||
| chr5:146486515 | A | G | 1 | a0001c0001t0003g0256 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2163+2886A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486515 | |||||||
| chr5:146486575 | C | T | 1 | a0001c0008t0009g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2163+2946C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486575 | |||||||
| chr5:146486646 | G | A | 1 | a0001c0001t0004g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2163+3017G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486646 | |||||||
| chr5:146486846 | A | G | 6 | a0001c0001t0001g0145 a0001c0001t0001g0181 a0003c0006t0001g0133 others(3): Show |
6 | HG00733.hp2 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.2163+3217A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486846 | |||||||
| chr5:146486895 | C | T | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.2163+3266C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486895 | |||||||
| chr5:146486980 | G | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(256): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.2163+3351G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146486980 | |||||||
| chr5:146487087 | C | CA | 152 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(149): Show |
173 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(170): Show |
intron_variant | MODIFIER | c.2163+3467dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146487087 | ||||||
| chr5:146487089 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2163+3460A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487089 | |||||||
| chr5:146487462 | T | A | 3 | a0001c0003t0001g0016 a0001c0003t0001g0176 a0005c0021t0001g0202 |
4 | HG02615.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2163+3833T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487462 | |||||||
| chr5:146487543 | T | G | 1 | a0001c0001t0007g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2163+3914T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487543 | |||||||
| chr5:146487592 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2163+3963A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487592 | |||||||
| chr5:146487612 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2163+3983A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487612 | |||||||
| chr5:146487731 | C | CA | 24 | a0001c0001t0001g0115 a0001c0001t0001g0131 a0001c0001t0001g0152 others(21): Show |
27 | HG01109.hp2 HG01167.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.2163+4120dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146487731 | ||||||
| chr5:146487731 | CA | C | 9 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(6): Show |
9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2163+4120delA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146487731 | ||||||
| chr5:146487731 | CAA | C | 7 | a0001c0001t0001g0032 a0001c0001t0001g0044 a0001c0001t0001g0075 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2163+4119_2163+412 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146487731 | ||||||
| chr5:146487731 | CAAA | C | 136 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(133): Show |
152 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(149): Show |
intron_variant | MODIFIER | c.2163+4118_2163+412 others(7): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146487731 | ||||||
| chr5:146487751 | C | G | 1 | a0001c0001t0008g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2163+4122C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487751 | |||||||
| chr5:146487754 | A | G | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.2163+4125A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487754 | |||||||
| chr5:146487867 | TAACTAA | T | 5 | a0001c0001t0005g0017 a0001c0001t0005g0195 a0001c0001t0005g0196 others(2): Show |
6 | HG01884.hp1 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2163+4242_2163+424 others(10): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146487867 | ||||||
| chr5:146487881 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(238): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.2163+4252C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487881 | |||||||
| chr5:146487898 | C | T | 1 | a0001c0001t0007g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2163+4269C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487898 | |||||||
| chr5:146487971 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2163+4342A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146487971 | |||||||
| chr5:146488012 | T | A | 1 | a0003c0019t0001g0236 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2163+4383T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146488012 | |||||||
| chr5:146488045 | A | G | 1 | a0001c0001t0004g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2163+4416A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146488045 | |||||||
| chr5:146488111 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2163+4482C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146488111 | |||||||
| chr5:146488260 | A | T | 8 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0195 others(5): Show |
10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2163+4631A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146488260 | |||||||
| chr5:146488335 | T | C | 1 | a0001c0001t0002g0091 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2164-4585T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146488335 | |||||||
| chr5:146488858 | T | C | 2 | a0002c0007t0001g0158 a0002c0007t0001g0165 |
2 | HG02572.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2164-4062T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146488858 | |||||||
| chr5:146489104 | T | G | 1 | a0001c0001t0002g0092 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2164-3816T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146489104 | |||||||
| chr5:146489127 | C | G | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.2164-3793C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146489127 | |||||||
| chr5:146489128 | G | A | 9 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(6): Show |
9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2164-3792G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146489128 | |||||||
| chr5:146489327 | A | G | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0005c0010t0001g0237 |
3 | HG02451.hp2 HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2164-3593A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146489327 | |||||||
| chr5:146489550 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2164-3370T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146489550 | |||||||
| chr5:146489632 | A | G | 36 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(33): Show |
36 | HG00738.hp2 HG01257.hp2 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.2164-3288A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146489632 | |||||||
| chr5:146489789 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2164-3131A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146489789 | |||||||
| chr5:146489865 | A | G | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.2164-3055A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146489865 | |||||||
| chr5:146490041 | G | A | 1 | a0001c0018t0002g0067 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2164-2879G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490041 | |||||||
| chr5:146490152 | A | C | 124 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(121): Show |
138 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.2164-2768A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490152 | |||||||
| chr5:146490183 | G | C | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2164-2737G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490183 | |||||||
| chr5:146490257 | A | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(263): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2164-2663A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490257 | |||||||
| chr5:146490409 | T | C | 1 | a0001c0001t0002g0093 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2164-2511T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490409 | |||||||
| chr5:146490516 | C | T | 1 | a0001c0001t0004g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2164-2404C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490516 | |||||||
| chr5:146490517 | G | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(81): Show |
98 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.2164-2403G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490517 | |||||||
| chr5:146490755 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2164-2165T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490755 | |||||||
| chr5:146490846 | T | C | 1 | a0001c0001t0007g0020 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2164-2074T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490846 | |||||||
| chr5:146490976 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2164-1944T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146490976 | |||||||
| chr5:146491014 | T | G | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2164-1906T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491014 | |||||||
| chr5:146491188 | C | T | 1 | a0001c0001t0006g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2164-1732C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491188 | |||||||
| chr5:146491318 | C | T | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(8): Show |
11 | HG00738.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2164-1602C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491318 | |||||||
| chr5:146491511 | G | A | 31 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(28): Show |
35 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2164-1409G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491511 | |||||||
| chr5:146491535 | A | T | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.2164-1385A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491535 | |||||||
| chr5:146491628 | C | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(72): Show |
93 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.2164-1292C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491628 | |||||||
| chr5:146491765 | A | G | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.2164-1155A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491765 | |||||||
| chr5:146491766 | T | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(84): Show |
106 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.2164-1154T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491766 | |||||||
| chr5:146491800 | C | T | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2164-1120C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146491800 | |||||||
| chr5:146491960 | A | AC | 144 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.2164-958dupC | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 146491960 | ||||||
| chr5:146492021 | T | G | 1 | a0001c0001t0005g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2164-899T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146492021 | |||||||
| chr5:146492527 | G | A | 3 | a0001c0002t0003g0005 a0001c0002t0003g0243 a0001c0002t0003g0244 |
6 | HG01261.hp2 HG01361.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2164-393G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146492527 | |||||||
| chr5:146492542 | C | T | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2164-378C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146492542 | |||||||
| chr5:146492555 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2164-365T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146492555 | |||||||
| chr5:146492710 | G | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2164-210G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146492710 | |||||||
| chr5:146492818 | T | A | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2164-102T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146492818 | |||||||
| chr5:146492888 | T | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02080.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.2164-32T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 15/22 | chr5 | 146492888 | |||||||
| chr5:146493274 | T | C | 3 | a0001c0001t0002g0082 a0001c0001t0002g0087 a0001c0001t0002g0094 |
3 | HG03491.hp1 NA18952.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2282+236T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493274 | |||||||
| chr5:146493288 | T | C | 1 | a0001c0001t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2282+250T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493288 | |||||||
| chr5:146493311 | C | T | 1 | a0001c0001t0010g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2282+273C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493311 | |||||||
| chr5:146493324 | T | C | 1 | a0001c0001t0004g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2282+286T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493324 | |||||||
| chr5:146493355 | A | G | 4 | a0002c0005t0004g0189 a0002c0005t0004g0190 a0002c0005t0004g0191 others(1): Show |
4 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2282+317A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493355 | |||||||
| chr5:146493700 | C | G | 8 | a0001c0002t0003g0005 a0001c0002t0003g0009 a0001c0002t0003g0241 others(5): Show |
13 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.2282+662C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493700 | |||||||
| chr5:146493802 | T | C | 143 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(140): Show |
159 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.2282+764T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493802 | |||||||
| chr5:146493968 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2282+930G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493968 | |||||||
| chr5:146493971 | A | T | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2282+933A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146493971 | |||||||
| chr5:146494048 | A | G | 4 | a0001c0001t0002g0091 a0001c0001t0002g0096 a0001c0001t0002g0097 others(1): Show |
4 | NA18954.hp2 NA19054.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.2282+1010A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146494048 | |||||||
| chr5:146494389 | G | A | 1 | a0001c0001t0004g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2282+1351G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146494389 | |||||||
| chr5:146494475 | C | A | 3 | a0001c0001t0003g0256 a0001c0001t0003g0257 a0001c0001t0003g0258 |
3 | HG02970.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2282+1437C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146494475 | |||||||
| chr5:146494718 | AGTAGAGC others(14): Show |
A | 1 | a0001c0001t0002g0088 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2282+1681_2282+170 others(25): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146494718 | |||||||
| chr5:146494852 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2282+1814T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146494852 | |||||||
| chr5:146494863 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(83): Show |
105 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.2282+1825T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146494863 | |||||||
| chr5:146495188 | T | G | 1 | a0001c0001t0002g0088 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2282+2150T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146495188 | |||||||
| chr5:146495222 | T | A | 1 | a0001c0001t0001g0213 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2282+2184T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146495222 | |||||||
| chr5:146495498 | T | C | 1 | a0001c0001t0005g0017 | 2 | HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2282+2460T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146495498 | |||||||
| chr5:146495534 | A | G | 145 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(142): Show |
161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.2282+2496A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146495534 | |||||||
| chr5:146495605 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2282+2567A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146495605 | |||||||
| chr5:146495696 | T | G | 18 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(15): Show |
23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.2282+2658T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146495696 | |||||||
| chr5:146495739 | CTTTGT | C | 36 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(33): Show |
36 | HG00738.hp2 HG01257.hp2 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.2282+2705_2282+270 others(9): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | 146495739 | ||||||
| chr5:146495880 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2283-2656C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146495880 | |||||||
| chr5:146495907 | C | G | 10 | a0001c0001t0007g0020 a0001c0002t0003g0005 a0001c0002t0003g0009 others(7): Show |
16 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.2283-2629C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146495907 | |||||||
| chr5:146496007 | G | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2283-2529G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496007 | |||||||
| chr5:146496077 | T | C | 3 | a0001c0001t0003g0256 a0001c0001t0003g0257 a0001c0001t0003g0258 |
3 | HG02970.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2283-2459T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496077 | |||||||
| chr5:146496107 | G | A | 1 | a0001c0001t0005g0199 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2283-2429G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496107 | |||||||
| chr5:146496129 | A | G | 3 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0248 |
3 | NA19002.hp1 NA19074.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.2283-2407A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496129 | |||||||
| chr5:146496235 | T | A | 1 | a0001c0001t0002g0088 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-2301T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496235 | |||||||
| chr5:146496507 | A | C | 3 | a0004c0014t0004g0186 a0006c0009t0004g0187 a0006c0009t0004g0188 |
3 | HG01496.hp2 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2283-2029A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496507 | |||||||
| chr5:146496558 | T | C | 124 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(121): Show |
138 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.2283-1978T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496558 | |||||||
| chr5:146496563 | A | T | 1 | a0001c0001t0002g0088 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-1973A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496563 | |||||||
| chr5:146496869 | G | GT | 11 | a0001c0001t0001g0119 a0001c0001t0001g0129 a0001c0001t0005g0018 others(8): Show |
12 | HG00673.hp1 HG01167.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.2283-1645dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | 146496869 | ||||||
| chr5:146496869 | GT | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(77): Show |
99 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.2283-1645delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | 146496869 | ||||||
| chr5:146496869 | GTT | G | 37 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(34): Show |
37 | HG00738.hp2 HG01257.hp2 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2283-1646_2283-164 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | 146496869 | ||||||
| chr5:146496869 | GTTT | G | 102 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(99): Show |
118 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.2283-1647_2283-164 others(7): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | 146496869 | ||||||
| chr5:146496877 | T | G | 1 | a0001c0001t0004g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2283-1659T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496877 | |||||||
| chr5:146496915 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0143 |
3 | HG01346.hp2 HG01496.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.2283-1621C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496915 | |||||||
| chr5:146496936 | T | G | 1 | a0001c0001t0004g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2283-1600T>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496936 | |||||||
| chr5:146496994 | A | T | 1 | a0001c0002t0003g0244 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2283-1542A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146496994 | |||||||
| chr5:146497023 | A | T | 1 | a0001c0001t0002g0088 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-1513A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497023 | |||||||
| chr5:146497111 | A | G | 85 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(82): Show |
99 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.2283-1425A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497111 | |||||||
| chr5:146497297 | A | T | 1 | a0001c0001t0002g0088 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-1239A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497297 | |||||||
| chr5:146497325 | T | C | 145 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(142): Show |
161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.2283-1211T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497325 | |||||||
| chr5:146497372 | C | T | 1 | a0001c0001t0002g0088 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-1164C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497372 | |||||||
| chr5:146497374 | T | C | 1 | a0001c0001t0002g0088 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-1162T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497374 | |||||||
| chr5:146497375 | G | T | 1 | a0001c0001t0002g0088 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-1161G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497375 | |||||||
| chr5:146497397 | T | A | 1 | a0001c0001t0002g0088 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-1139T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497397 | |||||||
| chr5:146497409 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(71): Show |
92 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.2283-1127C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497409 | |||||||
| chr5:146497584 | A | G | 1 | a0001c0015t0002g0105 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2283-952A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497584 | |||||||
| chr5:146497600 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2283-936A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497600 | |||||||
| chr5:146497689 | T | C | 6 | a0002c0005t0004g0189 a0002c0005t0004g0190 a0002c0005t0004g0191 others(3): Show |
6 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2283-847T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497689 | |||||||
| chr5:146497826 | C | T | 1 | a0001c0001t0003g0255 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2283-710C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497826 | |||||||
| chr5:146497837 | C | A | 1 | a0001c0001t0008g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2283-699C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497837 | |||||||
| chr5:146497934 | G | A | 24 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(21): Show |
24 | HG01257.hp2 HG01258.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.2283-602G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497934 | |||||||
| chr5:146497951 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2283-585T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146497951 | |||||||
| chr5:146498005 | C | G | 9 | a0001c0002t0003g0005 a0001c0002t0003g0009 a0001c0002t0003g0114 others(6): Show |
14 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.2283-531C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146498005 | |||||||
| chr5:146498089 | G | A | 3 | a0004c0014t0004g0186 a0006c0009t0004g0187 a0006c0009t0004g0188 |
3 | HG01496.hp2 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2283-447G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146498089 | |||||||
| chr5:146498094 | AC | A | 6 | a0002c0005t0004g0189 a0002c0005t0004g0190 a0002c0005t0004g0191 others(3): Show |
6 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2283-441delC | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146498094 | |||||||
| chr5:146498110 | A | G | 2 | a0001c0001t0003g0206 a0001c0001t0003g0207 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2283-426A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146498110 | |||||||
| chr5:146498311 | T | A | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2283-225T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146498311 | |||||||
| chr5:146498523 | A | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2283-13A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146498523 | |||||||
| chr5:146498524 | A | T | 1 | a0001c0001t0002g0088 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2283-12A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 16/22 | chr5 | 146498524 | |||||||
| chr5:146498764 | A | C | 1 | a0001c0001t0001g0142 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2433+78A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146498764 | |||||||
| chr5:146498809 | T | A | 1 | a0001c0001t0002g0088 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2433+123T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146498809 | |||||||
| chr5:146499150 | T | A | 1 | a0001c0001t0002g0088 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2433+464T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146499150 | |||||||
| chr5:146499186 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2433+500G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146499186 | |||||||
| chr5:146499187 | A | C | 2 | a0001c0004t0004g0250 a0001c0004t0004g0251 |
2 | HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.2433+501A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146499187 | |||||||
| chr5:146499449 | T | A | 1 | a0001c0001t0002g0088 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2433+763T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146499449 | |||||||
| chr5:146499647 | A | G | 1 | a0007c0017t0002g0036 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2433+961A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146499647 | |||||||
| chr5:146499750 | A | C | 163 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(160): Show |
184 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.2433+1064A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146499750 | |||||||
| chr5:146500103 | C | T | 3 | a0001c0001t0003g0256 a0001c0001t0003g0257 a0001c0001t0003g0258 |
3 | HG02970.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2433+1417C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146500103 | |||||||
| chr5:146500262 | C | G | 1 | a0001c0001t0002g0086 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2433+1576C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146500262 | |||||||
| chr5:146500319 | A | C | 1 | a0001c0001t0001g0130 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2433+1633A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146500319 | |||||||
| chr5:146500403 | TA | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(84): Show |
107 | HG00099.hp1 HG00140.hp2 HG00673.hp1 others(104): Show |
intron_variant | MODIFIER | c.2433+1729delA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146500403 | ||||||
| chr5:146500403 | TAA | T | 163 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(160): Show |
184 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.2433+1728_2433+172 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146500403 | ||||||
| chr5:146500469 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2433+1783G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146500469 | |||||||
| chr5:146500514 | A | C | 1 | a0001c0001t0007g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2433+1828A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146500514 | |||||||
| chr5:146500866 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2433+2180G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146500866 | |||||||
| chr5:146500891 | C | G | 1 | a0001c0001t0001g0229 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2433+2205C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146500891 | |||||||
| chr5:146500962 | G | A | 2 | a0001c0008t0009g0239 a0001c0008t0009g0240 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2433+2276G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146500962 | |||||||
| chr5:146501004 | C | CA | 10 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(7): Show |
10 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2433+2333dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501004 | ||||||
| chr5:146501004 | CA | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(238): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.2433+2333delA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501004 | ||||||
| chr5:146501004 | CAA | C | 6 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(3): Show |
6 | HG01099.hp2 HG01168.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.2433+2332_2433+233 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501004 | ||||||
| chr5:146501149 | A | T | 8 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0195 others(5): Show |
10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2434-2226A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146501149 | |||||||
| chr5:146501288 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2434-2087A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146501288 | |||||||
| chr5:146501346 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2434-2029G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146501346 | |||||||
| chr5:146501346 | G | GAT | 163 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(160): Show |
184 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.2434-2027_2434-202 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501346 | ||||||
| chr5:146501633 | G | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0110 |
5 | HG01256.hp1 HG01258.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2434-1742G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146501633 | |||||||
| chr5:146501688 | C | T | 18 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(15): Show |
23 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.2434-1687C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146501688 | |||||||
| chr5:146501887 | C | CT | 39 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0209 others(36): Show |
40 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.2434-1462dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501887 | ||||||
| chr5:146501887 | CT | C | 27 | a0001c0001t0001g0010 a0001c0001t0001g0151 a0001c0001t0001g0259 others(24): Show |
29 | HG01934.hp1 HG01943.hp1 HG02080.hp1 others(26): Show |
intron_variant | MODIFIER | c.2434-1462delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501887 | ||||||
| chr5:146501887 | CTT | C | 10 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0138 others(7): Show |
10 | HG01069.hp2 HG01891.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2434-1463_2434-146 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501887 | ||||||
| chr5:146501887 | CTTT | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(74): Show |
97 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.2434-1464_2434-146 others(7): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501887 | ||||||
| chr5:146501887 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | HG01243.hp2 HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2434-1474_2434-146 others(17): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501887 | ||||||
| chr5:146501915 | A | T | 1 | a0001c0001t0005g0196 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2434-1460A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146501915 | |||||||
| chr5:146501924 | TTTGC | T | 9 | a0001c0002t0003g0005 a0001c0002t0003g0009 a0001c0002t0003g0114 others(6): Show |
14 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.2434-1447_2434-144 others(8): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 146501924 | ||||||
| chr5:146501974 | C | A | 145 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(142): Show |
161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.2434-1401C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146501974 | |||||||
| chr5:146502031 | T | A | 164 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(161): Show |
185 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(182): Show |
intron_variant | MODIFIER | c.2434-1344T>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146502031 | |||||||
| chr5:146502228 | G | A | 88 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(85): Show |
102 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.2434-1147G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146502228 | |||||||
| chr5:146502420 | G | T | 4 | a0002c0005t0004g0189 a0002c0005t0004g0190 a0002c0005t0004g0191 others(1): Show |
4 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2434-955G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146502420 | |||||||
| chr5:146502742 | G | A | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2434-633G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146502742 | |||||||
| chr5:146502974 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2434-401A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146502974 | |||||||
| chr5:146503230 | A | C | 1 | a0001c0001t0001g0035 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2434-145A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 17/22 | chr5 | 146503230 | |||||||
| chr5:146503571 | T | C | 1 | a0001c0002t0003g0244 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2598+32T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 18/22 | chr5 | 146503571 | |||||||
| chr5:146503800 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02056.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.2599-24A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 18/22 | chr5 | 146503800 | |||||||
| chr5:146504054 | A | C | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2781+48A>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504054 | |||||||
| chr5:146504326 | G | A | 84 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(81): Show |
98 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.2781+320G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504326 | |||||||
| chr5:146504341 | T | C | 1 | a0001c0001t0007g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2781+335T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504341 | |||||||
| chr5:146504350 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2781+344C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504350 | |||||||
| chr5:146504866 | G | A | 1 | a0001c0001t0013g0204 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2781+860G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504866 | |||||||
| chr5:146504884 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2781+878T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504884 | |||||||
| chr5:146504903 | G | A | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2781+897G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504903 | |||||||
| chr5:146504913 | G | T | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2781+907G>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504913 | |||||||
| chr5:146504917 | G | C | 1 | a0001c0001t0001g0275 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2781+911G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504917 | |||||||
| chr5:146504968 | C | T | 8 | a0001c0002t0003g0005 a0001c0002t0003g0009 a0001c0002t0003g0241 others(5): Show |
13 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.2781+962C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504968 | |||||||
| chr5:146504987 | C | A | 154 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(151): Show |
170 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.2781+981C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146504987 | |||||||
| chr5:146505052 | A | G | 1 | a0001c0001t0003g0205 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2781+1046A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505052 | |||||||
| chr5:146505087 | T | TA | 19 | a0001c0001t0001g0131 a0001c0001t0001g0162 a0001c0001t0004g0113 others(16): Show |
25 | HG00733.hp1 HG01109.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.2781+1099dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | 146505087 | ||||||
| chr5:146505087 | TA | T | 136 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0043 others(133): Show |
154 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(151): Show |
intron_variant | MODIFIER | c.2781+1099delA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | 146505087 | ||||||
| chr5:146505087 | TAA | T | 10 | a0001c0001t0003g0205 a0001c0001t0003g0207 a0001c0001t0003g0255 others(7): Show |
10 | HG01934.hp1 HG02055.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.2781+1098_2781+109 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | 146505087 | ||||||
| chr5:146505118 | C | T | 1 | a0001c0001t0004g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2781+1112C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505118 | |||||||
| chr5:146505231 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2781+1225C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505231 | |||||||
| chr5:146505258 | C | G | 2 | a0001c0001t0002g0077 a0001c0001t0002g0078 |
2 | HG02040.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.2781+1252C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505258 | |||||||
| chr5:146505288 | C | T | 1 | a0001c0001t0010g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2781+1282C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505288 | |||||||
| chr5:146505294 | G | A | 154 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(151): Show |
170 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.2781+1288G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505294 | |||||||
| chr5:146505322 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2781+1316G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505322 | |||||||
| chr5:146505391 | C | A | 4 | a0001c0001t0006g0022 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
4 | HG02559.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2781+1385C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505391 | |||||||
| chr5:146505485 | C | A | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2781+1479C>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505485 | |||||||
| chr5:146505486 | A | AT | 259 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(256): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.2781+1482dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | 146505486 | ||||||
| chr5:146505490 | T | C | 154 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(151): Show |
170 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.2781+1484T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505490 | |||||||
| chr5:146505622 | G | GT | 8 | a0001c0002t0003g0005 a0001c0002t0003g0009 a0001c0002t0003g0241 others(5): Show |
13 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.2782-1405dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | 146505622 | ||||||
| chr5:146505626 | G | A | 3 | a0001c0002t0003g0005 a0001c0002t0003g0243 a0001c0002t0003g0244 |
6 | HG01261.hp2 HG01361.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2782-1402G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505626 | |||||||
| chr5:146505651 | A | G | 1 | a0001c0001t0002g0089 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2782-1377A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505651 | |||||||
| chr5:146505708 | C | T | 10 | a0001c0001t0007g0020 a0001c0002t0003g0005 a0001c0002t0003g0009 others(7): Show |
16 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.2782-1320C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505708 | |||||||
| chr5:146505717 | A | ACT | 154 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(151): Show |
170 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.2782-1310_2782-130 others(6): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | 146505717 | ||||||
| chr5:146505758 | A | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0027 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2782-1270A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505758 | |||||||
| chr5:146505808 | C | T | 1 | a0001c0004t0004g0249 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2782-1220C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505808 | |||||||
| chr5:146505886 | C | T | 123 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(120): Show |
137 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.2782-1142C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505886 | |||||||
| chr5:146505934 | A | T | 1 | a0001c0001t0005g0199 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2782-1094A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146505934 | |||||||
| chr5:146506035 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2782-993G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506035 | |||||||
| chr5:146506061 | G | A | 24 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(21): Show |
24 | HG01257.hp2 HG01258.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.2782-967G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506061 | |||||||
| chr5:146506120 | A | G | 153 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(150): Show |
169 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(166): Show |
intron_variant | MODIFIER | c.2782-908A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506120 | |||||||
| chr5:146506202 | A | T | 1 | a0001c0001t0001g0169 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2782-826A>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506202 | |||||||
| chr5:146506218 | G | C | 154 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(151): Show |
170 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.2782-810G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506218 | |||||||
| chr5:146506321 | G | A | 9 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(6): Show |
9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2782-707G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506321 | |||||||
| chr5:146506368 | C | T | 1 | a0001c0001t0004g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2782-660C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506368 | |||||||
| chr5:146506400 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2782-628G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506400 | |||||||
| chr5:146506467 | C | G | 1 | a0001c0001t0002g0068 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2782-561C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506467 | |||||||
| chr5:146506475 | C | T | 1 | a0001c0016t0001g0137 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2782-553C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 19/22 | chr5 | 146506475 | |||||||
| chr5:146507273 | G | A | 3 | a0003c0006t0001g0133 a0003c0006t0001g0134 a0003c0006t0001g0172 |
3 | HG00733.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2961+66G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 20/22 | chr5 | 146507273 | |||||||
| chr5:146507279 | A | G | 8 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0195 others(5): Show |
10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2961+72A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 20/22 | chr5 | 146507279 | |||||||
| chr5:146507357 | TG | T | 8 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0195 others(5): Show |
10 | HG01167.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2961+152delG | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | 146507357 | ||||||
| chr5:146507381 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02056.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.2961+174G>A | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 20/22 | chr5 | 146507381 | |||||||
| chr5:146507394 | A | G | 19 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
21 | HG01943.hp1 HG02074.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2961+187A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 20/22 | chr5 | 146507394 | |||||||
| chr5:146507532 | C | T | 1 | a0003c0019t0001g0236 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2961+325C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 20/22 | chr5 | 146507532 | |||||||
| chr5:146507573 | T | C | 164 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(161): Show |
185 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(182): Show |
intron_variant | MODIFIER | c.2962-300T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 20/22 | chr5 | 146507573 | |||||||
| chr5:146508325 | C | T | 9 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(6): Show |
9 | HG01934.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.3045+369C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 21/22 | chr5 | 146508325 | |||||||
| chr5:146508336 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(83): Show |
105 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.3045+380A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 21/22 | chr5 | 146508336 | |||||||
| chr5:146508521 | T | C | 1 | a0001c0001t0002g0083 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3045+565T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 21/22 | chr5 | 146508521 | |||||||
| chr5:146508748 | C | G | 145 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(142): Show |
161 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.3046-397C>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 21/22 | chr5 | 146508748 | |||||||
| chr5:146508752 | T | C | 8 | a0001c0002t0003g0005 a0001c0002t0003g0009 a0001c0002t0003g0241 others(5): Show |
13 | HG01256.hp2 HG01261.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.3046-393T>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 21/22 | chr5 | 146508752 | |||||||
| chr5:146509046 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3046-99A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 21/22 | chr5 | 146509046 | |||||||
| chr5:146509412 | C | CT | 63 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(60): Show |
67 | HG00738.hp2 HG01243.hp2 HG01257.hp2 others(64): Show |
intron_variant | MODIFIER | c.3146+181dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | 146509412 | ||||||
| chr5:146509412 | CT | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0143 a0001c0001t0001g0146 others(4): Show |
8 | HG00673.hp2 HG01346.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.3146+181delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | 146509412 | ||||||
| chr5:146509426 | T | TA | 3 | a0001c0001t0002g0037 a0001c0001t0002g0106 a0001c0015t0002g0105 |
3 | HG02027.hp2 NA18942.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.3146+184dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | 146509426 | ||||||
| chr5:146509492 | CT | C | 143 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0030 others(140): Show |
160 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.3146+261delT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | 146509492 | ||||||
| chr5:146509560 | G | C | 80 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0006 others(77): Show |
93 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.3146+315G>C | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | chr5 | 146509560 | |||||||
| chr5:146509672 | A | G | 85 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(82): Show |
99 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.3146+427A>G | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | chr5 | 146509672 | |||||||
| chr5:146509676 | A | AT | 13 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(10): Show |
13 | HG00738.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.3146+440dupT | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | 146509676 | ||||||
| chr5:146509714 | C | T | 2 | a0001c0001t0003g0206 a0001c0001t0003g0207 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3146+469C>T | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | chr5 | 146509714 | |||||||
| chr5:146510318 | T | TA | 7 | a0001c0001t0001g0015 a0001c0001t0001g0146 a0001c0001t0005g0017 others(4): Show |
9 | HG00738.hp1 HG01071.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.3147-100dupA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | 146510318 | ||||||
| chr5:146510318 | TA | T | 130 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0043 others(127): Show |
146 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.3147-100delA | TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | 146510318 | ||||||
| chr5:146510318 | TAA | T | 16 | a0001c0001t0001g0212 a0001c0001t0001g0219 a0001c0001t0001g0226 others(13): Show |
16 | HG01257.hp2 HG02451.hp2 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.3147-101_3147-100d others(4): Show |
TCERG1 | ENSG00000113649.14 | transcript | ENST00000679501.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | 146510318 |