Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6948 |
| ensemblid | ENSG00000185339.10 |
| hgncid | 11653 |
| symbol | TCN2 |
| name | transcobalamin 2 |
| refseq_nuc | NM_000355.4 |
| refseq_prot | NP_000346.2 |
| ensembl_nuc | ENST00000215838.8 |
| ensembl_prot | ENSP00000215838.3 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 30607174 |
| end | 30627271 |
| strand | + |
| ver | v1.2 |
| region | chr22:30607174-30627271 |
| region5000 | chr22:30602174-30632271 |
| regionname0 | TCN2_chr22_30607174_30627271 |
| regionname5000 | TCN2_chr22_30602174_30632271 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 427 | 175 | 26 | 30 | 105 | 3 | 11 | 81 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0002 | 1/1 | 427 | 161 | 2 | 27 | 97 | 6 | 27 | 76 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0003 | 0/0 | 427 | 33 | 12 | 13 | 0 | 5 | 3 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0004 | 0/0 | 427 | 26 | 23 | 2 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0005 | 0/0 | 427 | 22 | 16 | 5 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0006 | 0/0 | 427 | 10 | 5 | 2 | 1 | 0 | 2 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0007 | 0/0 | 427 | 9 | 7 | 1 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0008 | 0/0 | 427 | 8 | 0 | 0 | 8 | 0 | 0 | 7 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0009 | 0/0 | 427 | 5 | 0 | 3 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0010 | 0/0 | 427 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0011 | 0/0 | 427 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0012 | 0/0 | 427 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0013 | 0/0 | 427 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0014 | 0/0 | 427 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0015 | 0/0 | 427 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0016 | 0/0 | 427 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0017 | 0/0 | 427 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0018 | 0/0 | 427 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| a0019 | 0/0 | 427 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | MRHLG others(422): Show |
chr22 | 30602174 | 30632271 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1281 | 173 | 24 | 30 | 105 | 3 | 11 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0001c0014 | 0/0 | 1281 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0002c0002 | 1/1 | 1281 | 155 | 1 | 22 | 97 | 6 | 27 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0002c0010 | 0/0 | 1281 | 5 | 0 | 5 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0002c0021 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0003c0003 | 0/0 | 1281 | 32 | 12 | 13 | 0 | 5 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0003c0025 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0004c0004 | 0/0 | 1281 | 26 | 23 | 2 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0005c0005 | 0/0 | 1281 | 18 | 12 | 5 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0005c0011 | 0/0 | 1281 | 4 | 4 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0006c0006 | 0/0 | 1281 | 10 | 5 | 2 | 1 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0007c0007 | 0/0 | 1281 | 9 | 7 | 1 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0008c0008 | 0/0 | 1281 | 8 | 0 | 0 | 8 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0009c0009 | 0/0 | 1281 | 5 | 0 | 3 | 0 | 2 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0010c0012 | 0/0 | 1281 | 4 | 4 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0011c0013 | 0/0 | 1281 | 2 | 0 | 1 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0012c0015 | 0/0 | 1281 | 2 | 0 | 0 | 0 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0013c0018 | 0/0 | 1281 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0013c0019 | 0/0 | 1281 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0014c0016 | 0/0 | 1281 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0015c0024 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0016c0023 | 0/0 | 1281 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0017c0020 | 0/0 | 1281 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0018c0017 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 | ||
| a0019c0022 | 0/0 | 1281 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | ATGAG others(1276): Show |
chr22 | 30602174 | 30632271 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2192 | 4 | 2 | 1 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0001c0001t0002 | 0/0 | 2192 | 81 | 6 | 10 | 63 | 1 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0001c0001t0003 | 0/0 | 2192 | 64 | 6 | 9 | 40 | 1 | 8 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0001c0001t0006 | 0/0 | 2192 | 13 | 3 | 9 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0001c0001t0008 | 0/0 | 2192 | 5 | 5 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0001c0001t0010 | 0/0 | 2192 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0001c0001t0018 | 0/0 | 2193 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2188): Show |
chr22 | 30602174 | 30632271 |
| a0001c0001t0021 | 0/0 | 2193 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2188): Show |
chr22 | 30602174 | 30632271 |
| a0001c0001t0023 | 0/0 | 2192 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0001c0001t0024 | 0/0 | 2192 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0001c0014t0001 | 0/0 | 2192 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0002c0002t0001 | 1/1 | 2192 | 147 | 1 | 17 | 95 | 6 | 26 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0002c0002t0009 | 0/0 | 2192 | 4 | 0 | 4 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0002c0002t0013 | 0/0 | 2192 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0002c0002t0014 | 0/0 | 2192 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0002c0002t0017 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2188): Show |
chr22 | 30602174 | 30632271 |
| a0002c0002t0019 | 0/0 | 2192 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0002c0010t0001 | 0/0 | 2192 | 5 | 0 | 5 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0002c0021t0001 | 0/0 | 2192 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0003c0003t0004 | 0/0 | 2193 | 30 | 12 | 13 | 0 | 5 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2188): Show |
chr22 | 30602174 | 30632271 |
| a0003c0003t0007 | 0/0 | 2193 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2188): Show |
chr22 | 30602174 | 30632271 |
| a0003c0003t0012 | 0/0 | 2192 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0003c0025t0012 | 0/0 | 2192 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0004c0004t0001 | 0/0 | 2192 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0004c0004t0002 | 0/0 | 2192 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0004c0004t0005 | 0/0 | 2192 | 22 | 20 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0004c0004t0007 | 0/0 | 2193 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2188): Show |
chr22 | 30602174 | 30632271 |
| a0005c0005t0001 | 0/0 | 2192 | 12 | 8 | 3 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0005c0005t0002 | 0/0 | 2192 | 4 | 2 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0005c0005t0011 | 0/0 | 2192 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0005c0005t0015 | 0/0 | 2192 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0005c0011t0001 | 0/0 | 2192 | 4 | 4 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0006c0006t0001 | 0/0 | 2192 | 9 | 4 | 2 | 1 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0006c0006t0010 | 0/0 | 2192 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0007c0007t0004 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2188): Show |
chr22 | 30602174 | 30632271 |
| a0007c0007t0007 | 0/0 | 2193 | 8 | 6 | 1 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2188): Show |
chr22 | 30602174 | 30632271 |
| a0008c0008t0001 | 0/0 | 2192 | 8 | 0 | 0 | 8 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0009c0009t0003 | 0/0 | 2192 | 4 | 0 | 3 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0009c0009t0016 | 0/0 | 2192 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0010c0012t0001 | 0/0 | 2192 | 3 | 3 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0010c0012t0020 | 0/0 | 2192 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0011c0013t0011 | 0/0 | 2192 | 2 | 0 | 1 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0012c0015t0001 | 0/0 | 2192 | 2 | 0 | 0 | 0 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0013c0018t0002 | 0/0 | 2192 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0013c0019t0002 | 0/0 | 2192 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0014c0016t0001 | 0/0 | 2192 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0015c0024t0001 | 0/0 | 2192 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0016c0023t0001 | 0/0 | 2192 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0017c0020t0001 | 0/0 | 2192 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0018c0017t0022 | 0/0 | 2192 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| a0019c0022t0001 | 0/0 | 2192 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | GCAGA others(2187): Show |
chr22 | 30602174 | 30632271 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0008 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0066 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0067 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0068 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0006g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0006g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0006g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0006g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0006g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0008g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0008g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0008g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0008g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0010g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0010g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0018g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0021g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0023g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0001t0024g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0014t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0001c0014t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0001 | 0/0 | 12 | 0 | 1 | 8 | 2 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0005 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0006 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0061 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0063 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0064 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0268 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0298 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0009g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0009g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0009g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0013g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0014g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0017g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0002t0019g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0010t0001g0013 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0010t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0002c0021t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0044 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0007g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0003t0012g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0003c0025t0012g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0004c0004t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0004c0004t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0004c0004t0005g0002 | 0/0 | 12 | 12 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0004c0004t0005g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0004c0004t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0004c0004t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0004c0004t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0004c0004t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0004c0004t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0004c0004t0005g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0004c0004t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0004c0004t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0004c0004t0007g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0005t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0005t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0005t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0005t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0005t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0005t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0005t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0005t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0005t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0005t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0005t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0005t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0005t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0005t0011g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0005t0015g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0011t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0011t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0005c0011t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0006c0006t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0006c0006t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0006c0006t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0006c0006t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0006c0006t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0006c0006t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0006c0006t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0006c0006t0010g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0007c0007t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0007c0007t0007g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0007c0007t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0007c0007t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0007c0007t0007g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0007c0007t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0008c0008t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0008c0008t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0008c0008t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0008c0008t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0008c0008t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0008c0008t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0009c0009t0003g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0009c0009t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0009c0009t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0009c0009t0016g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0010c0012t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0010c0012t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0010c0012t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0010c0012t0020g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0011c0013t0011g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0011c0013t0011g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0012c0015t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0012c0015t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0013c0018t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0013c0019t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0014c0016t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0014c0016t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0015c0024t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0016c0023t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0017c0020t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0018c0017t0022g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| a0019c0022t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0059 | EUR | GBR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00099 | hp2 | a0011 | c0013 | t0011 | g0187 | EUR | GBR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00140 | hp1 | a0003 | c0003 | t0004 | g0213 | EUR | GBR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | GBR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00280 | hp1 | a0003 | c0003 | t0004 | g0215 | EUR | FIN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0018 | EUR | FIN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00323 | hp1 | a0009 | c0009 | t0016 | g0109 | EUR | FIN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0100 | EUR | FIN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00408 | hp1 | a0001 | c0001 | t0023 | g0167 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00597 | hp2 | a0008 | c0008 | t0001 | g0003 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0080 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0317 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00642 | hp2 | a0005 | c0005 | t0002 | g0073 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0279 | EAS | CHS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0322 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00733 | hp2 | a0003 | c0003 | t0004 | g0204 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0078 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0139 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0299 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00741 | hp1 | a0002 | c0002 | t0009 | g0050 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG00741 | hp2 | a0002 | c0010 | t0001 | g0013 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01069 | hp1 | a0002 | c0010 | t0001 | g0231 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01069 | hp2 | a0005 | c0005 | t0001 | g0041 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0021 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01071 | hp1 | a0005 | c0005 | t0001 | g0041 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0021 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0257 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01081 | hp1 | a0003 | c0003 | t0004 | g0206 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01081 | hp2 | a0003 | c0003 | t0004 | g0217 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0275 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01099 | hp2 | a0005 | c0005 | t0001 | g0192 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01106 | hp1 | a0011 | c0013 | t0011 | g0188 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01106 | hp2 | a0002 | c0010 | t0001 | g0013 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01109 | hp1 | a0002 | c0010 | t0001 | g0013 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0286 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0076 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01167 | hp2 | a0006 | c0006 | t0001 | g0046 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0321 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01168 | hp2 | a0002 | c0002 | t0009 | g0049 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01169 | hp1 | a0002 | c0002 | t0009 | g0049 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01169 | hp2 | a0006 | c0006 | t0001 | g0046 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01175 | hp1 | a0009 | c0009 | t0003 | g0106 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0287 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0015 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01192 | hp2 | a0005 | c0005 | t0002 | g0074 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01243 | hp2 | a0004 | c0004 | t0005 | g0119 | AMR | PUR | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0015 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0290 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01256 | hp1 | a0003 | c0003 | t0004 | g0194 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0061 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0137 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01257 | hp2 | a0009 | c0009 | t0003 | g0026 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0061 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01258 | hp2 | a0009 | c0009 | t0003 | g0026 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01261 | hp1 | a0007 | c0007 | t0007 | g0011 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01358 | hp1 | a0003 | c0003 | t0004 | g0209 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01361 | hp1 | a0002 | c0010 | t0001 | g0013 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0285 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0079 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01496 | hp1 | a0004 | c0004 | t0005 | g0114 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01515 | hp1 | a0003 | c0003 | t0004 | g0044 | EUR | IBS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0075 | EUR | IBS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01516 | hp1 | a0009 | c0009 | t0003 | g0110 | EUR | IBS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01516 | hp2 | a0015 | c0024 | t0001 | g0001 | EUR | IBS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01517 | hp1 | a0003 | c0003 | t0004 | g0044 | EUR | IBS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | IBS | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01884 | hp1 | a0004 | c0004 | t0005 | g0118 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01884 | hp2 | a0003 | c0003 | t0004 | g0201 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01891 | hp2 | a0004 | c0004 | t0005 | g0002 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01928 | hp2 | a0003 | c0003 | t0004 | g0222 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01943 | hp2 | a0003 | c0003 | t0004 | g0212 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01952 | hp2 | a0003 | c0003 | t0004 | g0210 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01978 | hp1 | a0003 | c0003 | t0004 | g0214 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01978 | hp2 | a0002 | c0002 | t0009 | g0240 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01981 | hp2 | a0001 | c0001 | t0021 | g0153 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01993 | hp1 | a0003 | c0003 | t0004 | g0043 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0325 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02040 | hp2 | a0016 | c0023 | t0001 | g0003 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02055 | hp1 | a0004 | c0004 | t0005 | g0002 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02055 | hp2 | a0007 | c0007 | t0007 | g0086 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | KHV | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02148 | hp2 | a0003 | c0003 | t0004 | g0043 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | CDX | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | CDX | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CDX | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02165 | hp2 | a0017 | c0020 | t0001 | g0006 | EAS | CDX | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02257 | hp1 | a0004 | c0004 | t0005 | g0002 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0320 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02258 | hp1 | a0003 | c0003 | t0004 | g0198 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0269 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0307 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | g0108 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0328 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0324 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02300 | hp1 | a0003 | c0003 | t0004 | g0045 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02300 | hp2 | a0003 | c0003 | t0004 | g0045 | AMR | PEL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02451 | hp1 | a0004 | c0004 | t0005 | g0002 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02451 | hp2 | a0003 | c0003 | t0004 | g0196 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02572 | hp2 | a0005 | c0005 | t0001 | g0082 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0148 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0297 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0319 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0309 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02622 | hp1 | a0005 | c0005 | t0001 | g0193 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02622 | hp2 | a0010 | c0012 | t0001 | g0225 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02630 | hp1 | a0007 | c0007 | t0007 | g0084 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02630 | hp2 | a0005 | c0005 | t0011 | g0329 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02647 | hp1 | a0007 | c0007 | t0007 | g0083 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02647 | hp2 | a0003 | c0003 | t0004 | g0230 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02683 | hp1 | a0006 | c0006 | t0001 | g0195 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02683 | hp2 | a0004 | c0004 | t0007 | g0125 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0053 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0315 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02717 | hp1 | a0004 | c0004 | t0005 | g0117 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02717 | hp2 | a0005 | c0005 | t0001 | g0040 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02723 | hp2 | a0005 | c0005 | t0001 | g0039 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0264 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0270 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02738 | hp1 | a0007 | c0007 | t0007 | g0085 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0260 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02809 | hp1 | a0004 | c0004 | t0005 | g0002 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02809 | hp2 | a0005 | c0005 | t0015 | g0071 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02818 | hp2 | a0010 | c0012 | t0001 | g0224 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02886 | hp1 | a0001 | c0014 | t0001 | g0227 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0312 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02895 | hp1 | a0003 | c0003 | t0004 | g0042 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02895 | hp2 | a0003 | c0003 | t0004 | g0199 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02896 | hp1 | a0007 | c0007 | t0007 | g0011 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02896 | hp2 | a0005 | c0011 | t0001 | g0022 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02897 | hp1 | a0003 | c0003 | t0004 | g0042 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02897 | hp2 | a0005 | c0011 | t0001 | g0022 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02922 | hp1 | a0004 | c0004 | t0005 | g0116 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02922 | hp2 | a0005 | c0005 | t0001 | g0190 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0303 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02965 | hp2 | a0010 | c0012 | t0020 | g0226 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02970 | hp1 | a0004 | c0004 | t0002 | g0029 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02970 | hp2 | a0007 | c0007 | t0004 | g0121 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02976 | hp1 | a0004 | c0004 | t0005 | g0002 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02976 | hp2 | a0004 | c0004 | t0005 | g0115 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0138 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0296 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03041 | hp1 | a0003 | c0003 | t0004 | g0203 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03041 | hp2 | a0005 | c0011 | t0001 | g0077 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03098 | hp1 | a0010 | c0012 | t0001 | g0223 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03098 | hp2 | a0004 | c0004 | t0005 | g0028 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03130 | hp1 | a0001 | c0014 | t0001 | g0228 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03139 | hp1 | a0004 | c0004 | t0005 | g0002 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03195 | hp1 | a0004 | c0004 | t0005 | g0002 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03195 | hp2 | a0003 | c0003 | t0004 | g0197 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0311 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0251 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03453 | hp1 | a0005 | c0005 | t0002 | g0072 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0326 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03486 | hp2 | a0007 | c0007 | t0007 | g0011 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03491 | hp1 | a0012 | c0015 | t0001 | g0248 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0183 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0267 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0182 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03516 | hp1 | a0003 | c0003 | t0004 | g0200 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ESN | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0313 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03540 | hp2 | a0007 | c0007 | t0007 | g0011 | AFR | GWD | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03579 | hp1 | a0004 | c0004 | t0005 | g0123 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03579 | hp2 | a0004 | c0004 | t0005 | g0002 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0136 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0289 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0132 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03688 | hp1 | a0006 | c0006 | t0001 | g0219 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0305 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0295 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0149 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0249 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03710 | hp2 | a0002 | c0002 | t0013 | g0054 | SAS | PJL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03831 | hp1 | a0003 | c0003 | t0012 | g0205 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0030 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03834 | hp1 | a0003 | c0003 | t0007 | g0216 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0306 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0030 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03927 | hp2 | a0003 | c0025 | t0012 | g0208 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0091 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0053 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0065 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0066 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG04184 | hp1 | a0005 | c0005 | t0001 | g0191 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG04184 | hp2 | a0012 | c0015 | t0001 | g0054 | SAS | BEB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG04199 | hp1 | a0001 | c0001 | t0018 | g0065 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0291 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0316 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0250 | SAS | STU | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18522 | hp1 | a0006 | c0006 | t0001 | g0069 | AFR | YRI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18522 | hp2 | a0018 | c0017 | t0022 | g0308 | AFR | YRI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | CHB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | CHB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | CHB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | CHB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18906 | hp1 | a0004 | c0004 | t0005 | g0002 | AFR | YRI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18906 | hp2 | a0006 | c0006 | t0010 | g0220 | AFR | YRI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18945 | hp1 | a0019 | c0022 | t0001 | g0278 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18949 | hp2 | a0013 | c0018 | t0002 | g0131 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18950 | hp2 | a0013 | c0019 | t0002 | g0294 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18956 | hp1 | a0008 | c0008 | t0001 | g0135 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18971 | hp1 | a0014 | c0016 | t0001 | g0006 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18974 | hp1 | a0002 | c0002 | t0017 | g0062 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18975 | hp1 | a0008 | c0008 | t0001 | g0031 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18982 | hp1 | a0006 | c0006 | t0001 | g0218 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18992 | hp2 | a0008 | c0008 | t0001 | g0003 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18998 | hp1 | a0002 | c0002 | t0019 | g0142 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19030 | hp1 | a0003 | c0003 | t0004 | g0202 | AFR | LWK | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19030 | hp2 | a0004 | c0004 | t0001 | g0124 | AFR | LWK | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19043 | hp1 | a0005 | c0005 | t0001 | g0039 | AFR | LWK | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0016 | AFR | LWK | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19059 | hp1 | a0008 | c0008 | t0001 | g0130 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19059 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19064 | hp2 | a0008 | c0008 | t0001 | g0145 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19085 | hp1 | a0001 | c0001 | t0024 | g0038 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19085 | hp2 | a0008 | c0008 | t0001 | g0144 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19089 | hp1 | a0008 | c0008 | t0001 | g0003 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19089 | hp2 | a0014 | c0016 | t0001 | g0051 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19240 | hp1 | a0004 | c0004 | t0002 | g0029 | AFR | YRI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA19240 | hp2 | a0004 | c0004 | t0005 | g0002 | AFR | YRI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA20129 | hp1 | a0005 | c0005 | t0001 | g0189 | AFR | ASW | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA20129 | hp2 | a0004 | c0004 | t0005 | g0122 | AFR | ASW | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0288 | EUR | TSI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0033 | EUR | TSI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA20805 | hp1 | a0003 | c0003 | t0004 | g0207 | EUR | TSI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0237 | EUR | TSI | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | GIH | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | GIH | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01123 | hp1 | a0002 | c0002 | t0014 | g0277 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02109 | hp1 | a0006 | c0006 | t0001 | g0221 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02109 | hp2 | a0005 | c0005 | t0002 | g0070 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02486 | hp1 | a0002 | c0021 | t0001 | g0059 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02486 | hp2 | a0006 | c0006 | t0001 | g0047 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0327 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0107 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG03471 | hp2 | a0004 | c0004 | t0005 | g0028 | AFR | MSL | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG06807 | hp1 | a0006 | c0006 | t0001 | g0047 | AFR | USA | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| HG06807 | hp2 | a0005 | c0005 | t0001 | g0040 | AFR | USA | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA20300 | hp1 | a0004 | c0004 | t0005 | g0002 | AFR | USA | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA20300 | hp2 | a0003 | c0003 | t0004 | g0211 | AFR | USA | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | LWK | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| NA21309 | hp2 | a0005 | c0011 | t0001 | g0081 | AFR | LWK | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0268 | REF | REF | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0298 | REF | REF | TCN2_chr22_30602174_30632271 | TCN2 | chr22 | 30602174 | 30632271 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:30610873 | A | G | 2 | a0003 a0006 |
43 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(40): Show |
missense_variant&splice_region_variant | MODERATE | c.67A>G | p.Ile23Val | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/9 | 225/2192 | 67/1284 | 23/427 | chr22 | 30610873 | |||
| chr22:30610895 | T | G | 1 | a0018 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.89T>G | p.Leu30Arg | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/9 | 247/2192 | 89/1284 | 30/427 | chr22 | 30610895 | |||
| chr22:30611036 | A | T | 1 | a0008 | 8 | HG00597.hp2 NA18956.hp1 NA18975.hp1 others(5): Show |
missense_variant | MODERATE | c.230A>T | p.Lys77Met | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/9 | 388/2192 | 230/1284 | 77/427 | chr22 | 30611036 | |||
| chr22:30612880 | T | C | 1 | a0011 | 2 | HG00099.hp2 HG01106.hp1 |
missense_variant | MODERATE | c.265T>C | p.Phe89Leu | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/9 | 423/2192 | 265/1284 | 89/427 | chr22 | 30612880 | |||
| chr22:30612901 | T | A | 1 | a0013 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.286T>A | p.Cys96Ser | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/9 | 444/2192 | 286/1284 | 96/427 | chr22 | 30612901 | |||
| chr22:30612902 | G | A | 1 | a0013 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.287G>A | p.Cys96Tyr | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/9 | 445/2192 | 287/1284 | 96/427 | chr22 | 30612902 | |||
| chr22:30613037 | C | G | 1 | a0015 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.422C>G | p.Ala141Gly | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/9 | 580/2192 | 422/1284 | 141/427 | chr22 | 30613037 | |||
| chr22:30613039 | A | G | 1 | a0016 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.424A>G | p.Ile142Val | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/9 | 582/2192 | 424/1284 | 142/427 | chr22 | 30613039 | |||
| chr22:30614430 | G | A | 1 | a0017 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.509G>A | p.Arg170Gln | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/9 | 667/2192 | 509/1284 | 170/427 | chr22 | 30614430 | |||
| chr22:30614475 | C | T | 1 | a0010 | 4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
missense_variant | MODERATE | c.554C>T | p.Pro185Leu | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/9 | 712/2192 | 554/1284 | 185/427 | chr22 | 30614475 | |||
| chr22:30615363 | C | T | 2 | a0004 a0018 |
27 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(24): Show |
missense_variant | MODERATE | c.643C>T | p.Arg215Trp | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 5/9 | 801/2192 | 643/1284 | 215/427 | chr22 | 30615363 | |||
| chr22:30615623 | G | C | 8 | a0001 a0003 a0004 others(5): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
missense_variant | MODERATE | c.776G>C | p.Arg259Pro | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/9 | 934/2192 | 776/1284 | 259/427 | chr22 | 30615623 | |||
| chr22:30615704 | C | T | 1 | a0019 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.857C>T | p.Ala286Val | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/9 | 1015/2192 | 857/1284 | 286/427 | chr22 | 30615704 | |||
| chr22:30617387 | C | T | 2 | a0014 a0017 |
3 | HG02165.hp2 NA18971.hp1 NA19089.hp2 |
missense_variant | MODERATE | c.998C>T | p.Thr333Met | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/9 | 1156/2192 | 998/1284 | 333/427 | chr22 | 30617387 | |||
| chr22:30617432 | C | T | 2 | a0003 a0007 |
42 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(39): Show |
missense_variant | MODERATE | c.1043C>T | p.Ser348Phe | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/9 | 1201/2192 | 1043/1284 | 348/427 | chr22 | 30617432 | |||
| chr22:30622988 | T | C | 1 | a0009 | 5 | HG00323.hp1 HG01175.hp1 HG01257.hp2 others(2): Show |
missense_variant | MODERATE | c.1127T>C | p.Leu376Ser | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/9 | 1285/2192 | 1127/1284 | 376/427 | chr22 | 30622988 | |||
| chr22:30623011 | G | A | 1 | a0012 | 2 | HG03491.hp1 HG04184.hp2 |
missense_variant | MODERATE | c.1150G>A | p.Val384Met | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/9 | 1308/2192 | 1150/1284 | 384/427 | chr22 | 30623011 | |||
| chr22:30623057 | G | A | 2 | a0005 a0011 |
24 | HG00099.hp2 HG00642.hp2 HG01069.hp2 others(21): Show |
missense_variant | MODERATE | c.1196G>A | p.Arg399Gln | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/9 | 1354/2192 | 1196/1284 | 399/427 | chr22 | 30623057 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:30612975 | G | A | 1 | a0005c0011 | 4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
synonymous_variant | LOW | c.360G>A | p.Arg120Arg | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/9 | 518/2192 | 360/1284 | 120/427 | chr22 | 30612975 | |||
| chr22:30614422 | C | T | 1 | a0003c0025 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.501C>T | p.His167His | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/9 | 659/2192 | 501/1284 | 167/427 | chr22 | 30614422 | |||
| chr22:30615687 | T | C | 1 | a0001c0014 | 2 | HG02886.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.840T>C | p.Asp280Asp | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/9 | 998/2192 | 840/1284 | 280/427 | chr22 | 30615687 | |||
| chr22:30615724 | C | T | 1 | a0002c0021 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.877C>T | p.Leu293Leu | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/9 | 1035/2192 | 877/1284 | 293/427 | chr22 | 30615724 | |||
| chr22:30617412 | G | A | 1 | a0002c0010 | 5 | HG00741.hp2 HG01069.hp1 HG01106.hp2 others(2): Show |
synonymous_variant | LOW | c.1023G>A | p.Pro341Pro | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/9 | 1181/2192 | 1023/1284 | 341/427 | chr22 | 30617412 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:30626550 | C | A | 1 | a0002c0002t0009 | 4 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*29C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 29 | chr22 | 30626550 | ||||||
| chr22:30626590 | T | C | 1 | a0002c0002t0013 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*69T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 69 | chr22 | 30626590 | ||||||
| chr22:30626603 | C | T | 7 | a0003c0003t0004 a0003c0003t0007 a0003c0003t0012 others(4): Show |
43 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*82C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 82 | chr22 | 30626603 | ||||||
| chr22:30626648 | C | T | 1 | a0001c0001t0006 | 13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*127C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 127 | chr22 | 30626648 | ||||||
| chr22:30626730 | G | C | 1 | a0002c0002t0014 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*209G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 209 | chr22 | 30626730 | ||||||
| chr22:30626733 | G | A | 1 | a0005c0005t0015 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*212G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 212 | chr22 | 30626733 | ||||||
| chr22:30626746 | A | T | 10 | a0001c0001t0002 a0001c0001t0021 a0001c0001t0023 others(7): Show |
115 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*225A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 225 | chr22 | 30626746 | ||||||
| chr22:30626804 | C | G | 1 | a0010c0012t0020 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*283C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 283 | chr22 | 30626804 | ||||||
| chr22:30626821 | T | G | 1 | a0009c0009t0016 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*300T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 300 | chr22 | 30626821 | ||||||
| chr22:30626828 | C | CA | 8 | a0001c0001t0018 a0001c0001t0021 a0002c0002t0017 others(5): Show |
44 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*313dupA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 314 | INFO_REALIGN_3_PRIME | chr22 | 30626828 | |||||
| chr22:30626836 | G | A | 1 | a0018c0017t0022 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*315G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 315 | chr22 | 30626836 | ||||||
| chr22:30626903 | C | T | 2 | a0005c0005t0011 a0011c0013t0011 |
3 | HG00099.hp2 HG01106.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*382C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 382 | chr22 | 30626903 | ||||||
| chr22:30626912 | G | A | 1 | a0002c0002t0019 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*391G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 391 | chr22 | 30626912 | ||||||
| chr22:30626926 | T | C | 1 | a0001c0001t0023 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*405T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 405 | chr22 | 30626926 | ||||||
| chr22:30626965 | C | T | 7 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0018 others(4): Show |
95 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*444C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 444 | chr22 | 30626965 | ||||||
| chr22:30627204 | A | G | 11 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(8): Show |
122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*683A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 9/9 | 683 | chr22 | 30627204 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:30607406 | C | T | 1 | a0005c0005t0011g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.64+11C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30607406 | |||||||
| chr22:30607467 | A | G | 10 | a0001c0001t0002g0004 a0002c0002t0001g0056 a0002c0002t0001g0057 others(7): Show |
12 | HG00597.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.64+72A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30607467 | |||||||
| chr22:30607474 | T | C | 2 | a0001c0001t0001g0020 a0006c0006t0001g0069 |
3 | HG01496.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.64+79T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30607474 | |||||||
| chr22:30607574 | A | G | 32 | a0001c0001t0003g0019 a0001c0001t0003g0065 a0001c0001t0003g0066 others(29): Show |
37 | HG00642.hp1 HG00733.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.64+179A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30607574 | |||||||
| chr22:30607620 | G | A | 5 | a0005c0005t0002g0070 a0005c0005t0002g0072 a0005c0005t0002g0073 others(2): Show |
5 | HG00642.hp2 HG01192.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+225G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30607620 | |||||||
| chr22:30607689 | C | T | 2 | a0001c0001t0002g0301 a0001c0001t0002g0302 |
2 | NA18975.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.64+294C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30607689 | |||||||
| chr22:30607927 | A | G | 1 | a0001c0001t0002g0300 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64+532A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30607927 | |||||||
| chr22:30608140 | G | A | 80 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(77): Show |
105 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.64+745G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608140 | |||||||
| chr22:30608201 | G | C | 101 | a0001c0001t0001g0020 a0001c0001t0002g0004 a0001c0001t0002g0008 others(98): Show |
148 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.64+806G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608201 | |||||||
| chr22:30608469 | C | T | 1 | a0002c0002t0001g0064 | 2 | NA19006.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.64+1074C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608469 | |||||||
| chr22:30608526 | C | CTGCATGT others(31): Show |
3 | a0001c0001t0002g0027 a0001c0001t0002g0112 a0001c0001t0002g0113 |
4 | HG01070.hp1 HG02559.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+1133_64+1170dup others(38): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 30608526 | ||||||
| chr22:30608610 | G | A | 11 | a0005c0005t0001g0039 a0005c0005t0001g0040 a0005c0005t0001g0041 others(8): Show |
14 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.64+1215G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608610 | |||||||
| chr22:30608639 | G | C | 156 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(153): Show |
204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.64+1244G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608639 | |||||||
| chr22:30608824 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.64+1429C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608824 | |||||||
| chr22:30608826 | C | T | 1 | a0003c0003t0004g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.64+1431C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608826 | |||||||
| chr22:30608841 | C | G | 11 | a0005c0005t0001g0039 a0005c0005t0001g0040 a0005c0005t0001g0041 others(8): Show |
14 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.64+1446C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608841 | |||||||
| chr22:30608858 | T | G | 2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | NA19011.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.64+1463T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608858 | |||||||
| chr22:30608877 | C | T | 1 | a0002c0002t0001g0299 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.64+1482C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30608877 | |||||||
| chr22:30609001 | G | A | 2 | a0002c0010t0001g0013 a0002c0010t0001g0231 |
5 | HG00741.hp2 HG01069.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+1606G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609001 | |||||||
| chr22:30609023 | T | C | 14 | a0001c0001t0002g0120 a0004c0004t0001g0124 a0004c0004t0002g0029 others(11): Show |
27 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.64+1628T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609023 | |||||||
| chr22:30609031 | A | G | 63 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(60): Show |
79 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.64+1636A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609031 | |||||||
| chr22:30609141 | C | T | 1 | a0002c0002t0001g0063 | 2 | NA18946.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.65-1730C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609141 | |||||||
| chr22:30609153 | C | G | 1 | a0001c0001t0008g0328 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.65-1718C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609153 | |||||||
| chr22:30609159 | CT | C | 19 | a0001c0001t0003g0087 a0001c0001t0003g0304 a0001c0001t0006g0075 others(16): Show |
19 | HG00099.hp2 HG01167.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.65-1698delT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 30609159 | ||||||
| chr22:30609233 | G | A | 1 | a0011c0013t0011g0187 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.65-1638G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609233 | |||||||
| chr22:30609234 | G | C | 3 | a0001c0001t0003g0023 a0001c0001t0003g0088 a0001c0001t0003g0089 |
4 | HG02040.hp1 HG02132.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-1637G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609234 | |||||||
| chr22:30609241 | G | A | 2 | a0001c0001t0003g0305 a0001c0001t0003g0306 |
2 | HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.65-1630G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609241 | |||||||
| chr22:30609246 | TCCCACCT others(3): Show |
T | 1 | a0001c0001t0003g0304 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.65-1622_65-1613del others(10): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 30609246 | ||||||
| chr22:30609257 | C | A | 11 | a0005c0005t0001g0039 a0005c0005t0001g0040 a0005c0005t0001g0041 others(8): Show |
14 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.65-1614C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609257 | |||||||
| chr22:30609263 | A | G | 14 | a0001c0001t0001g0229 a0001c0014t0001g0227 a0001c0014t0001g0228 others(11): Show |
17 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.65-1608A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609263 | |||||||
| chr22:30609306 | G | A | 135 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0003g0007 others(132): Show |
169 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.65-1565G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609306 | |||||||
| chr22:30609350 | T | C | 1 | a0001c0001t0003g0305 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.65-1521T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609350 | |||||||
| chr22:30609525 | C | T | 1 | a0001c0001t0002g0186 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.65-1346C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609525 | |||||||
| chr22:30609527 | G | C | 5 | a0005c0005t0002g0070 a0005c0005t0002g0072 a0005c0005t0002g0073 others(2): Show |
5 | HG00642.hp2 HG01192.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-1344G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609527 | |||||||
| chr22:30609547 | C | A | 1 | a0002c0002t0001g0238 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.65-1324C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609547 | |||||||
| chr22:30609589 | AGG | A | 260 | a0001c0001t0001g0020 a0001c0001t0001g0229 a0001c0001t0002g0004 others(257): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.65-1277_65-1276del others(2): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 30609589 | ||||||
| chr22:30609613 | A | G | 4 | a0010c0012t0001g0223 a0010c0012t0001g0224 a0010c0012t0001g0225 others(1): Show |
4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-1258A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609613 | |||||||
| chr22:30609879 | T | C | 3 | a0005c0005t0011g0329 a0011c0013t0011g0187 a0011c0013t0011g0188 |
3 | HG00099.hp2 HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.65-992T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609879 | |||||||
| chr22:30609971 | C | T | 1 | a0004c0004t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-900C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30609971 | |||||||
| chr22:30610000 | A | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0185 a0001c0001t0024g0038 |
3 | HG00673.hp1 HG02165.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.65-871A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610000 | |||||||
| chr22:30610017 | C | T | 11 | a0005c0005t0001g0039 a0005c0005t0001g0040 a0005c0005t0001g0041 others(8): Show |
14 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.65-854C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610017 | |||||||
| chr22:30610193 | A | G | 1 | a0002c0002t0001g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.65-678A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610193 | |||||||
| chr22:30610254 | A | G | 1 | a0004c0004t0005g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.65-617A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610254 | |||||||
| chr22:30610283 | C | A | 1 | a0004c0004t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-588C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610283 | |||||||
| chr22:30610518 | C | T | 2 | a0001c0001t0002g0010 a0001c0001t0002g0184 |
6 | NA18944.hp2 NA18952.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-353C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610518 | |||||||
| chr22:30610541 | C | A | 2 | a0002c0002t0001g0048 a0002c0002t0001g0239 |
3 | NA18972.hp1 NA19056.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.65-330C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610541 | |||||||
| chr22:30610543 | A | G | 1 | a0003c0003t0004g0222 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.65-328A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610543 | |||||||
| chr22:30610565 | G | A | 24 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(21): Show |
34 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.65-306G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610565 | |||||||
| chr22:30610626 | C | CT | 5 | a0007c0007t0007g0011 a0007c0007t0007g0083 a0007c0007t0007g0084 others(2): Show |
8 | HG01261.hp1 HG02055.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-244dupT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 30610626 | ||||||
| chr22:30610639 | A | G | 2 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.65-232A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610639 | |||||||
| chr22:30610644 | C | A | 1 | a0004c0004t0005g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.65-227C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610644 | |||||||
| chr22:30610715 | T | G | 5 | a0001c0001t0006g0015 a0001c0001t0006g0021 a0001c0001t0006g0075 others(2): Show |
8 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-156T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610715 | |||||||
| chr22:30610728 | A | G | 2 | a0002c0002t0001g0182 a0002c0002t0001g0183 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.65-143A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610728 | |||||||
| chr22:30610854 | C | T | 2 | a0011c0013t0011g0187 a0011c0013t0011g0188 |
2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.65-17C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 1/8 | chr22 | 30610854 | |||||||
| chr22:30611090 | T | C | 1 | a0001c0001t0003g0307 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.257+27T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611090 | |||||||
| chr22:30611157 | A | C | 1 | a0006c0006t0001g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.257+94A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611157 | |||||||
| chr22:30611201 | G | A | 1 | a0002c0002t0001g0132 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.257+138G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611201 | |||||||
| chr22:30611205 | A | G | 1 | a0004c0004t0005g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.257+142A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611205 | |||||||
| chr22:30611251 | G | T | 2 | a0011c0013t0011g0187 a0011c0013t0011g0188 |
2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.257+188G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611251 | |||||||
| chr22:30611276 | C | T | 1 | a0013c0019t0002g0294 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.257+213C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611276 | |||||||
| chr22:30611305 | A | G | 5 | a0007c0007t0007g0011 a0007c0007t0007g0083 a0007c0007t0007g0084 others(2): Show |
8 | HG01261.hp1 HG02055.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.257+242A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611305 | |||||||
| chr22:30611317 | ACT | A | 4 | a0010c0012t0001g0223 a0010c0012t0001g0224 a0010c0012t0001g0225 others(1): Show |
4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+257_257+258del others(2): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 30611317 | ||||||
| chr22:30611332 | G | A | 1 | a0003c0003t0004g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.257+269G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611332 | |||||||
| chr22:30611384 | T | C | 2 | a0011c0013t0011g0187 a0011c0013t0011g0188 |
2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.257+321T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611384 | |||||||
| chr22:30611533 | C | T | 3 | a0001c0001t0001g0229 a0001c0014t0001g0227 a0001c0014t0001g0228 |
3 | HG02886.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.257+470C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611533 | |||||||
| chr22:30611653 | G | A | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | HG02074.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.257+590G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611653 | |||||||
| chr22:30611750 | C | T | 2 | a0001c0001t0008g0326 a0001c0001t0008g0327 |
2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.257+687C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611750 | |||||||
| chr22:30611881 | G | A | 1 | a0005c0005t0002g0070 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.257+818G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611881 | |||||||
| chr22:30611932 | A | G | 79 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(76): Show |
104 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.257+869A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30611932 | |||||||
| chr22:30611949 | AAAG | A | 38 | a0003c0003t0004g0042 a0003c0003t0004g0043 a0003c0003t0004g0044 others(35): Show |
44 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.257+891_257+893del others(3): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 30611949 | ||||||
| chr22:30612138 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.258-735C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612138 | |||||||
| chr22:30612168 | C | T | 6 | a0001c0001t0002g0009 a0001c0001t0002g0180 a0001c0001t0002g0181 others(3): Show |
10 | NA18951.hp2 NA18953.hp2 NA18975.hp2 others(7): Show |
intron_variant | MODIFIER | c.258-705C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612168 | |||||||
| chr22:30612245 | T | TA | 35 | a0002c0002t0001g0050 a0002c0002t0009g0049 a0002c0002t0009g0050 others(32): Show |
40 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.258-616dupA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 30612245 | ||||||
| chr22:30612245 | TA | T | 58 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(55): Show |
84 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.258-616delA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 30612245 | ||||||
| chr22:30612252 | A | T | 5 | a0005c0005t0002g0070 a0005c0005t0002g0072 a0005c0005t0002g0073 others(2): Show |
5 | HG00642.hp2 HG01192.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.258-621A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612252 | |||||||
| chr22:30612253 | A | T | 64 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(61): Show |
81 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.258-620A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612253 | |||||||
| chr22:30612254 | A | T | 1 | a0002c0002t0001g0293 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.258-619A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612254 | |||||||
| chr22:30612258 | T | A | 1 | a0005c0005t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.258-615T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612258 | |||||||
| chr22:30612259 | A | T | 1 | a0013c0018t0002g0131 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.258-614A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612259 | |||||||
| chr22:30612298 | C | T | 20 | a0003c0003t0004g0043 a0003c0003t0004g0044 a0003c0003t0004g0045 others(17): Show |
23 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.258-575C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612298 | |||||||
| chr22:30612346 | C | T | 60 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(57): Show |
86 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.258-527C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612346 | |||||||
| chr22:30612449 | C | A | 11 | a0005c0005t0001g0039 a0005c0005t0001g0040 a0005c0005t0001g0041 others(8): Show |
14 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.258-424C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612449 | |||||||
| chr22:30612455 | C | T | 8 | a0005c0005t0001g0039 a0005c0005t0001g0040 a0005c0005t0001g0041 others(5): Show |
11 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.258-418C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612455 | |||||||
| chr22:30612475 | G | T | 3 | a0005c0005t0011g0329 a0011c0013t0011g0187 a0011c0013t0011g0188 |
3 | HG00099.hp2 HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.258-398G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612475 | |||||||
| chr22:30612504 | C | T | 1 | a0005c0005t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.258-369C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612504 | |||||||
| chr22:30612511 | C | G | 3 | a0005c0011t0001g0022 a0005c0011t0001g0077 a0005c0011t0001g0081 |
4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-362C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612511 | |||||||
| chr22:30612531 | CAA | C | 3 | a0005c0011t0001g0022 a0005c0011t0001g0077 a0005c0011t0001g0081 |
4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-341_258-340del others(2): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612531 | |||||||
| chr22:30612550 | C | T | 5 | a0001c0001t0003g0019 a0001c0001t0003g0068 a0001c0001t0003g0307 others(2): Show |
8 | HG01123.hp2 HG01943.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.258-323C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612550 | |||||||
| chr22:30612660 | G | T | 1 | a0001c0001t0001g0020 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.258-213G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612660 | |||||||
| chr22:30612758 | A | G | 20 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0021 others(17): Show |
29 | HG00639.hp2 HG00735.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.258-115A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612758 | |||||||
| chr22:30612764 | T | C | 1 | a0001c0001t0002g0112 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.258-109T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612764 | |||||||
| chr22:30612806 | G | A | 8 | a0005c0005t0001g0039 a0005c0005t0001g0040 a0005c0005t0001g0041 others(5): Show |
11 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.258-67G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | chr22 | 30612806 | |||||||
| chr22:30612828 | C | CG | 7 | a0001c0001t0002g0151 a0001c0001t0003g0090 a0001c0001t0003g0304 others(4): Show |
8 | HG01175.hp1 HG01496.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.258-41dupG | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 30612828 | ||||||
| chr22:30613059 | C | T | 2 | a0003c0003t0004g0202 a0003c0003t0004g0203 |
2 | HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.427+17C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613059 | |||||||
| chr22:30613131 | T | A | 62 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(59): Show |
78 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.427+89T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613131 | |||||||
| chr22:30613191 | G | A | 1 | a0001c0001t0006g0080 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.427+149G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613191 | |||||||
| chr22:30613191 | G | C | 1 | a0001c0001t0002g0032 | 2 | NA18979.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.427+149G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613191 | |||||||
| chr22:30613234 | T | C | 1 | a0010c0012t0001g0223 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.427+192T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613234 | |||||||
| chr22:30613247 | T | A | 1 | a0013c0018t0002g0131 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.427+205T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613247 | |||||||
| chr22:30613284 | G | C | 1 | a0001c0001t0001g0020 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.427+242G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613284 | |||||||
| chr22:30613390 | C | T | 130 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(127): Show |
161 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.427+348C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613390 | |||||||
| chr22:30613468 | G | T | 1 | a0005c0005t0011g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.427+426G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613468 | |||||||
| chr22:30613674 | T | C | 1 | a0005c0005t0001g0039 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.427+632T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613674 | |||||||
| chr22:30613765 | T | C | 77 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(74): Show |
117 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.428-584T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613765 | |||||||
| chr22:30613831 | C | G | 1 | a0002c0002t0001g0292 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.428-518C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613831 | |||||||
| chr22:30613833 | G | C | 190 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(187): Show |
259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.428-516G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613833 | |||||||
| chr22:30613852 | C | T | 77 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(74): Show |
117 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.428-497C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613852 | |||||||
| chr22:30613868 | C | T | 1 | a0005c0005t0001g0041 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.428-481C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30613868 | |||||||
| chr22:30614132 | C | T | 2 | a0002c0002t0001g0291 a0018c0017t0022g0308 |
2 | HG04204.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.428-217C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30614132 | |||||||
| chr22:30614253 | G | A | 13 | a0004c0004t0001g0124 a0004c0004t0002g0029 a0004c0004t0005g0002 others(10): Show |
26 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.428-96G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30614253 | |||||||
| chr22:30614255 | G | C | 70 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(67): Show |
91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.428-94G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30614255 | |||||||
| chr22:30614318 | G | A | 3 | a0005c0011t0001g0022 a0005c0011t0001g0077 a0005c0011t0001g0081 |
4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-31G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30614318 | |||||||
| chr22:30614326 | C | T | 4 | a0006c0006t0001g0047 a0006c0006t0001g0069 a0006c0006t0001g0221 others(1): Show |
5 | HG02109.hp1 HG02486.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-23C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 3/8 | chr22 | 30614326 | |||||||
| chr22:30614569 | C | G | 70 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(67): Show |
91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.580+68C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30614569 | |||||||
| chr22:30614662 | T | C | 207 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(204): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.580+161T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30614662 | |||||||
| chr22:30614765 | C | T | 1 | a0001c0001t0003g0111 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.580+264C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30614765 | |||||||
| chr22:30614841 | G | A | 1 | a0002c0002t0001g0242 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.580+340G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30614841 | |||||||
| chr22:30614953 | A | G | 1 | a0001c0001t0003g0306 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.581-348A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30614953 | |||||||
| chr22:30615010 | C | T | 73 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(70): Show |
112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.581-291C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30615010 | |||||||
| chr22:30615023 | TC | T | 4 | a0010c0012t0001g0223 a0010c0012t0001g0224 a0010c0012t0001g0225 others(1): Show |
4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-275delC | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 30615023 | ||||||
| chr22:30615082 | G | T | 8 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0021 others(5): Show |
13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.581-219G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30615082 | |||||||
| chr22:30615237 | G | GC | 4 | a0001c0001t0002g0150 a0003c0003t0004g0196 a0003c0003t0004g0197 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-60dupC | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 30615237 | ||||||
| chr22:30615293 | A | C | 69 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(66): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
splice_region_variant&intron_variant | LOW | c.581-8A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30615293 | |||||||
| chr22:30615293 | A | T | 4 | a0001c0001t0002g0037 a0001c0001t0002g0177 a0001c0001t0002g0178 others(1): Show |
5 | NA18962.hp1 NA18995.hp1 NA19072.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.581-8A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 4/8 | chr22 | 30615293 | |||||||
| chr22:30615516 | T | G | 1 | a0008c0008t0001g0135 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.753+43T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 5/8 | chr22 | 30615516 | |||||||
| chr22:30615517 | CAG | C | 27 | a0001c0001t0003g0019 a0001c0001t0003g0065 a0001c0001t0003g0066 others(24): Show |
33 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.753+45_753+46delAG | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 5/8 | chr22 | 30615517 | |||||||
| chr22:30615570 | T | C | 187 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(184): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.754-31T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 5/8 | chr22 | 30615570 | |||||||
| chr22:30615571 | T | A | 1 | a0004c0004t0005g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.754-30T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 5/8 | chr22 | 30615571 | |||||||
| chr22:30615818 | T | C | 3 | a0002c0002t0001g0136 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03491.hp2 HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.940+31T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30615818 | |||||||
| chr22:30615895 | A | T | 282 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(279): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.940+108A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30615895 | |||||||
| chr22:30615912 | G | A | 1 | a0003c0003t0004g0204 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.940+125G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30615912 | |||||||
| chr22:30615919 | C | T | 70 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(67): Show |
91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.940+132C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30615919 | |||||||
| chr22:30615936 | T | C | 73 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(70): Show |
112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.940+149T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30615936 | |||||||
| chr22:30616012 | A | G | 4 | a0010c0012t0001g0223 a0010c0012t0001g0224 a0010c0012t0001g0225 others(1): Show |
4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+225A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616012 | |||||||
| chr22:30616025 | T | TTGGA | 7 | a0001c0001t0003g0313 a0001c0001t0003g0323 a0001c0001t0008g0327 others(4): Show |
7 | HG01106.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.940+285_940+288dup others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616025 | ||||||
| chr22:30616025 | TTGGA | T | 145 | a0001c0001t0001g0094 a0001c0001t0002g0126 a0001c0001t0002g0127 others(142): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.940+285_940+288del others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616025 | ||||||
| chr22:30616025 | TTGGATGG others(1): Show |
T | 75 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(72): Show |
110 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.940+281_940+288del others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616025 | ||||||
| chr22:30616025 | TTGGATGG others(5): Show |
T | 23 | a0001c0001t0001g0020 a0001c0001t0002g0152 a0001c0001t0002g0300 others(20): Show |
38 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.940+277_940+288del others(12): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616025 | ||||||
| chr22:30616025 | TTGGATGG others(13): Show |
T | 2 | a0002c0002t0001g0243 a0006c0006t0001g0069 |
2 | NA18522.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.940+269_940+288del others(20): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616025 | ||||||
| chr22:30616025 | TTGGATGG others(17): Show |
T | 1 | a0006c0006t0001g0195 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.940+265_940+288del others(24): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616025 | ||||||
| chr22:30616025 | TTGGATGG others(21): Show |
T | 38 | a0001c0001t0001g0229 a0001c0014t0001g0227 a0001c0014t0001g0228 others(35): Show |
45 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.940+261_940+288del others(28): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616025 | ||||||
| chr22:30616103 | A | G | 1 | a0004c0004t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.940+316A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616103 | |||||||
| chr22:30616110 | A | G | 4 | a0010c0012t0001g0223 a0010c0012t0001g0224 a0010c0012t0001g0225 others(1): Show |
4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+323A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616110 | |||||||
| chr22:30616159 | C | G | 4 | a0010c0012t0001g0223 a0010c0012t0001g0224 a0010c0012t0001g0225 others(1): Show |
4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+372C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616159 | |||||||
| chr22:30616166 | C | G | 1 | a0002c0002t0001g0287 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.940+379C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616166 | |||||||
| chr22:30616190 | A | C | 1 | a0001c0001t0002g0175 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.940+403A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616190 | |||||||
| chr22:30616203 | G | A | 1 | a0004c0004t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.940+416G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616203 | |||||||
| chr22:30616255 | G | A | 1 | a0004c0004t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.940+468G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616255 | |||||||
| chr22:30616314 | T | C | 2 | a0003c0003t0004g0202 a0003c0003t0004g0203 |
2 | HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.940+527T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616314 | |||||||
| chr22:30616487 | C | CA | 16 | a0001c0001t0002g0173 a0001c0001t0002g0179 a0001c0001t0003g0092 others(13): Show |
16 | HG00735.hp1 HG02071.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.940+718dupA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616487 | ||||||
| chr22:30616487 | C | CAA | 91 | a0001c0001t0001g0020 a0001c0001t0001g0229 a0001c0001t0002g0004 others(88): Show |
125 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.940+717_940+718dup others(2): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616487 | ||||||
| chr22:30616487 | CA | C | 31 | a0001c0001t0003g0019 a0001c0001t0003g0068 a0001c0001t0003g0089 others(28): Show |
36 | HG00642.hp2 HG01069.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.940+718delA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616487 | ||||||
| chr22:30616487 | CAA | C | 14 | a0005c0005t0001g0040 a0005c0005t0001g0041 a0005c0005t0001g0082 others(11): Show |
17 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.940+717_940+718del others(2): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30616487 | ||||||
| chr22:30616492 | A | G | 4 | a0006c0006t0001g0047 a0006c0006t0001g0069 a0006c0006t0001g0221 others(1): Show |
5 | HG02109.hp1 HG02486.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.940+705A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616492 | |||||||
| chr22:30616583 | C | G | 1 | a0001c0001t0002g0152 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.941-747C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616583 | |||||||
| chr22:30616594 | A | G | 3 | a0003c0003t0004g0200 a0003c0003t0004g0201 a0007c0007t0004g0121 |
3 | HG01884.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.941-736A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616594 | |||||||
| chr22:30616645 | C | T | 1 | a0002c0010t0001g0231 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.941-685C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616645 | |||||||
| chr22:30616680 | A | G | 1 | a0001c0001t0008g0312 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.941-650A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616680 | |||||||
| chr22:30616686 | A | G | 8 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0021 others(5): Show |
13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.941-644A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616686 | |||||||
| chr22:30616769 | T | C | 187 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(184): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.941-561T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616769 | |||||||
| chr22:30616811 | A | G | 1 | a0004c0004t0002g0029 | 2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.941-519A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616811 | |||||||
| chr22:30616893 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0003g0091 |
2 | HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.941-437T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616893 | |||||||
| chr22:30616969 | CAG | C | 60 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(57): Show |
86 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.941-360_941-359del others(2): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30616969 | |||||||
| chr22:30617073 | C | G | 3 | a0005c0011t0001g0022 a0005c0011t0001g0077 a0005c0011t0001g0081 |
4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-257C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30617073 | |||||||
| chr22:30617093 | GGGTGGTG others(36): Show |
G | 2 | a0001c0001t0003g0323 a0003c0003t0004g0217 |
2 | HG01081.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.941-190_941-148del others(43): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 30617093 | ||||||
| chr22:30617103 | G | A | 2 | a0003c0003t0004g0044 a0003c0003t0004g0194 |
3 | HG01256.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.941-227G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30617103 | |||||||
| chr22:30617151 | A | T | 1 | a0001c0001t0002g0178 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.941-179A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30617151 | |||||||
| chr22:30617166 | C | T | 2 | a0011c0013t0011g0187 a0011c0013t0011g0188 |
2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.941-164C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30617166 | |||||||
| chr22:30617200 | C | T | 6 | a0001c0001t0002g0037 a0001c0001t0002g0126 a0001c0001t0002g0127 others(3): Show |
7 | NA18962.hp1 NA18995.hp1 NA19011.hp1 others(4): Show |
intron_variant | MODIFIER | c.941-130C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30617200 | |||||||
| chr22:30617309 | G | A | 73 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(70): Show |
112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.941-21G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30617309 | |||||||
| chr22:30617309 | G | C | 1 | a0001c0001t0002g0178 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.941-21G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30617309 | |||||||
| chr22:30617317 | C | T | 2 | a0002c0002t0001g0128 a0002c0002t0019g0142 |
2 | NA18960.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.941-13C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 6/8 | chr22 | 30617317 | |||||||
| chr22:30617562 | G | A | 70 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(67): Show |
91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1106+67G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617562 | |||||||
| chr22:30617588 | C | T | 1 | a0002c0002t0001g0292 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1106+93C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617588 | |||||||
| chr22:30617630 | A | T | 1 | a0002c0002t0001g0064 | 2 | NA19006.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1106+135A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617630 | |||||||
| chr22:30617681 | T | A | 1 | a0008c0008t0001g0135 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1106+186T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617681 | |||||||
| chr22:30617688 | T | A | 1 | a0002c0002t0001g0052 | 2 | HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1106+193T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617688 | |||||||
| chr22:30617689 | G | C | 1 | a0002c0002t0001g0052 | 2 | HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1106+194G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617689 | |||||||
| chr22:30617690 | A | T | 1 | a0002c0002t0001g0052 | 2 | HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1106+195A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617690 | |||||||
| chr22:30617788 | G | T | 1 | a0001c0001t0001g0020 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1106+293G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617788 | |||||||
| chr22:30617802 | C | T | 5 | a0007c0007t0007g0011 a0007c0007t0007g0083 a0007c0007t0007g0084 others(2): Show |
8 | HG01261.hp1 HG02055.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1106+307C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617802 | |||||||
| chr22:30617809 | A | T | 4 | a0010c0012t0001g0223 a0010c0012t0001g0224 a0010c0012t0001g0225 others(1): Show |
4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106+314A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617809 | |||||||
| chr22:30617841 | A | C | 1 | a0005c0005t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1106+346A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617841 | |||||||
| chr22:30617934 | G | T | 18 | a0001c0001t0001g0229 a0001c0014t0001g0227 a0001c0014t0001g0228 others(15): Show |
22 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1106+439G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30617934 | |||||||
| chr22:30618019 | C | T | 3 | a0005c0005t0011g0329 a0011c0013t0011g0187 a0011c0013t0011g0188 |
3 | HG00099.hp2 HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1106+524C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618019 | |||||||
| chr22:30618078 | T | C | 1 | a0005c0005t0011g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1106+583T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618078 | |||||||
| chr22:30618113 | A | AT | 8 | a0001c0001t0001g0229 a0002c0002t0001g0031 a0002c0002t0001g0140 others(5): Show |
8 | HG00423.hp1 HG03225.hp1 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.1106+638dupT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 30618113 | ||||||
| chr22:30618113 | AT | A | 175 | a0001c0001t0001g0020 a0001c0001t0002g0004 a0001c0001t0002g0008 others(172): Show |
238 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1106+638delT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 30618113 | ||||||
| chr22:30618113 | ATT | A | 30 | a0001c0001t0001g0094 a0001c0001t0002g0112 a0001c0001t0002g0113 others(27): Show |
40 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.1106+637_1106+638d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 30618113 | ||||||
| chr22:30618263 | G | T | 1 | a0002c0002t0001g0286 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1106+768G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618263 | |||||||
| chr22:30618272 | G | T | 1 | a0008c0008t0001g0135 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1106+777G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618272 | |||||||
| chr22:30618272 | GT | G | 183 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(180): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1106+788delT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 30618272 | ||||||
| chr22:30618273 | T | G | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG03654.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1106+778T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618273 | |||||||
| chr22:30618390 | C | T | 73 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(70): Show |
112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1106+895C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618390 | |||||||
| chr22:30618432 | A | G | 18 | a0001c0001t0001g0229 a0001c0014t0001g0227 a0001c0014t0001g0228 others(15): Show |
22 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1106+937A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618432 | |||||||
| chr22:30618433 | C | T | 1 | a0003c0003t0007g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1106+938C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618433 | |||||||
| chr22:30618435 | T | C | 1 | a0006c0006t0001g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1106+940T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618435 | |||||||
| chr22:30618487 | C | T | 202 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(199): Show |
274 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.1106+992C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618487 | |||||||
| chr22:30618497 | G | A | 3 | a0003c0003t0007g0216 a0004c0004t0001g0124 a0004c0004t0002g0029 |
4 | HG02970.hp1 HG03834.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106+1002G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618497 | |||||||
| chr22:30618526 | A | G | 4 | a0010c0012t0001g0223 a0010c0012t0001g0224 a0010c0012t0001g0225 others(1): Show |
4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106+1031A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618526 | |||||||
| chr22:30618567 | T | A | 1 | a0002c0002t0001g0247 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1106+1072T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618567 | |||||||
| chr22:30618585 | G | A | 74 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(71): Show |
113 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1106+1090G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618585 | |||||||
| chr22:30618659 | A | C | 1 | a0002c0002t0001g0246 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1106+1164A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618659 | |||||||
| chr22:30618674 | C | T | 1 | a0002c0002t0001g0266 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1106+1179C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618674 | |||||||
| chr22:30618680 | G | C | 1 | a0001c0001t0001g0020 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1106+1185G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618680 | |||||||
| chr22:30618730 | A | G | 6 | a0005c0005t0001g0039 a0005c0005t0001g0040 a0005c0005t0001g0189 others(3): Show |
8 | HG01099.hp2 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1106+1235A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618730 | |||||||
| chr22:30618758 | A | G | 1 | a0018c0017t0022g0308 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1106+1263A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618758 | |||||||
| chr22:30618839 | A | G | 1 | a0004c0004t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1106+1344A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618839 | |||||||
| chr22:30618873 | G | A | 73 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(70): Show |
112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1106+1378G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618873 | |||||||
| chr22:30618904 | G | A | 60 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(57): Show |
86 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1106+1409G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30618904 | |||||||
| chr22:30619012 | T | C | 8 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0021 others(5): Show |
13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1106+1517T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619012 | |||||||
| chr22:30619116 | A | T | 1 | a0004c0004t0005g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1106+1621A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619116 | |||||||
| chr22:30619231 | C | G | 3 | a0001c0001t0001g0229 a0001c0014t0001g0227 a0001c0014t0001g0228 |
3 | HG02886.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1106+1736C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619231 | |||||||
| chr22:30619243 | A | G | 1 | a0003c0003t0004g0215 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1106+1748A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619243 | |||||||
| chr22:30619251 | A | T | 1 | a0001c0001t0010g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1106+1756A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619251 | |||||||
| chr22:30619359 | C | T | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1106+1864C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619359 | |||||||
| chr22:30619395 | A | C | 1 | a0003c0003t0004g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1106+1900A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619395 | |||||||
| chr22:30619420 | C | T | 2 | a0002c0002t0001g0014 a0002c0002t0001g0265 |
5 | NA18944.hp1 NA18963.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.1106+1925C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619420 | |||||||
| chr22:30619426 | T | C | 1 | a0001c0001t0003g0314 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1106+1931T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619426 | |||||||
| chr22:30619514 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1106+2019G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619514 | |||||||
| chr22:30619575 | G | A | 73 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(70): Show |
112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1106+2080G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619575 | |||||||
| chr22:30619586 | C | A | 73 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(70): Show |
112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1106+2091C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619586 | |||||||
| chr22:30619617 | C | T | 1 | a0001c0001t0003g0309 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1106+2122C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619617 | |||||||
| chr22:30619671 | G | C | 1 | a0004c0004t0005g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1106+2176G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619671 | |||||||
| chr22:30619733 | C | T | 30 | a0003c0003t0004g0042 a0003c0003t0004g0043 a0003c0003t0004g0044 others(27): Show |
34 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1106+2238C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619733 | |||||||
| chr22:30619755 | G | A | 2 | a0002c0002t0001g0275 a0002c0002t0001g0288 |
2 | HG01099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1106+2260G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619755 | |||||||
| chr22:30619814 | T | C | 9 | a0002c0002t0001g0053 a0002c0002t0001g0249 a0002c0002t0001g0250 others(6): Show |
10 | HG02602.hp2 HG02698.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.1106+2319T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619814 | |||||||
| chr22:30619951 | T | C | 203 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(200): Show |
275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.1106+2456T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619951 | |||||||
| chr22:30619992 | A | G | 5 | a0002c0002t0001g0006 a0002c0002t0001g0051 a0002c0002t0001g0235 others(2): Show |
5 | HG00438.hp1 HG02071.hp1 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.1106+2497A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619992 | |||||||
| chr22:30619998 | A | T | 6 | a0001c0001t0003g0066 a0001c0001t0003g0319 a0001c0001t0003g0320 others(3): Show |
7 | HG00733.hp1 HG01168.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1106+2503A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30619998 | |||||||
| chr22:30620020 | G | C | 7 | a0003c0003t0004g0204 a0003c0003t0004g0206 a0003c0003t0004g0207 others(4): Show |
7 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1106+2525G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620020 | |||||||
| chr22:30620095 | G | A | 21 | a0004c0004t0001g0124 a0004c0004t0002g0029 a0004c0004t0005g0002 others(18): Show |
36 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.1106+2600G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620095 | |||||||
| chr22:30620114 | G | A | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1106+2619G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620114 | |||||||
| chr22:30620143 | CT | C | 47 | a0001c0001t0001g0020 a0001c0001t0002g0151 a0001c0001t0002g0154 others(44): Show |
55 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.1106+2663delT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 30620143 | ||||||
| chr22:30620159 | A | T | 3 | a0002c0002t0001g0237 a0002c0002t0001g0285 a0002c0002t0001g0286 |
3 | HG01109.hp2 HG01433.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1106+2664A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620159 | |||||||
| chr22:30620258 | C | T | 1 | a0010c0012t0001g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1107-2710C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620258 | |||||||
| chr22:30620259 | C | T | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1107-2709C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620259 | |||||||
| chr22:30620260 | G | A | 2 | a0003c0003t0004g0202 a0003c0003t0004g0203 |
2 | HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1107-2708G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620260 | |||||||
| chr22:30620423 | C | T | 1 | a0002c0002t0001g0284 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1107-2545C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620423 | |||||||
| chr22:30620511 | C | T | 1 | a0008c0008t0001g0135 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1107-2457C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620511 | |||||||
| chr22:30620552 | T | G | 35 | a0003c0003t0004g0042 a0003c0003t0004g0043 a0003c0003t0004g0044 others(32): Show |
42 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1107-2416T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620552 | |||||||
| chr22:30620658 | A | G | 8 | a0006c0006t0001g0046 a0006c0006t0001g0047 a0006c0006t0001g0069 others(5): Show |
10 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1107-2310A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620658 | |||||||
| chr22:30620685 | A | G | 4 | a0006c0006t0001g0047 a0006c0006t0001g0069 a0006c0006t0001g0221 others(1): Show |
5 | HG02109.hp1 HG02486.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1107-2283A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620685 | |||||||
| chr22:30620760 | C | T | 1 | a0002c0002t0001g0283 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1107-2208C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620760 | |||||||
| chr22:30620786 | C | T | 1 | a0001c0001t0002g0027 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1107-2182C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620786 | |||||||
| chr22:30620854 | A | T | 1 | a0001c0001t0002g0171 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1107-2114A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620854 | |||||||
| chr22:30620914 | G | C | 1 | a0001c0001t0002g0186 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1107-2054G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620914 | |||||||
| chr22:30620924 | A | G | 6 | a0005c0005t0001g0039 a0005c0005t0001g0040 a0005c0005t0001g0189 others(3): Show |
8 | HG01099.hp2 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1107-2044A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620924 | |||||||
| chr22:30620927 | G | A | 30 | a0003c0003t0004g0042 a0003c0003t0004g0043 a0003c0003t0004g0044 others(27): Show |
34 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1107-2041G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620927 | |||||||
| chr22:30620963 | C | G | 1 | a0001c0001t0003g0068 | 2 | NA19058.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1107-2005C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620963 | |||||||
| chr22:30620986 | G | GGGT | 24 | a0001c0001t0001g0229 a0001c0014t0001g0227 a0001c0014t0001g0228 others(21): Show |
28 | HG00099.hp2 HG00642.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1107-1975_1107-197 others(7): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 30620986 | ||||||
| chr22:30620996 | T | G | 212 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0002g0004 others(209): Show |
286 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.1107-1972T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620996 | |||||||
| chr22:30620999 | T | G | 11 | a0001c0001t0001g0020 a0001c0001t0002g0036 a0001c0001t0002g0037 others(8): Show |
15 | HG01346.hp2 HG01358.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1107-1969T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30620999 | |||||||
| chr22:30621317 | C | T | 1 | a0002c0002t0001g0262 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1107-1651C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621317 | |||||||
| chr22:30621332 | A | C | 2 | a0001c0001t0001g0020 a0004c0004t0007g0125 |
3 | HG01496.hp2 HG02683.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1107-1636A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621332 | |||||||
| chr22:30621335 | A | G | 95 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(92): Show |
121 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1107-1633A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621335 | |||||||
| chr22:30621338 | G | A | 1 | a0008c0008t0001g0144 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1107-1630G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621338 | |||||||
| chr22:30621356 | T | C | 70 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(67): Show |
91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1107-1612T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621356 | |||||||
| chr22:30621381 | A | T | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1107-1587A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621381 | |||||||
| chr22:30621384 | C | T | 3 | a0001c0001t0003g0067 a0001c0001t0003g0304 a0001c0001t0003g0323 |
4 | HG02071.hp2 NA18982.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1107-1584C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621384 | |||||||
| chr22:30621411 | T | C | 207 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(204): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1107-1557T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621411 | |||||||
| chr22:30621416 | C | T | 70 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(67): Show |
91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1107-1552C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621416 | |||||||
| chr22:30621417 | G | A | 2 | a0011c0013t0011g0187 a0011c0013t0011g0188 |
2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1107-1551G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621417 | |||||||
| chr22:30621434 | AG | A | 1 | a0002c0002t0001g0017 | 3 | NA18947.hp2 NA18960.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1107-1533delG | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621434 | |||||||
| chr22:30621470 | G | A | 72 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(69): Show |
111 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1107-1498G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621470 | |||||||
| chr22:30621470 | G | GTTA | 92 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0003g0007 others(89): Show |
118 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1107-1496_1107-149 others(7): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 30621470 | ||||||
| chr22:30621471 | T | A | 1 | a0001c0001t0002g0155 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1107-1497T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621471 | |||||||
| chr22:30621473 | T | A | 3 | a0001c0001t0001g0229 a0001c0014t0001g0227 a0001c0014t0001g0228 |
3 | HG02886.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1107-1495T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621473 | |||||||
| chr22:30621476 | TG | T | 3 | a0001c0001t0001g0229 a0001c0014t0001g0227 a0001c0014t0001g0228 |
3 | HG02886.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1107-1491delG | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621476 | |||||||
| chr22:30621480 | T | A | 13 | a0004c0004t0001g0124 a0004c0004t0002g0029 a0004c0004t0005g0002 others(10): Show |
26 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1107-1488T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621480 | |||||||
| chr22:30621607 | T | C | 2 | a0002c0002t0001g0140 a0002c0002t0001g0141 |
2 | NA18955.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1107-1361T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621607 | |||||||
| chr22:30621691 | C | G | 53 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(50): Show |
78 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1107-1277C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621691 | |||||||
| chr22:30621730 | C | T | 23 | a0001c0001t0001g0229 a0001c0014t0001g0227 a0001c0014t0001g0228 others(20): Show |
27 | HG00099.hp2 HG00642.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1107-1238C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621730 | |||||||
| chr22:30621749 | G | T | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1107-1219G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621749 | |||||||
| chr22:30621753 | G | T | 70 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(67): Show |
91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1107-1215G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621753 | |||||||
| chr22:30621790 | T | C | 95 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(92): Show |
121 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1107-1178T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621790 | |||||||
| chr22:30621856 | C | G | 4 | a0001c0001t0003g0007 a0001c0001t0003g0090 a0001c0001t0003g0102 others(1): Show |
8 | NA18939.hp2 NA18942.hp2 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.1107-1112C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621856 | |||||||
| chr22:30621899 | C | A | 1 | a0005c0005t0015g0071 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1107-1069C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621899 | |||||||
| chr22:30621982 | C | T | 1 | a0002c0002t0001g0282 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1107-986C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30621982 | |||||||
| chr22:30622029 | C | G | 1 | a0001c0014t0001g0228 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1107-939C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622029 | |||||||
| chr22:30622075 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1107-893C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622075 | |||||||
| chr22:30622085 | T | C | 73 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(70): Show |
112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1107-883T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622085 | |||||||
| chr22:30622091 | G | A | 73 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(70): Show |
112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1107-877G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622091 | |||||||
| chr22:30622137 | A | G | 23 | a0001c0001t0001g0229 a0001c0014t0001g0227 a0001c0014t0001g0228 others(20): Show |
27 | HG00099.hp2 HG00642.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1107-831A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622137 | |||||||
| chr22:30622238 | T | C | 93 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0003g0007 others(90): Show |
118 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1107-730T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622238 | |||||||
| chr22:30622574 | T | G | 71 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(68): Show |
92 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1107-394T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622574 | |||||||
| chr22:30622585 | G | A | 5 | a0003c0003t0004g0204 a0003c0003t0004g0206 a0003c0003t0004g0207 others(2): Show |
5 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1107-383G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622585 | |||||||
| chr22:30622618 | G | A | 1 | a0001c0001t0006g0080 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1107-350G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622618 | |||||||
| chr22:30622635 | C | T | 1 | a0001c0001t0002g0300 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1107-333C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622635 | |||||||
| chr22:30622659 | C | T | 70 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(67): Show |
91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1107-309C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622659 | |||||||
| chr22:30622782 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1107-186G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622782 | |||||||
| chr22:30622790 | G | A | 215 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(212): Show |
289 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1107-178G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622790 | |||||||
| chr22:30622830 | C | T | 70 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(67): Show |
91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1107-138C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622830 | |||||||
| chr22:30622897 | G | C | 65 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(62): Show |
82 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1107-71G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622897 | |||||||
| chr22:30622904 | A | T | 1 | a0002c0002t0001g0261 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1107-64A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 7/8 | chr22 | 30622904 | |||||||
| chr22:30623107 | G | C | 1 | a0001c0001t0001g0020 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1222+24G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623107 | |||||||
| chr22:30623199 | A | C | 1 | a0006c0006t0001g0047 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1222+116A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623199 | |||||||
| chr22:30623220 | G | A | 1 | a0002c0002t0001g0242 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1222+137G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623220 | |||||||
| chr22:30623247 | G | GC | 70 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(67): Show |
91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1222+164_1222+165i others(3): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623247 | |||||||
| chr22:30623248 | A | C | 70 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(67): Show |
91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1222+165A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623248 | |||||||
| chr22:30623296 | CA | C | 118 | a0001c0001t0001g0229 a0001c0001t0002g0004 a0001c0001t0002g0008 others(115): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1222+228delA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623296 | ||||||
| chr22:30623357 | C | T | 1 | a0002c0002t0001g0260 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1222+274C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623357 | |||||||
| chr22:30623371 | A | G | 1 | a0001c0001t0002g0036 | 2 | HG01346.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1222+288A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623371 | |||||||
| chr22:30623448 | G | A | 1 | a0002c0002t0001g0138 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1222+365G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623448 | |||||||
| chr22:30623461 | T | G | 8 | a0005c0005t0001g0039 a0005c0005t0001g0040 a0005c0005t0001g0041 others(5): Show |
11 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.1222+378T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623461 | |||||||
| chr22:30623470 | A | G | 90 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(87): Show |
115 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1222+387A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623470 | |||||||
| chr22:30623562 | AACTTTTC others(4): Show |
A | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+481_1222+491d others(13): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623562 | ||||||
| chr22:30623646 | G | A | 73 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(70): Show |
112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1222+563G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623646 | |||||||
| chr22:30623653 | A | G | 5 | a0005c0005t0002g0070 a0005c0005t0002g0072 a0005c0005t0002g0073 others(2): Show |
5 | HG00642.hp2 HG01192.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+570A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623653 | |||||||
| chr22:30623692 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1222+609T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623692 | |||||||
| chr22:30623699 | A | AAT | 3 | a0005c0011t0001g0022 a0005c0011t0001g0077 a0005c0011t0001g0081 |
4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+628_1222+629d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623699 | ||||||
| chr22:30623699 | AAT | A | 71 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(68): Show |
92 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1222+628_1222+629d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623699 | ||||||
| chr22:30623703 | T | C | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1222+620T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623703 | |||||||
| chr22:30623708 | A | G | 13 | a0004c0004t0001g0124 a0004c0004t0002g0029 a0004c0004t0005g0002 others(10): Show |
26 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1222+625A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623708 | |||||||
| chr22:30623709 | TATACAG | T | 2 | a0003c0003t0004g0042 a0003c0003t0004g0199 |
3 | HG02895.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1222+628_1222+633d others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623709 | ||||||
| chr22:30623711 | TAC | T | 5 | a0002c0002t0001g0006 a0007c0007t0007g0011 a0007c0007t0007g0083 others(2): Show |
8 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1222+630_1222+631d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623711 | ||||||
| chr22:30623711 | TACAG | T | 33 | a0001c0001t0001g0020 a0001c0001t0001g0229 a0001c0014t0001g0227 others(30): Show |
37 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1222+632_1222+635d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623711 | ||||||
| chr22:30623715 | G | C | 1 | a0003c0003t0004g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1222+632G>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623715 | |||||||
| chr22:30623715 | G | T | 4 | a0007c0007t0007g0011 a0007c0007t0007g0083 a0007c0007t0007g0084 others(1): Show |
7 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+632G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623715 | |||||||
| chr22:30623715 | GAC | G | 4 | a0010c0012t0001g0223 a0010c0012t0001g0224 a0010c0012t0001g0225 others(1): Show |
4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+638_1222+639d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623715 | ||||||
| chr22:30623717 | C | T | 1 | a0007c0007t0007g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1222+634C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623717 | |||||||
| chr22:30623721 | CAT | C | 4 | a0002c0002t0001g0063 a0002c0002t0001g0256 a0002c0002t0001g0257 others(1): Show |
5 | HG00408.hp2 HG01074.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+645_1222+646d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623721 | ||||||
| chr22:30623725 | T | C | 1 | a0005c0005t0015g0071 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1222+642T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623725 | |||||||
| chr22:30623733 | T | TACATATA others(3): Show |
1 | a0004c0004t0005g0116 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1222+659_1222+660i others(12): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623733 | ||||||
| chr22:30623741 | TATAC | T | 70 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(67): Show |
109 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1222+660_1222+663d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623741 | ||||||
| chr22:30623743 | T | C | 1 | a0004c0004t0005g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1222+660T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623743 | |||||||
| chr22:30623743 | TAC | T | 69 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(66): Show |
90 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.1222+666_1222+667d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623743 | ||||||
| chr22:30623745 | C | CATATATA others(3): Show |
1 | a0004c0004t0005g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1222+663_1222+664i others(12): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623745 | ||||||
| chr22:30623749 | CAT | C | 2 | a0005c0005t0001g0039 a0005c0005t0001g0191 |
3 | HG02723.hp2 HG04184.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1222+673_1222+674d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623749 | ||||||
| chr22:30623753 | T | TATATGTA others(247): Show |
1 | a0007c0007t0004g0121 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1222+679_1222+680i others(256): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623753 | ||||||
| chr22:30623753 | T | TATGTATA others(259): Show |
1 | a0003c0003t0004g0203 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1222+672_1222+673i others(268): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623753 | ||||||
| chr22:30623754 | ATATG | A | 8 | a0003c0003t0004g0042 a0003c0003t0004g0196 a0003c0003t0004g0197 others(5): Show |
9 | HG00642.hp2 HG01192.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1222+675_1222+678d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623754 | ||||||
| chr22:30623756 | A | G | 3 | a0005c0005t0002g0070 a0005c0005t0002g0072 a0005c0005t0015g0071 |
3 | HG02109.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1222+673A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623756 | |||||||
| chr22:30623757 | T | C | 1 | a0004c0004t0005g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1222+674T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623757 | |||||||
| chr22:30623758 | G | A | 5 | a0004c0004t0005g0116 a0004c0004t0005g0118 a0005c0005t0002g0070 others(2): Show |
5 | HG01884.hp1 HG02109.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+675G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623758 | |||||||
| chr22:30623758 | GTA | G | 68 | a0001c0001t0001g0020 a0002c0002t0001g0001 a0002c0002t0001g0050 others(65): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.1222+686_1222+687d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623758 | ||||||
| chr22:30623758 | GTATA | G | 3 | a0001c0001t0001g0229 a0001c0014t0001g0227 a0001c0014t0001g0228 |
3 | HG02886.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1222+684_1222+687d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623758 | ||||||
| chr22:30623759 | T | C | 2 | a0004c0004t0005g0116 a0004c0004t0005g0118 |
2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1222+676T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623759 | |||||||
| chr22:30623760 | A | G | 8 | a0003c0003t0004g0042 a0003c0003t0004g0196 a0003c0003t0004g0197 others(5): Show |
9 | HG00642.hp2 HG01192.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1222+677A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623760 | |||||||
| chr22:30623761 | T | C | 2 | a0004c0004t0005g0116 a0004c0004t0005g0118 |
2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1222+678T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623761 | |||||||
| chr22:30623763 | T | C | 150 | a0001c0001t0001g0094 a0001c0001t0002g0004 a0001c0001t0002g0008 others(147): Show |
213 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1222+680T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623763 | |||||||
| chr22:30623765 | T | C | 2 | a0003c0003t0004g0044 a0003c0003t0004g0194 |
3 | HG01256.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1222+682T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623765 | |||||||
| chr22:30623767 | TATAC | T | 60 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(57): Show |
86 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1222+686_1222+689d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623767 | ||||||
| chr22:30623769 | T | C | 2 | a0005c0005t0001g0191 a0005c0005t0011g0329 |
2 | HG02630.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1222+686T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623769 | |||||||
| chr22:30623769 | T | TATGAAAT others(14): Show |
1 | a0006c0006t0001g0195 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1222+687_1222+688i others(23): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623769 | ||||||
| chr22:30623771 | C | T | 63 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(60): Show |
79 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.1222+688C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623771 | |||||||
| chr22:30623773 | CACAT | C | 8 | a0004c0004t0005g0116 a0006c0006t0001g0046 a0006c0006t0001g0047 others(5): Show |
10 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1222+692_1222+695d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623773 | ||||||
| chr22:30623775 | C | T | 4 | a0003c0003t0004g0200 a0003c0003t0004g0201 a0004c0004t0005g0118 others(1): Show |
4 | HG01884.hp1 HG01884.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222+692C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623775 | |||||||
| chr22:30623777 | T | C | 65 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(62): Show |
81 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1222+694T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623777 | |||||||
| chr22:30623777 | T | TATATACA others(3): Show |
5 | a0004c0004t0005g0002 a0004c0004t0005g0115 a0004c0004t0005g0119 others(2): Show |
15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1222+699_1222+700i others(12): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623777 | ||||||
| chr22:30623779 | T | TATACAC | 2 | a0004c0004t0001g0124 a0004c0004t0002g0029 |
3 | HG02970.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1222+699_1222+700i others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623779 | ||||||
| chr22:30623779 | T | TATACACA others(1): Show |
3 | a0004c0004t0005g0028 a0004c0004t0005g0114 a0004c0004t0005g0117 |
4 | HG01496.hp1 HG02717.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+699_1222+700i others(10): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623779 | ||||||
| chr22:30623779 | T | TATACACA others(15): Show |
1 | a0005c0005t0001g0039 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1222+699_1222+700i others(24): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623779 | ||||||
| chr22:30623779 | T | TATACACA others(297): Show |
2 | a0003c0003t0004g0200 a0003c0003t0004g0201 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1222+699_1222+700i others(306): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623779 | ||||||
| chr22:30623780 | A | G | 2 | a0001c0001t0002g0032 a0001c0001t0002g0170 |
3 | HG00423.hp2 NA18979.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1222+697A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623780 | |||||||
| chr22:30623781 | T | C | 4 | a0005c0005t0001g0191 a0005c0011t0001g0022 a0005c0011t0001g0077 others(1): Show |
5 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+698T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623781 | |||||||
| chr22:30623782 | A | G | 9 | a0001c0001t0003g0100 a0001c0001t0006g0015 a0001c0001t0006g0016 others(6): Show |
14 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1222+699A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623782 | |||||||
| chr22:30623782 | ATG | A | 6 | a0005c0005t0002g0073 a0005c0005t0002g0074 a0005c0005t0011g0329 others(3): Show |
6 | HG00099.hp2 HG00642.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222+701_1222+702d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623782 | ||||||
| chr22:30623783 | T | C | 9 | a0005c0005t0001g0040 a0005c0005t0001g0041 a0005c0005t0001g0082 others(6): Show |
12 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+700T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623783 | |||||||
| chr22:30623784 | G | A | 36 | a0001c0001t0003g0100 a0001c0001t0006g0015 a0001c0001t0006g0016 others(33): Show |
58 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.1222+701G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623784 | |||||||
| chr22:30623785 | T | C | 18 | a0004c0004t0005g0116 a0004c0004t0005g0122 a0005c0005t0001g0040 others(15): Show |
20 | HG00099.hp2 HG00642.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.1222+702T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623785 | |||||||
| chr22:30623787 | T | C | 35 | a0001c0001t0003g0100 a0001c0001t0006g0015 a0001c0001t0006g0016 others(32): Show |
55 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1222+704T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623787 | |||||||
| chr22:30623789 | C | T | 20 | a0001c0001t0003g0100 a0001c0001t0006g0015 a0001c0001t0006g0016 others(17): Show |
28 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1222+706C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623789 | |||||||
| chr22:30623793 | T | C | 2 | a0005c0011t0001g0022 a0005c0011t0001g0077 |
3 | HG02896.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1222+710T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623793 | |||||||
| chr22:30623793 | TATACACA others(1): Show |
T | 4 | a0001c0001t0002g0181 a0007c0007t0007g0011 a0007c0007t0007g0083 others(1): Show |
7 | HG01261.hp1 HG02647.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+718_1222+725d others(10): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623793 | ||||||
| chr22:30623795 | T | C | 7 | a0003c0003t0004g0200 a0003c0003t0004g0201 a0005c0005t0001g0040 others(4): Show |
9 | HG01884.hp2 HG02717.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1222+712T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623795 | |||||||
| chr22:30623795 | T | TATAC | 61 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(58): Show |
77 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.1222+713_1222+714i others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623795 | ||||||
| chr22:30623795 | TAC | T | 9 | a0003c0003t0004g0196 a0003c0003t0004g0197 a0003c0003t0004g0198 others(6): Show |
9 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1222+718_1222+719d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623795 | ||||||
| chr22:30623797 | C | T | 10 | a0004c0004t0001g0124 a0004c0004t0002g0029 a0004c0004t0005g0002 others(7): Show |
23 | HG01243.hp2 HG01496.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1222+714C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623797 | |||||||
| chr22:30623799 | C | T | 2 | a0005c0011t0001g0022 a0005c0011t0001g0077 |
3 | HG02896.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1222+716C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623799 | |||||||
| chr22:30623801 | C | CAT | 10 | a0001c0001t0003g0100 a0001c0001t0006g0015 a0001c0001t0006g0016 others(7): Show |
15 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.1222+720_1222+721d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623801 | ||||||
| chr22:30623801 | C | CATAT | 7 | a0002c0002t0001g0249 a0004c0004t0002g0029 a0004c0004t0007g0125 others(4): Show |
8 | HG01099.hp2 HG01192.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1222+721_1222+722i others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623801 | ||||||
| chr22:30623801 | C | T | 148 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0002g0004 others(145): Show |
196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1222+718C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623801 | |||||||
| chr22:30623803 | T | C | 2 | a0001c0001t0002g0158 a0013c0019t0002g0294 |
2 | HG00609.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1222+720T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623803 | |||||||
| chr22:30623803 | T | TATAC | 8 | a0001c0001t0001g0229 a0001c0014t0001g0227 a0001c0014t0001g0228 others(5): Show |
8 | HG01884.hp1 HG02109.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1222+721_1222+722i others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623803 | ||||||
| chr22:30623803 | T | TATACACA others(13): Show |
2 | a0006c0006t0001g0046 a0006c0006t0001g0219 |
3 | HG01167.hp2 HG01169.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1222+721_1222+722i others(22): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623803 | ||||||
| chr22:30623803 | T | TATATAC | 78 | a0001c0001t0001g0020 a0001c0001t0002g0004 a0001c0001t0002g0008 others(75): Show |
120 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1222+721_1222+722i others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623803 | ||||||
| chr22:30623803 | T | TATATACA others(1): Show |
122 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(119): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1222+721_1222+722i others(10): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623803 | ||||||
| chr22:30623803 | T | TATATACA others(43): Show |
4 | a0010c0012t0001g0223 a0010c0012t0001g0224 a0010c0012t0001g0225 others(1): Show |
4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+721_1222+722i others(52): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623803 | ||||||
| chr22:30623803 | T | TATATATG others(27): Show |
1 | a0002c0002t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1222+721_1222+722i others(36): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623803 | ||||||
| chr22:30623803 | T | TATATATG others(59): Show |
1 | a0006c0006t0001g0195 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1222+721_1222+722i others(68): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623803 | ||||||
| chr22:30623803 | TACAC | T | 19 | a0001c0001t0002g0159 a0001c0001t0021g0153 a0003c0003t0004g0043 others(16): Show |
22 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.1222+722_1222+725d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623803 | ||||||
| chr22:30623805 | C | T | 14 | a0003c0003t0004g0196 a0003c0003t0004g0197 a0003c0003t0004g0198 others(11): Show |
14 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1222+722C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623805 | |||||||
| chr22:30623807 | C | T | 15 | a0001c0001t0002g0158 a0003c0003t0004g0196 a0003c0003t0004g0197 others(12): Show |
16 | HG00609.hp2 HG00733.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1222+724C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623807 | |||||||
| chr22:30623809 | T | C | 10 | a0002c0002t0001g0056 a0002c0002t0001g0148 a0002c0002t0001g0149 others(7): Show |
12 | HG01346.hp1 HG01884.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.1222+726T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623809 | |||||||
| chr22:30623811 | T | C | 9 | a0003c0003t0004g0196 a0003c0003t0004g0197 a0003c0003t0004g0198 others(6): Show |
9 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1222+728T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623811 | |||||||
| chr22:30623813 | T | C | 26 | a0001c0001t0001g0020 a0001c0001t0002g0159 a0001c0001t0021g0153 others(23): Show |
30 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1222+730T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623813 | |||||||
| chr22:30623813 | TACACACA others(1): Show |
T | 3 | a0007c0007t0007g0011 a0007c0007t0007g0083 a0007c0007t0007g0085 |
6 | HG01261.hp1 HG02647.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222+732_1222+739d others(10): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623813 | ||||||
| chr22:30623815 | C | T | 71 | a0001c0001t0001g0229 a0001c0001t0002g0004 a0001c0001t0002g0008 others(68): Show |
99 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1222+732C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623815 | |||||||
| chr22:30623817 | C | T | 10 | a0001c0001t0001g0020 a0003c0003t0004g0196 a0003c0003t0004g0197 others(7): Show |
11 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1222+734C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623817 | |||||||
| chr22:30623819 | C | CAT | 3 | a0001c0001t0002g0032 a0001c0001t0002g0170 a0005c0005t0002g0074 |
4 | HG00423.hp2 HG01192.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+737_1222+738i others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623819 | ||||||
| chr22:30623819 | C | T | 30 | a0001c0001t0001g0020 a0001c0001t0002g0159 a0001c0001t0003g0313 others(27): Show |
34 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1222+736C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623819 | |||||||
| chr22:30623821 | C | CAT | 8 | a0006c0006t0001g0047 a0006c0006t0001g0069 a0006c0006t0001g0221 others(5): Show |
9 | HG02109.hp1 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1222+740_1222+741d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623821 | ||||||
| chr22:30623821 | C | CATACATA others(77): Show |
1 | a0001c0001t0003g0316 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1222+743_1222+744i others(86): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623821 | ||||||
| chr22:30623821 | C | CATACATA others(69): Show |
3 | a0001c0001t0003g0066 a0001c0001t0003g0304 a0001c0001t0003g0318 |
4 | HG04115.hp2 NA18957.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222+743_1222+744i others(78): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623821 | ||||||
| chr22:30623821 | C | CATACATA others(81): Show |
20 | a0001c0001t0003g0019 a0001c0001t0003g0065 a0001c0001t0003g0067 others(17): Show |
24 | HG00642.hp1 HG00733.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1222+743_1222+744i others(90): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623821 | ||||||
| chr22:30623821 | C | CATACATA others(83): Show |
2 | a0001c0001t0010g0107 a0001c0001t0010g0108 |
2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1222+743_1222+744i others(92): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623821 | ||||||
| chr22:30623821 | C | CATAT | 69 | a0001c0001t0001g0229 a0001c0001t0002g0004 a0001c0001t0002g0008 others(66): Show |
98 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1222+741_1222+742i others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623821 | ||||||
| chr22:30623821 | C | CATATATA others(65): Show |
1 | a0001c0001t0003g0313 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1222+741_1222+742i others(74): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623821 | ||||||
| chr22:30623821 | C | T | 55 | a0001c0001t0001g0020 a0001c0001t0002g0032 a0001c0001t0002g0158 others(52): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.1222+738C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623821 | |||||||
| chr22:30623823 | TAC | T | 17 | a0002c0002t0001g0003 a0002c0002t0001g0031 a0002c0002t0001g0128 others(14): Show |
23 | HG00597.hp2 HG00738.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.1222+748_1222+749d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623823 | ||||||
| chr22:30623825 | C | CATATATA others(67): Show |
3 | a0001c0001t0008g0326 a0001c0001t0008g0327 a0001c0001t0008g0328 |
3 | HG02280.hp2 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1222+743_1222+744i others(76): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623825 | ||||||
| chr22:30623825 | C | CATATATA others(103): Show |
1 | a0001c0001t0003g0309 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1222+743_1222+744i others(112): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623825 | ||||||
| chr22:30623825 | C | CATATATA others(107): Show |
8 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0021 others(5): Show |
13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1222+743_1222+744i others(116): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623825 | ||||||
| chr22:30623825 | C | CATATATA others(69): Show |
2 | a0001c0001t0003g0095 a0001c0001t0003g0098 |
2 | HG00558.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1222+743_1222+744i others(78): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623825 | ||||||
| chr22:30623825 | C | CATATATA others(79): Show |
2 | a0001c0001t0003g0092 a0009c0009t0003g0026 |
3 | HG01257.hp2 HG01258.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1222+743_1222+744i others(88): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623825 | ||||||
| chr22:30623825 | C | CATATATA others(81): Show |
26 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(23): Show |
36 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1222+743_1222+744i others(90): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623825 | ||||||
| chr22:30623825 | C | T | 42 | a0001c0001t0001g0229 a0001c0001t0002g0032 a0001c0001t0002g0033 others(39): Show |
50 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.1222+742C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623825 | |||||||
| chr22:30623826 | A | G | 3 | a0003c0003t0004g0200 a0003c0003t0004g0201 a0007c0007t0004g0121 |
3 | HG01884.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1222+743A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623826 | |||||||
| chr22:30623827 | C | T | 10 | a0001c0001t0002g0033 a0001c0001t0002g0160 a0003c0003t0004g0200 others(7): Show |
12 | HG00639.hp1 HG01257.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+744C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623827 | |||||||
| chr22:30623829 | C | T | 6 | a0003c0003t0004g0200 a0003c0003t0004g0201 a0005c0005t0011g0329 others(3): Show |
6 | HG00099.hp2 HG01106.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1222+746C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623829 | |||||||
| chr22:30623829 | CACA | C | 2 | a0001c0001t0002g0033 a0001c0001t0002g0160 |
3 | HG00639.hp1 HG02148.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1222+747_1222+749d others(5): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623829 | |||||||
| chr22:30623831 | C | T | 125 | a0001c0001t0001g0020 a0001c0001t0002g0004 a0001c0001t0002g0008 others(122): Show |
172 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.1222+748C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623831 | |||||||
| chr22:30623833 | T | C | 4 | a0006c0006t0001g0047 a0006c0006t0001g0069 a0006c0006t0001g0221 others(1): Show |
5 | HG02109.hp1 HG02486.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+750T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623833 | |||||||
| chr22:30623833 | T | TAC | 4 | a0010c0012t0001g0223 a0010c0012t0001g0224 a0010c0012t0001g0225 others(1): Show |
4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+751_1222+752i others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623833 | ||||||
| chr22:30623835 | TAC | T | 7 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0021 others(4): Show |
12 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+760_1222+761d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623835 | ||||||
| chr22:30623837 | C | T | 155 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0002g0004 others(152): Show |
204 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1222+754C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623837 | |||||||
| chr22:30623839 | C | T | 6 | a0001c0001t0001g0229 a0001c0001t0002g0158 a0001c0014t0001g0227 others(3): Show |
6 | HG00609.hp2 HG02055.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222+756C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623839 | |||||||
| chr22:30623842 | A | ATGCACAC others(35): Show |
1 | a0001c0001t0008g0303 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1222+759_1222+760i others(44): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623842 | |||||||
| chr22:30623843 | C | CATAT | 4 | a0005c0005t0001g0040 a0005c0005t0001g0082 a0005c0005t0001g0189 others(1): Show |
5 | HG02572.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+763_1222+764i others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623843 | ||||||
| chr22:30623843 | C | T | 33 | a0001c0001t0001g0020 a0001c0001t0002g0032 a0001c0001t0002g0033 others(30): Show |
51 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1222+760C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623843 | |||||||
| chr22:30623845 | T | C | 4 | a0001c0001t0002g0158 a0005c0011t0001g0022 a0005c0011t0001g0077 others(1): Show |
5 | HG00609.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+762T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623845 | |||||||
| chr22:30623845 | TAC | T | 2 | a0001c0001t0003g0012 a0001c0001t0003g0087 |
5 | NA18947.hp1 NA18971.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+764_1222+765d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623845 | ||||||
| chr22:30623847 | C | T | 166 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0002g0004 others(163): Show |
213 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1222+764C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623847 | |||||||
| chr22:30623847 | CAT | C | 6 | a0001c0001t0002g0033 a0001c0001t0002g0160 a0001c0001t0003g0093 others(3): Show |
7 | HG00323.hp1 HG00639.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+766_1222+767d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623847 | ||||||
| chr22:30623848 | A | G | 2 | a0003c0003t0004g0203 a0007c0007t0004g0121 |
2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1222+765A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623848 | |||||||
| chr22:30623849 | T | C | 121 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0002g0004 others(118): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.1222+766T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623849 | |||||||
| chr22:30623849 | TACAC | T | 4 | a0002c0002t0001g0281 a0005c0011t0001g0022 a0005c0011t0001g0077 others(1): Show |
5 | HG02056.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+768_1222+771d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623849 | ||||||
| chr22:30623851 | C | CACACATA others(3): Show |
1 | a0005c0005t0001g0192 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1222+771_1222+772i others(12): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623851 | ||||||
| chr22:30623851 | C | T | 11 | a0001c0001t0008g0326 a0001c0001t0008g0327 a0001c0001t0008g0328 others(8): Show |
15 | HG01261.hp1 HG01884.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1222+768C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623851 | |||||||
| chr22:30623853 | C | CACAT | 3 | a0005c0005t0002g0070 a0005c0005t0002g0072 a0005c0005t0015g0071 |
3 | HG02109.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1222+771_1222+772i others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623853 | ||||||
| chr22:30623853 | C | T | 14 | a0003c0003t0004g0200 a0003c0003t0004g0201 a0004c0004t0001g0124 others(11): Show |
27 | HG01243.hp2 HG01496.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1222+770C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623853 | |||||||
| chr22:30623855 | T | C | 27 | a0001c0001t0001g0229 a0001c0001t0002g0032 a0001c0001t0002g0158 others(24): Show |
36 | HG00423.hp2 HG00609.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.1222+772T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623855 | |||||||
| chr22:30623857 | C | CATACACA others(5): Show |
1 | a0002c0002t0001g0289 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1222+802_1222+813d others(14): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623857 | ||||||
| chr22:30623857 | C | T | 188 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(185): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1222+774C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623857 | |||||||
| chr22:30623859 | T | C | 7 | a0003c0003t0004g0200 a0003c0003t0004g0201 a0004c0004t0007g0125 others(4): Show |
8 | HG01884.hp2 HG02683.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222+776T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623859 | |||||||
| chr22:30623859 | T | TACATAC | 4 | a0010c0012t0001g0223 a0010c0012t0001g0224 a0010c0012t0001g0225 others(1): Show |
4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+779_1222+780i others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623859 | ||||||
| chr22:30623859 | TAC | T | 3 | a0007c0007t0007g0011 a0007c0007t0007g0083 a0007c0007t0007g0085 |
6 | HG01261.hp1 HG02647.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222+782_1222+783d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623859 | ||||||
| chr22:30623860 | A | G | 1 | a0001c0001t0001g0020 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1222+777A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623860 | |||||||
| chr22:30623861 | C | T | 68 | a0001c0001t0001g0020 a0001c0001t0001g0229 a0001c0001t0002g0004 others(65): Show |
98 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1222+778C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623861 | |||||||
| chr22:30623863 | C | T | 4 | a0001c0001t0001g0020 a0003c0003t0004g0042 a0003c0003t0007g0216 others(1): Show |
6 | HG01496.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222+780C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623863 | |||||||
| chr22:30623865 | C | T | 5 | a0004c0004t0007g0125 a0005c0005t0001g0191 a0005c0011t0001g0022 others(2): Show |
6 | HG02683.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1222+782C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623865 | |||||||
| chr22:30623867 | T | C | 61 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(58): Show |
86 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1222+784T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623867 | |||||||
| chr22:30623870 | A | G | 1 | a0003c0003t0004g0203 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1222+787A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623870 | |||||||
| chr22:30623871 | T | C | 6 | a0001c0001t0001g0020 a0001c0001t0021g0153 a0004c0004t0007g0125 others(3): Show |
8 | HG01496.hp2 HG01981.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222+788T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623871 | |||||||
| chr22:30623871 | TAC | T | 27 | a0001c0001t0003g0019 a0001c0001t0003g0065 a0001c0001t0003g0067 others(24): Show |
31 | HG00642.hp1 HG00733.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.1222+794_1222+795d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623871 | ||||||
| chr22:30623872 | A | G | 16 | a0003c0003t0004g0200 a0003c0003t0004g0201 a0003c0003t0004g0202 others(13): Show |
29 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1222+789A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623872 | |||||||
| chr22:30623873 | C | T | 21 | a0001c0001t0002g0158 a0001c0001t0008g0326 a0001c0001t0008g0327 others(18): Show |
35 | HG00609.hp2 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.1222+790C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623873 | |||||||
| chr22:30623875 | C | CACACATA others(5): Show |
1 | a0007c0007t0004g0121 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1222+795_1222+796i others(14): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623875 | ||||||
| chr22:30623875 | C | CACACATA others(221): Show |
1 | a0003c0003t0007g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1222+795_1222+796i others(230): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623875 | ||||||
| chr22:30623875 | C | CACACATA others(197): Show |
1 | a0003c0003t0012g0205 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1222+795_1222+796i others(206): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623875 | ||||||
| chr22:30623875 | C | CACATATA others(65): Show |
1 | a0001c0001t0002g0173 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1222+812_1222+813i others(74): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623875 | ||||||
| chr22:30623875 | C | CACATATA others(53): Show |
2 | a0001c0001t0002g0032 a0001c0001t0002g0170 |
3 | HG00423.hp2 NA18979.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1222+800_1222+801i others(62): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623875 | ||||||
| chr22:30623875 | C | CATATATA others(249): Show |
1 | a0001c0001t0003g0304 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1222+793_1222+794i others(258): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623875 | ||||||
| chr22:30623875 | C | CATATGTA others(175): Show |
1 | a0003c0003t0004g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1222+793_1222+794i others(184): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623875 | ||||||
| chr22:30623875 | C | T | 42 | a0001c0001t0001g0229 a0001c0014t0001g0227 a0001c0014t0001g0228 others(39): Show |
58 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1222+792C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623875 | |||||||
| chr22:30623877 | C | CACATATA others(107): Show |
1 | a0001c0001t0001g0020 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1222+795_1222+796i others(116): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623877 | ||||||
| chr22:30623877 | C | CAT | 3 | a0005c0005t0002g0070 a0005c0005t0002g0072 a0005c0005t0015g0071 |
3 | HG02109.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1222+800_1222+801d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623877 | ||||||
| chr22:30623877 | C | T | 7 | a0001c0001t0002g0301 a0001c0001t0021g0153 a0005c0011t0001g0022 others(4): Show |
8 | HG00099.hp2 HG01106.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222+794C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623877 | |||||||
| chr22:30623877 | CAT | C | 2 | a0002c0010t0001g0013 a0002c0010t0001g0231 |
5 | HG00741.hp2 HG01069.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+800_1222+801d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623877 | ||||||
| chr22:30623877 | CATATATA others(21): Show |
C | 1 | a0002c0002t0001g0239 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1222+828_1222+855d others(30): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623877 | ||||||
| chr22:30623879 | T | C | 3 | a0001c0001t0001g0020 a0001c0001t0002g0158 a0005c0005t0001g0041 |
5 | HG00609.hp2 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+796T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623879 | |||||||
| chr22:30623879 | T | TATACAC | 4 | a0005c0005t0001g0040 a0005c0005t0001g0189 a0005c0005t0001g0191 others(1): Show |
5 | HG02622.hp1 HG02717.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+799_1222+800i others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623879 | ||||||
| chr22:30623879 | T | TATATATA others(61): Show |
1 | a0005c0005t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1222+801_1222+802i others(70): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623879 | ||||||
| chr22:30623879 | T | TATATGTA others(3): Show |
3 | a0005c0005t0001g0039 a0005c0005t0001g0190 a0005c0005t0001g0192 |
4 | HG01099.hp2 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+800_1222+801i others(12): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623879 | ||||||
| chr22:30623880 | A | G | 12 | a0003c0003t0004g0043 a0003c0003t0004g0044 a0003c0003t0004g0045 others(9): Show |
15 | HG00140.hp1 HG00280.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1222+797A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623880 | |||||||
| chr22:30623885 | C | T | 8 | a0005c0005t0001g0039 a0005c0005t0001g0040 a0005c0005t0001g0189 others(5): Show |
10 | HG01099.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1222+802C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623885 | |||||||
| chr22:30623885 | CACACATA others(7): Show |
C | 1 | a0007c0007t0007g0084 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1222+804_1222+817d others(16): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623885 | ||||||
| chr22:30623885 | CACACATA others(61): Show |
C | 1 | a0007c0007t0007g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1222+804_1222+871d others(70): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623885 | ||||||
| chr22:30623887 | CACAT | C | 3 | a0007c0007t0007g0011 a0007c0007t0007g0083 a0007c0007t0007g0085 |
6 | HG01261.hp1 HG02647.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222+806_1222+809d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623887 | ||||||
| chr22:30623889 | CAT | C | 80 | a0001c0001t0001g0229 a0001c0001t0002g0004 a0001c0001t0002g0008 others(77): Show |
117 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1222+813_1222+814d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623889 | ||||||
| chr22:30623891 | T | C | 30 | a0001c0001t0001g0020 a0001c0001t0003g0313 a0001c0001t0003g0318 others(27): Show |
37 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.1222+808T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623891 | |||||||
| chr22:30623891 | T | TATATACA others(193): Show |
1 | a0005c0005t0015g0071 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1222+813_1222+814i others(202): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623891 | ||||||
| chr22:30623891 | T | TATATACA others(215): Show |
1 | a0005c0005t0002g0070 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1222+813_1222+814i others(224): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623891 | ||||||
| chr22:30623891 | T | TATATGTA others(167): Show |
1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1222+812_1222+813i others(176): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623891 | ||||||
| chr22:30623893 | T | C | 16 | a0001c0001t0001g0229 a0001c0001t0003g0304 a0001c0014t0001g0227 others(13): Show |
16 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.1222+810T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623893 | |||||||
| chr22:30623893 | T | TATACACA others(135): Show |
1 | a0005c0005t0002g0072 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1222+813_1222+814i others(144): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623893 | ||||||
| chr22:30623893 | T | TATATACA others(149): Show |
1 | a0005c0005t0002g0073 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1222+814_1222+815i others(158): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623893 | ||||||
| chr22:30623893 | T | TATGTATA others(237): Show |
1 | a0003c0003t0004g0202 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1222+812_1222+813i others(246): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623893 | ||||||
| chr22:30623893 | T | TATGTATA others(133): Show |
1 | a0003c0003t0004g0194 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1222+812_1222+813i others(142): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623893 | ||||||
| chr22:30623893 | T | TATGTATA others(131): Show |
6 | a0003c0003t0004g0043 a0003c0003t0004g0044 a0003c0003t0004g0209 others(3): Show |
7 | HG01358.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+812_1222+813i others(140): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623893 | ||||||
| chr22:30623893 | T | TATGTATA others(129): Show |
3 | a0003c0003t0004g0043 a0003c0003t0004g0045 a0003c0003t0004g0214 |
4 | HG01978.hp1 HG01993.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222+812_1222+813i others(138): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623893 | ||||||
| chr22:30623893 | T | TATGTATA others(127): Show |
1 | a0003c0003t0004g0222 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1222+812_1222+813i others(136): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623893 | ||||||
| chr22:30623897 | T | TACACAC | 2 | a0005c0011t0001g0022 a0005c0011t0001g0081 |
3 | HG02896.hp2 HG02897.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1222+814_1222+815i others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623897 | |||||||
| chr22:30623898 | G | A | 10 | a0001c0001t0002g0158 a0001c0001t0002g0184 a0005c0011t0001g0022 others(7): Show |
14 | HG00099.hp2 HG00609.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1222+815G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623898 | |||||||
| chr22:30623899 | T | C | 8 | a0005c0005t0002g0074 a0005c0005t0011g0329 a0005c0011t0001g0077 others(5): Show |
11 | HG00099.hp2 HG01106.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1222+816T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623899 | |||||||
| chr22:30623901 | T | C | 6 | a0001c0001t0021g0153 a0005c0005t0002g0074 a0005c0005t0011g0329 others(3): Show |
6 | HG00099.hp2 HG01106.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1222+818T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623901 | |||||||
| chr22:30623902 | A | G | 1 | a0001c0001t0002g0158 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1222+819A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623902 | |||||||
| chr22:30623903 | C | CACACATA others(5): Show |
1 | a0001c0001t0002g0184 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1222+821_1222+822i others(14): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623903 | ||||||
| chr22:30623903 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1222+820C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623903 | |||||||
| chr22:30623903 | CAT | C | 26 | a0001c0001t0002g0173 a0003c0003t0004g0043 a0003c0003t0004g0044 others(23): Show |
41 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(38): Show |
intron_variant | MODIFIER | c.1222+828_1222+829d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623903 | ||||||
| chr22:30623905 | T | C | 4 | a0001c0001t0021g0153 a0005c0005t0002g0074 a0005c0011t0001g0022 others(1): Show |
5 | HG01192.hp2 HG01981.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+822T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623905 | |||||||
| chr22:30623905 | T | TATATACA others(19): Show |
1 | a0002c0002t0001g0030 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1222+827_1222+828i others(28): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623905 | ||||||
| chr22:30623905 | T | TATATACA others(17): Show |
2 | a0002c0002t0001g0279 a0002c0002t0001g0283 |
2 | HG00673.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1222+827_1222+828i others(26): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623905 | ||||||
| chr22:30623905 | T | TATATACA others(195): Show |
1 | a0001c0001t0003g0306 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1222+827_1222+828i others(204): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623905 | ||||||
| chr22:30623905 | T | TATATACA others(87): Show |
3 | a0004c0004t0002g0029 a0004c0004t0005g0116 a0004c0004t0005g0118 |
4 | HG01884.hp1 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222+827_1222+828i others(96): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623905 | ||||||
| chr22:30623905 | T | TATATATA others(19): Show |
4 | a0006c0006t0001g0046 a0006c0006t0001g0195 a0006c0006t0001g0218 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+836_1222+861d others(28): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623905 | ||||||
| chr22:30623907 | T | C | 2 | a0001c0001t0002g0158 a0001c0001t0002g0184 |
2 | HG00609.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1222+824T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623907 | |||||||
| chr22:30623907 | T | TATACACA others(13): Show |
1 | a0005c0005t0001g0040 | 2 | HG02717.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1222+827_1222+828i others(22): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623907 | ||||||
| chr22:30623907 | T | TATACACA others(37): Show |
1 | a0005c0005t0001g0193 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1222+827_1222+828i others(46): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623907 | ||||||
| chr22:30623909 | T | C | 4 | a0005c0005t0011g0329 a0005c0011t0001g0077 a0011c0013t0011g0187 others(1): Show |
4 | HG00099.hp2 HG01106.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+826T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623909 | |||||||
| chr22:30623909 | TATAC | T | 60 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(57): Show |
87 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1222+828_1222+831d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623909 | ||||||
| chr22:30623911 | T | C | 29 | a0001c0001t0001g0229 a0001c0001t0002g0032 a0001c0001t0002g0170 others(26): Show |
34 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.1222+828T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623911 | |||||||
| chr22:30623913 | C | T | 8 | a0001c0001t0002g0158 a0001c0001t0002g0184 a0005c0005t0001g0040 others(5): Show |
9 | HG00099.hp2 HG00609.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1222+830C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623913 | |||||||
| chr22:30623915 | C | T | 4 | a0005c0005t0011g0329 a0005c0011t0001g0077 a0011c0013t0011g0187 others(1): Show |
4 | HG00099.hp2 HG01106.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+832C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623915 | |||||||
| chr22:30623915 | CACATAT | C | 2 | a0001c0001t0002g0032 a0001c0001t0002g0170 |
3 | HG00423.hp2 NA18979.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1222+834_1222+839d others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623915 | ||||||
| chr22:30623917 | C | T | 1 | a0005c0005t0002g0074 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+834C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623917 | |||||||
| chr22:30623917 | CAT | C | 8 | a0001c0001t0021g0153 a0002c0002t0001g0255 a0002c0002t0001g0260 others(5): Show |
8 | HG00642.hp2 HG01069.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222+841_1222+842d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623917 | ||||||
| chr22:30623917 | CATAT | C | 7 | a0001c0001t0001g0229 a0005c0011t0001g0022 a0005c0011t0001g0081 others(4): Show |
11 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1222+839_1222+842d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623917 | ||||||
| chr22:30623919 | T | C | 88 | a0001c0001t0001g0020 a0001c0001t0002g0004 a0001c0001t0002g0008 others(85): Show |
120 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1222+836T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623919 | |||||||
| chr22:30623919 | T | TATATATG others(19): Show |
28 | a0002c0002t0001g0003 a0002c0002t0001g0030 a0002c0002t0001g0031 others(25): Show |
35 | HG00597.hp2 HG00735.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1222+838_1222+863d others(28): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623919 | ||||||
| chr22:30623919 | T | TATATATG others(45): Show |
1 | a0002c0002t0019g0142 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1222+863_1222+864i others(54): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623919 | ||||||
| chr22:30623919 | T | TATATATG others(43): Show |
1 | a0002c0002t0001g0271 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1222+861_1222+862i others(52): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623919 | ||||||
| chr22:30623919 | T | TATATGTA others(17): Show |
4 | a0002c0002t0001g0272 a0002c0002t0001g0276 a0002c0002t0009g0049 others(1): Show |
5 | HG01168.hp2 HG01169.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+840_1222+841i others(26): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623919 | ||||||
| chr22:30623921 | T | C | 6 | a0001c0001t0003g0304 a0001c0001t0003g0306 a0005c0005t0011g0329 others(3): Show |
6 | HG00099.hp2 HG01106.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1222+838T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | |||||||
| chr22:30623921 | T | TACACACA others(189): Show |
1 | a0001c0001t0003g0007 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1222+839_1222+840i others(198): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(197): Show |
1 | a0001c0001t0003g0319 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1222+841_1222+842i others(206): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(195): Show |
1 | a0001c0001t0003g0322 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1222+841_1222+842i others(204): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(197): Show |
1 | a0001c0001t0003g0111 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1222+841_1222+842i others(206): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(201): Show |
18 | a0001c0001t0003g0007 a0001c0001t0003g0023 a0001c0001t0003g0024 others(15): Show |
24 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1222+841_1222+842i others(210): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(251): Show |
1 | a0001c0001t0003g0093 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1222+841_1222+842i others(260): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(199): Show |
1 | a0001c0001t0003g0314 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1222+841_1222+842i others(208): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(199): Show |
19 | a0001c0001t0003g0065 a0001c0001t0003g0066 a0001c0001t0003g0067 others(16): Show |
20 | HG00642.hp1 HG01168.hp1 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1222+841_1222+842i others(208): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(225): Show |
1 | a0001c0001t0003g0066 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1222+841_1222+842i others(234): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(199): Show |
2 | a0001c0001t0003g0012 a0001c0001t0003g0087 |
5 | NA18947.hp1 NA18971.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+841_1222+842i others(208): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(199): Show |
1 | a0001c0001t0003g0019 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1222+841_1222+842i others(208): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(197): Show |
4 | a0001c0001t0003g0019 a0001c0001t0003g0068 a0001c0001t0003g0307 others(1): Show |
5 | HG01981.hp1 HG02273.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+841_1222+842i others(206): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(195): Show |
1 | a0001c0001t0003g0019 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1222+841_1222+842i others(204): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(197): Show |
1 | a0001c0001t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1222+841_1222+842i others(206): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(195): Show |
1 | a0001c0001t0003g0091 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1222+841_1222+842i others(204): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(197): Show |
1 | a0001c0001t0003g0315 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1222+841_1222+842i others(206): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(197): Show |
1 | a0001c0001t0003g0305 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1222+841_1222+842i others(206): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(195): Show |
2 | a0001c0001t0010g0107 a0001c0001t0010g0108 |
2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1222+841_1222+842i others(204): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(259): Show |
1 | a0001c0001t0006g0076 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1222+841_1222+842i others(268): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(153): Show |
1 | a0001c0001t0006g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1222+841_1222+842i others(162): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(125): Show |
4 | a0001c0001t0006g0015 a0001c0001t0006g0021 a0001c0001t0006g0078 others(1): Show |
7 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1222+841_1222+842i others(134): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(151): Show |
1 | a0001c0001t0006g0075 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1222+841_1222+842i others(160): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATACACA others(151): Show |
1 | a0001c0001t0006g0016 | 2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1222+841_1222+842i others(160): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TATGCACA others(201): Show |
1 | a0001c0001t0003g0092 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1222+840_1222+841i others(210): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623921 | ||||||
| chr22:30623921 | T | TGTATACA others(325): Show |
1 | a0003c0003t0004g0206 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1222+838_1222+839i others(334): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | |||||||
| chr22:30623921 | T | TGTATACA others(303): Show |
1 | a0003c0025t0012g0208 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1222+838_1222+839i others(312): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | |||||||
| chr22:30623921 | T | TGTATACA others(303): Show |
1 | a0003c0003t0004g0207 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1222+838_1222+839i others(312): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | |||||||
| chr22:30623921 | T | TGTATACA others(301): Show |
1 | a0003c0003t0004g0204 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1222+838_1222+839i others(310): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | |||||||
| chr22:30623921 | T | TGTATACA others(301): Show |
1 | a0003c0003t0004g0217 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1222+838_1222+839i others(310): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | |||||||
| chr22:30623921 | T | TGTATACA others(57): Show |
1 | a0003c0003t0012g0205 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1222+838_1222+839i others(66): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | |||||||
| chr22:30623921 | T | TGTATACA others(81): Show |
1 | a0003c0003t0007g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1222+838_1222+839i others(90): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | |||||||
| chr22:30623921 | T | TGTATACA others(37): Show |
1 | a0003c0003t0004g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1222+838_1222+839i others(46): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | |||||||
| chr22:30623921 | T | TGTATACA others(87): Show |
1 | a0003c0003t0004g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1222+838_1222+839i others(96): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | |||||||
| chr22:30623921 | T | TGTATACA others(113): Show |
2 | a0003c0003t0004g0197 a0003c0003t0004g0198 |
2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1222+838_1222+839i others(122): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | |||||||
| chr22:30623921 | T | TGTATACA others(285): Show |
1 | a0003c0003t0004g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1222+838_1222+839i others(294): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | |||||||
| chr22:30623921 | T | TGTATACA others(33): Show |
1 | a0003c0003t0004g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1222+838_1222+839i others(42): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | |||||||
| chr22:30623921 | T | TGTATACA others(35): Show |
1 | a0003c0003t0004g0215 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1222+838_1222+839i others(44): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | |||||||
| chr22:30623921 | T | TGTATACA others(57): Show |
1 | a0003c0003t0004g0213 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1222+838_1222+839i others(66): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | |||||||
| chr22:30623921 | T | TGTATACA others(229): Show |
2 | a0001c0014t0001g0227 a0001c0014t0001g0228 |
2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1222+838_1222+839i others(238): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623921 | |||||||
| chr22:30623923 | T | C | 3 | a0001c0014t0001g0227 a0001c0014t0001g0228 a0005c0005t0002g0074 |
3 | HG01192.hp2 HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1222+840T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623923 | |||||||
| chr22:30623923 | T | TACACACA others(171): Show |
4 | a0009c0009t0003g0026 a0009c0009t0003g0106 a0009c0009t0003g0110 others(1): Show |
5 | HG00323.hp1 HG01175.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+841_1222+842i others(180): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623923 | ||||||
| chr22:30623923 | T | TACACACA others(171): Show |
1 | a0001c0001t0003g0325 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1222+841_1222+842i others(180): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623923 | ||||||
| chr22:30623925 | T | C | 1 | a0005c0005t0002g0074 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+842T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623925 | |||||||
| chr22:30623926 | G | A | 1 | a0005c0005t0002g0074 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+843G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623926 | |||||||
| chr22:30623927 | T | C | 1 | a0005c0005t0002g0074 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+844T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623927 | |||||||
| chr22:30623931 | C | T | 1 | a0005c0005t0002g0074 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+848C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623931 | |||||||
| chr22:30623933 | T | C | 1 | a0005c0005t0002g0074 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+850T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623933 | |||||||
| chr22:30623933 | T | TATATACA others(17): Show |
1 | a0002c0002t0001g0149 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1222+863_1222+864i others(26): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623933 | ||||||
| chr22:30623935 | T | C | 1 | a0005c0005t0002g0074 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+852T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623935 | |||||||
| chr22:30623937 | TAC | T | 77 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(74): Show |
107 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1222+864_1222+865d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623937 | ||||||
| chr22:30623937 | TACAC | T | 4 | a0001c0001t0021g0153 a0004c0004t0002g0029 a0004c0004t0005g0116 others(1): Show |
5 | HG01884.hp1 HG01981.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+862_1222+865d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623937 | ||||||
| chr22:30623939 | C | CACACATA others(69): Show |
3 | a0005c0011t0001g0022 a0005c0011t0001g0077 a0005c0011t0001g0081 |
4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+861_1222+862i others(78): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623939 | ||||||
| chr22:30623939 | C | T | 10 | a0001c0001t0001g0229 a0001c0001t0006g0080 a0004c0004t0007g0125 others(7): Show |
12 | HG00639.hp2 HG01099.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+856C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623939 | |||||||
| chr22:30623941 | C | CACATATA others(111): Show |
6 | a0004c0004t0001g0124 a0004c0004t0005g0002 a0004c0004t0005g0114 others(3): Show |
17 | HG01243.hp2 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1222+861_1222+862i others(120): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623941 | ||||||
| chr22:30623941 | C | CACATATA others(109): Show |
1 | a0018c0017t0022g0308 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1222+861_1222+862i others(118): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623941 | ||||||
| chr22:30623941 | C | CACATATA others(63): Show |
1 | a0005c0005t0001g0189 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1222+861_1222+862i others(72): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623941 | ||||||
| chr22:30623941 | C | CATATATA others(11): Show |
1 | a0005c0005t0015g0071 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1222+859_1222+860i others(20): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623941 | ||||||
| chr22:30623941 | C | T | 2 | a0001c0001t0002g0169 a0005c0005t0002g0074 |
2 | HG01192.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1222+858C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623941 | |||||||
| chr22:30623943 | C | CACATATA others(73): Show |
1 | a0001c0001t0006g0080 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1222+863_1222+864i others(82): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623943 | ||||||
| chr22:30623943 | C | T | 1 | a0005c0005t0015g0071 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1222+860C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623943 | |||||||
| chr22:30623945 | C | CATATATA others(23): Show |
1 | a0010c0012t0020g0226 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1222+863_1222+864i others(32): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623945 | ||||||
| chr22:30623945 | C | T | 76 | a0001c0001t0001g0094 a0001c0001t0002g0032 a0001c0001t0002g0158 others(73): Show |
98 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1222+862C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623945 | |||||||
| chr22:30623947 | C | T | 163 | a0001c0001t0001g0020 a0001c0001t0002g0004 a0001c0001t0002g0008 others(160): Show |
223 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.1222+864C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623947 | |||||||
| chr22:30623949 | T | C | 1 | a0001c0001t0006g0080 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1222+866T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623949 | |||||||
| chr22:30623956 | A | G | 1 | a0001c0001t0002g0173 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1222+873A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623956 | |||||||
| chr22:30623957 | C | T | 1 | a0001c0001t0003g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1222+874C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623957 | |||||||
| chr22:30623963 | TAC | T | 65 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(62): Show |
97 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1222+888_1222+889d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623963 | ||||||
| chr22:30623965 | C | CACACACA others(45): Show |
24 | a0002c0002t0001g0001 a0002c0002t0001g0050 a0002c0002t0001g0058 others(21): Show |
33 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1222+889_1222+890i others(54): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | ||||||
| chr22:30623965 | C | CACACACA others(71): Show |
2 | a0002c0002t0001g0001 a0002c0002t0009g0050 |
2 | HG00741.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1222+889_1222+890i others(80): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | ||||||
| chr22:30623965 | C | CACACACA others(43): Show |
5 | a0002c0002t0001g0001 a0002c0002t0001g0237 a0002c0002t0001g0285 others(2): Show |
7 | HG00140.hp2 HG01109.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1222+889_1222+890i others(52): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | ||||||
| chr22:30623965 | C | CACACACA others(41): Show |
1 | a0002c0002t0017g0062 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1222+889_1222+890i others(50): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | ||||||
| chr22:30623965 | C | CACACACA others(45): Show |
1 | a0002c0002t0001g0238 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1222+907_1222+908i others(54): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | ||||||
| chr22:30623965 | C | CACACACA others(19): Show |
11 | a0002c0002t0001g0017 a0002c0002t0001g0271 a0002c0002t0001g0272 others(8): Show |
16 | HG00423.hp1 HG00673.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1222+942_1222+967d others(28): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | ||||||
| chr22:30623965 | C | CACACACA others(45): Show |
1 | a0002c0002t0001g0293 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1222+916_1222+967d others(54): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | ||||||
| chr22:30623965 | C | CACACACA others(71): Show |
2 | a0002c0002t0001g0001 a0002c0002t0001g0241 |
3 | NA18940.hp2 NA18956.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1222+894_1222+895i others(80): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | ||||||
| chr22:30623965 | C | T | 86 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0002g0173 others(83): Show |
116 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.1222+882C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623965 | |||||||
| chr22:30623965 | CACACACA others(19): Show |
C | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG03654.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1222+942_1222+967d others(28): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623965 | ||||||
| chr22:30623967 | C | CACACACA others(43): Show |
1 | a0002c0002t0001g0280 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1222+889_1222+890i others(52): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623967 | ||||||
| chr22:30623967 | C | CACATATA others(37): Show |
1 | a0005c0005t0002g0074 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+887_1222+888i others(46): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623967 | ||||||
| chr22:30623967 | C | CATATATG others(3): Show |
1 | a0001c0001t0002g0172 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1222+885_1222+886i others(12): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623967 | ||||||
| chr22:30623969 | CACAT | C | 9 | a0001c0001t0002g0032 a0001c0001t0002g0127 a0001c0001t0002g0160 others(6): Show |
12 | HG00423.hp2 HG00639.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+888_1222+891d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623969 | ||||||
| chr22:30623971 | C | T | 2 | a0001c0001t0002g0172 a0005c0005t0001g0190 |
2 | HG02922.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1222+888C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623971 | |||||||
| chr22:30623971 | CAT | C | 21 | a0001c0001t0001g0020 a0001c0001t0002g0173 a0002c0002t0001g0146 others(18): Show |
24 | HG00099.hp2 HG00733.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1222+895_1222+896d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623971 | ||||||
| chr22:30623971 | CATAT | C | 9 | a0001c0014t0001g0227 a0001c0014t0001g0228 a0003c0003t0004g0213 others(6): Show |
12 | HG00140.hp1 HG01261.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+893_1222+896d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623971 | ||||||
| chr22:30623973 | T | C | 4 | a0001c0001t0001g0229 a0002c0002t0001g0280 a0003c0003t0004g0199 others(1): Show |
4 | HG01192.hp2 HG02895.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222+890T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623973 | |||||||
| chr22:30623973 | T | TATATGTA others(17): Show |
1 | a0006c0006t0001g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1222+894_1222+895i others(26): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623973 | ||||||
| chr22:30623973 | T | TATGTATA others(205): Show |
1 | a0003c0003t0004g0215 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1222+892_1222+893i others(214): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623973 | ||||||
| chr22:30623975 | T | C | 64 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(61): Show |
85 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1222+892T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623975 | |||||||
| chr22:30623975 | T | TATGTATA others(111): Show |
2 | a0003c0003t0004g0197 a0003c0003t0004g0198 |
2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1222+894_1222+895i others(120): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623975 | ||||||
| chr22:30623975 | T | TATGTATA others(35): Show |
1 | a0005c0005t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1222+894_1222+895i others(44): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623975 | ||||||
| chr22:30623975 | T | TGTATACA others(103): Show |
1 | a0003c0003t0004g0209 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1222+892_1222+893i others(112): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623975 | |||||||
| chr22:30623975 | T | TGTATACA others(77): Show |
9 | a0003c0003t0004g0043 a0003c0003t0004g0044 a0003c0003t0004g0045 others(6): Show |
12 | HG01256.hp1 HG01515.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.1222+892_1222+893i others(86): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623975 | |||||||
| chr22:30623975 | T | TGTATACA others(11): Show |
1 | a0005c0005t0001g0190 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1222+892_1222+893i others(20): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623975 | |||||||
| chr22:30623975 | T | TGTATACA others(181): Show |
1 | a0003c0003t0004g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1222+892_1222+893i others(190): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623975 | |||||||
| chr22:30623977 | T | TGTATACA others(91): Show |
1 | a0001c0001t0001g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1222+894_1222+895i others(100): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623977 | |||||||
| chr22:30623984 | A | G | 2 | a0001c0001t0002g0032 a0001c0001t0002g0170 |
3 | HG00423.hp2 NA18979.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1222+901A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623984 | |||||||
| chr22:30623985 | C | CAT | 42 | a0001c0001t0003g0019 a0001c0001t0003g0065 a0001c0001t0003g0066 others(39): Show |
48 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.1222+908_1222+909d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623985 | ||||||
| chr22:30623985 | C | CATATATA others(51): Show |
1 | a0010c0012t0001g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1222+915_1222+916i others(60): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623985 | ||||||
| chr22:30623985 | C | CATATATA others(39): Show |
2 | a0005c0005t0002g0072 a0005c0005t0002g0073 |
2 | HG00642.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1222+909_1222+910i others(48): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623985 | ||||||
| chr22:30623991 | T | C | 4 | a0001c0001t0002g0037 a0001c0001t0002g0177 a0001c0001t0002g0178 others(1): Show |
5 | NA18962.hp1 NA18995.hp1 NA19072.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+908T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623991 | |||||||
| chr22:30623991 | T | TAC | 7 | a0001c0001t0006g0076 a0002c0002t0001g0146 a0002c0002t0001g0239 others(4): Show |
8 | HG01167.hp1 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222+914_1222+915d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623991 | ||||||
| chr22:30623993 | C | CACACACA others(49): Show |
1 | a0010c0012t0001g0223 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1222+915_1222+916i others(58): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623993 | ||||||
| chr22:30623993 | C | T | 6 | a0001c0001t0002g0032 a0001c0001t0002g0170 a0001c0001t0002g0173 others(3): Show |
8 | HG00423.hp2 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1222+910C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623993 | |||||||
| chr22:30623995 | CACATAT | C | 4 | a0001c0001t0002g0037 a0001c0001t0002g0177 a0001c0001t0002g0178 others(1): Show |
5 | NA18962.hp1 NA18995.hp1 NA19072.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+914_1222+919d others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623995 | ||||||
| chr22:30623997 | CAT | C | 7 | a0001c0014t0001g0227 a0001c0014t0001g0228 a0003c0003t0004g0042 others(4): Show |
9 | HG01069.hp2 HG01071.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1222+921_1222+922d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623997 | ||||||
| chr22:30623997 | CATAT | C | 45 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(42): Show |
68 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.1222+919_1222+922d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623997 | ||||||
| chr22:30623997 | CATATAT | C | 3 | a0001c0001t0002g0027 a0001c0001t0002g0112 a0001c0001t0002g0113 |
4 | HG01070.hp1 HG02559.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+917_1222+922d others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623997 | ||||||
| chr22:30623999 | T | C | 45 | a0001c0001t0001g0020 a0001c0001t0001g0229 a0001c0001t0002g0032 others(42): Show |
54 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.1222+916T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30623999 | |||||||
| chr22:30623999 | T | TATGTATA others(65): Show |
1 | a0001c0001t0002g0300 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1222+918_1222+919i others(74): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30623999 | ||||||
| chr22:30624001 | T | C | 16 | a0001c0001t0003g0066 a0001c0001t0003g0311 a0001c0001t0003g0320 others(13): Show |
22 | HG00733.hp1 HG00735.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1222+918T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624001 | |||||||
| chr22:30624001 | T | TATGTATA others(9): Show |
1 | a0004c0004t0005g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1222+920_1222+921i others(18): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624001 | ||||||
| chr22:30624001 | T | TATGTATA others(13): Show |
3 | a0004c0004t0005g0028 a0004c0004t0005g0123 a0011c0013t0011g0188 |
4 | HG01106.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+920_1222+921i others(22): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624001 | ||||||
| chr22:30624001 | T | TATGTATA others(83): Show |
1 | a0011c0013t0011g0187 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1222+920_1222+921i others(92): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624001 | ||||||
| chr22:30624001 | T | TGTATACA others(11): Show |
1 | a0013c0018t0002g0131 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1222+918_1222+919i others(20): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624001 | |||||||
| chr22:30624002 | A | G | 10 | a0004c0004t0001g0124 a0004c0004t0002g0029 a0004c0004t0005g0002 others(7): Show |
22 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1222+919A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624002 | |||||||
| chr22:30624004 | A | G | 5 | a0005c0005t0001g0039 a0005c0005t0001g0040 a0005c0005t0001g0192 others(2): Show |
7 | HG01099.hp2 HG01192.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+921A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624004 | |||||||
| chr22:30624004 | ATG | A | 10 | a0004c0004t0001g0124 a0004c0004t0002g0029 a0004c0004t0005g0002 others(7): Show |
22 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1222+923_1222+924d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624004 | ||||||
| chr22:30624005 | TGTATACA others(49): Show |
T | 4 | a0007c0007t0007g0011 a0007c0007t0007g0083 a0007c0007t0007g0084 others(1): Show |
7 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+923_1222+978d others(58): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624005 | |||||||
| chr22:30624006 | G | A | 5 | a0005c0005t0001g0039 a0005c0005t0001g0040 a0005c0005t0001g0192 others(2): Show |
7 | HG01099.hp2 HG01192.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+923G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624006 | |||||||
| chr22:30624009 | T | C | 15 | a0004c0004t0001g0124 a0004c0004t0002g0029 a0004c0004t0005g0002 others(12): Show |
29 | HG01099.hp2 HG01192.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1222+926T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624009 | |||||||
| chr22:30624011 | C | CAT | 70 | a0001c0001t0001g0094 a0001c0001t0002g0032 a0001c0001t0002g0170 others(67): Show |
87 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1222+934_1222+935d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624011 | ||||||
| chr22:30624011 | C | CATATATA others(93): Show |
1 | a0001c0001t0021g0153 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1222+944_1222+945i others(102): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624011 | ||||||
| chr22:30624011 | C | CATATATA others(15): Show |
1 | a0005c0005t0001g0189 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1222+939_1222+940i others(24): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624011 | ||||||
| chr22:30624011 | C | T | 17 | a0004c0004t0001g0124 a0004c0004t0002g0029 a0004c0004t0005g0002 others(14): Show |
31 | HG01099.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1222+928C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624011 | |||||||
| chr22:30624019 | C | T | 5 | a0001c0001t0008g0303 a0005c0005t0001g0082 a0005c0005t0002g0070 others(2): Show |
5 | HG01106.hp1 HG02109.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+936C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624019 | |||||||
| chr22:30624023 | CAT | C | 10 | a0001c0001t0002g0036 a0001c0001t0002g0180 a0001c0001t0002g0181 others(7): Show |
12 | HG01069.hp2 HG01071.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+947_1222+948d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624023 | ||||||
| chr22:30624025 | T | C | 40 | a0001c0001t0001g0020 a0001c0001t0001g0229 a0001c0001t0008g0303 others(37): Show |
45 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.1222+942T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624025 | |||||||
| chr22:30624027 | T | C | 12 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0021 others(9): Show |
17 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1222+944T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624027 | |||||||
| chr22:30624027 | T | TGTATACA others(125): Show |
1 | a0001c0001t0001g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1222+944_1222+945i others(134): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624027 | |||||||
| chr22:30624032 | G | A | 3 | a0003c0003t0004g0201 a0007c0007t0004g0121 a0009c0009t0016g0109 |
3 | HG00323.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1222+949G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624032 | |||||||
| chr22:30624033 | T | C | 1 | a0005c0005t0015g0071 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1222+950T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624033 | |||||||
| chr22:30624035 | T | C | 2 | a0005c0005t0002g0070 a0005c0005t0015g0071 |
2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1222+952T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624035 | |||||||
| chr22:30624037 | C | T | 2 | a0005c0005t0002g0072 a0005c0005t0002g0073 |
2 | HG00642.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1222+954C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624037 | |||||||
| chr22:30624039 | T | C | 2 | a0005c0005t0002g0070 a0005c0005t0015g0071 |
2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1222+956T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624039 | |||||||
| chr22:30624039 | T | TATATACA others(53): Show |
1 | a0005c0011t0001g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1222+965_1222+966i others(62): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624039 | ||||||
| chr22:30624041 | T | C | 2 | a0005c0005t0002g0070 a0005c0005t0015g0071 |
2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1222+958T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624041 | |||||||
| chr22:30624043 | T | C | 3 | a0003c0003t0004g0210 a0005c0005t0002g0070 a0005c0005t0015g0071 |
3 | HG01952.hp2 HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1222+960T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624043 | |||||||
| chr22:30624043 | T | TACACATA others(59): Show |
1 | a0005c0005t0001g0190 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1222+965_1222+966i others(68): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | ||||||
| chr22:30624043 | T | TACACATA others(61): Show |
2 | a0005c0011t0001g0022 a0005c0011t0001g0077 |
3 | HG02896.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1222+965_1222+966i others(70): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | ||||||
| chr22:30624043 | T | TATACACA others(87): Show |
1 | a0005c0005t0001g0039 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1222+961_1222+962i others(96): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | ||||||
| chr22:30624043 | T | TATACACA others(89): Show |
3 | a0005c0005t0001g0040 a0005c0005t0001g0192 a0005c0005t0001g0193 |
4 | HG01099.hp2 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+961_1222+962i others(98): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | ||||||
| chr22:30624043 | T | TATACACA others(9): Show |
1 | a0005c0005t0001g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1222+961_1222+962i others(18): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | ||||||
| chr22:30624043 | T | TATACACA others(11): Show |
2 | a0005c0005t0001g0041 a0005c0005t0001g0189 |
3 | HG01069.hp2 HG01071.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1222+961_1222+962i others(20): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | ||||||
| chr22:30624043 | T | TATACACA others(13): Show |
2 | a0005c0005t0001g0082 a0011c0013t0011g0187 |
2 | HG00099.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1222+961_1222+962i others(22): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | ||||||
| chr22:30624043 | T | TATACACA others(15): Show |
2 | a0005c0005t0002g0072 a0005c0005t0002g0073 |
2 | HG00642.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1222+961_1222+962i others(24): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | ||||||
| chr22:30624043 | T | TATACACA others(109): Show |
1 | a0005c0005t0011g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1222+961_1222+962i others(118): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | ||||||
| chr22:30624043 | T | TATACATA others(85): Show |
1 | a0011c0013t0011g0188 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1222+961_1222+962i others(94): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | ||||||
| chr22:30624043 | T | TATACATA others(115): Show |
1 | a0005c0005t0002g0074 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1222+961_1222+962i others(124): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | ||||||
| chr22:30624043 | TAC | T | 14 | a0001c0014t0001g0227 a0001c0014t0001g0228 a0002c0002t0001g0266 others(11): Show |
27 | HG01081.hp1 HG01243.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.1222+978_1222+979d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | ||||||
| chr22:30624043 | TACAC | T | 11 | a0001c0001t0001g0229 a0003c0003t0004g0196 a0003c0003t0004g0207 others(8): Show |
11 | HG00280.hp1 HG01081.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.1222+976_1222+979d others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | ||||||
| chr22:30624043 | TACACAC | T | 3 | a0001c0001t0003g0093 a0001c0001t0003g0304 a0009c0009t0016g0109 |
3 | HG00323.hp1 NA19001.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1222+974_1222+979d others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624043 | ||||||
| chr22:30624045 | C | CACACACA others(103): Show |
1 | a0010c0012t0001g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1222+969_1222+970i others(112): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624045 | ||||||
| chr22:30624045 | C | T | 77 | a0001c0001t0001g0094 a0001c0001t0002g0032 a0001c0001t0002g0170 others(74): Show |
96 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1222+962C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624045 | |||||||
| chr22:30624047 | C | T | 8 | a0004c0004t0002g0029 a0004c0004t0005g0002 a0004c0004t0005g0114 others(5): Show |
20 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1222+964C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624047 | |||||||
| chr22:30624049 | C | CATATATG others(35): Show |
1 | a0003c0003t0004g0198 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1222+967_1222+968i others(44): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | ||||||
| chr22:30624049 | C | CATATATG others(37): Show |
1 | a0003c0003t0004g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1222+967_1222+968i others(46): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | ||||||
| chr22:30624049 | C | CATATATG others(91): Show |
1 | a0001c0001t0002g0161 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1222+967_1222+968i others(100): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | ||||||
| chr22:30624049 | C | CATATATG others(63): Show |
2 | a0001c0001t0002g0164 a0001c0001t0002g0165 |
2 | HG02027.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1222+967_1222+968i others(72): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | ||||||
| chr22:30624049 | C | CATATATG others(65): Show |
3 | a0001c0001t0002g0035 a0013c0018t0002g0131 a0013c0019t0002g0294 |
4 | NA18949.hp2 NA18950.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222+967_1222+968i others(74): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | ||||||
| chr22:30624049 | C | CATATATG others(67): Show |
37 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0010 others(34): Show |
57 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1222+967_1222+968i others(76): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | ||||||
| chr22:30624049 | C | CATATATG others(95): Show |
1 | a0001c0001t0002g0150 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1222+967_1222+968i others(104): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | ||||||
| chr22:30624049 | C | CATATATG others(65): Show |
1 | a0001c0001t0002g0166 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1222+967_1222+968i others(74): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | ||||||
| chr22:30624049 | C | CATATATG others(67): Show |
8 | a0001c0001t0002g0009 a0001c0001t0002g0171 a0001c0001t0002g0172 others(5): Show |
12 | HG00408.hp1 HG04199.hp2 NA18951.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+967_1222+968i others(76): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | ||||||
| chr22:30624049 | C | CATATATG others(67): Show |
1 | a0001c0001t0002g0180 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1222+967_1222+968i others(76): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | ||||||
| chr22:30624049 | C | CATATATG others(65): Show |
1 | a0001c0001t0002g0168 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1222+967_1222+968i others(74): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | ||||||
| chr22:30624049 | C | CATATGTA others(37): Show |
1 | a0004c0004t0005g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1222+967_1222+968i others(46): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | ||||||
| chr22:30624049 | C | CATATGTA others(89): Show |
1 | a0004c0004t0005g0028 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1222+967_1222+968i others(98): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | ||||||
| chr22:30624049 | C | CATATGTA others(87): Show |
1 | a0004c0004t0005g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1222+967_1222+968i others(96): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624049 | ||||||
| chr22:30624051 | C | CATACATA others(125): Show |
3 | a0001c0001t0006g0015 a0001c0001t0006g0075 a0001c0001t0006g0078 |
5 | HG00735.hp1 HG01074.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+969_1222+970i others(134): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | ||||||
| chr22:30624051 | C | CATACATA others(153): Show |
1 | a0001c0001t0006g0079 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1222+969_1222+970i others(162): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | ||||||
| chr22:30624051 | C | CATACATA others(181): Show |
1 | a0001c0001t0006g0016 | 3 | HG02572.hp1 HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1222+969_1222+970i others(190): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | ||||||
| chr22:30624051 | C | CATACATA others(125): Show |
1 | a0001c0001t0006g0021 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1222+969_1222+970i others(134): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | ||||||
| chr22:30624051 | C | CATATATA others(11): Show |
1 | a0003c0003t0004g0200 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1222+969_1222+970i others(20): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | ||||||
| chr22:30624051 | C | CATATATA others(13): Show |
2 | a0009c0009t0003g0026 a0009c0009t0003g0106 |
3 | HG01175.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1222+969_1222+970i others(22): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | ||||||
| chr22:30624051 | C | CATATATA others(11): Show |
1 | a0001c0001t0003g0322 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1222+969_1222+970i others(20): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | ||||||
| chr22:30624051 | C | CATATATA others(13): Show |
51 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(48): Show |
65 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1222+969_1222+970i others(22): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | ||||||
| chr22:30624051 | C | CATATATA others(145): Show |
1 | a0001c0001t0001g0020 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1222+969_1222+970i others(154): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | ||||||
| chr22:30624051 | C | CATATATA others(15): Show |
2 | a0001c0001t0003g0111 a0004c0004t0007g0125 |
2 | HG02683.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1222+969_1222+970i others(24): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | ||||||
| chr22:30624051 | C | CATATATA others(41): Show |
4 | a0001c0001t0003g0066 a0001c0001t0003g0102 a0001c0001t0003g0320 others(1): Show |
5 | HG02004.hp1 HG02257.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+969_1222+970i others(50): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | ||||||
| chr22:30624051 | C | CATATATG others(11): Show |
10 | a0003c0003t0004g0043 a0003c0003t0004g0044 a0003c0003t0004g0045 others(7): Show |
13 | HG01256.hp1 HG01515.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.1222+969_1222+970i others(20): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | ||||||
| chr22:30624051 | C | CATATGTA others(175): Show |
1 | a0003c0003t0004g0213 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1222+969_1222+970i others(184): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | ||||||
| chr22:30624051 | C | CATATGTA others(135): Show |
1 | a0003c0003t0004g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1222+969_1222+970i others(144): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624051 | ||||||
| chr22:30624051 | C | T | 8 | a0001c0001t0002g0035 a0001c0001t0002g0164 a0001c0001t0002g0165 others(5): Show |
9 | HG00639.hp2 HG02027.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1222+968C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624051 | |||||||
| chr22:30624053 | C | CATATGTA others(203): Show |
1 | a0001c0001t0006g0080 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1222+971_1222+972i others(212): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624053 | ||||||
| chr22:30624053 | C | T | 5 | a0001c0001t0002g0164 a0001c0001t0002g0165 a0001c0001t0003g0322 others(2): Show |
5 | HG00733.hp1 HG00733.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222+970C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624053 | |||||||
| chr22:30624055 | C | T | 15 | a0001c0001t0002g0032 a0001c0001t0002g0170 a0001c0001t0002g0173 others(12): Show |
16 | HG00423.hp2 HG00733.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1222+972C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624055 | |||||||
| chr22:30624057 | C | T | 37 | a0001c0001t0001g0229 a0001c0001t0002g0032 a0001c0001t0002g0170 others(34): Show |
51 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1222+974C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624057 | |||||||
| chr22:30624059 | C | T | 137 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0002g0004 others(134): Show |
186 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1222+976C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624059 | |||||||
| chr22:30624060 | A | G | 1 | a0001c0001t0006g0076 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1222+977A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624060 | |||||||
| chr22:30624061 | C | CAT | 5 | a0002c0002t0001g0058 a0002c0002t0001g0132 a0002c0002t0001g0243 others(2): Show |
6 | HG03669.hp2 HG03710.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.1222+997_1222+998d others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624061 | ||||||
| chr22:30624061 | C | T | 177 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(174): Show |
244 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.1222+978C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624061 | |||||||
| chr22:30624063 | T | C | 9 | a0002c0002t0001g0060 a0002c0002t0001g0276 a0002c0002t0001g0292 others(6): Show |
11 | HG00544.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1222+980T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624063 | |||||||
| chr22:30624064 | A | ATG | 56 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(53): Show |
72 | HG00558.hp2 HG00609.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1222+982_1222+983i others(4): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624064 | ||||||
| chr22:30624064 | A | G | 3 | a0001c0001t0003g0093 a0001c0001t0003g0304 a0009c0009t0016g0109 |
3 | HG00323.hp1 NA19001.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1222+981A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624064 | |||||||
| chr22:30624068 | A | G | 6 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0021 others(3): Show |
11 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1222+985A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624068 | |||||||
| chr22:30624070 | A | G | 1 | a0001c0001t0006g0080 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1222+987A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624070 | |||||||
| chr22:30624076 | A | G | 1 | a0002c0002t0001g0003 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1222+993A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624076 | |||||||
| chr22:30624077 | TA | T | 3 | a0001c0001t0002g0032 a0001c0001t0002g0173 a0001c0001t0021g0153 |
4 | HG01981.hp2 NA18979.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222+995delA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624077 | |||||||
| chr22:30624078 | A | AT | 3 | a0001c0001t0002g0170 a0005c0005t0001g0082 a0011c0013t0011g0187 |
3 | HG00099.hp2 HG00423.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1222+996dupT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624078 | ||||||
| chr22:30624078 | A | T | 16 | a0001c0001t0001g0229 a0001c0014t0001g0227 a0002c0002t0001g0254 others(13): Show |
19 | HG00642.hp2 HG01192.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.1222+995A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624078 | |||||||
| chr22:30624080 | A | AT | 12 | a0001c0001t0002g0027 a0001c0001t0002g0113 a0001c0001t0002g0120 others(9): Show |
14 | HG01070.hp1 HG01106.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1222+1009dupT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624080 | ||||||
| chr22:30624080 | A | ATAT | 9 | a0001c0001t0002g0008 a0001c0001t0002g0133 a0001c0001t0002g0134 others(6): Show |
13 | HG00621.hp1 HG01261.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.1222+998_1222+999i others(5): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624080 | ||||||
| chr22:30624080 | A | ATATT | 8 | a0003c0003t0004g0044 a0003c0003t0004g0194 a0003c0003t0004g0200 others(5): Show |
9 | HG01256.hp1 HG01515.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1222+998_1222+999i others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624080 | ||||||
| chr22:30624080 | A | ATATTT | 11 | a0001c0001t0002g0038 a0001c0001t0002g0171 a0001c0001t0002g0185 others(8): Show |
16 | HG00673.hp1 HG00735.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1222+998_1222+999i others(7): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624080 | ||||||
| chr22:30624080 | A | ATT | 5 | a0001c0001t0002g0162 a0002c0002t0001g0053 a0004c0004t0005g0123 others(2): Show |
6 | HG02698.hp1 HG03579.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222+1008_1222+100 others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624080 | ||||||
| chr22:30624080 | A | ATTT | 31 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
49 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1222+1007_1222+100 others(7): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624080 | ||||||
| chr22:30624080 | A | ATTTT | 6 | a0001c0001t0001g0020 a0003c0003t0004g0043 a0003c0003t0004g0045 others(3): Show |
10 | HG00140.hp1 HG01496.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.1222+1006_1222+100 others(8): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624080 | ||||||
| chr22:30624080 | A | T | 59 | a0001c0001t0001g0229 a0001c0001t0002g0032 a0001c0001t0002g0170 others(56): Show |
82 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1222+997A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624080 | |||||||
| chr22:30624082 | T | A | 62 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(59): Show |
80 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1222+999T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624082 | |||||||
| chr22:30624084 | T | A | 21 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(18): Show |
31 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.1222+1001T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624084 | |||||||
| chr22:30624085 | T | A | 4 | a0010c0012t0001g0223 a0010c0012t0001g0224 a0010c0012t0001g0225 others(1): Show |
4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+1002T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624085 | |||||||
| chr22:30624103 | C | T | 70 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(67): Show |
91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1222+1020C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624103 | |||||||
| chr22:30624126 | G | A | 203 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(200): Show |
275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.1222+1043G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624126 | |||||||
| chr22:30624127 | T | C | 38 | a0001c0001t0001g0229 a0001c0014t0001g0227 a0001c0014t0001g0228 others(35): Show |
45 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.1222+1044T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624127 | |||||||
| chr22:30624165 | T | C | 203 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(200): Show |
275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.1222+1082T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624165 | |||||||
| chr22:30624293 | C | CA | 3 | a0005c0011t0001g0022 a0005c0011t0001g0077 a0005c0011t0001g0081 |
4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+1213dupA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624293 | ||||||
| chr22:30624354 | G | T | 40 | a0001c0001t0001g0020 a0001c0001t0001g0229 a0001c0014t0001g0227 others(37): Show |
48 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.1222+1271G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624354 | |||||||
| chr22:30624403 | C | T | 1 | a0005c0005t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1222+1320C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624403 | |||||||
| chr22:30624413 | T | C | 215 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0229 others(212): Show |
289 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1222+1330T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624413 | |||||||
| chr22:30624514 | C | A | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1431C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624514 | |||||||
| chr22:30624517 | A | C | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1434A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624517 | |||||||
| chr22:30624518 | G | T | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1435G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624518 | |||||||
| chr22:30624520 | G | A | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1437G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624520 | |||||||
| chr22:30624523 | C | A | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1440C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624523 | |||||||
| chr22:30624524 | C | G | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1441C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624524 | |||||||
| chr22:30624525 | C | A | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1442C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624525 | |||||||
| chr22:30624526 | A | G | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1443A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624526 | |||||||
| chr22:30624527 | C | G | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1444C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624527 | |||||||
| chr22:30624529 | A | G | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1446A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624529 | |||||||
| chr22:30624532 | A | G | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1449A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624532 | |||||||
| chr22:30624533 | A | G | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1450A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624533 | |||||||
| chr22:30624534 | G | T | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1451G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624534 | |||||||
| chr22:30624535 | C | G | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1452C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624535 | |||||||
| chr22:30624536 | A | ATTC | 70 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(67): Show |
91 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1222+1456_1222+145 others(7): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30624536 | ||||||
| chr22:30624542 | T | G | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1459T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624542 | |||||||
| chr22:30624544 | C | G | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1461C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624544 | |||||||
| chr22:30624547 | G | T | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1222+1464G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624547 | |||||||
| chr22:30624548 | C | T | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1222+1465C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624548 | |||||||
| chr22:30624550 | C | A | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1467C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624550 | |||||||
| chr22:30624556 | C | T | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1473C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624556 | |||||||
| chr22:30624561 | T | C | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1222+1478T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624561 | |||||||
| chr22:30624647 | C | T | 1 | a0005c0005t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1222+1564C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624647 | |||||||
| chr22:30624669 | C | A | 1 | a0002c0002t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1222+1586C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624669 | |||||||
| chr22:30624693 | A | G | 5 | a0005c0005t0002g0070 a0005c0005t0002g0072 a0005c0005t0002g0073 others(2): Show |
5 | HG00642.hp2 HG01192.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222+1610A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624693 | |||||||
| chr22:30624732 | C | T | 1 | a0004c0004t0005g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1222+1649C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624732 | |||||||
| chr22:30624783 | C | T | 3 | a0001c0001t0002g0027 a0001c0001t0002g0112 a0001c0001t0002g0113 |
4 | HG01070.hp1 HG02559.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1223-1677C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624783 | |||||||
| chr22:30624816 | A | G | 4 | a0010c0012t0001g0223 a0010c0012t0001g0224 a0010c0012t0001g0225 others(1): Show |
4 | HG02622.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1223-1644A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624816 | |||||||
| chr22:30624853 | T | C | 3 | a0005c0011t0001g0022 a0005c0011t0001g0077 a0005c0011t0001g0081 |
4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1223-1607T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624853 | |||||||
| chr22:30624857 | G | T | 1 | a0001c0001t0003g0111 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1223-1603G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624857 | |||||||
| chr22:30624915 | C | G | 1 | a0001c0001t0010g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1223-1545C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624915 | |||||||
| chr22:30624973 | T | C | 1 | a0005c0005t0002g0070 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1223-1487T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624973 | |||||||
| chr22:30624988 | A | C | 62 | a0001c0001t0001g0094 a0001c0001t0003g0007 a0001c0001t0003g0012 others(59): Show |
78 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1223-1472A>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30624988 | |||||||
| chr22:30625062 | C | G | 60 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(57): Show |
86 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1223-1398C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625062 | |||||||
| chr22:30625113 | G | A | 1 | a0003c0003t0004g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1223-1347G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625113 | |||||||
| chr22:30625223 | T | A | 5 | a0005c0005t0002g0070 a0005c0005t0002g0072 a0005c0005t0002g0073 others(2): Show |
5 | HG00642.hp2 HG01192.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1223-1237T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625223 | |||||||
| chr22:30625297 | C | T | 1 | a0003c0003t0004g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1223-1163C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625297 | |||||||
| chr22:30625315 | GGGGCCCA others(28): Show |
G | 1 | a0003c0003t0004g0203 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1223-1144_1223-111 others(39): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625315 | |||||||
| chr22:30625348 | GT | G | 14 | a0002c0002t0001g0003 a0002c0002t0001g0031 a0002c0002t0001g0128 others(11): Show |
16 | HG00597.hp2 HG02015.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.1223-1110delT | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30625348 | ||||||
| chr22:30625366 | G | A | 2 | a0002c0002t0001g0137 a0002c0002t0001g0139 |
2 | HG00735.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1223-1094G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625366 | |||||||
| chr22:30625378 | T | A | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0163 |
3 | HG02074.hp2 HG02083.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1223-1082T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625378 | |||||||
| chr22:30625402 | TA | T | 35 | a0003c0003t0004g0042 a0003c0003t0004g0043 a0003c0003t0004g0044 others(32): Show |
42 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1223-1046delA | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30625402 | ||||||
| chr22:30625402 | TAA | T | 234 | a0001c0001t0001g0020 a0001c0001t0001g0229 a0001c0001t0002g0004 others(231): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.1223-1047_1223-104 others(6): Show |
TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 30625402 | ||||||
| chr22:30625405 | A | T | 5 | a0005c0005t0001g0041 a0005c0005t0001g0191 a0005c0005t0011g0329 others(2): Show |
6 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1223-1055A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625405 | |||||||
| chr22:30625411 | A | T | 1 | a0007c0007t0007g0085 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1223-1049A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625411 | |||||||
| chr22:30625413 | A | T | 8 | a0003c0003t0004g0200 a0003c0003t0004g0201 a0007c0007t0004g0121 others(5): Show |
11 | HG01261.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1223-1047A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625413 | |||||||
| chr22:30625415 | T | A | 1 | a0001c0001t0010g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1223-1045T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625415 | |||||||
| chr22:30625425 | G | T | 60 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(57): Show |
86 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1223-1035G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625425 | |||||||
| chr22:30625469 | A | T | 1 | a0002c0002t0001g0147 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1223-991A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625469 | |||||||
| chr22:30625470 | T | A | 7 | a0001c0001t0001g0020 a0002c0002t0001g0272 a0002c0002t0001g0276 others(4): Show |
8 | HG01496.hp2 HG02056.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.1223-990T>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625470 | |||||||
| chr22:30625595 | T | G | 1 | a0003c0003t0004g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1223-865T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625595 | |||||||
| chr22:30625623 | C | A | 73 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(70): Show |
112 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1223-837C>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625623 | |||||||
| chr22:30625690 | C | T | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1223-770C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625690 | |||||||
| chr22:30625823 | C | G | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1223-637C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625823 | |||||||
| chr22:30625830 | C | G | 4 | a0009c0009t0003g0026 a0009c0009t0003g0106 a0009c0009t0003g0110 others(1): Show |
5 | HG00323.hp1 HG01175.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1223-630C>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30625830 | |||||||
| chr22:30626067 | A | T | 2 | a0001c0001t0002g0120 a0001c0001t0002g0157 |
2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1223-393A>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626067 | |||||||
| chr22:30626097 | T | G | 1 | a0001c0001t0002g0027 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1223-363T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626097 | |||||||
| chr22:30626108 | T | G | 60 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(57): Show |
86 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1223-352T>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626108 | |||||||
| chr22:30626166 | C | T | 1 | a0004c0004t0007g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1223-294C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626166 | |||||||
| chr22:30626213 | A | G | 1 | a0001c0001t0003g0104 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1223-247A>G | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626213 | |||||||
| chr22:30626254 | C | T | 1 | a0010c0012t0020g0226 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1223-206C>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626254 | |||||||
| chr22:30626275 | G | T | 5 | a0003c0003t0004g0204 a0003c0003t0004g0206 a0003c0003t0004g0207 others(2): Show |
5 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1223-185G>T | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626275 | |||||||
| chr22:30626285 | G | A | 202 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0002g0004 others(199): Show |
273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1223-175G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626285 | |||||||
| chr22:30626292 | T | C | 13 | a0004c0004t0001g0124 a0004c0004t0002g0029 a0004c0004t0005g0002 others(10): Show |
26 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1223-168T>C | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626292 | |||||||
| chr22:30626314 | G | A | 35 | a0003c0003t0004g0042 a0003c0003t0004g0043 a0003c0003t0004g0044 others(32): Show |
42 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1223-146G>A | TCN2 | ENSG00000185339.10 | transcript | ENST00000215838.8 | protein_coding | 8/8 | chr22 | 30626314 |