Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 94160 |
| ensemblid | ENSG00000140798.17 |
| hgncid | 14640 |
| symbol | ABCC12 |
| name | ATP binding cassette subfamily C member 12 |
| refseq_nuc | NM_001393797.1 |
| refseq_prot | NP_001380726.1 |
| ensembl_nuc | ENST00000311303.8 |
| ensembl_prot | ENSP00000311030.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 48080882 |
| end | 48155993 |
| strand | - |
| ver | v1.2 |
| region | chr16:48080882-48155993 |
| region5000 | chr16:48075882-48160993 |
| regionname0 | ABCC12_chr16_48080882_48155993 |
| regionname5000 | ABCC12_chr16_48075882_48160993 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1359 | 36 | 11 | 7 | 9 | 1 | 8 | 2 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0002 | 1/0 | 1359 | 26 | 13 | 4 | 4 | 1 | 3 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0003 | 0/0 | 1359 | 9 | 5 | 0 | 3 | 0 | 1 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0004 | 0/0 | 1359 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0005 | 0/0 | 82 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(77): Show |
chr16 | 48075882 | 48160993 |
| a0006 | 0/0 | 1359 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0007 | 0/0 | 1359 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0008 | 0/0 | 1359 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0009 | 0/0 | 1359 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0010 | 0/0 | 1359 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0011 | 0/1 | 1359 | 2 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0012 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0013 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0014 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0015 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0016 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0017 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0018 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0019 | 0/0 | 1023 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1018): Show |
chr16 | 48075882 | 48160993 |
| a0020 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0021 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0022 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0023 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| a0024 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | MVGEG others(1354): Show |
chr16 | 48075882 | 48160993 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4077 | 28 | 10 | 4 | 9 | 0 | 5 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0001c0004 | 0/0 | 4077 | 8 | 1 | 3 | 0 | 1 | 3 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0002c0002 | 1/0 | 4077 | 26 | 13 | 4 | 4 | 1 | 3 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0003c0003 | 0/0 | 4077 | 9 | 5 | 0 | 3 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0004c0007 | 0/0 | 4077 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0004c0013 | 0/0 | 4077 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0005c0010 | 0/0 | 4075 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4070): Show |
chr16 | 48075882 | 48160993 | ||
| a0005c0021 | 0/0 | 4075 | 2 | 1 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4070): Show |
chr16 | 48075882 | 48160993 | ||
| a0005c0029 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4070): Show |
chr16 | 48075882 | 48160993 | ||
| a0005c0030 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4070): Show |
chr16 | 48075882 | 48160993 | ||
| a0006c0005 | 0/0 | 4077 | 7 | 7 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0007c0006 | 0/0 | 4077 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0008c0009 | 0/0 | 4077 | 5 | 5 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0009c0008 | 0/0 | 4077 | 5 | 5 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0010c0018 | 0/0 | 4077 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0010c0026 | 0/0 | 4077 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0011c0019 | 0/1 | 4077 | 2 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0012c0016 | 0/0 | 4077 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0013c0017 | 0/0 | 4077 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0014c0012 | 0/0 | 4077 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0015c0020 | 0/0 | 4077 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0016c0015 | 0/0 | 4077 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0017c0011 | 0/0 | 4077 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0018c0014 | 0/0 | 4077 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0019c0027 | 0/0 | 4077 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0020c0022 | 0/0 | 4077 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0021c0024 | 0/0 | 4077 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0022c0023 | 0/0 | 4077 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0023c0025 | 0/0 | 4077 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 | ||
| a0024c0028 | 0/0 | 4077 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | ATGGT others(4072): Show |
chr16 | 48075882 | 48160993 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7385 | 27 | 10 | 4 | 9 | 0 | 4 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0001c0001t0013 | 0/0 | 7385 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0001c0004t0001 | 0/0 | 7385 | 7 | 1 | 2 | 0 | 1 | 3 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0001c0004t0017 | 0/0 | 7385 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0002c0002t0001 | 1/0 | 7385 | 24 | 12 | 4 | 3 | 1 | 3 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0002c0002t0019 | 0/0 | 7385 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0002c0002t0020 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0003c0003t0001 | 0/0 | 7385 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0003c0003t0004 | 0/0 | 7385 | 7 | 4 | 0 | 3 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0003c0003t0014 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0004c0007t0003 | 0/0 | 7385 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0004c0013t0003 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0005c0010t0002 | 0/0 | 7383 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7378): Show |
chr16 | 48075882 | 48160993 |
| a0005c0021t0002 | 0/0 | 7383 | 2 | 1 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7378): Show |
chr16 | 48075882 | 48160993 |
| a0005c0029t0018 | 0/0 | 7383 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7378): Show |
chr16 | 48075882 | 48160993 |
| a0005c0030t0001 | 0/0 | 7383 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7378): Show |
chr16 | 48075882 | 48160993 |
| a0006c0005t0001 | 0/0 | 7385 | 7 | 7 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0007c0006t0001 | 0/0 | 7385 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0008c0009t0001 | 0/0 | 7385 | 5 | 5 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0009c0008t0009 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0009c0008t0010 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0009c0008t0015 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0010c0018t0011 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0010c0026t0016 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0011c0019t0001 | 0/1 | 7385 | 2 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0012c0016t0005 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0013c0017t0002 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0014c0012t0007 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0015c0020t0005 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0016c0015t0008 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0017c0011t0006 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0018c0014t0001 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0019c0027t0001 | 0/0 | 7385 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0020c0022t0012 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0021c0024t0001 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0022c0023t0006 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0023c0025t0001 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| a0024c0028t0002 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | AGTTG others(7380): Show |
chr16 | 48075882 | 48160993 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0001t0013g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0004t0001g0010 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0004t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0004t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0004t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0001c0004t0017g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0019g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0002c0002t0020g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0003c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0003c0003t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0003c0003t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0003c0003t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0003c0003t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0003c0003t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0003c0003t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0003c0003t0014g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0004c0007t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0004c0007t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0004c0007t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0004c0007t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0004c0007t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0004c0007t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0004c0013t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0004c0013t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0005c0010t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0005c0010t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0005c0010t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0005c0021t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0005c0021t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0005c0029t0018g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0005c0030t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0006c0005t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0006c0005t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0006c0005t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0006c0005t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0006c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0006c0005t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0007c0006t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0007c0006t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0007c0006t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0007c0006t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0007c0006t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0008c0009t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0008c0009t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0008c0009t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0008c0009t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0009c0008t0009g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0009c0008t0010g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0009c0008t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0009c0008t0015g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0010c0018t0011g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0010c0018t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0010c0026t0016g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0011c0019t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0011c0019t0001g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0012c0016t0005g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0013c0017t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0013c0017t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0014c0012t0007g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0015c0020t0005g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0016c0015t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0016c0015t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0017c0011t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0017c0011t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0018c0014t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0018c0014t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0019c0027t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0020c0022t0012g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0021c0024t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0022c0023t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0023c0025t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| a0024c0028t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | CHS | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG00558 | hp1 | a0003 | c0003 | t0004 | g0045 | EAS | CHS | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | CHS | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG00741 | hp1 | a0011 | c0019 | t0001 | g0072 | AMR | PUR | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG00741 | hp2 | a0001 | c0004 | t0001 | g0081 | AMR | PUR | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG01074 | hp2 | a0001 | c0004 | t0001 | g0098 | AMR | PUR | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | CLM | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG01256 | hp1 | a0019 | c0027 | t0001 | g0059 | AMR | CLM | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG01496 | hp2 | a0005 | c0021 | t0002 | g0026 | AMR | CLM | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG01517 | hp1 | a0001 | c0004 | t0001 | g0010 | EUR | IBS | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0006 | EUR | IBS | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG01884 | hp1 | a0012 | c0016 | t0005 | g0004 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0060 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG01891 | hp1 | a0013 | c0017 | t0002 | g0109 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG01891 | hp2 | a0004 | c0007 | t0003 | g0103 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02040 | hp1 | a0003 | c0003 | t0004 | g0061 | EAS | KHV | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02055 | hp2 | a0004 | c0013 | t0003 | g0108 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | KHV | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02083 | hp1 | a0002 | c0002 | t0019 | g0050 | EAS | KHV | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02129 | hp2 | a0003 | c0003 | t0004 | g0062 | EAS | KHV | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02257 | hp1 | a0007 | c0006 | t0001 | g0011 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02258 | hp1 | a0006 | c0005 | t0001 | g0042 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02258 | hp2 | a0004 | c0007 | t0003 | g0102 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02280 | hp1 | a0020 | c0022 | t0012 | g0028 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02572 | hp1 | a0014 | c0012 | t0007 | g0012 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02572 | hp2 | a0015 | c0020 | t0005 | g0007 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02602 | hp1 | a0001 | c0004 | t0001 | g0099 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0058 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02615 | hp1 | a0016 | c0015 | t0008 | g0041 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0055 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0044 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02622 | hp2 | a0005 | c0021 | t0002 | g0025 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02630 | hp1 | a0008 | c0009 | t0001 | g0020 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02630 | hp2 | a0021 | c0024 | t0001 | g0092 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02647 | hp1 | a0005 | c0010 | t0002 | g0027 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02647 | hp2 | a0006 | c0005 | t0001 | g0064 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0095 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02717 | hp1 | a0007 | c0006 | t0001 | g0090 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02717 | hp2 | a0022 | c0023 | t0006 | g0037 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02723 | hp1 | a0010 | c0018 | t0011 | g0021 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02723 | hp2 | a0005 | c0010 | t0002 | g0024 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02809 | hp2 | a0008 | c0009 | t0001 | g0018 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02895 | hp1 | a0009 | c0008 | t0010 | g0014 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02895 | hp2 | a0015 | c0020 | t0005 | g0007 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02896 | hp1 | a0005 | c0029 | t0018 | g0029 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02896 | hp2 | a0006 | c0005 | t0001 | g0065 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02897 | hp1 | a0006 | c0005 | t0001 | g0031 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02897 | hp2 | a0009 | c0008 | t0010 | g0015 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02922 | hp1 | a0006 | c0005 | t0001 | g0009 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02965 | hp1 | a0013 | c0017 | t0002 | g0111 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02965 | hp2 | a0003 | c0003 | t0004 | g0008 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02970 | hp1 | a0023 | c0025 | t0001 | g0110 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02970 | hp2 | a0009 | c0008 | t0009 | g0005 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03017 | hp1 | a0003 | c0003 | t0001 | g0088 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03041 | hp1 | a0017 | c0011 | t0006 | g0117 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03098 | hp1 | a0004 | c0007 | t0003 | g0101 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03098 | hp2 | a0002 | c0002 | t0020 | g0063 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03130 | hp1 | a0008 | c0009 | t0001 | g0003 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03130 | hp2 | a0004 | c0007 | t0003 | g0116 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03139 | hp2 | a0005 | c0010 | t0002 | g0023 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03195 | hp1 | a0018 | c0014 | t0001 | g0106 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03195 | hp2 | a0003 | c0003 | t0004 | g0085 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03209 | hp1 | a0003 | c0003 | t0014 | g0068 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03209 | hp2 | a0009 | c0008 | t0015 | g0016 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03225 | hp1 | a0018 | c0014 | t0001 | g0107 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03225 | hp2 | a0006 | c0005 | t0001 | g0009 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03453 | hp1 | a0024 | c0028 | t0002 | g0017 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03453 | hp2 | a0009 | c0008 | t0009 | g0005 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03486 | hp1 | a0007 | c0006 | t0001 | g0091 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03486 | hp2 | a0016 | c0015 | t0008 | g0112 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03516 | hp1 | a0003 | c0003 | t0004 | g0008 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03516 | hp2 | a0006 | c0005 | t0001 | g0066 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03540 | hp2 | a0007 | c0006 | t0001 | g0011 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03579 | hp1 | a0017 | c0011 | t0006 | g0115 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03579 | hp2 | a0003 | c0003 | t0004 | g0100 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03704 | hp2 | a0001 | c0004 | t0001 | g0035 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03710 | hp2 | a0001 | c0004 | t0001 | g0083 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0097 | SAS | STU | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG04115 | hp2 | a0001 | c0001 | t0013 | g0078 | SAS | STU | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| NA18522 | hp1 | a0010 | c0026 | t0016 | g0084 | AFR | YRI | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0034 | AFR | YRI | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| NA18906 | hp2 | a0004 | c0013 | t0003 | g0114 | AFR | YRI | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0040 | AFR | LWK | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| NA19030 | hp2 | a0007 | c0006 | t0001 | g0093 | AFR | LWK | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| NA20129 | hp1 | a0012 | c0016 | t0005 | g0004 | AFR | ASW | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG01123 | hp1 | a0001 | c0004 | t0017 | g0118 | AMR | CLM | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0048 | AMR | CLM | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02109 | hp1 | a0004 | c0007 | t0003 | g0104 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02109 | hp2 | a0008 | c0009 | t0001 | g0019 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02486 | hp2 | a0014 | c0012 | t0007 | g0012 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG02559 | hp2 | a0004 | c0007 | t0003 | g0105 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG03471 | hp2 | a0010 | c0018 | t0011 | g0039 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG06807 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | USA | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0056 | AFR | USA | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| NA20300 | hp1 | a0008 | c0009 | t0001 | g0003 | AFR | USA | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| NA20300 | hp2 | a0005 | c0030 | t0001 | g0119 | AFR | USA | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| NA21309 | hp2 | a0007 | c0006 | t0001 | g0094 | AFR | LWK | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| homoSapiens | chm13v2 | a0011 | c0019 | t0001 | g0079 | REF | REF | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0057 | REF | REF | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48087989 | T | G | 3 | a0005 a0020 a0024 |
7 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
missense_variant | MODERATE | c.3572A>C | p.Glu1191Ala | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/31 | 4044/7385 | 3572/4080 | 1191/1359 | chr16 | 48087989 | |||
| chr16:48088001 | A | G | 7 | a0004 a0005 a0010 others(4): Show |
20 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
missense_variant | MODERATE | c.3560T>C | p.Ile1187Thr | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/31 | 4032/7385 | 3560/4080 | 1187/1359 | chr16 | 48088001 | |||
| chr16:48088076 | G | A | 1 | a0014 | 2 | HG02486.hp2 HG02572.hp1 |
missense_variant | MODERATE | c.3485C>T | p.Ser1162Leu | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/31 | 3957/7385 | 3485/4080 | 1162/1359 | chr16 | 48088076 | |||
| chr16:48088545 | C | T | 3 | a0012 a0015 a0016 |
6 | HG01884.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
missense_variant&splice_region_variant | MODERATE | c.3475G>A | p.Gly1159Arg | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 26/31 | 3947/7385 | 3475/4080 | 1159/1359 | chr16 | 48088545 | |||
| chr16:48088671 | G | A | 4 | a0001 a0005 a0011 others(1): Show |
39 | HG00544.hp1 HG00735.hp1 HG00741.hp1 others(36): Show |
missense_variant | MODERATE | c.3349C>T | p.Arg1117Cys | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 26/31 | 3821/7385 | 3349/4080 | 1117/1359 | chr16 | 48088671 | |||
| chr16:48088694 | G | T | 1 | a0023 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.3326C>A | p.Thr1109Asn | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 26/31 | 3798/7385 | 3326/4080 | 1109/1359 | chr16 | 48088694 | |||
| chr16:48096870 | C | T | 1 | a0019 | 1 | HG01256.hp1 | stop_gained | HIGH | c.3071G>A | p.Trp1024* | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/31 | 3543/7385 | 3071/4080 | 1024/1359 | chr16 | 48096870 | |||
| chr16:48100873 | A | G | 12 | a0004 a0005 a0009 others(9): Show |
36 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(33): Show |
missense_variant&splice_region_variant | MODERATE | c.3037T>C | p.Tyr1013His | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/31 | 3509/7385 | 3037/4080 | 1013/1359 | chr16 | 48100873 | |||
| chr16:48100912 | T | C | 2 | a0005 a0024 |
3 | HG01496.hp2 HG02622.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.2998A>G | p.Ile1000Val | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/31 | 3470/7385 | 2998/4080 | 1000/1359 | chr16 | 48100912 | |||
| chr16:48100945 | T | A | 12 | a0004 a0005 a0009 others(9): Show |
36 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(33): Show |
missense_variant | MODERATE | c.2965A>T | p.Thr989Ser | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/31 | 3437/7385 | 2965/4080 | 989/1359 | chr16 | 48100945 | |||
| chr16:48104361 | T | A | 1 | a0006 | 7 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
missense_variant | MODERATE | c.2681A>T | p.Lys894Met | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/31 | 3153/7385 | 2681/4080 | 894/1359 | chr16 | 48104361 | |||
| chr16:48105152 | G | A | 1 | a0012 | 2 | HG01884.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.2660C>T | p.Thr887Met | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 21/31 | 3132/7385 | 2660/4080 | 887/1359 | chr16 | 48105152 | |||
| chr16:48105263 | A | G | 1 | a0011 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.2549T>C | p.Val850Ala | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 21/31 | 3021/7385 | 2549/4080 | 850/1359 | chr16 | 48105263 | |||
| chr16:48111793 | G | A | 1 | a0005 | 1 | NA20300.hp2 | stop_gained | HIGH | c.2107C>T | p.Arg703* | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 16/31 | 2579/7385 | 2107/4080 | 703/1359 | chr16 | 48111793 | |||
| chr16:48111831 | T | A | 2 | a0003 a0008 |
14 | HG00558.hp1 HG02040.hp1 HG02109.hp2 others(11): Show |
missense_variant | MODERATE | c.2069A>T | p.Glu690Val | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 16/31 | 2541/7385 | 2069/4080 | 690/1359 | chr16 | 48111831 | |||
| chr16:48115458 | G | A | 2 | a0013 a0023 |
3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
missense_variant | MODERATE | c.1946C>T | p.Thr649Met | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/31 | 2418/7385 | 1946/4080 | 649/1359 | chr16 | 48115458 | |||
| chr16:48117287 | T | A | 7 | a0007 a0012 a0014 others(4): Show |
16 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
missense_variant | MODERATE | c.1759A>T | p.Asn587Tyr | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/31 | 2231/7385 | 1759/4080 | 587/1359 | chr16 | 48117287 | |||
| chr16:48139215 | C | A | 2 | a0013 a0023 |
3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
missense_variant | MODERATE | c.779G>T | p.Gly260Val | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 7/31 | 1251/7385 | 779/4080 | 260/1359 | chr16 | 48139215 | |||
| chr16:48141324 | G | T | 16 | a0004 a0005 a0007 others(13): Show |
48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
missense_variant | MODERATE | c.305C>A | p.Ala102Glu | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 5/31 | 777/7385 | 305/4080 | 102/1359 | chr16 | 48141324 | |||
| chr16:48143965 | C | T | 1 | a0017 | 2 | HG03041.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.220G>A | p.Val74Ile | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/31 | 692/7385 | 220/4080 | 74/1359 | chr16 | 48143965 | |||
| chr16:48143986 | CTT | C | 1 | a0005 | 7 | HG01496.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
frameshift_variant | HIGH | c.197_198delAA | p.Lys66fs | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/31 | 670/7385 | 197/4080 | 66/1359 | chr16 | 48143986 | |||
| chr16:48146349 | C | T | 3 | a0014 a0017 a0020 |
5 | HG02280.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
missense_variant | MODERATE | c.76G>A | p.Asp26Asn | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/31 | 548/7385 | 76/4080 | 26/1359 | chr16 | 48146349 | |||
| chr16:48146400 | T | G | 4 | a0005 a0008 a0009 others(1): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
missense_variant | MODERATE | c.25A>C | p.Ile9Leu | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/31 | 497/7385 | 25/4080 | 9/1359 | chr16 | 48146400 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48083763 | C | T | 1 | a0009c0008 | 5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
synonymous_variant | LOW | c.4032G>A | p.Lys1344Lys | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 4504/7385 | 4032/4080 | 1344/1359 | chr16 | 48083763 | |||
| chr16:48086786 | A | G | 16 | a0004c0007 a0004c0013 a0005c0010 others(13): Show |
35 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(32): Show |
synonymous_variant | LOW | c.3669T>C | p.Asp1223Asp | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 28/31 | 4141/7385 | 3669/4080 | 1223/1359 | chr16 | 48086786 | |||
| chr16:48104348 | A | G | 17 | a0004c0007 a0004c0013 a0005c0010 others(14): Show |
36 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(33): Show |
synonymous_variant | LOW | c.2694T>C | p.Ser898Ser | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/31 | 3166/7385 | 2694/4080 | 898/1359 | chr16 | 48104348 | |||
| chr16:48115556 | A | G | 10 | a0004c0007 a0007c0006 a0009c0008 others(7): Show |
29 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(26): Show |
synonymous_variant | LOW | c.1848T>C | p.Ala616Ala | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/31 | 2320/7385 | 1848/4080 | 616/1359 | chr16 | 48115556 | |||
| chr16:48130866 | T | C | 1 | a0001c0004 | 8 | HG00741.hp2 HG01074.hp2 HG01123.hp1 others(5): Show |
synonymous_variant | LOW | c.1158A>G | p.Val386Val | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/31 | 1630/7385 | 1158/4080 | 386/1359 | chr16 | 48130866 | |||
| chr16:48138274 | C | A | 1 | a0004c0007 | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
synonymous_variant | LOW | c.933G>T | p.Leu311Leu | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/31 | 1405/7385 | 933/4080 | 311/1359 | chr16 | 48138274 | |||
| chr16:48140828 | G | T | 1 | a0010c0018 | 2 | HG02723.hp1 HG03471.hp2 |
synonymous_variant | LOW | c.516C>A | p.Thr172Thr | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/31 | 988/7385 | 516/4080 | 172/1359 | chr16 | 48140828 | |||
| chr16:48140855 | A | G | 7 | a0005c0010 a0005c0021 a0005c0029 others(4): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
synonymous_variant | LOW | c.489T>C | p.Ile163Ile | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/31 | 961/7385 | 489/4080 | 163/1359 | chr16 | 48140855 | |||
| chr16:48144023 | G | A | 4 | a0004c0007 a0014c0012 a0017c0011 others(1): Show |
11 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
synonymous_variant | LOW | c.162C>T | p.Phe54Phe | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/31 | 634/7385 | 162/4080 | 54/1359 | chr16 | 48144023 | |||
| chr16:48146356 | T | C | 7 | a0005c0010 a0005c0021 a0005c0029 others(4): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
synonymous_variant | LOW | c.69A>G | p.Glu23Glu | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/31 | 541/7385 | 69/4080 | 23/1359 | chr16 | 48146356 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48080939 | G | A | 1 | a0003c0003t0004 | 7 | HG00558.hp1 HG02040.hp1 HG02129.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2776C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2776 | chr16 | 48080939 | ||||||
| chr16:48081090 | T | C | 19 | a0004c0007t0003 a0004c0013t0003 a0005c0010t0002 others(16): Show |
37 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2625A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2625 | chr16 | 48081090 | ||||||
| chr16:48081255 | T | C | 1 | a0020c0022t0012 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2460A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2460 | chr16 | 48081255 | ||||||
| chr16:48081326 | G | A | 3 | a0009c0008t0009 a0009c0008t0010 a0009c0008t0015 |
5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2389C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2389 | chr16 | 48081326 | ||||||
| chr16:48081434 | T | C | 1 | a0016c0015t0008 | 2 | HG02615.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2281A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2281 | chr16 | 48081434 | ||||||
| chr16:48081509 | C | A | 3 | a0009c0008t0009 a0009c0008t0010 a0009c0008t0015 |
5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2206G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2206 | chr16 | 48081509 | ||||||
| chr16:48081579 | T | A | 2 | a0004c0007t0003 a0004c0013t0003 |
8 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2136A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2136 | chr16 | 48081579 | ||||||
| chr16:48081660 | C | T | 1 | a0010c0018t0011 | 2 | HG02723.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2055G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2055 | chr16 | 48081660 | ||||||
| chr16:48081670 | G | A | 2 | a0005c0029t0018 a0010c0018t0011 |
3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2045C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2045 | chr16 | 48081670 | ||||||
| chr16:48081879 | T | C | 1 | a0009c0008t0010 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1836A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 1836 | chr16 | 48081879 | ||||||
| chr16:48082448 | G | A | 1 | a0010c0026t0016 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1267C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 1267 | chr16 | 48082448 | ||||||
| chr16:48082498 | C | T | 2 | a0017c0011t0006 a0022c0023t0006 |
3 | HG02717.hp2 HG03041.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1217G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 1217 | chr16 | 48082498 | ||||||
| chr16:48082716 | C | T | 1 | a0001c0004t0017 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*999G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 999 | chr16 | 48082716 | ||||||
| chr16:48082852 | T | C | 3 | a0012c0016t0005 a0015c0020t0005 a0016c0015t0008 |
6 | HG01884.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*863A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 863 | chr16 | 48082852 | ||||||
| chr16:48082854 | A | G | 4 | a0009c0008t0009 a0009c0008t0010 a0009c0008t0015 others(1): Show |
6 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*861T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 861 | chr16 | 48082854 | ||||||
| chr16:48083065 | C | T | 2 | a0003c0003t0004 a0003c0003t0014 |
8 | HG00558.hp1 HG02040.hp1 HG02129.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*650G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 650 | chr16 | 48083065 | ||||||
| chr16:48083178 | A | T | 2 | a0001c0001t0013 a0009c0008t0009 |
3 | HG02970.hp2 HG03453.hp2 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*537T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 537 | chr16 | 48083178 | ||||||
| chr16:48083185 | T | A | 1 | a0002c0002t0019 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*530A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 530 | chr16 | 48083185 | ||||||
| chr16:48083269 | G | A | 1 | a0002c0002t0020 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*446C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 446 | chr16 | 48083269 | ||||||
| chr16:48083503 | C | T | 4 | a0012c0016t0005 a0014c0012t0007 a0015c0020t0005 others(1): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*212G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 212 | chr16 | 48083503 | ||||||
| chr16:48083505 | G | A | 2 | a0004c0007t0003 a0004c0013t0003 |
8 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*210C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 210 | chr16 | 48083505 | ||||||
| chr16:48083712 | C | T | 1 | a0020c0022t0012 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 3 | chr16 | 48083712 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48084131 | C | T | 23 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(20): Show |
26 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.3829-58G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48084131 | |||||||
| chr16:48084232 | C | T | 1 | a0003c0003t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3829-159G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48084232 | |||||||
| chr16:48084300 | T | C | 1 | a0010c0026t0016g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3829-227A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48084300 | |||||||
| chr16:48084437 | TA | T | 14 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(11): Show |
17 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.3829-365delT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48084437 | |||||||
| chr16:48084456 | A | G | 17 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(14): Show |
20 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.3829-383T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48084456 | |||||||
| chr16:48084948 | G | A | 3 | a0017c0011t0006g0115 a0017c0011t0006g0117 a0022c0023t0006g0037 |
3 | HG02717.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3828+645C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48084948 | |||||||
| chr16:48084991 | A | T | 2 | a0009c0008t0010g0014 a0009c0008t0010g0015 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3828+602T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48084991 | |||||||
| chr16:48085177 | G | A | 4 | a0009c0008t0009g0005 a0009c0008t0010g0014 a0009c0008t0010g0015 others(1): Show |
5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3828+416C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48085177 | |||||||
| chr16:48085185 | T | C | 8 | a0005c0029t0018g0029 a0010c0018t0011g0021 a0010c0018t0011g0039 others(5): Show |
11 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.3828+408A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48085185 | |||||||
| chr16:48085214 | A | G | 8 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(5): Show |
8 | HG00544.hp2 HG00735.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.3828+379T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48085214 | |||||||
| chr16:48085363 | G | A | 3 | a0005c0029t0018g0029 a0010c0018t0011g0021 a0010c0018t0011g0039 |
3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3828+230C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48085363 | |||||||
| chr16:48085374 | A | C | 17 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(14): Show |
20 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.3828+219T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48085374 | |||||||
| chr16:48085396 | G | A | 6 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(3): Show |
6 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.3828+197C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48085396 | |||||||
| chr16:48085514 | C | T | 6 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(3): Show |
6 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.3828+79G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48085514 | |||||||
| chr16:48086003 | A | G | 24 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(21): Show |
27 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.3715-297T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 28/30 | chr16 | 48086003 | |||||||
| chr16:48086057 | T | G | 1 | a0007c0006t0001g0093 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3715-351A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 28/30 | chr16 | 48086057 | |||||||
| chr16:48086253 | G | A | 3 | a0005c0029t0018g0029 a0010c0018t0011g0021 a0010c0018t0011g0039 |
3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3714+488C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 28/30 | chr16 | 48086253 | |||||||
| chr16:48086525 | T | A | 2 | a0005c0010t0002g0023 a0005c0010t0002g0024 |
2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3714+216A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 28/30 | chr16 | 48086525 | |||||||
| chr16:48086615 | C | T | 1 | a0001c0004t0001g0083 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3714+126G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 28/30 | chr16 | 48086615 | |||||||
| chr16:48086671 | A | T | 1 | a0002c0002t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3714+70T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 28/30 | chr16 | 48086671 | |||||||
| chr16:48086875 | G | T | 3 | a0005c0029t0018g0029 a0010c0018t0011g0021 a0010c0018t0011g0039 |
3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3636-56C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/30 | chr16 | 48086875 | |||||||
| chr16:48087182 | T | C | 15 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(12): Show |
18 | HG01496.hp2 HG01884.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.3636-363A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/30 | chr16 | 48087182 | |||||||
| chr16:48087538 | C | T | 31 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(28): Show |
35 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.3635+388G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/30 | chr16 | 48087538 | |||||||
| chr16:48087722 | T | C | 8 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3635+204A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/30 | chr16 | 48087722 | |||||||
| chr16:48087757 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3635+169C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/30 | chr16 | 48087757 | |||||||
| chr16:48087794 | C | T | 8 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3635+132G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/30 | chr16 | 48087794 | |||||||
| chr16:48087796 | C | G | 1 | a0008c0009t0001g0018 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3635+130G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/30 | chr16 | 48087796 | |||||||
| chr16:48088116 | C | G | 2 | a0009c0008t0010g0014 a0009c0008t0010g0015 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3476-31G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 26/30 | chr16 | 48088116 | |||||||
| chr16:48088538 | T | C | 8 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.3475+7A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 26/30 | chr16 | 48088538 | |||||||
| chr16:48088990 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3286-256C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48088990 | |||||||
| chr16:48089009 | T | C | 12 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3286-275A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48089009 | |||||||
| chr16:48089109 | G | A | 4 | a0009c0008t0009g0005 a0009c0008t0010g0014 a0009c0008t0010g0015 others(1): Show |
5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3286-375C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48089109 | |||||||
| chr16:48089414 | A | C | 7 | a0009c0008t0009g0005 a0009c0008t0010g0014 a0009c0008t0010g0015 others(4): Show |
8 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.3286-680T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48089414 | |||||||
| chr16:48089668 | A | T | 1 | a0004c0013t0003g0114 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3286-934T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48089668 | |||||||
| chr16:48089945 | T | G | 3 | a0005c0029t0018g0029 a0010c0018t0011g0021 a0010c0018t0011g0039 |
3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3285+1175A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48089945 | |||||||
| chr16:48089956 | CAAG | C | 8 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3285+1161_3285+116 others(7): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48089956 | |||||||
| chr16:48089994 | T | TA | 17 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(14): Show |
20 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.3285+1125dupT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48089994 | |||||||
| chr16:48090079 | T | C | 1 | a0023c0025t0001g0110 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3285+1041A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48090079 | |||||||
| chr16:48090278 | A | C | 1 | a0023c0025t0001g0110 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3285+842T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48090278 | |||||||
| chr16:48090401 | C | CT | 9 | a0001c0001t0013g0078 a0002c0002t0020g0063 a0005c0029t0018g0029 others(6): Show |
10 | HG02723.hp1 HG02895.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.3285+718dupA | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48090401 | |||||||
| chr16:48090401 | CT | C | 18 | a0003c0003t0004g0061 a0003c0003t0004g0062 a0004c0007t0003g0101 others(15): Show |
21 | HG01884.hp1 HG01891.hp2 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.3285+718delA | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48090401 | |||||||
| chr16:48090655 | C | T | 5 | a0012c0016t0005g0004 a0014c0012t0007g0012 a0015c0020t0005g0007 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3285+465G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48090655 | |||||||
| chr16:48091395 | C | A | 4 | a0009c0008t0009g0005 a0009c0008t0010g0014 a0009c0008t0010g0015 others(1): Show |
5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3196-186G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48091395 | |||||||
| chr16:48091677 | T | C | 1 | a0016c0015t0008g0041 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3196-468A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48091677 | |||||||
| chr16:48091885 | T | C | 8 | a0005c0029t0018g0029 a0010c0018t0011g0021 a0010c0018t0011g0039 others(5): Show |
11 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.3196-676A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48091885 | |||||||
| chr16:48091897 | C | T | 29 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(26): Show |
33 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.3196-688G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48091897 | |||||||
| chr16:48092239 | C | T | 1 | a0005c0021t0002g0026 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3196-1030G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092239 | |||||||
| chr16:48092240 | G | A | 3 | a0005c0029t0018g0029 a0010c0018t0011g0021 a0010c0018t0011g0039 |
3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3196-1031C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092240 | |||||||
| chr16:48092277 | G | C | 3 | a0002c0002t0001g0055 a0002c0002t0001g0056 a0002c0002t0001g0060 |
3 | HG01884.hp2 HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3196-1068C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092277 | |||||||
| chr16:48092313 | C | T | 26 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(23): Show |
30 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.3196-1104G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092313 | |||||||
| chr16:48092348 | C | T | 1 | a0002c0002t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3196-1139G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092348 | |||||||
| chr16:48092493 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3196-1284G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092493 | |||||||
| chr16:48092621 | G | T | 4 | a0009c0008t0009g0005 a0009c0008t0010g0014 a0009c0008t0010g0015 others(1): Show |
5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3196-1412C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092621 | |||||||
| chr16:48092764 | G | A | 8 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3196-1555C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092764 | |||||||
| chr16:48092924 | C | T | 3 | a0005c0029t0018g0029 a0010c0018t0011g0021 a0010c0018t0011g0039 |
3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3196-1715G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092924 | |||||||
| chr16:48093369 | T | C | 1 | a0002c0002t0001g0046 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3196-2160A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48093369 | |||||||
| chr16:48093497 | C | T | 1 | a0005c0010t0002g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3196-2288G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48093497 | |||||||
| chr16:48094070 | T | C | 7 | a0002c0002t0001g0040 a0006c0005t0001g0009 a0006c0005t0001g0031 others(4): Show |
8 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.3195+2676A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48094070 | |||||||
| chr16:48094710 | GA | G | 5 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(2): Show |
5 | HG01496.hp2 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3195+2035delT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48094710 | |||||||
| chr16:48094764 | C | T | 5 | a0012c0016t0005g0004 a0014c0012t0007g0012 a0015c0020t0005g0007 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3195+1982G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48094764 | |||||||
| chr16:48094793 | A | G | 9 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.3195+1953T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48094793 | |||||||
| chr16:48095177 | G | A | 1 | a0020c0022t0012g0028 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3195+1569C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48095177 | |||||||
| chr16:48095252 | T | C | 5 | a0012c0016t0005g0004 a0014c0012t0007g0012 a0015c0020t0005g0007 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3195+1494A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48095252 | |||||||
| chr16:48095290 | A | C | 1 | a0001c0004t0001g0081 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3195+1456T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48095290 | |||||||
| chr16:48095341 | GC | G | 20 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(17): Show |
25 | HG01496.hp2 HG01884.hp1 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.3195+1404delG | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48095341 | |||||||
| chr16:48095485 | TA | T | 8 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0052 others(5): Show |
8 | HG00544.hp1 HG00544.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.3195+1260delT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48095485 | |||||||
| chr16:48096391 | A | C | 1 | a0002c0002t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3195+355T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48096391 | |||||||
| chr16:48096913 | C | T | 4 | a0012c0016t0005g0004 a0015c0020t0005g0007 a0016c0015t0008g0041 others(1): Show |
6 | HG01884.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3039-11G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48096913 | |||||||
| chr16:48096923 | C | T | 3 | a0002c0002t0001g0055 a0002c0002t0001g0056 a0002c0002t0001g0060 |
3 | HG01884.hp2 HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3039-21G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48096923 | |||||||
| chr16:48097184 | C | T | 1 | a0003c0003t0004g0045 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3039-282G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48097184 | |||||||
| chr16:48097520 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3039-618C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48097520 | |||||||
| chr16:48097559 | C | T | 5 | a0012c0016t0005g0004 a0014c0012t0007g0012 a0015c0020t0005g0007 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3039-657G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48097559 | |||||||
| chr16:48097818 | G | A | 5 | a0012c0016t0005g0004 a0014c0012t0007g0012 a0015c0020t0005g0007 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3039-916C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48097818 | |||||||
| chr16:48097828 | T | A | 9 | a0007c0006t0001g0011 a0007c0006t0001g0090 a0007c0006t0001g0091 others(6): Show |
11 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.3039-926A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48097828 | |||||||
| chr16:48097930 | G | C | 3 | a0005c0029t0018g0029 a0010c0018t0011g0021 a0010c0018t0011g0039 |
3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3039-1028C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48097930 | |||||||
| chr16:48097945 | G | A | 1 | a0001c0004t0017g0118 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3039-1043C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48097945 | |||||||
| chr16:48098017 | A | T | 3 | a0005c0029t0018g0029 a0010c0018t0011g0021 a0010c0018t0011g0039 |
3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3039-1115T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098017 | |||||||
| chr16:48098090 | G | GAC | 19 | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0004t0001g0081 others(16): Show |
20 | HG00558.hp1 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.3039-1190_3039-118 others(6): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098090 | |||||||
| chr16:48098090 | G | GACACAC | 3 | a0013c0017t0002g0109 a0013c0017t0002g0111 a0014c0012t0007g0012 |
4 | HG01891.hp1 HG02486.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.3039-1194_3039-118 others(10): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098090 | |||||||
| chr16:48098090 | GAC | G | 21 | a0001c0001t0001g0067 a0001c0001t0001g0096 a0002c0002t0001g0002 others(18): Show |
24 | HG00735.hp2 HG01496.hp2 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.3039-1190_3039-118 others(6): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098090 | |||||||
| chr16:48098090 | GACAC | G | 11 | a0001c0001t0001g0052 a0001c0001t0001g0074 a0001c0001t0001g0077 others(8): Show |
11 | HG00544.hp1 HG00544.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.3039-1192_3039-118 others(8): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098090 | |||||||
| chr16:48098090 | GACACAC | G | 3 | a0001c0001t0001g0032 a0009c0008t0010g0014 a0009c0008t0010g0015 |
3 | HG02895.hp1 HG02897.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3039-1194_3039-118 others(10): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098090 | |||||||
| chr16:48098090 | GACACACA others(3): Show |
G | 1 | a0004c0007t0003g0104 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3039-1198_3039-118 others(14): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098090 | |||||||
| chr16:48098130 | CACACACA others(3): Show |
C | 1 | a0016c0015t0008g0112 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3039-1238_3039-122 others(14): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098130 | |||||||
| chr16:48098134 | CACACAG | C | 1 | a0015c0020t0005g0007 | 2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.3039-1238_3039-123 others(10): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098134 | |||||||
| chr16:48098140 | G | C | 5 | a0005c0029t0018g0029 a0010c0018t0011g0021 a0010c0018t0011g0039 others(2): Show |
7 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3039-1238C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098140 | |||||||
| chr16:48098494 | C | G | 1 | a0001c0004t0001g0035 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3039-1592G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098494 | |||||||
| chr16:48098538 | CA | C | 2 | a0003c0003t0004g0061 a0003c0003t0004g0062 |
2 | HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.3039-1637delT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098538 | |||||||
| chr16:48098936 | C | T | 13 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(10): Show |
14 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.3038+1936G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098936 | |||||||
| chr16:48098960 | T | A | 5 | a0012c0016t0005g0004 a0014c0012t0007g0012 a0015c0020t0005g0007 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3038+1912A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098960 | |||||||
| chr16:48099008 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3038+1864C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48099008 | |||||||
| chr16:48099305 | G | A | 1 | a0010c0026t0016g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3038+1567C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48099305 | |||||||
| chr16:48099464 | T | G | 1 | a0001c0004t0001g0035 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3038+1408A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48099464 | |||||||
| chr16:48099831 | C | A | 1 | a0002c0002t0001g0048 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3038+1041G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48099831 | |||||||
| chr16:48099962 | C | CT | 13 | a0004c0007t0003g0104 a0004c0007t0003g0105 a0004c0013t0003g0108 others(10): Show |
16 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3038+909dupA | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48099962 | |||||||
| chr16:48100148 | T | C | 5 | a0012c0016t0005g0004 a0014c0012t0007g0012 a0015c0020t0005g0007 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3038+724A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48100148 | |||||||
| chr16:48100351 | G | T | 6 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(3): Show |
6 | HG01496.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3038+521C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48100351 | |||||||
| chr16:48100496 | A | T | 1 | a0002c0002t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3038+376T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48100496 | |||||||
| chr16:48100672 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3038+200G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48100672 | |||||||
| chr16:48101154 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2901-145G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48101154 | |||||||
| chr16:48101210 | G | C | 1 | a0002c0002t0001g0048 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2901-201C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48101210 | |||||||
| chr16:48101587 | C | T | 5 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2901-578G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48101587 | |||||||
| chr16:48101755 | A | T | 11 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(8): Show |
11 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2901-746T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48101755 | |||||||
| chr16:48102068 | A | T | 11 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(8): Show |
11 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2901-1059T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48102068 | |||||||
| chr16:48102094 | C | T | 3 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 |
3 | HG02647.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2901-1085G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48102094 | |||||||
| chr16:48102117 | A | G | 1 | a0009c0008t0009g0005 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2901-1108T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48102117 | |||||||
| chr16:48102368 | T | A | 2 | a0009c0008t0010g0014 a0009c0008t0010g0015 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2901-1359A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48102368 | |||||||
| chr16:48102558 | C | A | 1 | a0001c0001t0001g0033 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2901-1549G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48102558 | |||||||
| chr16:48102562 | G | A | 1 | a0002c0002t0019g0050 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2901-1553C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48102562 | |||||||
| chr16:48102880 | C | T | 1 | a0021c0024t0001g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2900+1262G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48102880 | |||||||
| chr16:48102881 | G | C | 3 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 |
3 | HG02647.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2900+1261C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48102881 | |||||||
| chr16:48103208 | C | T | 3 | a0005c0029t0018g0029 a0010c0018t0011g0021 a0010c0018t0011g0039 |
3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2900+934G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48103208 | |||||||
| chr16:48103337 | G | C | 13 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(10): Show |
14 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2900+805C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48103337 | |||||||
| chr16:48103489 | T | C | 1 | a0014c0012t0007g0012 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2900+653A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48103489 | |||||||
| chr16:48103644 | A | G | 34 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(31): Show |
38 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.2900+498T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48103644 | |||||||
| chr16:48103794 | C | T | 4 | a0004c0007t0003g0104 a0004c0007t0003g0105 a0004c0013t0003g0108 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2900+348G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48103794 | |||||||
| chr16:48103811 | C | A | 2 | a0010c0018t0011g0021 a0010c0018t0011g0039 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2900+331G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48103811 | |||||||
| chr16:48103975 | G | A | 4 | a0004c0007t0003g0104 a0004c0007t0003g0105 a0004c0013t0003g0108 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2900+167C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48103975 | |||||||
| chr16:48104040 | G | C | 1 | a0005c0021t0002g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2900+102C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48104040 | |||||||
| chr16:48104408 | G | A | 2 | a0004c0007t0003g0102 a0004c0007t0003g0103 |
2 | HG01891.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2674-40C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 21/30 | chr16 | 48104408 | |||||||
| chr16:48104445 | T | C | 2 | a0001c0001t0001g0067 a0003c0003t0014g0068 |
2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2674-77A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 21/30 | chr16 | 48104445 | |||||||
| chr16:48104595 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0089 |
2 | HG01496.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2674-227G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 21/30 | chr16 | 48104595 | |||||||
| chr16:48104604 | C | G | 1 | a0005c0029t0018g0029 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2674-236G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 21/30 | chr16 | 48104604 | |||||||
| chr16:48104655 | C | T | 1 | a0005c0030t0001g0119 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2674-287G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 21/30 | chr16 | 48104655 | |||||||
| chr16:48104806 | G | A | 3 | a0001c0001t0001g0074 a0001c0004t0001g0098 a0001c0004t0001g0099 |
3 | HG01074.hp2 HG01255.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.2673+333C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 21/30 | chr16 | 48104806 | |||||||
| chr16:48105403 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2476-67C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48105403 | |||||||
| chr16:48105419 | G | A | 4 | a0009c0008t0009g0005 a0009c0008t0010g0014 a0009c0008t0010g0015 others(1): Show |
5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2476-83C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48105419 | |||||||
| chr16:48105615 | T | A | 1 | a0001c0001t0001g0075 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2476-279A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48105615 | |||||||
| chr16:48105617 | C | T | 1 | a0011c0019t0001g0072 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2476-281G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48105617 | |||||||
| chr16:48105633 | C | T | 4 | a0009c0008t0009g0005 a0009c0008t0010g0014 a0009c0008t0010g0015 others(1): Show |
5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2476-297G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48105633 | |||||||
| chr16:48105916 | G | A | 3 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 |
3 | HG02647.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2476-580C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48105916 | |||||||
| chr16:48106140 | T | A | 1 | a0002c0002t0019g0050 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2476-804A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48106140 | |||||||
| chr16:48106326 | G | A | 3 | a0017c0011t0006g0115 a0017c0011t0006g0117 a0022c0023t0006g0037 |
3 | HG02717.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2476-990C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48106326 | |||||||
| chr16:48106343 | T | C | 7 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(4): Show |
7 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2475+979A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48106343 | |||||||
| chr16:48106392 | G | A | 3 | a0017c0011t0006g0115 a0017c0011t0006g0117 a0022c0023t0006g0037 |
3 | HG02717.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2475+930C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48106392 | |||||||
| chr16:48106712 | C | T | 31 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(28): Show |
35 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.2475+610G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48106712 | |||||||
| chr16:48106778 | A | G | 9 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(6): Show |
10 | HG01891.hp2 HG02258.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2475+544T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48106778 | |||||||
| chr16:48106917 | A | T | 1 | a0001c0004t0001g0081 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2475+405T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48106917 | |||||||
| chr16:48106948 | G | A | 3 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 |
3 | HG02647.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2475+374C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48106948 | |||||||
| chr16:48107196 | C | T | 2 | a0009c0008t0010g0014 a0009c0008t0010g0015 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2475+126G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48107196 | |||||||
| chr16:48107446 | C | T | 1 | a0002c0002t0020g0063 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2372-21G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 19/30 | chr16 | 48107446 | |||||||
| chr16:48107578 | T | A | 8 | a0012c0016t0005g0004 a0014c0012t0007g0012 a0015c0020t0005g0007 others(5): Show |
11 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2372-153A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 19/30 | chr16 | 48107578 | |||||||
| chr16:48108200 | C | T | 2 | a0013c0017t0002g0109 a0013c0017t0002g0111 |
2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2371+240G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 19/30 | chr16 | 48108200 | |||||||
| chr16:48108245 | T | A | 2 | a0002c0002t0001g0002 a0002c0002t0001g0013 |
4 | HG02486.hp1 HG02559.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2371+195A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 19/30 | chr16 | 48108245 | |||||||
| chr16:48108282 | C | T | 4 | a0004c0007t0003g0104 a0004c0007t0003g0105 a0004c0013t0003g0108 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2371+158G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 19/30 | chr16 | 48108282 | |||||||
| chr16:48108366 | C | T | 1 | a0010c0026t0016g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2371+74G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 19/30 | chr16 | 48108366 | |||||||
| chr16:48108630 | G | A | 1 | a0002c0002t0001g0038 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2282-101C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48108630 | |||||||
| chr16:48108790 | A | G | 1 | a0010c0026t0016g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2282-261T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48108790 | |||||||
| chr16:48108830 | C | T | 7 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(4): Show |
7 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2282-301G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48108830 | |||||||
| chr16:48108863 | T | C | 4 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2282-334A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48108863 | |||||||
| chr16:48109493 | C | T | 1 | a0002c0002t0001g0006 | 2 | HG01255.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2282-964G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48109493 | |||||||
| chr16:48109726 | C | T | 1 | a0002c0002t0001g0058 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2282-1197G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48109726 | |||||||
| chr16:48109787 | C | T | 4 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2282-1258G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48109787 | |||||||
| chr16:48109835 | C | T | 2 | a0013c0017t0002g0109 a0013c0017t0002g0111 |
2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2282-1306G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48109835 | |||||||
| chr16:48109900 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2282-1371C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48109900 | |||||||
| chr16:48109927 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0080 a0001c0001t0013g0078 |
3 | HG03017.hp2 HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2282-1398C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48109927 | |||||||
| chr16:48109941 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG02055.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2282-1412G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48109941 | |||||||
| chr16:48109942 | G | A | 4 | a0004c0007t0003g0104 a0004c0007t0003g0105 a0004c0013t0003g0108 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2282-1413C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48109942 | |||||||
| chr16:48110024 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2281+1412C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110024 | |||||||
| chr16:48110027 | G | T | 1 | a0017c0011t0006g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2281+1409C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110027 | |||||||
| chr16:48110072 | G | A | 1 | a0014c0012t0007g0012 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2281+1364C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110072 | |||||||
| chr16:48110175 | G | A | 3 | a0002c0002t0001g0002 a0002c0002t0001g0013 a0002c0002t0001g0022 |
5 | HG02451.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2281+1261C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110175 | |||||||
| chr16:48110233 | TCTTTCCC others(1): Show |
T | 4 | a0004c0007t0003g0104 a0004c0007t0003g0105 a0004c0013t0003g0108 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2281+1195_2281+120 others(12): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110233 | |||||||
| chr16:48110303 | A | C | 1 | a0002c0002t0001g0071 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2281+1133T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110303 | |||||||
| chr16:48110322 | T | C | 2 | a0001c0001t0001g0067 a0003c0003t0014g0068 |
2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2281+1114A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110322 | |||||||
| chr16:48110585 | C | A | 8 | a0007c0006t0001g0011 a0007c0006t0001g0091 a0007c0006t0001g0093 others(5): Show |
9 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2281+851G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110585 | |||||||
| chr16:48110673 | C | A | 1 | a0001c0001t0001g0077 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2281+763G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110673 | |||||||
| chr16:48110726 | G | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0032 others(102): Show |
119 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.2281+710C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110726 | |||||||
| chr16:48110770 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0032 others(113): Show |
131 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.2281+666T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110770 | |||||||
| chr16:48110778 | T | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0032 others(73): Show |
86 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.2281+658A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110778 | |||||||
| chr16:48110996 | G | A | 2 | a0004c0013t0003g0108 a0004c0013t0003g0114 |
2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2281+440C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110996 | |||||||
| chr16:48111089 | A | G | 1 | a0001c0001t0001g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2281+347T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48111089 | |||||||
| chr16:48111097 | T | C | 1 | a0005c0010t0002g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2281+339A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48111097 | |||||||
| chr16:48111113 | T | A | 1 | a0001c0001t0013g0078 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2281+323A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48111113 | |||||||
| chr16:48111674 | A | G | 1 | a0002c0002t0001g0051 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2125-12T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 16/30 | chr16 | 48111674 | |||||||
| chr16:48111738 | G | T | 38 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(35): Show |
42 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.2124+38C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 16/30 | chr16 | 48111738 | |||||||
| chr16:48112049 | A | T | 1 | a0005c0030t0001g0119 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1990-139T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112049 | |||||||
| chr16:48112088 | T | A | 1 | a0001c0001t0001g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1990-178A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112088 | |||||||
| chr16:48112118 | C | T | 1 | a0005c0030t0001g0119 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1990-208G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112118 | |||||||
| chr16:48112350 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1990-440G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112350 | |||||||
| chr16:48112376 | A | G | 21 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(18): Show |
24 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1990-466T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112376 | |||||||
| chr16:48112527 | G | A | 2 | a0016c0015t0008g0041 a0016c0015t0008g0112 |
2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1990-617C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112527 | |||||||
| chr16:48112604 | A | C | 2 | a0002c0002t0001g0044 a0010c0026t0016g0084 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1990-694T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112604 | |||||||
| chr16:48112773 | G | A | 2 | a0004c0013t0003g0108 a0004c0013t0003g0114 |
2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1990-863C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112773 | |||||||
| chr16:48112980 | G | C | 3 | a0013c0017t0002g0109 a0013c0017t0002g0111 a0023c0025t0001g0110 |
3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1990-1070C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112980 | |||||||
| chr16:48113362 | T | C | 13 | a0007c0006t0001g0011 a0007c0006t0001g0090 a0007c0006t0001g0091 others(10): Show |
16 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1990-1452A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48113362 | |||||||
| chr16:48113377 | C | A | 1 | a0005c0029t0018g0029 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1990-1467G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48113377 | |||||||
| chr16:48113444 | T | C | 2 | a0017c0011t0006g0115 a0017c0011t0006g0117 |
2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1990-1534A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48113444 | |||||||
| chr16:48113491 | C | T | 4 | a0002c0002t0020g0063 a0018c0014t0001g0106 a0018c0014t0001g0107 others(1): Show |
4 | HG02717.hp2 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1990-1581G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48113491 | |||||||
| chr16:48113530 | T | C | 1 | a0002c0002t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1990-1620A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48113530 | |||||||
| chr16:48113608 | G | A | 2 | a0017c0011t0006g0115 a0017c0011t0006g0117 |
2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1990-1698C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48113608 | |||||||
| chr16:48113815 | C | T | 2 | a0017c0011t0006g0115 a0017c0011t0006g0117 |
2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1989+1600G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48113815 | |||||||
| chr16:48113941 | C | A | 1 | a0005c0029t0018g0029 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1989+1474G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48113941 | |||||||
| chr16:48114479 | A | G | 4 | a0009c0008t0009g0005 a0009c0008t0010g0014 a0009c0008t0010g0015 others(1): Show |
5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1989+936T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48114479 | |||||||
| chr16:48114588 | G | T | 1 | a0001c0001t0001g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1989+827C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48114588 | |||||||
| chr16:48114647 | C | G | 3 | a0005c0021t0002g0025 a0005c0021t0002g0026 a0024c0028t0002g0017 |
3 | HG01496.hp2 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1989+768G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48114647 | |||||||
| chr16:48114857 | A | G | 4 | a0009c0008t0009g0005 a0009c0008t0010g0014 a0009c0008t0010g0015 others(1): Show |
5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1989+558T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48114857 | |||||||
| chr16:48115345 | A | G | 6 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1989+70T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48115345 | |||||||
| chr16:48115702 | A | T | 2 | a0004c0013t0003g0108 a0004c0013t0003g0114 |
2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1786-84T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48115702 | |||||||
| chr16:48115803 | T | C | 1 | a0002c0002t0020g0063 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1786-185A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48115803 | |||||||
| chr16:48115859 | C | T | 2 | a0013c0017t0002g0109 a0023c0025t0001g0110 |
2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1786-241G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48115859 | |||||||
| chr16:48115874 | T | G | 13 | a0007c0006t0001g0011 a0007c0006t0001g0090 a0007c0006t0001g0091 others(10): Show |
16 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1786-256A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48115874 | |||||||
| chr16:48116172 | A | C | 4 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1786-554T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48116172 | |||||||
| chr16:48116328 | G | A | 6 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1786-710C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48116328 | |||||||
| chr16:48116642 | T | G | 6 | a0009c0008t0009g0005 a0009c0008t0010g0014 a0009c0008t0010g0015 others(3): Show |
7 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1785+619A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48116642 | |||||||
| chr16:48116733 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1785+528T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48116733 | |||||||
| chr16:48116756 | A | G | 6 | a0009c0008t0009g0005 a0009c0008t0010g0014 a0009c0008t0010g0015 others(3): Show |
7 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1785+505T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48116756 | |||||||
| chr16:48117075 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1785+186C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48117075 | |||||||
| chr16:48117123 | T | C | 38 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(35): Show |
42 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.1785+138A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48117123 | |||||||
| chr16:48117149 | C | T | 6 | a0009c0008t0009g0005 a0009c0008t0010g0014 a0009c0008t0010g0015 others(3): Show |
7 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1785+112G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48117149 | |||||||
| chr16:48117219 | T | C | 6 | a0009c0008t0009g0005 a0009c0008t0010g0014 a0009c0008t0010g0015 others(3): Show |
7 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1785+42A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48117219 | |||||||
| chr16:48117254 | C | T | 2 | a0004c0007t0003g0104 a0004c0007t0003g0105 |
2 | HG02109.hp1 HG02559.hp2 |
splice_region_variant&intron_variant | LOW | c.1785+7G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48117254 | |||||||
| chr16:48117374 | C | T | 6 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1713-41G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48117374 | |||||||
| chr16:48117452 | T | C | 25 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(22): Show |
29 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1713-119A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48117452 | |||||||
| chr16:48117552 | G | C | 1 | a0010c0026t0016g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1713-219C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48117552 | |||||||
| chr16:48117578 | T | C | 27 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(24): Show |
31 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1713-245A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48117578 | |||||||
| chr16:48117639 | G | C | 30 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(27): Show |
34 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1713-306C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48117639 | |||||||
| chr16:48117694 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1713-361C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48117694 | |||||||
| chr16:48117877 | T | C | 1 | a0002c0002t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1713-544A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48117877 | |||||||
| chr16:48118108 | C | T | 13 | a0007c0006t0001g0011 a0007c0006t0001g0090 a0007c0006t0001g0091 others(10): Show |
16 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1713-775G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48118108 | |||||||
| chr16:48118173 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1713-840G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48118173 | |||||||
| chr16:48118223 | G | T | 13 | a0007c0006t0001g0011 a0007c0006t0001g0090 a0007c0006t0001g0091 others(10): Show |
16 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1713-890C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48118223 | |||||||
| chr16:48118334 | C | A | 2 | a0010c0018t0011g0021 a0010c0018t0011g0039 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1713-1001G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48118334 | |||||||
| chr16:48118842 | G | C | 2 | a0005c0021t0002g0025 a0005c0021t0002g0026 |
2 | HG01496.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1713-1509C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48118842 | |||||||
| chr16:48119297 | T | C | 2 | a0001c0001t0001g0053 a0002c0002t0001g0006 |
3 | HG01255.hp1 HG01256.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1713-1964A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48119297 | |||||||
| chr16:48119664 | C | T | 3 | a0013c0017t0002g0109 a0013c0017t0002g0111 a0023c0025t0001g0110 |
3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1712+2052G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48119664 | |||||||
| chr16:48120136 | T | C | 1 | a0009c0008t0009g0005 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1712+1580A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48120136 | |||||||
| chr16:48120551 | G | T | 1 | a0009c0008t0009g0005 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1712+1165C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48120551 | |||||||
| chr16:48120558 | GT | G | 39 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(36): Show |
43 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1712+1157delA | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48120558 | |||||||
| chr16:48120587 | G | T | 2 | a0016c0015t0008g0041 a0016c0015t0008g0112 |
2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1712+1129C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48120587 | |||||||
| chr16:48120833 | C | T | 3 | a0013c0017t0002g0109 a0013c0017t0002g0111 a0023c0025t0001g0110 |
3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1712+883G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48120833 | |||||||
| chr16:48121017 | C | A | 1 | a0001c0001t0001g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1712+699G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48121017 | |||||||
| chr16:48121224 | T | C | 3 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 |
3 | HG02647.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1712+492A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48121224 | |||||||
| chr16:48121489 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1712+227G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48121489 | |||||||
| chr16:48121534 | C | T | 32 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(29): Show |
36 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.1712+182G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48121534 | |||||||
| chr16:48121535 | G | A | 1 | a0002c0002t0001g0038 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1712+181C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48121535 | |||||||
| chr16:48121636 | T | A | 1 | a0005c0021t0002g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1712+80A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48121636 | |||||||
| chr16:48122380 | C | T | 2 | a0004c0013t0003g0108 a0004c0013t0003g0114 |
2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1588-540G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48122380 | |||||||
| chr16:48122381 | A | T | 2 | a0004c0013t0003g0108 a0004c0013t0003g0114 |
2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1588-541T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48122381 | |||||||
| chr16:48122522 | G | A | 2 | a0004c0013t0003g0108 a0004c0013t0003g0114 |
2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1588-682C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48122522 | |||||||
| chr16:48122531 | C | T | 2 | a0001c0001t0001g0053 a0002c0002t0001g0006 |
3 | HG01255.hp1 HG01256.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1588-691G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48122531 | |||||||
| chr16:48122568 | A | C | 3 | a0005c0029t0018g0029 a0010c0018t0011g0021 a0010c0018t0011g0039 |
3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1588-728T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48122568 | |||||||
| chr16:48122605 | C | T | 4 | a0009c0008t0009g0005 a0009c0008t0010g0014 a0009c0008t0010g0015 others(1): Show |
5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1588-765G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48122605 | |||||||
| chr16:48122943 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1588-1103C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48122943 | |||||||
| chr16:48123082 | C | T | 1 | a0002c0002t0001g0038 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1587+1131G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48123082 | |||||||
| chr16:48123225 | A | G | 19 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(16): Show |
22 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1587+988T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48123225 | |||||||
| chr16:48123304 | C | T | 3 | a0013c0017t0002g0109 a0013c0017t0002g0111 a0023c0025t0001g0110 |
3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1587+909G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48123304 | |||||||
| chr16:48123591 | G | T | 2 | a0001c0001t0001g0067 a0003c0003t0014g0068 |
2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1587+622C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48123591 | |||||||
| chr16:48124352 | GC | G | 2 | a0004c0007t0003g0104 a0004c0007t0003g0105 |
2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1516-69delG | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48124352 | |||||||
| chr16:48125370 | C | T | 3 | a0013c0017t0002g0109 a0013c0017t0002g0111 a0023c0025t0001g0110 |
3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1516-1086G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48125370 | |||||||
| chr16:48125388 | T | C | 13 | a0007c0006t0001g0011 a0007c0006t0001g0090 a0007c0006t0001g0091 others(10): Show |
16 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1516-1104A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48125388 | |||||||
| chr16:48125540 | C | G | 1 | a0002c0002t0001g0038 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1516-1256G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48125540 | |||||||
| chr16:48126231 | C | T | 13 | a0007c0006t0001g0011 a0007c0006t0001g0090 a0007c0006t0001g0091 others(10): Show |
16 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1516-1947G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48126231 | |||||||
| chr16:48126260 | T | C | 1 | a0002c0002t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1516-1976A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48126260 | |||||||
| chr16:48126499 | C | T | 19 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(16): Show |
22 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1515+1960G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48126499 | |||||||
| chr16:48126517 | G | A | 1 | a0001c0004t0017g0118 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1515+1942C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48126517 | |||||||
| chr16:48126525 | T | A | 13 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(10): Show |
14 | HG01496.hp2 HG02622.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1515+1934A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48126525 | |||||||
| chr16:48126749 | C | G | 2 | a0002c0002t0001g0055 a0002c0002t0001g0056 |
2 | HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1515+1710G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48126749 | |||||||
| chr16:48126754 | G | C | 6 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1515+1705C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48126754 | |||||||
| chr16:48126919 | C | A | 2 | a0016c0015t0008g0041 a0016c0015t0008g0112 |
2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1515+1540G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48126919 | |||||||
| chr16:48127008 | T | C | 19 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(16): Show |
22 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1515+1451A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48127008 | |||||||
| chr16:48127064 | T | C | 9 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(6): Show |
9 | HG01496.hp2 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1515+1395A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48127064 | |||||||
| chr16:48127143 | C | G | 6 | a0007c0006t0001g0011 a0007c0006t0001g0090 a0007c0006t0001g0091 others(3): Show |
7 | HG02257.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1515+1316G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48127143 | |||||||
| chr16:48127245 | C | T | 1 | a0020c0022t0012g0028 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1515+1214G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48127245 | |||||||
| chr16:48127360 | C | T | 1 | a0005c0021t0002g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1515+1099G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48127360 | |||||||
| chr16:48127731 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1515+728T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48127731 | |||||||
| chr16:48127806 | T | C | 1 | a0009c0008t0009g0005 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1515+653A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48127806 | |||||||
| chr16:48127997 | T | C | 13 | a0007c0006t0001g0011 a0007c0006t0001g0090 a0007c0006t0001g0091 others(10): Show |
16 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1515+462A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48127997 | |||||||
| chr16:48128160 | C | G | 19 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(16): Show |
22 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1515+299G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48128160 | |||||||
| chr16:48128889 | G | T | 2 | a0005c0021t0002g0025 a0005c0021t0002g0026 |
2 | HG01496.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1237-152C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48128889 | |||||||
| chr16:48128921 | A | G | 13 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(10): Show |
14 | HG01496.hp2 HG02622.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1237-184T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48128921 | |||||||
| chr16:48129348 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1237-611G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48129348 | |||||||
| chr16:48129624 | G | A | 10 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(7): Show |
11 | HG01496.hp2 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1237-887C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48129624 | |||||||
| chr16:48129625 | T | C | 1 | a0006c0005t0001g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1237-888A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48129625 | |||||||
| chr16:48129895 | T | C | 5 | a0004c0013t0003g0108 a0004c0013t0003g0114 a0013c0017t0002g0109 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1236+893A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48129895 | |||||||
| chr16:48130062 | G | A | 16 | a0007c0006t0001g0011 a0007c0006t0001g0090 a0007c0006t0001g0091 others(13): Show |
19 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.1236+726C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48130062 | |||||||
| chr16:48130093 | A | G | 1 | a0014c0012t0007g0012 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1236+695T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48130093 | |||||||
| chr16:48130465 | T | C | 1 | a0002c0002t0001g0038 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1236+323A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48130465 | |||||||
| chr16:48130553 | A | G | 2 | a0010c0018t0011g0021 a0010c0018t0011g0039 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1236+235T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48130553 | |||||||
| chr16:48130573 | T | C | 22 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(19): Show |
25 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1236+215A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48130573 | |||||||
| chr16:48131003 | G | A | 22 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(19): Show |
25 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1129-108C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48131003 | |||||||
| chr16:48131093 | T | C | 2 | a0004c0013t0003g0108 a0004c0013t0003g0114 |
2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1129-198A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48131093 | |||||||
| chr16:48131457 | A | G | 3 | a0013c0017t0002g0109 a0013c0017t0002g0111 a0023c0025t0001g0110 |
3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1129-562T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48131457 | |||||||
| chr16:48131594 | A | G | 1 | a0014c0012t0007g0012 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1129-699T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48131594 | |||||||
| chr16:48131667 | A | G | 22 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(19): Show |
25 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1129-772T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48131667 | |||||||
| chr16:48131778 | C | G | 17 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(14): Show |
18 | HG01496.hp2 HG01891.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1129-883G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48131778 | |||||||
| chr16:48131936 | C | T | 11 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(8): Show |
12 | HG01496.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1129-1041G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48131936 | |||||||
| chr16:48132140 | T | C | 2 | a0004c0013t0003g0108 a0004c0013t0003g0114 |
2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1129-1245A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48132140 | |||||||
| chr16:48132345 | A | T | 2 | a0004c0013t0003g0108 a0004c0013t0003g0114 |
2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1128+1342T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48132345 | |||||||
| chr16:48132515 | TTCTC | T | 1 | a0012c0016t0005g0004 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1128+1168_1128+117 others(8): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48132515 | |||||||
| chr16:48132716 | C | T | 2 | a0017c0011t0006g0115 a0017c0011t0006g0117 |
2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1128+971G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48132716 | |||||||
| chr16:48132766 | G | A | 22 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(19): Show |
25 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1128+921C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48132766 | |||||||
| chr16:48132793 | A | G | 1 | a0012c0016t0005g0004 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1128+894T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48132793 | |||||||
| chr16:48133357 | T | C | 9 | a0007c0006t0001g0011 a0007c0006t0001g0090 a0007c0006t0001g0091 others(6): Show |
10 | HG02257.hp1 HG02630.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1128+330A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48133357 | |||||||
| chr16:48133482 | C | T | 22 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(19): Show |
25 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1128+205G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48133482 | |||||||
| chr16:48133527 | G | GA | 10 | a0007c0006t0001g0011 a0007c0006t0001g0090 a0007c0006t0001g0093 others(7): Show |
13 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1128+159dupT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48133527 | |||||||
| chr16:48133527 | GA | G | 5 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1128+159delT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48133527 | |||||||
| chr16:48133663 | C | G | 22 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(19): Show |
25 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1128+24G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48133663 | |||||||
| chr16:48133933 | C | T | 2 | a0002c0002t0001g0034 a0002c0002t0001g0040 |
2 | NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.980-98G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48133933 | |||||||
| chr16:48134058 | T | G | 3 | a0001c0001t0001g0049 a0002c0002t0001g0051 a0002c0002t0019g0050 |
3 | HG00544.hp2 HG02083.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.980-223A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48134058 | |||||||
| chr16:48134295 | C | T | 1 | a0014c0012t0007g0012 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.980-460G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48134295 | |||||||
| chr16:48134324 | T | A | 1 | a0020c0022t0012g0028 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.980-489A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48134324 | |||||||
| chr16:48134659 | G | A | 4 | a0009c0008t0009g0005 a0009c0008t0010g0014 a0009c0008t0010g0015 others(1): Show |
5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.980-824C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48134659 | |||||||
| chr16:48134747 | C | G | 1 | a0024c0028t0002g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.980-912G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48134747 | |||||||
| chr16:48134890 | A | C | 6 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.980-1055T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48134890 | |||||||
| chr16:48134926 | C | A | 6 | a0006c0005t0001g0009 a0006c0005t0001g0031 a0006c0005t0001g0042 others(3): Show |
7 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.980-1091G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48134926 | |||||||
| chr16:48135023 | G | A | 2 | a0005c0021t0002g0025 a0005c0021t0002g0026 |
2 | HG01496.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.980-1188C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48135023 | |||||||
| chr16:48135049 | C | CA | 4 | a0001c0001t0001g0082 a0009c0008t0009g0005 a0009c0008t0010g0015 others(1): Show |
5 | HG00735.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.980-1215dupT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48135049 | |||||||
| chr16:48135283 | C | T | 1 | a0012c0016t0005g0004 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.980-1448G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48135283 | |||||||
| chr16:48135543 | G | T | 1 | a0010c0026t0016g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.980-1708C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48135543 | |||||||
| chr16:48135547 | AT | A | 3 | a0012c0016t0005g0004 a0017c0011t0006g0115 a0017c0011t0006g0117 |
4 | HG01884.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.980-1713delA | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48135547 | |||||||
| chr16:48135609 | T | C | 6 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.980-1774A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48135609 | |||||||
| chr16:48135611 | T | C | 1 | a0002c0002t0001g0051 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.980-1776A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48135611 | |||||||
| chr16:48135739 | T | A | 2 | a0010c0018t0011g0021 a0010c0018t0011g0039 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.980-1904A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48135739 | |||||||
| chr16:48135960 | G | A | 3 | a0013c0017t0002g0109 a0013c0017t0002g0111 a0023c0025t0001g0110 |
3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.980-2125C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48135960 | |||||||
| chr16:48136108 | G | T | 1 | a0002c0002t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.979+2120C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48136108 | |||||||
| chr16:48136173 | A | T | 1 | a0005c0029t0018g0029 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.979+2055T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48136173 | |||||||
| chr16:48136390 | C | G | 4 | a0009c0008t0009g0005 a0009c0008t0010g0014 a0009c0008t0010g0015 others(1): Show |
5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.979+1838G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48136390 | |||||||
| chr16:48136761 | G | A | 2 | a0010c0018t0011g0021 a0010c0018t0011g0039 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.979+1467C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48136761 | |||||||
| chr16:48136851 | C | T | 2 | a0014c0012t0007g0012 a0020c0022t0012g0028 |
3 | HG02280.hp1 HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.979+1377G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48136851 | |||||||
| chr16:48137021 | A | G | 39 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(36): Show |
43 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.979+1207T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48137021 | |||||||
| chr16:48137050 | C | T | 10 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(7): Show |
11 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.979+1178G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48137050 | |||||||
| chr16:48137132 | G | GC | 21 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(18): Show |
23 | HG01496.hp2 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.979+1095dupG | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48137132 | |||||||
| chr16:48137581 | C | T | 2 | a0014c0012t0007g0012 a0020c0022t0012g0028 |
3 | HG02280.hp1 HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.979+647G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48137581 | |||||||
| chr16:48137802 | T | C | 11 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(8): Show |
12 | HG01496.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.979+426A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48137802 | |||||||
| chr16:48137827 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.979+401T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48137827 | |||||||
| chr16:48137943 | GT | G | 10 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(7): Show |
11 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.979+284delA | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48137943 | |||||||
| chr16:48138787 | C | T | 2 | a0004c0007t0003g0104 a0004c0007t0003g0105 |
2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.831+376G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 7/30 | chr16 | 48138787 | |||||||
| chr16:48138805 | AT | A | 35 | a0004c0007t0003g0104 a0004c0007t0003g0105 a0004c0013t0003g0108 others(32): Show |
39 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.831+357delA | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 7/30 | chr16 | 48138805 | |||||||
| chr16:48138973 | CAAAAACA others(5): Show |
C | 18 | a0004c0013t0003g0108 a0004c0013t0003g0114 a0007c0006t0001g0011 others(15): Show |
20 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.831+178_831+189del others(12): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 7/30 | chr16 | 48138973 | |||||||
| chr16:48138992 | AAAAC | A | 4 | a0001c0004t0001g0083 a0005c0010t0002g0023 a0005c0010t0002g0024 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+167_831+170del others(4): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 7/30 | chr16 | 48138992 | |||||||
| chr16:48139444 | C | T | 2 | a0014c0012t0007g0012 a0020c0022t0012g0028 |
3 | HG02280.hp1 HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.658-108G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139444 | |||||||
| chr16:48139470 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0032 others(28): Show |
35 | HG00544.hp1 HG00558.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.658-134C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139470 | |||||||
| chr16:48139493 | T | C | 28 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(25): Show |
31 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.658-157A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139493 | |||||||
| chr16:48139520 | T | C | 43 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(40): Show |
48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.658-184A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139520 | |||||||
| chr16:48139627 | C | A | 1 | a0012c0016t0005g0004 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.658-291G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139627 | |||||||
| chr16:48139794 | A | C | 17 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(14): Show |
20 | HG01496.hp2 HG01884.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.658-458T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139794 | |||||||
| chr16:48139910 | CATG | C | 17 | a0004c0013t0003g0108 a0004c0013t0003g0114 a0007c0006t0001g0011 others(14): Show |
19 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.658-577_658-575del others(3): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139910 | |||||||
| chr16:48139918 | C | G | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.658-582G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139918 | |||||||
| chr16:48139973 | G | A | 6 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.658-637C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139973 | |||||||
| chr16:48140036 | T | A | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.657+651A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48140036 | |||||||
| chr16:48140136 | C | T | 4 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.657+551G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48140136 | |||||||
| chr16:48140176 | A | G | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.657+511T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48140176 | |||||||
| chr16:48140243 | T | TAAGGATT others(8): Show |
16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.657+443_657+444ins others(15): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48140243 | |||||||
| chr16:48140421 | C | T | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.657+266G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48140421 | |||||||
| chr16:48140453 | C | T | 6 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.657+234G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48140453 | |||||||
| chr16:48140523 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.657+164C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48140523 | |||||||
| chr16:48140648 | G | A | 43 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(40): Show |
48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.657+39C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48140648 | |||||||
| chr16:48140938 | G | C | 1 | a0003c0003t0004g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.424-18C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 5/30 | chr16 | 48140938 | |||||||
| chr16:48141368 | CAG | C | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-17_276-16delCT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48141368 | |||||||
| chr16:48141444 | C | T | 1 | a0001c0001t0001g0033 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.276-91G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48141444 | |||||||
| chr16:48141667 | G | A | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-314C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48141667 | |||||||
| chr16:48141943 | A | G | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-590T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48141943 | |||||||
| chr16:48141944 | T | A | 6 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.276-591A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48141944 | |||||||
| chr16:48142097 | C | T | 1 | a0005c0029t0018g0029 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.276-744G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142097 | |||||||
| chr16:48142098 | C | G | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-745G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142098 | |||||||
| chr16:48142182 | CT | C | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-830delA | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142182 | |||||||
| chr16:48142184 | A | C | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-831T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142184 | |||||||
| chr16:48142277 | T | C | 43 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(40): Show |
48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.276-924A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142277 | |||||||
| chr16:48142319 | C | A | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-966G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142319 | |||||||
| chr16:48142322 | C | T | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-969G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142322 | |||||||
| chr16:48142328 | T | C | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-975A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142328 | |||||||
| chr16:48142336 | G | C | 17 | a0004c0013t0003g0108 a0004c0013t0003g0114 a0007c0006t0001g0011 others(14): Show |
19 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.276-983C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142336 | |||||||
| chr16:48142382 | T | A | 43 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(40): Show |
48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.276-1029A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142382 | |||||||
| chr16:48142385 | A | T | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-1032T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142385 | |||||||
| chr16:48142585 | G | A | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-1232C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142585 | |||||||
| chr16:48142618 | G | C | 6 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.276-1265C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142618 | |||||||
| chr16:48142732 | C | T | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.275+1178G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142732 | |||||||
| chr16:48142864 | A | G | 6 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.275+1046T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142864 | |||||||
| chr16:48142950 | C | T | 1 | a0014c0012t0007g0012 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.275+960G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142950 | |||||||
| chr16:48143151 | G | T | 17 | a0004c0013t0003g0108 a0004c0013t0003g0114 a0007c0006t0001g0011 others(14): Show |
19 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.275+759C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143151 | |||||||
| chr16:48143160 | A | G | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.275+750T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143160 | |||||||
| chr16:48143233 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.275+677G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143233 | |||||||
| chr16:48143309 | T | C | 43 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(40): Show |
48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.275+601A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143309 | |||||||
| chr16:48143377 | C | A | 1 | a0001c0001t0001g0086 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.275+533G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143377 | |||||||
| chr16:48143422 | T | G | 43 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(40): Show |
48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.275+488A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143422 | |||||||
| chr16:48143651 | T | A | 17 | a0004c0013t0003g0108 a0004c0013t0003g0114 a0007c0006t0001g0011 others(14): Show |
19 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.275+259A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143651 | |||||||
| chr16:48143720 | C | G | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.275+190G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143720 | |||||||
| chr16:48143787 | C | A | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.275+123G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143787 | |||||||
| chr16:48144300 | A | C | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-235T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144300 | |||||||
| chr16:48144351 | T | C | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-286A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144351 | |||||||
| chr16:48144436 | C | A | 6 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.120-371G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144436 | |||||||
| chr16:48144484 | C | A | 17 | a0004c0013t0003g0108 a0004c0013t0003g0114 a0007c0006t0001g0011 others(14): Show |
19 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.120-419G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144484 | |||||||
| chr16:48144561 | C | A | 1 | a0001c0001t0001g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.120-496G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144561 | |||||||
| chr16:48144651 | T | G | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-586A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144651 | |||||||
| chr16:48144665 | C | A | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-600G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144665 | |||||||
| chr16:48144868 | A | G | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-803T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144868 | |||||||
| chr16:48144910 | A | G | 43 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(40): Show |
48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.120-845T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144910 | |||||||
| chr16:48144962 | G | A | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-897C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144962 | |||||||
| chr16:48145033 | T | A | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-968A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145033 | |||||||
| chr16:48145071 | C | T | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-1006G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145071 | |||||||
| chr16:48145134 | A | G | 1 | a0012c0016t0005g0004 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.120-1069T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145134 | |||||||
| chr16:48145243 | G | A | 2 | a0017c0011t0006g0115 a0017c0011t0006g0117 |
2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.119+1063C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145243 | |||||||
| chr16:48145266 | G | A | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.119+1040C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145266 | |||||||
| chr16:48145380 | T | C | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.119+926A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145380 | |||||||
| chr16:48145496 | C | A | 1 | a0002c0002t0001g0046 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.119+810G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145496 | |||||||
| chr16:48145663 | A | G | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.119+643T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145663 | |||||||
| chr16:48145701 | G | A | 6 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.119+605C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145701 | |||||||
| chr16:48145712 | C | T | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.119+594G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145712 | |||||||
| chr16:48145749 | C | T | 1 | a0007c0006t0001g0090 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.119+557G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145749 | |||||||
| chr16:48146072 | T | C | 17 | a0004c0013t0003g0108 a0004c0013t0003g0114 a0007c0006t0001g0011 others(14): Show |
19 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.119+234A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48146072 | |||||||
| chr16:48146072 | T | TC | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.119+233dupG | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48146072 | |||||||
| chr16:48146171 | C | T | 43 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(40): Show |
48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.119+135G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48146171 | |||||||
| chr16:48146199 | C | T | 6 | a0001c0001t0001g0049 a0002c0002t0001g0046 a0002c0002t0001g0047 others(3): Show |
6 | HG00544.hp2 HG00735.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.119+107G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48146199 | |||||||
| chr16:48146209 | G | A | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.119+97C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48146209 | |||||||
| chr16:48146287 | T | C | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.119+19A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48146287 | |||||||
| chr16:48146288 | G | A | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.119+18C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48146288 | |||||||
| chr16:48146480 | G | A | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.-50-6C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48146480 | |||||||
| chr16:48146941 | C | T | 1 | a0002c0002t0001g0046 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-50-467G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48146941 | |||||||
| chr16:48146942 | G | C | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-468C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48146942 | |||||||
| chr16:48146949 | G | A | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-475C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48146949 | |||||||
| chr16:48146970 | C | T | 1 | a0005c0029t0018g0029 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-50-496G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48146970 | |||||||
| chr16:48146975 | A | G | 2 | a0005c0010t0002g0023 a0005c0010t0002g0024 |
2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-50-501T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48146975 | |||||||
| chr16:48147028 | T | G | 43 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(40): Show |
48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.-50-554A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147028 | |||||||
| chr16:48147069 | G | A | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-595C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147069 | |||||||
| chr16:48147082 | A | G | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-608T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147082 | |||||||
| chr16:48147090 | T | C | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-616A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147090 | |||||||
| chr16:48147382 | G | A | 17 | a0001c0001t0001g0087 a0005c0010t0002g0023 a0005c0010t0002g0024 others(14): Show |
19 | HG01496.hp2 HG02109.hp2 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50-908C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147382 | |||||||
| chr16:48147439 | G | A | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-965C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147439 | |||||||
| chr16:48147446 | C | T | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-972G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147446 | |||||||
| chr16:48147448 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-50-974A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147448 | |||||||
| chr16:48147708 | C | T | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-1234G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147708 | |||||||
| chr16:48147812 | G | A | 1 | a0014c0012t0007g0012 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-50-1338C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147812 | |||||||
| chr16:48147843 | G | A | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-1369C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147843 | |||||||
| chr16:48147956 | G | GGTT | 43 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(40): Show |
48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.-50-1485_-50-1483d others(5): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147956 | |||||||
| chr16:48148134 | G | C | 1 | a0003c0003t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-50-1660C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148134 | |||||||
| chr16:48148165 | A | C | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-1691T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148165 | |||||||
| chr16:48148227 | C | T | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-1753G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148227 | |||||||
| chr16:48148237 | CA | C | 23 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(20): Show |
26 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-50-1764delT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148237 | |||||||
| chr16:48148237 | CAA | C | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-1765_-50-1764d others(4): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148237 | |||||||
| chr16:48148348 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-50-1874G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148348 | |||||||
| chr16:48148524 | T | C | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-2050A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148524 | |||||||
| chr16:48148536 | T | C | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-2062A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148536 | |||||||
| chr16:48148596 | A | G | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-2122T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148596 | |||||||
| chr16:48148602 | G | A | 33 | a0004c0013t0003g0108 a0004c0013t0003g0114 a0005c0010t0002g0023 others(30): Show |
37 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.-50-2128C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148602 | |||||||
| chr16:48148911 | T | A | 37 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(34): Show |
41 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.-50-2437A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148911 | |||||||
| chr16:48148945 | C | T | 6 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50-2471G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148945 | |||||||
| chr16:48148964 | A | G | 1 | a0003c0003t0004g0045 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-50-2490T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148964 | |||||||
| chr16:48148966 | C | T | 1 | a0002c0002t0001g0044 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-50-2492G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148966 | |||||||
| chr16:48148967 | G | A | 27 | a0004c0013t0003g0108 a0004c0013t0003g0114 a0005c0010t0002g0023 others(24): Show |
30 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.-50-2493C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148967 | |||||||
| chr16:48148970 | A | G | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-2496T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148970 | |||||||
| chr16:48149014 | T | A | 16 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(13): Show |
18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-2540A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149014 | |||||||
| chr16:48149040 | T | C | 1 | a0002c0002t0001g0095 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-50-2566A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149040 | |||||||
| chr16:48149146 | T | C | 2 | a0001c0001t0001g0096 a0002c0002t0001g0097 |
2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-50-2672A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149146 | |||||||
| chr16:48149244 | CA | C | 6 | a0001c0001t0001g0030 a0001c0001t0001g0043 a0005c0029t0018g0029 others(3): Show |
6 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-2771delT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149244 | |||||||
| chr16:48149244 | CAA | C | 13 | a0004c0013t0003g0108 a0004c0013t0003g0114 a0012c0016t0005g0004 others(10): Show |
15 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-50-2772_-50-2771d others(4): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149244 | |||||||
| chr16:48149244 | CAAA | C | 6 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50-2773_-50-2771d others(5): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149244 | |||||||
| chr16:48149263 | AG | A | 14 | a0005c0010t0002g0023 a0005c0010t0002g0024 a0005c0010t0002g0027 others(11): Show |
16 | HG01496.hp2 HG02622.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-50-2790delC | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149263 | |||||||
| chr16:48149388 | T | C | 11 | a0004c0013t0003g0108 a0004c0013t0003g0114 a0012c0016t0005g0004 others(8): Show |
12 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-50-2914A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149388 | |||||||
| chr16:48149649 | A | ACAGATGT others(8): Show |
20 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(17): Show |
21 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-50-3176_-50-3175i others(17): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149649 | |||||||
| chr16:48149837 | A | G | 4 | a0005c0029t0018g0029 a0017c0011t0006g0115 a0017c0011t0006g0117 others(1): Show |
4 | HG02280.hp1 HG02896.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-3363T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149837 | |||||||
| chr16:48150024 | A | G | 7 | a0002c0002t0001g0040 a0004c0007t0003g0101 a0004c0007t0003g0102 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-3550T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48150024 | |||||||
| chr16:48150204 | C | T | 1 | a0001c0004t0001g0098 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-51+3412G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48150204 | |||||||
| chr16:48150405 | C | G | 10 | a0002c0002t0001g0013 a0008c0009t0001g0003 a0008c0009t0001g0018 others(7): Show |
12 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+3211G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48150405 | |||||||
| chr16:48150459 | T | C | 1 | a0004c0013t0003g0114 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-51+3157A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48150459 | |||||||
| chr16:48150816 | G | A | 2 | a0017c0011t0006g0115 a0017c0011t0006g0117 |
2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-51+2800C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48150816 | |||||||
| chr16:48151257 | C | T | 11 | a0001c0001t0001g0113 a0002c0002t0001g0038 a0004c0013t0003g0108 others(8): Show |
11 | HG01074.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-51+2359G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48151257 | |||||||
| chr16:48151412 | T | G | 5 | a0008c0009t0001g0003 a0008c0009t0001g0018 a0008c0009t0001g0019 others(2): Show |
6 | HG02109.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51+2204A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48151412 | |||||||
| chr16:48151891 | A | G | 1 | a0012c0016t0005g0004 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-51+1725T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48151891 | |||||||
| chr16:48152049 | G | A | 2 | a0001c0004t0001g0098 a0001c0004t0001g0099 |
2 | HG01074.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-51+1567C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48152049 | |||||||
| chr16:48152284 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-51+1332T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48152284 | |||||||
| chr16:48152462 | A | C | 42 | a0001c0001t0001g0036 a0001c0001t0001g0113 a0002c0002t0001g0002 others(39): Show |
47 | HG01074.hp1 HG01496.hp2 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.-51+1154T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48152462 | |||||||
| chr16:48152943 | C | T | 1 | a0001c0004t0001g0035 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-51+673G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48152943 | |||||||
| chr16:48153065 | T | C | 12 | a0002c0002t0001g0002 a0002c0002t0001g0022 a0005c0010t0002g0023 others(9): Show |
15 | HG01496.hp2 HG01884.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-51+551A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48153065 | |||||||
| chr16:48153129 | T | C | 7 | a0004c0007t0003g0101 a0004c0007t0003g0102 a0004c0007t0003g0103 others(4): Show |
8 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-51+487A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48153129 | |||||||
| chr16:48153384 | A | AT | 28 | a0002c0002t0001g0002 a0002c0002t0001g0013 a0002c0002t0001g0022 others(25): Show |
33 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.-51+231dupA | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48153384 | |||||||
| chr16:48153448 | A | G | 1 | a0005c0030t0001g0119 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-51+168T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48153448 | |||||||
| chr16:48153950 | G | A | 1 | a0001c0001t0001g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-319-66C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48153950 | |||||||
| chr16:48154440 | C | T | 21 | a0002c0002t0001g0002 a0002c0002t0001g0013 a0002c0002t0001g0022 others(18): Show |
25 | HG01496.hp2 HG01884.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-319-556G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48154440 | |||||||
| chr16:48154939 | C | G | 1 | a0002c0002t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-320+902G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48154939 | |||||||
| chr16:48155019 | C | T | 1 | a0001c0001t0001g0033 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-320+822G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48155019 | |||||||
| chr16:48155193 | G | C | 1 | a0003c0003t0004g0100 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-320+648C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48155193 | |||||||
| chr16:48155376 | TA | T | 40 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0113 others(37): Show |
45 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.-320+464delT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48155376 | |||||||
| chr16:48155436 | T | G | 2 | a0005c0029t0018g0029 a0020c0022t0012g0028 |
2 | HG02280.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-320+405A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48155436 | |||||||
| chr16:48155452 | T | G | 19 | a0001c0001t0001g0113 a0001c0004t0017g0118 a0004c0007t0003g0101 others(16): Show |
20 | HG01123.hp1 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-320+389A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48155452 | |||||||
| chr16:48155727 | CCACA | C | 21 | a0002c0002t0001g0002 a0002c0002t0001g0013 a0002c0002t0001g0022 others(18): Show |
25 | HG01496.hp2 HG01884.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-320+110_-320+113d others(6): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48155727 | |||||||
| chr16:48155754 | G | A | 1 | a0005c0030t0001g0119 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-320+87C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48155754 |