Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9735 |
|---|---|
| ensemblid | ENSG00000184445.12 |
| hgncid | 17255 |
| symbol | KNTC1 |
| name | kinetochore associated 1 |
| refseq_nuc | NM_014708.6 |
| refseq_prot | NP_055523.1 |
| ensembl_nuc | ENST00000333479.12 |
| ensembl_prot | ENSP00000328236.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 122527249 |
| end | 122626396 |
| strand | + |
| ver | v1.2 |
| region | chr12:122527249-122626396 |
| region5000 | chr12:122522249-122631396 |
| regionname0 | KNTC1_chr12_122527249_122626396 |
| regionname5000 | KNTC1_chr12_122522249_122631396 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 2209 | 243 | 34 | 56 | 109 | 11 | 31 | 84 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0002 | 0/0 | 2209 | 17 | 15 | 2 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0003 | 0/0 | 2209 | 16 | 0 | 6 | 0 | 3 | 7 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0004 | 0/0 | 2209 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0005 | 0/0 | 2209 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0006 | 0/0 | 2209 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0007 | 0/0 | 2209 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0008 | 0/0 | 2209 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0009 | 0/0 | 2209 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0010 | 0/0 | 2209 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0011 | 0/0 | 2209 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0012 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0013 | 0/0 | 2209 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0014 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0015 | 0/0 | 2209 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0016 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0017 | 0/0 | 2209 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0018 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0019 | 0/0 | 2209 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0020 | 0/0 | 2209 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0021 | 0/0 | 2209 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0022 | 0/0 | 2209 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0023 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0024 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 6630 | 148 | 25 | 39 | 59 | 7 | 17 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0002 | 0/1 | 6630 | 81 | 5 | 16 | 43 | 4 | 12 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0003 | 0/0 | 6630 | 13 | 12 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0004 | 0/0 | 6630 | 12 | 0 | 4 | 0 | 3 | 5 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0005 | 0/0 | 6630 | 9 | 9 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0006 | 0/0 | 6630 | 5 | 5 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0007 | 0/0 | 6630 | 5 | 0 | 0 | 5 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0008 | 0/0 | 6630 | 4 | 0 | 2 | 0 | 0 | 2 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0009 | 0/0 | 6630 | 4 | 3 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0010 | 0/0 | 6630 | 3 | 3 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0011 | 0/0 | 6630 | 3 | 0 | 0 | 3 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0012 | 0/0 | 6630 | 3 | 3 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0013 | 0/0 | 6630 | 3 | 3 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0014 | 0/0 | 6630 | 2 | 0 | 0 | 0 | 0 | 2 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0015 | 0/0 | 6630 | 2 | 2 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0016 | 0/0 | 6630 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0017 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0018 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0019 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0020 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0021 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0022 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0023 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0024 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0025 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0026 | 0/0 | 6630 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0027 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0028 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0029 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0030 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0031 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0032 | 0/0 | 6630 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0033 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0034 | 0/0 | 6630 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0035 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0036 | 0/0 | 6630 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0037 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| c0038 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 345 | 316 | 78 | 63 | 120 | 14 | 39 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| t0002 | 0/0 | 345 | 2 | 0 | 2 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| t0003 | 0/0 | 345 | 2 | 0 | 1 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 6630 | 148 | 25 | 39 | 59 | 7 | 17 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0002 | 0/1 | 6630 | 81 | 5 | 16 | 43 | 4 | 12 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0010 | 0/0 | 6630 | 3 | 3 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0011 | 0/0 | 6630 | 3 | 0 | 0 | 3 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0016 | 0/0 | 6630 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0021 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0023 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0025 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0026 | 0/0 | 6630 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0031 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0034 | 0/0 | 6630 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0038 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0002c0003 | 0/0 | 6630 | 13 | 12 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0002c0009 | 0/0 | 6630 | 4 | 3 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0003c0004 | 0/0 | 6630 | 12 | 0 | 4 | 0 | 3 | 5 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0003c0008 | 0/0 | 6630 | 4 | 0 | 2 | 0 | 0 | 2 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0004c0005 | 0/0 | 6630 | 9 | 9 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0005c0007 | 0/0 | 6630 | 5 | 0 | 0 | 5 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0006c0006 | 0/0 | 6630 | 5 | 5 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0007c0013 | 0/0 | 6630 | 3 | 3 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0008c0012 | 0/0 | 6630 | 3 | 3 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0009c0014 | 0/0 | 6630 | 2 | 0 | 0 | 0 | 0 | 2 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0010c0029 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0010c0033 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0011c0015 | 0/0 | 6630 | 2 | 2 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0012c0022 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0013c0024 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0014c0027 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0015c0030 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0016c0028 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0017c0020 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0018c0019 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0019c0032 | 0/0 | 6630 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0020c0037 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0021c0036 | 0/0 | 6630 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0022c0035 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0023c0018 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0024c0017 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6974 | 148 | 25 | 39 | 59 | 7 | 17 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0002t0001 | 0/1 | 6974 | 79 | 5 | 15 | 43 | 4 | 11 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0002t0003 | 0/0 | 6974 | 2 | 0 | 1 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0010t0001 | 0/0 | 6974 | 3 | 3 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0011t0001 | 0/0 | 6974 | 3 | 0 | 0 | 3 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0016t0001 | 0/0 | 6974 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0021t0001 | 0/0 | 6974 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0023t0001 | 0/0 | 6974 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0025t0001 | 0/0 | 6974 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0026t0001 | 0/0 | 6974 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0031t0001 | 0/0 | 6974 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0034t0001 | 0/0 | 6974 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0001c0038t0001 | 0/0 | 6974 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0002c0003t0001 | 0/0 | 6974 | 13 | 12 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0002c0009t0001 | 0/0 | 6974 | 4 | 3 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0003c0004t0001 | 0/0 | 6974 | 12 | 0 | 4 | 0 | 3 | 5 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0003c0008t0001 | 0/0 | 6974 | 2 | 0 | 0 | 0 | 0 | 2 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0003c0008t0002 | 0/0 | 6974 | 2 | 0 | 2 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0004c0005t0001 | 0/0 | 6974 | 9 | 9 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0005c0007t0001 | 0/0 | 6974 | 5 | 0 | 0 | 5 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0006c0006t0001 | 0/0 | 6974 | 5 | 5 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0007c0013t0001 | 0/0 | 6974 | 3 | 3 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0008c0012t0001 | 0/0 | 6974 | 3 | 3 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0009c0014t0001 | 0/0 | 6974 | 2 | 0 | 0 | 0 | 0 | 2 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0010c0029t0001 | 0/0 | 6974 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0010c0033t0001 | 0/0 | 6974 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0011c0015t0001 | 0/0 | 6974 | 2 | 2 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0012c0022t0001 | 0/0 | 6974 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0013c0024t0001 | 0/0 | 6974 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0014c0027t0001 | 0/0 | 6974 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0015c0030t0001 | 0/0 | 6974 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0016c0028t0001 | 0/0 | 6974 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0017c0020t0001 | 0/0 | 6974 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0018c0019t0001 | 0/0 | 6974 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0019c0032t0001 | 0/0 | 6974 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0020c0037t0001 | 0/0 | 6974 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0021c0036t0001 | 0/0 | 6974 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0022c0035t0001 | 0/0 | 6974 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0023c0018t0001 | 0/0 | 6974 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| a0024c0017t0001 | 0/0 | 6974 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | copy fasta | chr12 | 122522249 | 122631396 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0010t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0010t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0010t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0011t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0011t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0011t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0016t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0021t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0023t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0025t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0026t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0031t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0034t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0001c0038t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0002c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0002c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0002c0003t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0002c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0002c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0002c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0002c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0002c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0002c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0002c0003t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0002c0003t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0002c0003t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0002c0003t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0002c0009t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0002c0009t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0002c0009t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0002c0009t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0003c0004t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0003c0004t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0003c0004t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0003c0004t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0003c0004t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0003c0004t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0003c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0003c0004t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0003c0004t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0003c0004t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0003c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0003c0004t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0003c0008t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0003c0008t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0003c0008t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0003c0008t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0004c0005t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0004c0005t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0004c0005t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0004c0005t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0004c0005t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0004c0005t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0004c0005t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0004c0005t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0005c0007t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0005c0007t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0005c0007t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0005c0007t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0005c0007t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0006c0006t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0006c0006t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0006c0006t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0006c0006t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0006c0006t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0007c0013t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0007c0013t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0007c0013t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0008c0012t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0008c0012t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0008c0012t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0009c0014t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0010c0029t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0010c0033t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0011c0015t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0011c0015t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0012c0022t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0013c0024t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0014c0027t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0015c0030t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0016c0028t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0017c0020t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0018c0019t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0019c0032t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0020c0037t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0021c0036t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0022c0035t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0023c0018t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| a0024c0017t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | GBR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0048 | EUR | GBR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | FIN | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00280 | hp2 | a0003 | c0004 | t0001 | g0028 | EUR | FIN | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0252 | EUR | FIN | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0034 | EUR | FIN | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | CHS | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00423 | hp2 | a0001 | c0011 | t0001 | g0218 | EAS | CHS | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | CHS | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00597 | hp1 | a0023 | c0018 | t0001 | g0064 | EAS | CHS | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | CHS | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0084 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00639 | hp2 | a0003 | c0004 | t0001 | g0016 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0038 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0086 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01099 | hp1 | a0019 | c0032 | t0001 | g0127 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01106 | hp1 | a0003 | c0008 | t0002 | g0017 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0090 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01109 | hp1 | a0002 | c0009 | t0001 | g0202 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0079 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01168 | hp2 | a0003 | c0004 | t0001 | g0021 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01169 | hp2 | a0003 | c0004 | t0001 | g0020 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01243 | hp1 | a0021 | c0036 | t0001 | g0013 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01243 | hp2 | a0002 | c0003 | t0001 | g0278 | AMR | PUR | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | CLM | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | CLM | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | CLM | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01346 | hp1 | a0003 | c0008 | t0002 | g0018 | AMR | CLM | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | CLM | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | CLM | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01515 | hp1 | a0003 | c0004 | t0001 | g0023 | EUR | IBS | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0109 | EUR | IBS | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | IBS | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0085 | EUR | IBS | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | IBS | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01517 | hp2 | a0003 | c0004 | t0001 | g0024 | EUR | IBS | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01884 | hp1 | a0015 | c0030 | t0001 | g0280 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01884 | hp2 | a0008 | c0012 | t0001 | g0125 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01891 | hp1 | a0004 | c0005 | t0001 | g0313 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01928 | hp2 | a0001 | c0034 | t0001 | g0229 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0087 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01975 | hp1 | a0003 | c0004 | t0001 | g0019 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02056 | hp1 | a0016 | c0028 | t0001 | g0082 | EAS | KHV | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02071 | hp1 | a0018 | c0019 | t0001 | g0131 | EAS | KHV | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | KHV | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | KHV | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | KHV | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | KHV | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | KHV | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02145 | hp1 | a0002 | c0009 | t0001 | g0264 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CDX | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CDX | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0290 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02257 | hp2 | a0006 | c0006 | t0001 | g0246 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02258 | hp1 | a0001 | c0031 | t0001 | g0118 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02280 | hp2 | a0011 | c0015 | t0001 | g0274 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0277 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | KHV | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02572 | hp1 | a0011 | c0015 | t0001 | g0276 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02602 | hp1 | a0003 | c0004 | t0001 | g0026 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0072 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02630 | hp1 | a0004 | c0005 | t0001 | g0311 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0289 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02717 | hp1 | a0010 | c0029 | t0001 | g0314 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02723 | hp1 | a0001 | c0010 | t0001 | g0284 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02723 | hp2 | a0002 | c0003 | t0001 | g0291 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02735 | hp1 | a0003 | c0008 | t0001 | g0014 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0047 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02738 | hp2 | a0003 | c0004 | t0001 | g0027 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02895 | hp1 | a0007 | c0013 | t0001 | g0030 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02896 | hp1 | a0004 | c0005 | t0001 | g0004 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02897 | hp2 | a0004 | c0005 | t0001 | g0004 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02922 | hp1 | a0001 | c0010 | t0001 | g0282 | AFR | ESN | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02922 | hp2 | a0008 | c0012 | t0001 | g0005 | AFR | ESN | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02976 | hp1 | a0004 | c0005 | t0001 | g0309 | AFR | ESN | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03017 | hp2 | a0003 | c0004 | t0001 | g0008 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0272 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03041 | hp2 | a0020 | c0037 | t0001 | g0292 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | MSL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03139 | hp1 | a0004 | c0005 | t0001 | g0316 | AFR | ESN | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03139 | hp2 | a0002 | c0003 | t0001 | g0294 | AFR | ESN | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0296 | AFR | MSL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03225 | hp2 | a0007 | c0013 | t0001 | g0203 | AFR | MSL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03453 | hp1 | a0002 | c0003 | t0001 | g0273 | AFR | MSL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03453 | hp2 | a0017 | c0020 | t0001 | g0310 | AFR | MSL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03486 | hp1 | a0004 | c0005 | t0001 | g0312 | AFR | MSL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03486 | hp2 | a0004 | c0005 | t0001 | g0308 | AFR | MSL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03491 | hp1 | a0001 | c0016 | t0001 | g0076 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03491 | hp2 | a0009 | c0014 | t0001 | g0003 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03492 | hp1 | a0009 | c0014 | t0001 | g0003 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0295 | AFR | ESN | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03516 | hp2 | a0004 | c0005 | t0001 | g0307 | AFR | ESN | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | GWD | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0046 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0057 | SAS | BEB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03927 | hp1 | a0001 | c0026 | t0001 | g0081 | SAS | BEB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03942 | hp1 | a0003 | c0004 | t0001 | g0025 | SAS | BEB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03942 | hp2 | a0001 | c0002 | t0003 | g0093 | SAS | BEB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0110 | SAS | BEB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG04199 | hp1 | a0003 | c0004 | t0001 | g0022 | SAS | STU | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG04204 | hp1 | a0003 | c0008 | t0001 | g0015 | SAS | STU | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0056 | SAS | STU | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18522 | hp1 | a0002 | c0009 | t0001 | g0263 | AFR | YRI | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18522 | hp2 | a0002 | c0009 | t0001 | g0201 | AFR | YRI | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | CHB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | YRI | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | YRI | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18940 | hp1 | a0005 | c0007 | t0001 | g0279 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18941 | hp1 | a0005 | c0007 | t0001 | g0187 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18951 | hp2 | a0024 | c0017 | t0001 | g0065 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18963 | hp1 | a0014 | c0027 | t0001 | g0162 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18964 | hp2 | a0001 | c0038 | t0001 | g0173 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18973 | hp2 | a0001 | c0021 | t0001 | g0133 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18979 | hp1 | a0012 | c0022 | t0001 | g0043 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18986 | hp2 | a0001 | c0025 | t0001 | g0207 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19003 | hp1 | a0005 | c0007 | t0001 | g0167 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19010 | hp1 | a0001 | c0023 | t0001 | g0184 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19030 | hp2 | a0010 | c0033 | t0001 | g0315 | AFR | LWK | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19043 | hp1 | a0007 | c0013 | t0001 | g0204 | AFR | LWK | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | LWK | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19062 | hp1 | a0005 | c0007 | t0001 | g0136 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19067 | hp1 | a0001 | c0011 | t0001 | g0237 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19068 | hp2 | a0001 | c0011 | t0001 | g0305 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0078 | AFR | YRI | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA19240 | hp2 | a0006 | c0006 | t0001 | g0247 | AFR | YRI | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0275 | AFR | ASW | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ASW | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | TSI | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | TSI | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | GIH | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0261 | SAS | GIH | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02109 | hp1 | a0006 | c0006 | t0001 | g0248 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02109 | hp2 | a0001 | c0010 | t0001 | g0283 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02486 | hp2 | a0022 | c0035 | t0001 | g0029 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02559 | hp1 | a0008 | c0012 | t0001 | g0126 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03471 | hp1 | a0002 | c0003 | t0001 | g0124 | AFR | MSL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG06807 | hp1 | a0002 | c0003 | t0001 | g0293 | AFR | USA | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| HG06807 | hp2 | a0006 | c0006 | t0001 | g0245 | AFR | USA | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18955 | hp1 | a0005 | c0007 | t0001 | g0195 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | USA | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA20300 | hp2 | a0013 | c0024 | t0001 | g0119 | AFR | USA | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| NA21309 | hp2 | a0006 | c0006 | t0001 | g0249 | AFR | LWK | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0106 | REF | REF | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0227 | REF | REF | KNTC1_chr12_122522249_122631396 | KNTC1 | chr12 | 122522249 | 122631396 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122530096
|
T | A | 1 | a0024 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.33T>A | p.Asp11Glu | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/64 | 209/6974 | 33/6630 | 11/2209 | chr12 | 122530096 | ||
| chr12:122534703
|
G | A | 1 | a0023 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.169G>A | p.Asp57Asn | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/64 | 345/6974 | 169/6630 | 57/2209 | chr12 | 122534703 | ||
| chr12:122538449
|
A | G | 1 | a0024 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.361A>G | p.Thr121Ala | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 4/64 | 537/6974 | 361/6630 | 121/2209 | chr12 | 122538449 | ||
| chr12:122544192
|
A | G | 1 | a0005 | 5 | NA18940.hp1 NA18941.hp1 NA18955.hp1 others(2): Show |
missense_variant | MODERATE | c.592A>G | p.Thr198Ala | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 8/64 | 768/6974 | 592/6630 | 198/2209 | chr12 | 122544192 | ||
| chr12:122546241
|
G | T | 8 | a0002a0003a0007others(5): Show | 44 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(41): Show |
missense_variant | MODERATE | c.735G>T | p.Lys245Asn | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 9/64 | 911/6974 | 735/6630 | 245/2209 | chr12 | 122546241 | ||
| chr12:122547958
|
G | C | 1 | a0011 | 2 | HG02280.hp2 HG02572.hp1 |
missense_variant | MODERATE | c.976G>C | p.Ala326Pro | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/64 | 1152/6974 | 976/6630 | 326/2209 | chr12 | 122547958 | ||
| chr12:122549853
|
G | A | 2 | a0021a0022 | 2 | HG01243.hp1 HG02486.hp2 |
missense_variant | MODERATE | c.1075G>A | p.Gly359Arg | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/64 | 1251/6974 | 1075/6630 | 359/2209 | chr12 | 122549853 | ||
| chr12:122557457
|
C | A | 1 | a0007 | 3 | HG02895.hp1 HG03225.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.1346C>A | p.Thr449Asn | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 17/64 | 1522/6974 | 1346/6630 | 449/2209 | chr12 | 122557457 | ||
| chr12:122569780
|
A | G | 1 | a0021 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.1816A>G | p.Asn606Asp | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 22/64 | 1992/6974 | 1816/6630 | 606/2209 | chr12 | 122569780 | ||
| chr12:122573245
|
A | G | 1 | a0019 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.2243A>G | p.His748Arg | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 26/64 | 2419/6974 | 2243/6630 | 748/2209 | chr12 | 122573245 | ||
| chr12:122575885
|
A | G | 1 | a0009 | 2 | HG03491.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.2572A>G | p.Asn858Asp | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/64 | 2748/6974 | 2572/6630 | 858/2209 | chr12 | 122575885 | ||
| chr12:122577672
|
G | A | 1 | a0018 | 1 | HG02071.hp1 | missense_variant&splice_region_variant | MODERATE | c.2722G>A | p.Gly908Ser | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/64 | 2898/6974 | 2722/6630 | 908/2209 | chr12 | 122577672 | ||
| chr12:122582969
|
G | A | 1 | a0017 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.3247G>A | p.Ala1083Thr | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 34/64 | 3423/6974 | 3247/6630 | 1083/2209 | chr12 | 122582969 | ||
| chr12:122588725
|
C | T | 1 | a0020 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.3908C>T | p.Thr1303Ile | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/64 | 4084/6974 | 3908/6630 | 1303/2209 | chr12 | 122588725 | ||
| chr12:122597738
|
C | G | 1 | a0006 | 5 | HG02109.hp1 HG02257.hp2 HG06807.hp2 others(2): Show |
missense_variant | MODERATE | c.4363C>G | p.Gln1455Glu | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/64 | 4539/6974 | 4363/6630 | 1455/2209 | chr12 | 122597738 | ||
| chr12:122597892
|
C | T | 1 | a0010 | 2 | HG02717.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.4517C>T | p.Thr1506Met | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/64 | 4693/6974 | 4517/6630 | 1506/2209 | chr12 | 122597892 | ||
| chr12:122597910
|
T | G | 1 | a0012 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.4535T>G | p.Val1512Gly | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/64 | 4711/6974 | 4535/6630 | 1512/2209 | chr12 | 122597910 | ||
| chr12:122597918
|
C | G | 1 | a0016 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.4543C>G | p.Leu1515Val | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/64 | 4719/6974 | 4543/6630 | 1515/2209 | chr12 | 122597918 | ||
| chr12:122601541
|
T | G | 1 | a0015 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.4569T>G | p.Asp1523Glu | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 45/64 | 4745/6974 | 4569/6630 | 1523/2209 | chr12 | 122601541 | ||
| chr12:122602620
|
G | A | 1 | a0013 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.4705G>A | p.Val1569Met | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 46/64 | 4881/6974 | 4705/6630 | 1569/2209 | chr12 | 122602620 | ||
| chr12:122605408
|
C | T | 3 | a0004a0010a0017 | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
missense_variant | MODERATE | c.5489C>T | p.Pro1830Leu | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/64 | 5665/6974 | 5489/6630 | 1830/2209 | chr12 | 122605408 | ||
| chr12:122618374
|
T | G | 3 | a0003a0021a0022 | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
missense_variant | MODERATE | c.6062T>G | p.Val2021Gly | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 58/64 | 6238/6974 | 6062/6630 | 2021/2209 | chr12 | 122618374 | ||
| chr12:122624665
|
A | G | 1 | a0008 | 3 | HG01884.hp2 HG02559.hp1 HG02922.hp2 |
missense_variant | MODERATE | c.6583A>G | p.Thr2195Ala | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/64 | 6759/6974 | 6583/6630 | 2195/2209 | chr12 | 122624665 | ||
| chr12:122624681
|
T | G | 1 | a0014 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.6599T>G | p.Ile2200Ser | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/64 | 6775/6974 | 6599/6630 | 2200/2209 | chr12 | 122624681 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122530081
|
G | A | 1 | a0001c0016 | 1 | HG03491.hp1 | synonymous_variant | LOW | c.18G>A | p.Glu6Glu | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/64 | 194/6974 | 18/6630 | 6/2209 | chr12 | 122530081 | ||
| chr12:122530138
|
A | G | 1 | a0001c0038 | 1 | NA18964.hp2 | synonymous_variant | LOW | c.75A>G | p.Glu25Glu | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/64 | 251/6974 | 75/6630 | 25/2209 | chr12 | 122530138 | ||
| chr12:122534723
|
C | T | 2 | a0002c0009a0007c0013 | 7 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
synonymous_variant | LOW | c.189C>T | p.Ala63Ala | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/64 | 365/6974 | 189/6630 | 63/2209 | chr12 | 122534723 | ||
| chr12:122547417
|
C | T | 1 | a0001c0034 | 1 | HG01928.hp2 | splice_region_variant&synonymous_variant | LOW | c.819C>T | p.Asn273Asn | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 11/64 | 995/6974 | 819/6630 | 273/2209 | chr12 | 122547417 | ||
| chr12:122551482
|
G | C | 2 | a0002c0009a0007c0013 | 7 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
synonymous_variant | LOW | c.1155G>C | p.Val385Val | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 15/64 | 1331/6974 | 1155/6630 | 385/2209 | chr12 | 122551482 | ||
| chr12:122557458
|
C | T | 1 | a0010c0033 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1347C>T | p.Thr449Thr | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 17/64 | 1523/6974 | 1347/6630 | 449/2209 | chr12 | 122557458 | ||
| chr12:122557479
|
C | T | 1 | a0010c0033 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1368C>T | p.Asp456Asp | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 17/64 | 1544/6974 | 1368/6630 | 456/2209 | chr12 | 122557479 | ||
| chr12:122582890
|
A | T | 2 | a0001c0031a0015c0030 | 2 | HG01884.hp1 HG02258.hp1 |
synonymous_variant | LOW | c.3168A>T | p.Ala1056Ala | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 34/64 | 3344/6974 | 3168/6630 | 1056/2209 | chr12 | 122582890 | ||
| chr12:122585671
|
G | A | 1 | a0003c0008 | 4 | HG01106.hp1 HG01346.hp1 HG02735.hp1 others(1): Show |
synonymous_variant | LOW | c.3570G>A | p.Glu1190Glu | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/64 | 3746/6974 | 3570/6630 | 1190/2209 | chr12 | 122585671 | ||
| chr12:122585773
|
T | G | 1 | a0001c0021 | 1 | NA18973.hp2 | splice_region_variant&synonymous_variant | LOW | c.3672T>G | p.Ala1224Ala | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/64 | 3848/6974 | 3672/6630 | 1224/2209 | chr12 | 122585773 | ||
| chr12:122587718
|
C | T | 1 | a0001c0011 | 3 | HG00423.hp2 NA19067.hp1 NA19068.hp2 |
synonymous_variant | LOW | c.3738C>T | p.Gly1246Gly | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 39/64 | 3914/6974 | 3738/6630 | 1246/2209 | chr12 | 122587718 | ||
| chr12:122594317
|
G | A | 2 | a0002c0009a0007c0013 | 7 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
synonymous_variant | LOW | c.4287G>A | p.Lys1429Lys | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/64 | 4463/6974 | 4287/6630 | 1429/2209 | chr12 | 122594317 | ||
| chr12:122597911
|
C | T | 1 | a0012c0022 | 1 | NA18979.hp1 | synonymous_variant | LOW | c.4536C>T | p.Val1512Val | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/64 | 4712/6974 | 4536/6630 | 1512/2209 | chr12 | 122597911 | ||
| chr12:122601547
|
T | C | 1 | a0001c0023 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.4575T>C | p.Tyr1525Tyr | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 45/64 | 4751/6974 | 4575/6630 | 1525/2209 | chr12 | 122601547 | ||
| chr12:122604939
|
G | A | 1 | a0001c0025 | 1 | NA18986.hp2 | synonymous_variant | LOW | c.5238G>A | p.Ser1746Ser | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 50/64 | 5414/6974 | 5238/6630 | 1746/2209 | chr12 | 122604939 | ||
| chr12:122605397
|
T | C | 1 | a0001c0026 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.5478T>C | p.Pro1826Pro | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/64 | 5654/6974 | 5478/6630 | 1826/2209 | chr12 | 122605397 | ||
| chr12:122610838
|
C | T | 1 | a0024c0017 | 1 | NA18951.hp2 | synonymous_variant | LOW | c.5560C>T | p.Leu1854Leu | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/64 | 5736/6974 | 5560/6630 | 1854/2209 | chr12 | 122610838 | ||
| chr12:122615017
|
T | C | 1 | a0001c0010 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
synonymous_variant | LOW | c.5904T>C | p.Cys1968Cys | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 56/64 | 6080/6974 | 5904/6630 | 1968/2209 | chr12 | 122615017 | ||
| chr12:122615026
|
C | T | 1 | a0001c0010 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
synonymous_variant | LOW | c.5913C>T | p.Tyr1971Tyr | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 56/64 | 6089/6974 | 5913/6630 | 1971/2209 | chr12 | 122615026 | ||
| chr12:122620596
|
C | T | 7 | a0001c0002a0001c0016a0001c0026others(4): Show | 87 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(84): Show |
synonymous_variant | LOW | c.6267C>T | p.His2089His | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 60/64 | 6443/6974 | 6267/6630 | 2089/2209 | chr12 | 122620596 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122626238
|
C | A | 1 | a0003c0008t0002 | 2 | HG01106.hp1 HG01346.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 64/64 | 10 | chr12 | 122626238 | |||||
| chr12:122626363
|
T | A | 1 | a0001c0002t0003 | 2 | HG01106.hp2 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*135T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 64/64 | 135 | chr12 | 122626363 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122527443
|
T | C | 1 | a0008c0012t0001g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-74+92T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122527443 | ||||||
| chr12:122527564
|
G | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-74+213G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122527564 | ||||||
| chr12:122527579
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-74+228T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122527579 | ||||||
| chr12:122527683
|
T | C | 1 | a0001c0002t0001g0007 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-74+332T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122527683 | ||||||
| chr12:122527786
|
T | C | 22 | a0001c0001t0001g0011a0001c0002t0001g0009a0001c0002t0001g0010others(19): Show | 22 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.-74+435T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122527786 | ||||||
| chr12:122527824
|
C | G | 2 | a0001c0001t0001g0306a0008c0012t0001g0005 | 2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-74+473C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122527824 | ||||||
| chr12:122527911
|
C | T | 1 | a0001c0011t0001g0305 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-74+560C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122527911 | ||||||
| chr12:122527964
|
C | T | 1 | a0001c0001t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-74+613C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122527964 | ||||||
| chr12:122528057
|
C | T | 7 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(4): Show | 7 | HG02080.hp2 HG02135.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.-74+706C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122528057 | ||||||
| chr12:122528079
|
CA | C | 8 | a0002c0003t0001g0289a0002c0003t0001g0290a0002c0003t0001g0291others(5): Show | 8 | HG02257.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-74+730delA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | INFO_REALIGN_3_PRIME | chr12 | 122528079 | |||||
| chr12:122528240
|
CCTT | C | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-74+894_-74+896del others(3): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | INFO_REALIGN_3_PRIME | chr12 | 122528240 | |||||
| chr12:122528502
|
G | A | 1 | a0003c0004t0001g0008 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-74+1151G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122528502 | ||||||
| chr12:122528543
|
C | T | 1 | a0001c0001t0001g0288 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-74+1192C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122528543 | ||||||
| chr12:122528764
|
C | T | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-73-1227C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122528764 | ||||||
| chr12:122528797
|
C | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-73-1194C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122528797 | ||||||
| chr12:122528809
|
G | A | 7 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(4): Show | 7 | HG02080.hp2 HG02135.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.-73-1182G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122528809 | ||||||
| chr12:122528829
|
C | T | 1 | a0001c0002t0001g0281 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-73-1162C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122528829 | ||||||
| chr12:122528848
|
A | T | 12 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(9): Show | 13 | HG01884.hp1 HG01891.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-73-1143A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122528848 | ||||||
| chr12:122528850
|
T | A | 1 | a0007c0013t0001g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-73-1141T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122528850 | ||||||
| chr12:122528867
|
GT | G | 114 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(111): Show | 115 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-73-1121delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | INFO_REALIGN_3_PRIME | chr12 | 122528867 | |||||
| chr12:122528930
|
C | T | 1 | a0005c0007t0001g0279 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-73-1061C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122528930 | ||||||
| chr12:122528950
|
C | G | 15 | a0002c0003t0001g0272a0002c0003t0001g0273a0002c0003t0001g0275others(12): Show | 15 | HG01243.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-73-1041C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122528950 | ||||||
| chr12:122529053
|
A | T | 1 | a0022c0035t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-73-938A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122529053 | ||||||
| chr12:122529087
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-73-904A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122529087 | ||||||
| chr12:122529126
|
G | T | 1 | a0001c0001t0001g0270 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-73-865G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122529126 | ||||||
| chr12:122529133
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-73-858C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122529133 | ||||||
| chr12:122529135
|
C | T | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG02165.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.-73-856C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122529135 | ||||||
| chr12:122529312
|
G | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-73-679G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122529312 | ||||||
| chr12:122529399
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-73-592A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122529399 | ||||||
| chr12:122529583
|
C | G | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02165.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.-73-408C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122529583 | ||||||
| chr12:122529808
|
A | G | 12 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(9): Show | 13 | HG01884.hp1 HG01891.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-73-183A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122529808 | ||||||
| chr12:122529872
|
T | C | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-73-119T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 1/63 | chr12 | 122529872 | ||||||
| chr12:122530237
|
G | A | 1 | a0019c0032t0001g0127 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.129+45G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122530237 | ||||||
| chr12:122530377
|
C | CA | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0288 | 3 | HG01081.hp1 HG01993.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.129+186dupA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | INFO_REALIGN_3_PRIME | chr12 | 122530377 | |||||
| chr12:122530383
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.129+191T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122530383 | ||||||
| chr12:122530530
|
A | G | 8 | a0002c0003t0001g0289a0002c0003t0001g0290a0002c0003t0001g0291others(5): Show | 8 | HG02257.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.129+338A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122530530 | ||||||
| chr12:122530608
|
G | A | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.129+416G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122530608 | ||||||
| chr12:122531048
|
CT | C | 20 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(17): Show | 20 | HG01243.hp2 HG01884.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.129+868delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | INFO_REALIGN_3_PRIME | chr12 | 122531048 | |||||
| chr12:122531081
|
A | T | 1 | a0001c0001t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.129+889A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122531081 | ||||||
| chr12:122531188
|
T | C | 2 | a0002c0003t0001g0272a0002c0003t0001g0273 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.129+996T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122531188 | ||||||
| chr12:122531215
|
G | C | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.129+1023G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122531215 | ||||||
| chr12:122531276
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.129+1084G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122531276 | ||||||
| chr12:122531321
|
C | T | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.129+1129C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122531321 | ||||||
| chr12:122531533
|
G | T | 1 | a0001c0011t0001g0305 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.129+1341G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122531533 | ||||||
| chr12:122531599
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.129+1407C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122531599 | ||||||
| chr12:122531614
|
CATT | C | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.129+1426_129+1428d others(5): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | INFO_REALIGN_3_PRIME | chr12 | 122531614 | |||||
| chr12:122531776
|
C | T | 2 | a0002c0009t0001g0263a0002c0009t0001g0264 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.129+1584C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122531776 | ||||||
| chr12:122531803
|
A | G | 14 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.129+1611A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122531803 | ||||||
| chr12:122531853
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.129+1661C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122531853 | ||||||
| chr12:122531878
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.129+1686C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122531878 | ||||||
| chr12:122531981
|
G | C | 2 | a0001c0002t0001g0031a0001c0002t0001g0032 | 2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.129+1789G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122531981 | ||||||
| chr12:122532037
|
G | GT | 93 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0260others(90): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.129+1859dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | INFO_REALIGN_3_PRIME | chr12 | 122532037 | |||||
| chr12:122532191
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(84): Show | 89 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(86): Show |
intron_variant | MODIFIER | c.129+1999G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122532191 | ||||||
| chr12:122532206
|
C | CT | 9 | a0001c0001t0001g0006a0001c0001t0001g0258a0001c0001t0001g0259others(6): Show | 9 | HG00438.hp2 HG00597.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.129+2035dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | INFO_REALIGN_3_PRIME | chr12 | 122532206 | |||||
| chr12:122532206
|
CT | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0111others(118): Show | 125 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.129+2035delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | INFO_REALIGN_3_PRIME | chr12 | 122532206 | |||||
| chr12:122532206
|
CTT | C | 11 | a0001c0001t0001g0270a0001c0010t0001g0282a0001c0010t0001g0283others(8): Show | 11 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.129+2034_129+2035d others(4): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | INFO_REALIGN_3_PRIME | chr12 | 122532206 | |||||
| chr12:122532206
|
CTTT | C | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.129+2033_129+2035d others(5): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | INFO_REALIGN_3_PRIME | chr12 | 122532206 | |||||
| chr12:122532212
|
T | C | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | NA18968.hp1 NA19009.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.129+2020T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122532212 | ||||||
| chr12:122532213
|
T | C | 18 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(15): Show | 19 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.129+2021T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122532213 | ||||||
| chr12:122532214
|
T | C | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.129+2022T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122532214 | ||||||
| chr12:122532233
|
G | A | 1 | a0021c0036t0001g0013 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.129+2041G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122532233 | ||||||
| chr12:122532234
|
A | G | 164 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(161): Show | 165 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.129+2042A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122532234 | ||||||
| chr12:122532270
|
G | A | 1 | a0015c0030t0001g0280 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.129+2078G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122532270 | ||||||
| chr12:122532431
|
T | C | 1 | a0009c0014t0001g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.130-2233T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122532431 | ||||||
| chr12:122532664
|
T | C | 2 | a0003c0008t0001g0014a0003c0008t0001g0015 | 2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.130-2000T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122532664 | ||||||
| chr12:122533100
|
C | G | 1 | a0005c0007t0001g0195 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.130-1564C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122533100 | ||||||
| chr12:122533114
|
G | T | 1 | a0001c0001t0001g0194 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.130-1550G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122533114 | ||||||
| chr12:122533181
|
T | C | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | NA18986.hp1 NA19010.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.130-1483T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122533181 | ||||||
| chr12:122533312
|
G | A | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.130-1352G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122533312 | ||||||
| chr12:122533315
|
C | T | 1 | a0001c0002t0001g0106 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.130-1349C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122533315 | ||||||
| chr12:122533444
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.130-1220C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122533444 | ||||||
| chr12:122533525
|
G | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.130-1139G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122533525 | ||||||
| chr12:122533737
|
TTGGGGAA others(207): Show |
T | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.130-923_130-710del | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | INFO_REALIGN_3_PRIME | chr12 | 122533737 | |||||
| chr12:122533864
|
C | T | 7 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-800C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122533864 | ||||||
| chr12:122533896
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.130-768C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122533896 | ||||||
| chr12:122533928
|
T | C | 2 | a0001c0001t0001g0270a0019c0032t0001g0127 | 2 | HG01099.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.130-736T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122533928 | ||||||
| chr12:122533936
|
T | C | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.130-728T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122533936 | ||||||
| chr12:122533999
|
C | G | 1 | a0001c0002t0001g0105 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.130-665C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122533999 | ||||||
| chr12:122534111
|
T | A | 13 | a0002c0003t0001g0275a0002c0003t0001g0277a0002c0003t0001g0278others(10): Show | 13 | HG01243.hp2 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.130-553T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122534111 | ||||||
| chr12:122534215
|
A | G | 93 | a0001c0001t0001g0011a0001c0001t0001g0128a0001c0001t0001g0260others(90): Show | 93 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.130-449A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122534215 | ||||||
| chr12:122534347
|
T | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.130-317T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122534347 | ||||||
| chr12:122534432
|
A | C | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.130-232A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122534432 | ||||||
| chr12:122534493
|
A | G | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.130-171A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 2/63 | chr12 | 122534493 | ||||||
| chr12:122535063
|
T | C | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.250+279T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122535063 | ||||||
| chr12:122535164
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.250+380T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122535164 | ||||||
| chr12:122535173
|
T | C | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.250+389T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122535173 | ||||||
| chr12:122535243
|
G | C | 1 | a0005c0007t0001g0136 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.250+459G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122535243 | ||||||
| chr12:122535249
|
C | T | 1 | a0003c0004t0001g0026 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.250+465C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122535249 | ||||||
| chr12:122535354
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.250+570T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122535354 | ||||||
| chr12:122535388
|
C | T | 88 | a0001c0001t0001g0011a0001c0002t0001g0007a0001c0002t0001g0009others(85): Show | 88 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.250+604C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122535388 | ||||||
| chr12:122535428
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.250+644C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122535428 | ||||||
| chr12:122535487
|
A | C | 7 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.250+703A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122535487 | ||||||
| chr12:122535504
|
G | C | 7 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.250+720G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122535504 | ||||||
| chr12:122535765
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.250+981A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122535765 | ||||||
| chr12:122535859
|
G | T | 13 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.250+1075G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122535859 | ||||||
| chr12:122535889
|
G | GT | 12 | a0001c0001t0001g0134a0001c0001t0001g0188a0001c0001t0001g0189others(9): Show | 12 | HG02056.hp2 HG02738.hp2 HG03098.hp1 others(9): Show |
intron_variant | MODIFIER | c.250+1123dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | INFO_REALIGN_3_PRIME | chr12 | 122535889 | |||||
| chr12:122535889
|
GT | G | 12 | a0001c0001t0001g0137a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG00609.hp2 HG01109.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.250+1123delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | INFO_REALIGN_3_PRIME | chr12 | 122535889 | |||||
| chr12:122536049
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.250+1265A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122536049 | ||||||
| chr12:122536107
|
G | A | 5 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(2): Show | 5 | HG02055.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.250+1323G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122536107 | ||||||
| chr12:122536125
|
G | A | 1 | a0021c0036t0001g0013 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.250+1341G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122536125 | ||||||
| chr12:122536232
|
T | A | 5 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.250+1448T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122536232 | ||||||
| chr12:122536276
|
G | A | 116 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(113): Show | 117 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.250+1492G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122536276 | ||||||
| chr12:122536403
|
T | C | 1 | a0012c0022t0001g0043 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.250+1619T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122536403 | ||||||
| chr12:122536469
|
G | A | 16 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(13): Show | 16 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.250+1685G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122536469 | ||||||
| chr12:122536474
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(86): Show | 91 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.250+1690G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122536474 | ||||||
| chr12:122536501
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.250+1717C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122536501 | ||||||
| chr12:122536521
|
C | CT | 19 | a0001c0001t0001g0116a0001c0001t0001g0122a0001c0001t0001g0185others(16): Show | 19 | HG01175.hp1 HG01175.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.250+1751dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | INFO_REALIGN_3_PRIME | chr12 | 122536521 | |||||
| chr12:122536658
|
T | C | 1 | a0001c0001t0001g0260 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.251-1681T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122536658 | ||||||
| chr12:122536732
|
G | A | 2 | a0001c0002t0001g0044a0001c0002t0001g0045 | 2 | HG02071.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.251-1607G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122536732 | ||||||
| chr12:122536969
|
T | C | 12 | a0001c0001t0001g0111a0004c0005t0001g0004a0004c0005t0001g0307others(9): Show | 13 | HG01891.hp1 HG02572.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.251-1370T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122536969 | ||||||
| chr12:122536997
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.251-1342A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122536997 | ||||||
| chr12:122537038
|
T | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0137a0001c0001t0001g0138others(2): Show | 6 | NA18952.hp1 NA18954.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-1301T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122537038 | ||||||
| chr12:122537052
|
TTGTGGCG others(3): Show |
T | 1 | a0001c0002t0001g0044 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.251-1285_251-1276d others(12): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | INFO_REALIGN_3_PRIME | chr12 | 122537052 | |||||
| chr12:122537226
|
C | T | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.251-1113C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122537226 | ||||||
| chr12:122537375
|
C | G | 1 | a0001c0001t0001g0270 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.251-964C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122537375 | ||||||
| chr12:122537421
|
A | AT | 7 | a0001c0001t0001g0011a0001c0001t0001g0193a0001c0001t0001g0306others(4): Show | 7 | HG02698.hp2 HG03017.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-903dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | INFO_REALIGN_3_PRIME | chr12 | 122537421 | |||||
| chr12:122537421
|
AT | A | 11 | a0001c0001t0001g0134a0001c0002t0001g0046a0001c0002t0001g0281others(8): Show | 11 | HG00639.hp2 HG01109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.251-903delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | INFO_REALIGN_3_PRIME | chr12 | 122537421 | |||||
| chr12:122537480
|
G | A | 1 | a0002c0003t0001g0272 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.251-859G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122537480 | ||||||
| chr12:122537528
|
C | T | 2 | a0001c0001t0001g0183a0001c0023t0001g0184 | 2 | NA18982.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.251-811C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122537528 | ||||||
| chr12:122537574
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.251-765A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122537574 | ||||||
| chr12:122537638
|
G | A | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02055.hp2 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-701G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122537638 | ||||||
| chr12:122537669
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.251-670C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122537669 | ||||||
| chr12:122537816
|
A | G | 7 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.251-523A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122537816 | ||||||
| chr12:122537830
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.251-509G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | chr12 | 122537830 | ||||||
| chr12:122537976
|
T | TA | 89 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0002t0001g0007others(86): Show | 89 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.251-362dupA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 3/63 | INFO_REALIGN_3_PRIME | chr12 | 122537976 | |||||
| chr12:122538667
|
C | T | 1 | a0001c0010t0001g0284 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.366+213C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 4/63 | chr12 | 122538667 | ||||||
| chr12:122538718
|
G | GT | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.366+265dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 4/63 | INFO_REALIGN_3_PRIME | chr12 | 122538718 | |||||
| chr12:122538784
|
G | T | 1 | a0001c0002t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.366+330G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 4/63 | chr12 | 122538784 | ||||||
| chr12:122538989
|
G | A | 6 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG01258.hp1 HG01346.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.366+535G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 4/63 | chr12 | 122538989 | ||||||
| chr12:122539019
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.366+565G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 4/63 | chr12 | 122539019 | ||||||
| chr12:122539026
|
A | G | 1 | a0001c0001t0001g0211 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.366+572A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 4/63 | chr12 | 122539026 | ||||||
| chr12:122539062
|
T | C | 1 | a0009c0014t0001g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.366+608T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 4/63 | chr12 | 122539062 | ||||||
| chr12:122539342
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.367-334A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 4/63 | chr12 | 122539342 | ||||||
| chr12:122539381
|
A | T | 7 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.367-295A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 4/63 | chr12 | 122539381 | ||||||
| chr12:122539394
|
C | T | 3 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0001t0001g0267 | 3 | NA18964.hp1 NA19001.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.367-282C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 4/63 | chr12 | 122539394 | ||||||
| chr12:122539785
|
C | CT | 103 | a0001c0001t0001g0011a0001c0001t0001g0134a0001c0001t0001g0260others(100): Show | 104 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.445+47dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122539785 | |||||
| chr12:122539834
|
T | G | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.445+80T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122539834 | ||||||
| chr12:122539884
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.445+130C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122539884 | ||||||
| chr12:122539929
|
G | T | 7 | a0001c0001t0001g0130a0001c0001t0001g0251a0001c0001t0001g0252others(4): Show | 7 | HG00280.hp1 HG00323.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.445+175G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122539929 | ||||||
| chr12:122540053
|
G | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.445+299G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122540053 | ||||||
| chr12:122540071
|
A | T | 1 | a0001c0002t0001g0101 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.445+317A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122540071 | ||||||
| chr12:122540138
|
T | G | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.445+384T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122540138 | ||||||
| chr12:122540175
|
G | GT | 47 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(44): Show | 47 | HG01109.hp1 HG01243.hp2 HG01433.hp2 others(44): Show |
intron_variant | MODIFIER | c.445+435dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122540175 | |||||
| chr12:122540235
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.445+481C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122540235 | ||||||
| chr12:122540247
|
A | G | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.445+493A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122540247 | ||||||
| chr12:122540264
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.445+510C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122540264 | ||||||
| chr12:122540300
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0188 | 3 | HG02145.hp2 HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.445+546G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122540300 | ||||||
| chr12:122540337
|
T | TAATTTTT others(13): Show |
1 | a0001c0001t0001g0134 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.445+584_445+603dup others(20): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122540337 | |||||
| chr12:122540505
|
T | G | 1 | a0001c0001t0001g0146 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.445+751T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122540505 | ||||||
| chr12:122540535
|
A | T | 1 | a0004c0005t0001g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.445+781A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122540535 | ||||||
| chr12:122540948
|
A | G | 1 | a0001c0002t0001g0109 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.446-1102A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122540948 | ||||||
| chr12:122540998
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(85): Show | 90 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.446-1052G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122540998 | ||||||
| chr12:122541008
|
C | T | 1 | a0003c0004t0001g0027 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.446-1042C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541008 | ||||||
| chr12:122541029
|
C | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(250): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.446-1021C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541029 | ||||||
| chr12:122541135
|
C | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0197 | 3 | HG01168.hp1 HG01175.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.446-915C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541135 | ||||||
| chr12:122541136
|
G | T | 7 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(4): Show | 7 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.446-914G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541136 | ||||||
| chr12:122541209
|
A | C | 3 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0002t0001g0108 | 3 | HG02080.hp1 NA18955.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.446-841A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541209 | ||||||
| chr12:122541261
|
T | TTGCC | 11 | a0003c0008t0002g0017a0003c0008t0002g0018a0004c0005t0001g0004others(8): Show | 12 | HG01106.hp1 HG01346.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.446-763_446-760dup others(4): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541261 | |||||
| chr12:122541283
|
G | GCCTT | 4 | a0001c0002t0001g0098a0002c0009t0001g0263a0002c0009t0001g0264others(1): Show | 4 | HG02145.hp1 HG02486.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.446-764_446-763ins others(4): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541283 | |||||
| chr12:122541287
|
G | GCCTGCCT others(33): Show |
1 | a0002c0003t0001g0124 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.446-760_446-759ins others(40): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTGCCT others(37): Show |
1 | a0008c0012t0001g0125 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.446-760_446-759ins others(44): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTGCCT others(41): Show |
1 | a0008c0012t0001g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.446-760_446-759ins others(48): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTGCCT others(29): Show |
1 | a0008c0012t0001g0126 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.446-760_446-759ins others(36): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTGCCT others(17): Show |
1 | a0002c0003t0001g0278 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.446-760_446-759ins others(24): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTGCCT others(25): Show |
1 | a0002c0003t0001g0290 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.446-760_446-759ins others(32): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTGCCT others(33): Show |
1 | a0011c0015t0001g0274 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.446-760_446-759ins others(40): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTGCCT others(13): Show |
2 | a0002c0003t0001g0275a0002c0003t0001g0291 | 2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.446-760_446-759ins others(20): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTGCCT others(17): Show |
1 | a0020c0037t0001g0292 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.446-760_446-759ins others(24): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTGCCT others(21): Show |
5 | a0002c0003t0001g0289a0002c0003t0001g0293a0002c0003t0001g0294others(2): Show | 5 | HG02647.hp1 HG03139.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.446-760_446-759ins others(28): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTGCCT others(29): Show |
2 | a0002c0003t0001g0272a0002c0003t0001g0273 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.446-760_446-759ins others(36): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTGCCT others(37): Show |
1 | a0011c0015t0001g0276 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.446-760_446-759ins others(44): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTGCCT others(5): Show |
1 | a0001c0001t0001g0262 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.446-760_446-759ins others(12): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTGCCT others(25): Show |
1 | a0002c0003t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.446-760_446-759ins others(32): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTGCCT others(1): Show |
4 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0298others(1): Show | 4 | HG01074.hp2 HG01255.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-760_446-759ins others(8): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTGCCT others(5): Show |
68 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(65): Show | 69 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.446-760_446-759ins others(12): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTGCCT others(9): Show |
14 | a0001c0001t0001g0002a0001c0001t0001g0135a0001c0001t0001g0143others(11): Show | 15 | HG01261.hp1 HG01346.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.446-760_446-759ins others(16): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTGCCT others(13): Show |
1 | a0001c0002t0001g0039 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.446-760_446-759ins others(20): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTT | 12 | a0001c0001t0001g0285a0001c0002t0001g0055a0001c0002t0001g0056others(9): Show | 13 | HG01515.hp1 HG01517.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.446-728_446-725dup others(4): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTTCCT others(1): Show |
50 | a0001c0001t0001g0146a0001c0001t0001g0175a0001c0001t0001g0176others(47): Show | 50 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.446-732_446-725dup others(8): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTTCCT others(5): Show |
46 | a0001c0001t0001g0011a0001c0001t0001g0198a0001c0001t0001g0199others(43): Show | 46 | HG00323.hp2 HG00438.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.446-736_446-725dup others(12): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTTCCT others(9): Show |
8 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0095others(5): Show | 8 | HG01433.hp2 HG01496.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-740_446-725dup others(16): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTTCCT others(13): Show |
3 | a0001c0002t0001g0096a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.446-744_446-725dup others(20): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCCTTCCT others(17): Show |
2 | a0001c0002t0001g0097a0001c0002t0001g0106 | 2 | NA19070.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.446-748_446-725dup others(24): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | GCGCCTGC others(11): Show |
1 | a0001c0001t0001g0134 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.446-762_446-761ins others(18): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541287 | |||||
| chr12:122541287
|
G | T | 7 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0002t0001g0098others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.446-763G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541287 | ||||||
| chr12:122541291
|
T | G | 10 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(7): Show | 11 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.446-759T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541291 | ||||||
| chr12:122541295
|
T | G | 1 | a0004c0005t0001g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.446-755T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541295 | ||||||
| chr12:122541299
|
T | G | 1 | a0001c0001t0001g0174 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.446-751T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541299 | ||||||
| chr12:122541314
|
TTCCTTCC others(5): Show |
T | 2 | a0003c0004t0001g0019a0003c0004t0001g0028 | 2 | HG00280.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.446-727_446-716del others(12): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541314 | |||||
| chr12:122541318
|
TTCCTTCC others(1): Show |
T | 13 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.446-724_446-717del others(8): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541318 | |||||
| chr12:122541326
|
G | T | 148 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0001t0001g0285others(145): Show | 149 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.446-724G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541326 | ||||||
| chr12:122541435
|
T | C | 1 | a0001c0002t0001g0046 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.446-615T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541435 | ||||||
| chr12:122541441
|
G | T | 1 | a0003c0008t0001g0015 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.446-609G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541441 | ||||||
| chr12:122541588
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.446-462A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541588 | ||||||
| chr12:122541592
|
G | A | 6 | a0001c0002t0001g0033a0001c0002t0001g0058a0001c0002t0001g0059others(3): Show | 6 | HG01099.hp2 HG02717.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.446-458G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541592 | ||||||
| chr12:122541614
|
G | T | 1 | a0002c0009t0001g0201 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.446-436G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541614 | ||||||
| chr12:122541634
|
T | C | 2 | a0006c0006t0001g0245a0006c0006t0001g0248 | 2 | HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.446-416T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541634 | ||||||
| chr12:122541660
|
CTCTT | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(86): Show | 91 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.446-385_446-382del others(4): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | 122541660 | |||||
| chr12:122541834
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.446-216C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541834 | ||||||
| chr12:122541880
|
A | G | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.446-170A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541880 | ||||||
| chr12:122541964
|
G | A | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.446-86G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122541964 | ||||||
| chr12:122542013
|
C | A | 2 | a0011c0015t0001g0274a0011c0015t0001g0276 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.446-37C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | chr12 | 122542013 | ||||||
| chr12:122542164
|
G | A | 2 | a0002c0009t0001g0263a0002c0009t0001g0264 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.523+37G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | chr12 | 122542164 | ||||||
| chr12:122542203
|
T | A | 1 | a0001c0001t0001g0134 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.523+76T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | chr12 | 122542203 | ||||||
| chr12:122542259
|
A | G | 1 | a0001c0002t0001g0105 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.523+132A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | chr12 | 122542259 | ||||||
| chr12:122542364
|
T | A | 1 | a0001c0002t0001g0257 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.523+237T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | chr12 | 122542364 | ||||||
| chr12:122542492
|
G | A | 2 | a0002c0009t0001g0263a0002c0009t0001g0264 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.523+365G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | chr12 | 122542492 | ||||||
| chr12:122542718
|
C | G | 1 | a0001c0001t0001g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.523+591C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | chr12 | 122542718 | ||||||
| chr12:122542764
|
CA | C | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.523+648delA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | INFO_REALIGN_3_PRIME | chr12 | 122542764 | |||||
| chr12:122542907
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.524-693A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | chr12 | 122542907 | ||||||
| chr12:122542968
|
A | G | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.524-632A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | chr12 | 122542968 | ||||||
| chr12:122542979
|
A | T | 4 | a0002c0003t0001g0124a0008c0012t0001g0005a0008c0012t0001g0125others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.524-621A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | chr12 | 122542979 | ||||||
| chr12:122542995
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.524-605C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | chr12 | 122542995 | ||||||
| chr12:122543101
|
C | T | 2 | a0003c0008t0002g0017a0003c0008t0002g0018 | 2 | HG01106.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.524-499C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | chr12 | 122543101 | ||||||
| chr12:122543114
|
T | C | 1 | a0011c0015t0001g0276 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.524-486T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | chr12 | 122543114 | ||||||
| chr12:122543264
|
T | C | 89 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0002t0001g0007others(86): Show | 89 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.524-336T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | chr12 | 122543264 | ||||||
| chr12:122543267
|
A | G | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.524-333A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | chr12 | 122543267 | ||||||
| chr12:122543282
|
AT | A | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.524-315delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | INFO_REALIGN_3_PRIME | chr12 | 122543282 | |||||
| chr12:122543317
|
C | T | 1 | a0001c0016t0001g0076 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.524-283C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | chr12 | 122543317 | ||||||
| chr12:122543327
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.524-273A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | chr12 | 122543327 | ||||||
| chr12:122543549
|
T | C | 92 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0001t0001g0285others(89): Show | 92 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.524-51T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 6/63 | chr12 | 122543549 | ||||||
| chr12:122543918
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.559-241C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 7/63 | chr12 | 122543918 | ||||||
| chr12:122543950
|
T | C | 4 | a0001c0002t0001g0038a0001c0002t0001g0040a0001c0002t0001g0041others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.559-209T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 7/63 | chr12 | 122543950 | ||||||
| chr12:122543990
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.559-169G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 7/63 | chr12 | 122543990 | ||||||
| chr12:122544006
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.559-153G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 7/63 | chr12 | 122544006 | ||||||
| chr12:122544371
|
C | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.669+102C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 8/63 | chr12 | 122544371 | ||||||
| chr12:122544638
|
A | T | 32 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(29): Show | 33 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.669+369A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 8/63 | chr12 | 122544638 | ||||||
| chr12:122544787
|
A | C | 1 | a0001c0002t0001g0075 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.669+518A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 8/63 | chr12 | 122544787 | ||||||
| chr12:122544811
|
C | G | 2 | a0011c0015t0001g0274a0011c0015t0001g0276 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.669+542C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 8/63 | chr12 | 122544811 | ||||||
| chr12:122544932
|
C | T | 1 | a0010c0029t0001g0314 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.669+663C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 8/63 | chr12 | 122544932 | ||||||
| chr12:122545007
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.669+738C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 8/63 | chr12 | 122545007 | ||||||
| chr12:122545238
|
T | C | 7 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.670-938T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 8/63 | chr12 | 122545238 | ||||||
| chr12:122545318
|
C | T | 124 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(121): Show | 125 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.670-858C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 8/63 | chr12 | 122545318 | ||||||
| chr12:122545432
|
AAG | A | 21 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.670-738_670-737del others(2): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 8/63 | INFO_REALIGN_3_PRIME | chr12 | 122545432 | |||||
| chr12:122545701
|
C | T | 11 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(8): Show | 11 | HG00609.hp2 HG02165.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.670-475C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 8/63 | chr12 | 122545701 | ||||||
| chr12:122545738
|
A | G | 163 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(160): Show | 164 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.670-438A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 8/63 | chr12 | 122545738 | ||||||
| chr12:122545757
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG01261.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.670-419G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 8/63 | chr12 | 122545757 | ||||||
| chr12:122545792
|
A | C | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.670-384A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 8/63 | chr12 | 122545792 | ||||||
| chr12:122545819
|
T | G | 14 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.670-357T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 8/63 | chr12 | 122545819 | ||||||
| chr12:122545950
|
T | TA | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(232): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.670-210dupA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 8/63 | INFO_REALIGN_3_PRIME | chr12 | 122545950 | |||||
| chr12:122546152
|
T | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.670-24T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 8/63 | chr12 | 122546152 | ||||||
| chr12:122546329
|
A | G | 1 | a0009c0014t0001g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.763+60A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 9/63 | chr12 | 122546329 | ||||||
| chr12:122546378
|
A | G | 1 | a0001c0025t0001g0207 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.763+109A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 9/63 | chr12 | 122546378 | ||||||
| chr12:122546708
|
T | C | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.816+34T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 10/63 | chr12 | 122546708 | ||||||
| chr12:122546783
|
A | G | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.816+109A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 10/63 | chr12 | 122546783 | ||||||
| chr12:122546832
|
AT | A | 103 | a0001c0001t0001g0011a0001c0001t0001g0112a0001c0001t0001g0113others(100): Show | 103 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.816+175delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 10/63 | INFO_REALIGN_3_PRIME | chr12 | 122546832 | |||||
| chr12:122547189
|
C | A | 14 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.817-226C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 10/63 | chr12 | 122547189 | ||||||
| chr12:122547243
|
T | G | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.817-172T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 10/63 | chr12 | 122547243 | ||||||
| chr12:122547363
|
A | G | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.817-52A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 10/63 | chr12 | 122547363 | ||||||
| chr12:122547660
|
A | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG00735.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.932+130A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 11/63 | chr12 | 122547660 | ||||||
| chr12:122548271
|
C | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.987+302C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122548271 | ||||||
| chr12:122548275
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.987+306C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122548275 | ||||||
| chr12:122548328
|
G | C | 2 | a0001c0002t0001g0048a0001c0002t0001g0079 | 2 | HG00099.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.987+359G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122548328 | ||||||
| chr12:122548362
|
G | A | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.987+393G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122548362 | ||||||
| chr12:122548423
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.987+454C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122548423 | ||||||
| chr12:122548497
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.987+528A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122548497 | ||||||
| chr12:122548583
|
C | T | 1 | a0001c0011t0001g0237 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.987+614C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122548583 | ||||||
| chr12:122548642
|
G | A | 2 | a0001c0001t0001g0183a0001c0023t0001g0184 | 2 | NA18982.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.987+673G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122548642 | ||||||
| chr12:122548683
|
A | G | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.987+714A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122548683 | ||||||
| chr12:122548716
|
C | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.987+747C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122548716 | ||||||
| chr12:122548824
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.987+855C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122548824 | ||||||
| chr12:122548908
|
C | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(85): Show | 90 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.988-858C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122548908 | ||||||
| chr12:122548954
|
C | T | 14 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.988-812C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122548954 | ||||||
| chr12:122549009
|
C | T | 1 | a0005c0007t0001g0195 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.988-757C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122549009 | ||||||
| chr12:122549017
|
T | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.988-749T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122549017 | ||||||
| chr12:122549107
|
G | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.988-659G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122549107 | ||||||
| chr12:122549130
|
A | G | 25 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(22): Show | 26 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.988-636A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122549130 | ||||||
| chr12:122549338
|
G | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.988-428G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122549338 | ||||||
| chr12:122549380
|
C | T | 5 | a0005c0007t0001g0136a0005c0007t0001g0167a0005c0007t0001g0187others(2): Show | 5 | NA18940.hp1 NA18941.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-386C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122549380 | ||||||
| chr12:122549466
|
C | T | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.988-300C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122549466 | ||||||
| chr12:122549475
|
C | A | 92 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0001t0001g0285others(89): Show | 92 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.988-291C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122549475 | ||||||
| chr12:122549552
|
G | A | 25 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(22): Show | 26 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.988-214G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122549552 | ||||||
| chr12:122549651
|
C | G | 4 | a0002c0003t0001g0124a0008c0012t0001g0005a0008c0012t0001g0125others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.988-115C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122549651 | ||||||
| chr12:122549658
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.988-108G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 12/63 | chr12 | 122549658 | ||||||
| chr12:122549958
|
T | G | 7 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1086+94T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/63 | chr12 | 122549958 | ||||||
| chr12:122550169
|
A | ACATATTT others(14): Show |
3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1086+319_1086+320i others(23): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/63 | INFO_REALIGN_3_PRIME | chr12 | 122550169 | |||||
| chr12:122550169
|
A | ACATATTT others(14): Show |
160 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(157): Show | 161 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1086+325_1086+326i others(23): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/63 | INFO_REALIGN_3_PRIME | chr12 | 122550169 | |||||
| chr12:122550192
|
A | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(85): Show | 90 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.1086+328A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/63 | chr12 | 122550192 | ||||||
| chr12:122550291
|
C | T | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1086+427C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/63 | chr12 | 122550291 | ||||||
| chr12:122550376
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG00438.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1086+512A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/63 | chr12 | 122550376 | ||||||
| chr12:122550384
|
A | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(83): Show | 88 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(85): Show |
intron_variant | MODIFIER | c.1086+520A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/63 | chr12 | 122550384 | ||||||
| chr12:122550429
|
A | G | 92 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0001t0001g0285others(89): Show | 92 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1086+565A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/63 | chr12 | 122550429 | ||||||
| chr12:122550443
|
AT | A | 19 | a0001c0001t0001g0134a0003c0004t0001g0008a0003c0004t0001g0016others(16): Show | 19 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.1086+588delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/63 | INFO_REALIGN_3_PRIME | chr12 | 122550443 | |||||
| chr12:122550480
|
C | G | 1 | a0001c0001t0001g0137 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1086+616C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/63 | chr12 | 122550480 | ||||||
| chr12:122550500
|
TTTG | T | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1086+653_1086+655d others(5): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/63 | INFO_REALIGN_3_PRIME | chr12 | 122550500 | |||||
| chr12:122550561
|
C | T | 1 | a0006c0006t0001g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1086+697C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/63 | chr12 | 122550561 | ||||||
| chr12:122550701
|
C | T | 1 | a0001c0002t0001g0053 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1087-618C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/63 | chr12 | 122550701 | ||||||
| chr12:122550703
|
A | G | 2 | a0001c0031t0001g0118a0015c0030t0001g0280 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1087-616A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/63 | chr12 | 122550703 | ||||||
| chr12:122551147
|
T | TA | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1087-172_1087-171i others(3): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/63 | chr12 | 122551147 | ||||||
| chr12:122551148
|
G | GT | 153 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(150): Show | 153 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.1087-161dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/63 | INFO_REALIGN_3_PRIME | chr12 | 122551148 | |||||
| chr12:122551148
|
G | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1087-171G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 13/63 | chr12 | 122551148 | ||||||
| chr12:122551534
|
A | T | 1 | a0007c0013t0001g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1196+11A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 15/63 | chr12 | 122551534 | ||||||
| chr12:122552032
|
C | T | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1272+336C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122552032 | ||||||
| chr12:122552314
|
C | G | 3 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0094 | 3 | HG02129.hp2 NA19000.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1272+618C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122552314 | ||||||
| chr12:122552539
|
A | G | 8 | a0002c0003t0001g0289a0002c0003t0001g0290a0002c0003t0001g0291others(5): Show | 8 | HG02257.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272+843A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122552539 | ||||||
| chr12:122552636
|
T | G | 1 | a0001c0001t0001g0138 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1272+940T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122552636 | ||||||
| chr12:122552761
|
T | C | 92 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0001t0001g0285others(89): Show | 92 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1272+1065T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122552761 | ||||||
| chr12:122552924
|
A | G | 163 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(160): Show | 164 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1272+1228A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122552924 | ||||||
| chr12:122553052
|
G | T | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG02602.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1272+1356G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122553052 | ||||||
| chr12:122553160
|
G | GA | 41 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(38): Show | 41 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.1272+1479dupA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122553160 | |||||
| chr12:122553276
|
T | C | 1 | a0001c0002t0001g0055 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1272+1580T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122553276 | ||||||
| chr12:122553284
|
C | T | 2 | a0004c0005t0001g0307a0004c0005t0001g0308 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1272+1588C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122553284 | ||||||
| chr12:122553285
|
G | A | 5 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0123others(2): Show | 5 | HG01884.hp1 HG02258.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1272+1589G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122553285 | ||||||
| chr12:122553498
|
C | T | 117 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(114): Show | 118 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1272+1802C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122553498 | ||||||
| chr12:122553543
|
A | T | 1 | a0022c0035t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1272+1847A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122553543 | ||||||
| chr12:122553682
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1272+1986A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122553682 | ||||||
| chr12:122553745
|
A | G | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1272+2049A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122553745 | ||||||
| chr12:122553792
|
T | C | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1272+2096T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122553792 | ||||||
| chr12:122553866
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1272+2170A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122553866 | ||||||
| chr12:122554000
|
G | A | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1272+2304G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122554000 | ||||||
| chr12:122554064
|
T | TAAA | 12 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037others(9): Show | 12 | HG01256.hp2 HG03831.hp1 HG04228.hp2 others(9): Show |
intron_variant | MODIFIER | c.1272+2379_1272+238 others(7): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554064 | |||||
| chr12:122554064
|
T | TAAAA | 15 | a0001c0002t0001g0010a0001c0002t0001g0031a0001c0002t0001g0032others(12): Show | 15 | HG01258.hp2 HG01261.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.1272+2378_1272+238 others(8): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554064 | |||||
| chr12:122554064
|
TA | T | 11 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(8): Show | 11 | HG00609.hp2 HG02165.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.1272+2381delA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554064 | |||||
| chr12:122554064
|
TAA | T | 8 | a0001c0001t0001g0255a0002c0003t0001g0289a0002c0003t0001g0290others(5): Show | 8 | HG02257.hp1 HG02273.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272+2380_1272+238 others(6): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554064 | |||||
| chr12:122554071
|
AAAAAAAT others(6): Show |
A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1272+2377_1272+238 others(17): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554071 | |||||
| chr12:122554072
|
A | AATAT | 7 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 8 | HG01074.hp2 HG03669.hp2 HG04228.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272+2377_1272+237 others(8): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554072 | |||||
| chr12:122554074
|
A | AAT | 37 | a0001c0001t0001g0111a0001c0001t0001g0128a0001c0001t0001g0132others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1272+2379_1272+238 others(6): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554074 | |||||
| chr12:122554074
|
A | AATAT | 18 | a0001c0001t0001g0116a0001c0001t0001g0134a0001c0001t0001g0137others(15): Show | 18 | HG01099.hp1 HG01243.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.1272+2379_1272+238 others(8): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554074 | |||||
| chr12:122554074
|
A | AT | 6 | a0001c0001t0001g0304a0005c0007t0001g0136a0005c0007t0001g0167others(3): Show | 7 | HG03491.hp2 HG03492.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.1272+2378_1272+237 others(5): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122554074 | ||||||
| chr12:122554074
|
A | ATAT | 7 | a0001c0001t0001g0002a0001c0001t0001g0152a0001c0001t0001g0166others(4): Show | 8 | HG00438.hp1 HG01884.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272+2378_1272+237 others(7): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122554074 | ||||||
| chr12:122554074
|
A | ATATAT | 7 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(4): Show | 7 | HG01258.hp1 HG01346.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.1272+2378_1272+237 others(9): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122554074 | ||||||
| chr12:122554074
|
A | T | 14 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(11): Show | 15 | HG01074.hp2 HG01168.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1272+2378A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122554074 | ||||||
| chr12:122554074
|
AAAAT | A | 6 | a0002c0003t0001g0124a0002c0009t0001g0202a0002c0009t0001g0263others(3): Show | 6 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1272+2380_1272+238 others(8): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554074 | |||||
| chr12:122554076
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1272+2381_1272+238 others(25): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554076 | |||||
| chr12:122554076
|
A | AAAAAAAT others(16): Show |
2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1272+2381_1272+238 others(27): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554076 | |||||
| chr12:122554076
|
A | AAAAAATA others(15): Show |
1 | a0001c0001t0001g0209 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1272+2381_1272+238 others(26): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554076 | |||||
| chr12:122554076
|
A | AAAAT | 22 | a0001c0001t0001g0011a0001c0001t0001g0123a0001c0002t0001g0038others(19): Show | 22 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.1272+2381_1272+238 others(8): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554076 | |||||
| chr12:122554076
|
A | AAAATATA others(11): Show |
1 | a0001c0001t0001g0210 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1272+2381_1272+238 others(22): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554076 | |||||
| chr12:122554076
|
A | AAAT | 12 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(9): Show | 12 | HG00323.hp2 HG00738.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.1272+2381_1272+238 others(7): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554076 | |||||
| chr12:122554076
|
A | AAT | 16 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0149others(13): Show | 16 | HG01081.hp1 HG01261.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.1272+2403_1272+240 others(6): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554076 | |||||
| chr12:122554076
|
A | AATAT | 20 | a0001c0001t0001g0120a0001c0001t0001g0154a0001c0001t0001g0260others(17): Show | 20 | HG00438.hp2 HG01099.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1272+2401_1272+240 others(8): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554076 | |||||
| chr12:122554076
|
A | AATATATA others(13): Show |
1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1272+2385_1272+240 others(24): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554076 | |||||
| chr12:122554076
|
A | AT | 7 | a0001c0001t0001g0215a0001c0002t0001g0094a0005c0007t0001g0195others(4): Show | 7 | HG02109.hp1 HG02738.hp1 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.1272+2380_1272+238 others(5): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122554076 | ||||||
| chr12:122554076
|
A | ATAT | 3 | a0001c0002t0001g0051a0001c0016t0001g0076a0001c0031t0001g0118 | 3 | HG00423.hp1 HG02258.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1272+2380_1272+238 others(7): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122554076 | ||||||
| chr12:122554076
|
A | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0111others(112): Show | 118 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1272+2380A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122554076 | ||||||
| chr12:122554076
|
AATATAT | A | 8 | a0004c0005t0001g0004a0004c0005t0001g0311a0004c0005t0001g0312others(5): Show | 9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1272+2399_1272+240 others(10): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122554076 | |||||
| chr12:122554078
|
T | A | 2 | a0001c0001t0001g0216a0012c0022t0001g0043 | 2 | HG02027.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1272+2382T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122554078 | ||||||
| chr12:122554084
|
T | A | 1 | a0010c0033t0001g0315 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1272+2388T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122554084 | ||||||
| chr12:122554100
|
T | C | 7 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1272+2404T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122554100 | ||||||
| chr12:122554231
|
G | A | 2 | a0001c0002t0001g0077a0001c0002t0001g0078 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1272+2535G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122554231 | ||||||
| chr12:122554787
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1273-2597T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122554787 | ||||||
| chr12:122555188
|
A | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1273-2196A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122555188 | ||||||
| chr12:122555377
|
C | T | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0188 | 3 | HG02145.hp2 HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1273-2007C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122555377 | ||||||
| chr12:122555380
|
T | C | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1273-2004T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122555380 | ||||||
| chr12:122555388
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1273-1996C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122555388 | ||||||
| chr12:122555394
|
A | C | 14 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1273-1990A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122555394 | ||||||
| chr12:122555570
|
C | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1273-1814C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122555570 | ||||||
| chr12:122555575
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1273-1809C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122555575 | ||||||
| chr12:122555763
|
C | T | 1 | a0023c0018t0001g0064 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1273-1621C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122555763 | ||||||
| chr12:122555835
|
C | T | 92 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0001t0001g0285others(89): Show | 92 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1273-1549C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122555835 | ||||||
| chr12:122556075
|
C | T | 1 | a0002c0003t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1273-1309C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122556075 | ||||||
| chr12:122556142
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1273-1242G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122556142 | ||||||
| chr12:122556214
|
T | C | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1273-1170T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122556214 | ||||||
| chr12:122556226
|
C | G | 16 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(13): Show | 16 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1273-1158C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122556226 | ||||||
| chr12:122556283
|
G | T | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1273-1101G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122556283 | ||||||
| chr12:122556341
|
A | G | 1 | a0024c0017t0001g0065 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1273-1043A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122556341 | ||||||
| chr12:122556359
|
C | T | 3 | a0001c0001t0001g0111a0001c0031t0001g0118a0015c0030t0001g0280 | 3 | HG01884.hp1 HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1273-1025C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122556359 | ||||||
| chr12:122556438
|
T | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.1273-946T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122556438 | ||||||
| chr12:122556449
|
C | T | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1273-935C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122556449 | ||||||
| chr12:122556484
|
C | CT | 121 | a0001c0001t0001g0011a0001c0001t0001g0139a0001c0001t0001g0182others(118): Show | 122 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1273-881dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122556484 | |||||
| chr12:122556484
|
C | CTT | 29 | a0001c0002t0001g0257a0002c0003t0001g0124a0002c0003t0001g0272others(26): Show | 29 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1273-882_1273-881d others(4): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122556484 | |||||
| chr12:122556524
|
T | C | 92 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0001t0001g0285others(89): Show | 92 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1273-860T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122556524 | ||||||
| chr12:122556705
|
C | A | 1 | a0002c0009t0001g0201 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1273-679C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122556705 | ||||||
| chr12:122556876
|
A | G | 2 | a0002c0009t0001g0201a0002c0009t0001g0202 | 2 | HG01109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1273-508A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122556876 | ||||||
| chr12:122556917
|
C | CT | 165 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0129others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1273-444dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122556917 | |||||
| chr12:122556917
|
C | CTT | 24 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0137others(21): Show | 25 | HG01243.hp2 HG01884.hp2 HG02135.hp1 others(22): Show |
intron_variant | MODIFIER | c.1273-445_1273-444d others(4): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122556917 | |||||
| chr12:122556917
|
C | CTTT | 16 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(13): Show | 16 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1273-446_1273-444d others(5): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | INFO_REALIGN_3_PRIME | chr12 | 122556917 | |||||
| chr12:122556940
|
T | TTTA | 17 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(14): Show | 17 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1273-444_1273-443i others(5): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122556940 | ||||||
| chr12:122556979
|
C | T | 1 | a0002c0003t0001g0290 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1273-405C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122556979 | ||||||
| chr12:122556981
|
C | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(85): Show | 90 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.1273-403C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122556981 | ||||||
| chr12:122557367
|
G | C | 1 | a0002c0003t0001g0289 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1273-17G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 16/63 | chr12 | 122557367 | ||||||
| chr12:122557697
|
C | T | 1 | a0001c0002t0001g0037 | 1 | NA19063.hp1 | splice_region_variant&intron_variant | LOW | c.1488+8C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122557697 | ||||||
| chr12:122557721
|
G | T | 14 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1488+32G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122557721 | ||||||
| chr12:122557789
|
T | C | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1488+100T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122557789 | ||||||
| chr12:122557791
|
T | C | 14 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1488+102T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122557791 | ||||||
| chr12:122557792
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1488+103G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122557792 | ||||||
| chr12:122558095
|
A | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(249): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.1488+406A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122558095 | ||||||
| chr12:122558142
|
A | T | 1 | a0001c0001t0001g0129 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1488+453A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122558142 | ||||||
| chr12:122558207
|
T | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1488+518T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122558207 | ||||||
| chr12:122558508
|
C | T | 14 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1488+819C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122558508 | ||||||
| chr12:122558523
|
G | C | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1488+834G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122558523 | ||||||
| chr12:122558598
|
G | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(249): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.1488+909G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122558598 | ||||||
| chr12:122558769
|
G | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0160 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1488+1080G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122558769 | ||||||
| chr12:122558937
|
C | G | 2 | a0002c0003t0001g0272a0002c0003t0001g0273 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1488+1248C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122558937 | ||||||
| chr12:122559077
|
G | A | 1 | a0009c0014t0001g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1488+1388G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122559077 | ||||||
| chr12:122559153
|
T | C | 40 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284others(37): Show | 40 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.1488+1464T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122559153 | ||||||
| chr12:122559191
|
CA | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(85): Show | 90 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.1488+1508delA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | INFO_REALIGN_3_PRIME | chr12 | 122559191 | |||||
| chr12:122559197
|
A | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(85): Show | 90 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.1488+1508A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122559197 | ||||||
| chr12:122559217
|
A | G | 163 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(160): Show | 164 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1488+1528A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122559217 | ||||||
| chr12:122559226
|
C | T | 1 | a0001c0002t0001g0103 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1488+1537C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122559226 | ||||||
| chr12:122559262
|
C | T | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1488+1573C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122559262 | ||||||
| chr12:122559561
|
C | A | 40 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284others(37): Show | 40 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.1488+1872C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122559561 | ||||||
| chr12:122559573
|
AAAAAATA others(2): Show |
A | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(85): Show | 90 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.1488+1885_1488+189 others(13): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122559573 | ||||||
| chr12:122559698
|
A | G | 1 | a0008c0012t0001g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1488+2009A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122559698 | ||||||
| chr12:122559722
|
G | A | 1 | a0001c0002t0001g0047 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1488+2033G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122559722 | ||||||
| chr12:122559947
|
A | G | 1 | a0001c0001t0001g0194 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1489-1974A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122559947 | ||||||
| chr12:122559987
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1489-1934A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122559987 | ||||||
| chr12:122560047
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1489-1874A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122560047 | ||||||
| chr12:122560149
|
A | C | 2 | a0003c0004t0001g0019a0003c0004t0001g0028 | 2 | HG00280.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1489-1772A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122560149 | ||||||
| chr12:122560403
|
T | C | 165 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(162): Show | 166 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1489-1518T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122560403 | ||||||
| chr12:122560715
|
T | A | 1 | a0001c0001t0001g0172 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1489-1206T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122560715 | ||||||
| chr12:122560852
|
T | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1489-1069T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122560852 | ||||||
| chr12:122561021
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1489-900T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122561021 | ||||||
| chr12:122561320
|
A | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1489-601A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122561320 | ||||||
| chr12:122561323
|
A | T | 17 | a0001c0001t0001g0117a0001c0001t0001g0149a0001c0001t0001g0150others(14): Show | 18 | HG01261.hp2 HG02109.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1489-598A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122561323 | ||||||
| chr12:122561326
|
T | A | 21 | a0001c0001t0001g0006a0001c0001t0001g0191a0001c0001t0001g0211others(18): Show | 21 | HG00423.hp2 HG00597.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1489-595T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122561326 | ||||||
| chr12:122561389
|
T | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0171 | 2 | NA18944.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1489-532T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122561389 | ||||||
| chr12:122561423
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1489-498A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122561423 | ||||||
| chr12:122561524
|
G | T | 1 | a0015c0030t0001g0280 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1489-397G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122561524 | ||||||
| chr12:122561564
|
G | A | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1489-357G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122561564 | ||||||
| chr12:122561701
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG01261.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1489-220G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122561701 | ||||||
| chr12:122561734
|
G | A | 7 | a0004c0005t0001g0004a0004c0005t0001g0309a0004c0005t0001g0311others(4): Show | 8 | HG01891.hp1 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1489-187G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122561734 | ||||||
| chr12:122561764
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1489-157T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 18/63 | chr12 | 122561764 | ||||||
| chr12:122561984
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1542+10C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | chr12 | 122561984 | ||||||
| chr12:122562378
|
A | G | 1 | a0001c0001t0001g0250 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1543-260A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | chr12 | 122562378 | ||||||
| chr12:122562436
|
G | GTT | 3 | a0001c0001t0001g0111a0004c0005t0001g0307a0004c0005t0001g0309 | 3 | HG02572.hp2 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1543-199_1543-198d others(4): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | INFO_REALIGN_3_PRIME | chr12 | 122562436 | |||||
| chr12:122562439
|
T | TTG | 4 | a0001c0001t0001g0150a0003c0004t0001g0019a0003c0008t0001g0014others(1): Show | 4 | HG01975.hp1 HG02683.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543-159_1543-158d others(4): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | INFO_REALIGN_3_PRIME | chr12 | 122562439 | |||||
| chr12:122562439
|
T | TTGTG | 6 | a0003c0004t0001g0008a0003c0004t0001g0026a0003c0004t0001g0028others(3): Show | 6 | HG00280.hp2 HG01106.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1543-161_1543-158d others(6): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | INFO_REALIGN_3_PRIME | chr12 | 122562439 | |||||
| chr12:122562439
|
T | TTGTGTG | 3 | a0003c0004t0001g0016a0003c0004t0001g0020a0003c0004t0001g0021 | 3 | HG00639.hp2 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1543-163_1543-158d others(8): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | INFO_REALIGN_3_PRIME | chr12 | 122562439 | |||||
| chr12:122562439
|
T | TTGTGTGT others(1): Show |
5 | a0003c0004t0001g0023a0003c0004t0001g0024a0003c0004t0001g0025others(2): Show | 5 | HG01515.hp1 HG01517.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1543-165_1543-158d others(10): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | INFO_REALIGN_3_PRIME | chr12 | 122562439 | |||||
| chr12:122562439
|
T | TTTTG | 10 | a0001c0001t0001g0121a0004c0005t0001g0004a0004c0005t0001g0308others(7): Show | 11 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1543-198_1543-197i others(6): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | INFO_REALIGN_3_PRIME | chr12 | 122562439 | |||||
| chr12:122562439
|
TTG | T | 22 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115others(19): Show | 22 | HG01167.hp1 HG01243.hp2 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.1543-159_1543-158d others(4): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | INFO_REALIGN_3_PRIME | chr12 | 122562439 | |||||
| chr12:122562439
|
TTGTG | T | 56 | a0001c0001t0001g0006a0001c0001t0001g0117a0001c0001t0001g0130others(53): Show | 57 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1543-161_1543-158d others(6): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | INFO_REALIGN_3_PRIME | chr12 | 122562439 | |||||
| chr12:122562439
|
TTGTGTG | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(74): Show | 79 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(76): Show |
intron_variant | MODIFIER | c.1543-163_1543-158d others(8): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | INFO_REALIGN_3_PRIME | chr12 | 122562439 | |||||
| chr12:122562439
|
TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0001g0164a0002c0009t0001g0201a0002c0009t0001g0202 | 3 | HG01109.hp1 HG04204.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1543-165_1543-158d others(10): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | INFO_REALIGN_3_PRIME | chr12 | 122562439 | |||||
| chr12:122562439
|
TTGTGTGT others(3): Show |
T | 6 | a0001c0001t0001g0148a0001c0001t0001g0174a0001c0010t0001g0282others(3): Show | 6 | HG01255.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1543-167_1543-158d others(12): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | INFO_REALIGN_3_PRIME | chr12 | 122562439 | |||||
| chr12:122562439
|
TTGTGTGT others(5): Show |
T | 5 | a0001c0002t0001g0007a0001c0002t0001g0053a0001c0002t0001g0086others(2): Show | 5 | HG01074.hp1 HG02145.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1543-169_1543-158d others(14): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | INFO_REALIGN_3_PRIME | chr12 | 122562439 | |||||
| chr12:122562439
|
TTGTGTGT others(7): Show |
T | 83 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0002t0001g0009others(80): Show | 83 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1543-171_1543-158d others(16): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | INFO_REALIGN_3_PRIME | chr12 | 122562439 | |||||
| chr12:122562439
|
TTGTGTGT others(9): Show |
T | 2 | a0001c0002t0001g0048a0001c0002t0001g0079 | 2 | HG00099.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1543-173_1543-158d others(18): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | INFO_REALIGN_3_PRIME | chr12 | 122562439 | |||||
| chr12:122562441
|
G | T | 6 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0122others(3): Show | 6 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1543-197G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | chr12 | 122562441 | ||||||
| chr12:122562443
|
G | T | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115others(1): Show | 4 | HG02055.hp2 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1543-195G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | chr12 | 122562443 | ||||||
| chr12:122562445
|
G | T | 2 | a0001c0001t0001g0117a0015c0030t0001g0280 | 2 | HG01884.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1543-193G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | chr12 | 122562445 | ||||||
| chr12:122562467
|
GTGTGTGT others(7): Show |
G | 1 | a0001c0002t0001g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1543-162_1543-149d others(16): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | INFO_REALIGN_3_PRIME | chr12 | 122562467 | |||||
| chr12:122562471
|
GTGTGTGT others(3): Show |
G | 1 | a0018c0019t0001g0131 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1543-158_1543-149d others(12): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | INFO_REALIGN_3_PRIME | chr12 | 122562471 | |||||
| chr12:122562589
|
T | C | 2 | a0004c0005t0001g0307a0004c0005t0001g0308 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1543-49T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | chr12 | 122562589 | ||||||
| chr12:122562594
|
ATTG | A | 9 | a0004c0005t0001g0004a0004c0005t0001g0309a0004c0005t0001g0311others(6): Show | 10 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1543-40_1543-38del others(3): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | INFO_REALIGN_3_PRIME | chr12 | 122562594 | |||||
| chr12:122562597
|
G | A | 2 | a0004c0005t0001g0307a0004c0005t0001g0308 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1543-41G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 19/63 | chr12 | 122562597 | ||||||
| chr12:122562759
|
C | T | 2 | a0002c0003t0001g0275a0002c0003t0001g0278 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1604+60C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122562759 | ||||||
| chr12:122562988
|
G | A | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1604+289G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122562988 | ||||||
| chr12:122563008
|
C | CA | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(85): Show | 90 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.1604+322dupA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | INFO_REALIGN_3_PRIME | chr12 | 122563008 | |||||
| chr12:122563008
|
CA | C | 22 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(19): Show | 23 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1604+322delA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | INFO_REALIGN_3_PRIME | chr12 | 122563008 | |||||
| chr12:122563021
|
A | T | 1 | a0007c0013t0001g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1604+322A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122563021 | ||||||
| chr12:122563022
|
T | A | 4 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284others(1): Show | 4 | HG01169.hp2 HG02109.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1604+323T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122563022 | ||||||
| chr12:122563038
|
A | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1604+339A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122563038 | ||||||
| chr12:122563213
|
C | G | 1 | a0016c0028t0001g0082 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1604+514C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122563213 | ||||||
| chr12:122563508
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG01261.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1604+809G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122563508 | ||||||
| chr12:122563618
|
C | T | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1604+919C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122563618 | ||||||
| chr12:122563663
|
C | T | 2 | a0001c0001t0001g0134a0001c0021t0001g0133 | 2 | NA18973.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1604+964C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122563663 | ||||||
| chr12:122563725
|
G | T | 1 | a0014c0027t0001g0162 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1604+1026G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122563725 | ||||||
| chr12:122563759
|
C | T | 14 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1604+1060C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122563759 | ||||||
| chr12:122563766
|
C | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1604+1067C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122563766 | ||||||
| chr12:122563788
|
A | T | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1604+1089A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122563788 | ||||||
| chr12:122563854
|
T | C | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1604+1155T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122563854 | ||||||
| chr12:122563891
|
G | A | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1604+1192G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122563891 | ||||||
| chr12:122564056
|
C | A | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1604+1357C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122564056 | ||||||
| chr12:122564071
|
A | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.1604+1372A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122564071 | ||||||
| chr12:122564449
|
C | T | 2 | a0001c0002t0001g0007a0001c0002t0001g0053 | 2 | NA18954.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1604+1750C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122564449 | ||||||
| chr12:122564459
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1604+1760T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122564459 | ||||||
| chr12:122564602
|
G | A | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1604+1903G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122564602 | ||||||
| chr12:122564685
|
C | T | 2 | a0001c0001t0001g0183a0001c0023t0001g0184 | 2 | NA18982.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1604+1986C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122564685 | ||||||
| chr12:122565052
|
C | T | 8 | a0002c0003t0001g0289a0002c0003t0001g0290a0002c0003t0001g0291others(5): Show | 8 | HG02257.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1604+2353C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122565052 | ||||||
| chr12:122565055
|
A | G | 1 | a0001c0034t0001g0229 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1604+2356A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122565055 | ||||||
| chr12:122565101
|
G | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1604+2402G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122565101 | ||||||
| chr12:122565199
|
G | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(84): Show | 89 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(86): Show |
intron_variant | MODIFIER | c.1604+2500G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122565199 | ||||||
| chr12:122565240
|
G | GT | 26 | a0001c0001t0001g0132a0001c0001t0001g0152a0001c0001t0001g0161others(23): Show | 26 | HG01884.hp2 HG01975.hp1 HG02129.hp1 others(23): Show |
intron_variant | MODIFIER | c.1604+2553dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | INFO_REALIGN_3_PRIME | chr12 | 122565240 | |||||
| chr12:122565240
|
G | GTT | 18 | a0001c0002t0001g0069a0003c0004t0001g0008a0003c0004t0001g0016others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1604+2552_1604+255 others(6): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | INFO_REALIGN_3_PRIME | chr12 | 122565240 | |||||
| chr12:122565252
|
T | A | 14 | a0001c0001t0001g0138a0001c0001t0001g0179a0001c0001t0001g0213others(11): Show | 14 | HG00423.hp2 HG00609.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.1604+2553T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122565252 | ||||||
| chr12:122565252
|
T | TA | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(70): Show | 75 | HG00099.hp1 HG00438.hp1 HG01074.hp2 others(72): Show |
intron_variant | MODIFIER | c.1604+2566dupA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | INFO_REALIGN_3_PRIME | chr12 | 122565252 | |||||
| chr12:122565252
|
TA | T | 10 | a0001c0001t0001g0258a0001c0002t0001g0054a0001c0002t0001g0062others(7): Show | 10 | HG01256.hp1 HG02109.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.1604+2566delA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | INFO_REALIGN_3_PRIME | chr12 | 122565252 | |||||
| chr12:122565253
|
A | T | 121 | a0001c0001t0001g0011a0001c0001t0001g0130a0001c0001t0001g0209others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1604+2554A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122565253 | ||||||
| chr12:122565254
|
A | T | 114 | a0001c0002t0001g0007a0001c0002t0001g0009a0001c0002t0001g0010others(111): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1604+2555A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122565254 | ||||||
| chr12:122565255
|
A | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1604+2556A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122565255 | ||||||
| chr12:122565259
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1604+2560A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122565259 | ||||||
| chr12:122565287
|
A | G | 1 | a0003c0004t0001g0025 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1604+2588A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122565287 | ||||||
| chr12:122565392
|
T | C | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1604+2693T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122565392 | ||||||
| chr12:122565515
|
A | AT | 15 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1605-2734dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | INFO_REALIGN_3_PRIME | chr12 | 122565515 | |||||
| chr12:122565515
|
AT | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(91): Show | 97 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(94): Show |
intron_variant | MODIFIER | c.1605-2734delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | INFO_REALIGN_3_PRIME | chr12 | 122565515 | |||||
| chr12:122565518
|
T | A | 4 | a0002c0003t0001g0124a0008c0012t0001g0005a0008c0012t0001g0125others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1605-2743T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122565518 | ||||||
| chr12:122565666
|
C | T | 1 | a0002c0003t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1605-2595C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122565666 | ||||||
| chr12:122565886
|
A | T | 1 | a0021c0036t0001g0013 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1605-2375A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122565886 | ||||||
| chr12:122565952
|
C | CT | 112 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(109): Show | 112 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1605-2291dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | INFO_REALIGN_3_PRIME | chr12 | 122565952 | |||||
| chr12:122565952
|
CT | C | 21 | a0001c0001t0001g0211a0001c0001t0001g0298a0002c0009t0001g0201others(18): Show | 22 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1605-2291delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | INFO_REALIGN_3_PRIME | chr12 | 122565952 | |||||
| chr12:122566029
|
G | A | 2 | a0002c0009t0001g0263a0002c0009t0001g0264 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1605-2232G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122566029 | ||||||
| chr12:122566162
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1605-2099C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122566162 | ||||||
| chr12:122566188
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1605-2073G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122566188 | ||||||
| chr12:122566217
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1605-2044A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122566217 | ||||||
| chr12:122566302
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1605-1959C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122566302 | ||||||
| chr12:122566321
|
C | T | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1605-1940C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122566321 | ||||||
| chr12:122566410
|
AT | A | 118 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(115): Show | 119 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.1605-1839delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | INFO_REALIGN_3_PRIME | chr12 | 122566410 | |||||
| chr12:122566471
|
A | G | 164 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(161): Show | 165 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1605-1790A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122566471 | ||||||
| chr12:122566474
|
A | T | 117 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(114): Show | 118 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1605-1787A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122566474 | ||||||
| chr12:122566499
|
T | G | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1605-1762T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122566499 | ||||||
| chr12:122566530
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1605-1731C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122566530 | ||||||
| chr12:122566558
|
C | G | 1 | a0001c0001t0001g0155 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1605-1703C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122566558 | ||||||
| chr12:122566560
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(86): Show | 91 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.1605-1701A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122566560 | ||||||
| chr12:122566758
|
G | GT | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(202): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1605-1482dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | INFO_REALIGN_3_PRIME | chr12 | 122566758 | |||||
| chr12:122566758
|
G | GTT | 16 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0001g0153others(13): Show | 16 | HG01081.hp1 HG01243.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.1605-1483_1605-148 others(6): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | INFO_REALIGN_3_PRIME | chr12 | 122566758 | |||||
| chr12:122566758
|
GT | G | 6 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(3): Show | 6 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1605-1482delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | INFO_REALIGN_3_PRIME | chr12 | 122566758 | |||||
| chr12:122566811
|
G | A | 14 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1605-1450G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122566811 | ||||||
| chr12:122566906
|
G | A | 1 | a0001c0002t0001g0035 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1605-1355G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122566906 | ||||||
| chr12:122566994
|
G | A | 1 | a0003c0008t0001g0015 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1605-1267G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122566994 | ||||||
| chr12:122567045
|
C | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1605-1216C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122567045 | ||||||
| chr12:122567219
|
T | C | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1605-1042T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122567219 | ||||||
| chr12:122567249
|
T | C | 5 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0179others(2): Show | 5 | HG01074.hp2 HG01168.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1605-1012T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122567249 | ||||||
| chr12:122567633
|
G | T | 1 | a0001c0001t0001g0256 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1605-628G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122567633 | ||||||
| chr12:122567738
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1605-523T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122567738 | ||||||
| chr12:122567847
|
G | C | 1 | a0011c0015t0001g0274 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1605-414G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122567847 | ||||||
| chr12:122568035
|
A | G | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG02258.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1605-226A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122568035 | ||||||
| chr12:122568158
|
T | C | 1 | a0001c0002t0001g0046 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1605-103T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 20/63 | chr12 | 122568158 | ||||||
| chr12:122568389
|
T | G | 14 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1716+17T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 21/63 | chr12 | 122568389 | ||||||
| chr12:122568477
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1716+105A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 21/63 | chr12 | 122568477 | ||||||
| chr12:122568554
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1716+182G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 21/63 | chr12 | 122568554 | ||||||
| chr12:122568830
|
C | T | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1716+458C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 21/63 | chr12 | 122568830 | ||||||
| chr12:122568880
|
T | C | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(303): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1716+508T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 21/63 | chr12 | 122568880 | ||||||
| chr12:122568941
|
A | G | 96 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0002t0001g0007others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1716+569A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 21/63 | chr12 | 122568941 | ||||||
| chr12:122569306
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1717-375T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 21/63 | chr12 | 122569306 | ||||||
| chr12:122569485
|
C | T | 12 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1717-196C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 21/63 | chr12 | 122569485 | ||||||
| chr12:122569492
|
C | T | 1 | a0001c0002t0001g0084 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1717-189C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 21/63 | chr12 | 122569492 | ||||||
| chr12:122569493
|
G | A | 1 | a0007c0013t0001g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1717-188G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 21/63 | chr12 | 122569493 | ||||||
| chr12:122569508
|
A | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(88): Show | 93 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(90): Show |
intron_variant | MODIFIER | c.1717-173A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 21/63 | chr12 | 122569508 | ||||||
| chr12:122569910
|
A | G | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG02165.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1860+86A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 22/63 | chr12 | 122569910 | ||||||
| chr12:122569994
|
C | T | 7 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1860+170C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 22/63 | chr12 | 122569994 | ||||||
| chr12:122570064
|
A | G | 1 | a0001c0002t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1860+240A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 22/63 | chr12 | 122570064 | ||||||
| chr12:122570388
|
A | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1861-488A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 22/63 | chr12 | 122570388 | ||||||
| chr12:122570593
|
A | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1861-283A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 22/63 | chr12 | 122570593 | ||||||
| chr12:122570677
|
T | A | 315 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(312): Show | 319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.1861-199T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 22/63 | chr12 | 122570677 | ||||||
| chr12:122571495
|
A | C | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | HG01255.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.2019+369A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 24/63 | chr12 | 122571495 | ||||||
| chr12:122571499
|
C | A | 1 | a0001c0002t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2019+373C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 24/63 | chr12 | 122571499 | ||||||
| chr12:122571517
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2019+391C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 24/63 | chr12 | 122571517 | ||||||
| chr12:122571678
|
A | T | 6 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0236others(3): Show | 6 | HG00423.hp2 HG02027.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.2019+552A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 24/63 | chr12 | 122571678 | ||||||
| chr12:122572046
|
A | G | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.2020-891A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 24/63 | chr12 | 122572046 | ||||||
| chr12:122572120
|
G | A | 25 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(22): Show | 25 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.2020-817G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 24/63 | chr12 | 122572120 | ||||||
| chr12:122572141
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2020-796C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 24/63 | chr12 | 122572141 | ||||||
| chr12:122572310
|
G | T | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2020-627G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 24/63 | chr12 | 122572310 | ||||||
| chr12:122572428
|
CT | C | 12 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(9): Show | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.2020-507delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 24/63 | INFO_REALIGN_3_PRIME | chr12 | 122572428 | |||||
| chr12:122572446
|
T | C | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2020-491T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 24/63 | chr12 | 122572446 | ||||||
| chr12:122572671
|
C | G | 1 | a0001c0001t0001g0135 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2020-266C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 24/63 | chr12 | 122572671 | ||||||
| chr12:122573105
|
G | C | 1 | a0001c0001t0001g0235 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2140-37G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 25/63 | chr12 | 122573105 | ||||||
| chr12:122573317
|
T | A | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.2283+32T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 26/63 | chr12 | 122573317 | ||||||
| chr12:122573325
|
A | G | 1 | a0003c0008t0002g0018 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2283+40A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 26/63 | chr12 | 122573325 | ||||||
| chr12:122573417
|
A | C | 1 | a0007c0013t0001g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2283+132A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 26/63 | chr12 | 122573417 | ||||||
| chr12:122573455
|
G | C | 14 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.2283+170G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 26/63 | chr12 | 122573455 | ||||||
| chr12:122573713
|
C | T | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.2283+428C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 26/63 | chr12 | 122573713 | ||||||
| chr12:122573866
|
G | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0255 | 2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2284-416G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 26/63 | chr12 | 122573866 | ||||||
| chr12:122574000
|
T | C | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2284-282T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 26/63 | chr12 | 122574000 | ||||||
| chr12:122574109
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2284-173A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 26/63 | chr12 | 122574109 | ||||||
| chr12:122574159
|
T | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2284-123T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 26/63 | chr12 | 122574159 | ||||||
| chr12:122574438
|
C | G | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2382+58C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 27/63 | chr12 | 122574438 | ||||||
| chr12:122574988
|
C | T | 2 | a0004c0005t0001g0307a0004c0005t0001g0308 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2383-555C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 27/63 | chr12 | 122574988 | ||||||
| chr12:122575072
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2383-471G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 27/63 | chr12 | 122575072 | ||||||
| chr12:122575125
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2383-418G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 27/63 | chr12 | 122575125 | ||||||
| chr12:122575287
|
T | C | 2 | a0001c0001t0001g0183a0001c0023t0001g0184 | 2 | NA18982.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.2383-256T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 27/63 | chr12 | 122575287 | ||||||
| chr12:122575498
|
G | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2383-45G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 27/63 | chr12 | 122575498 | ||||||
| chr12:122575506
|
G | A | 1 | a0024c0017t0001g0065 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2383-37G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 27/63 | chr12 | 122575506 | ||||||
| chr12:122575694
|
T | C | 2 | a0002c0003t0001g0272a0002c0003t0001g0273 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2486+48T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 28/63 | chr12 | 122575694 | ||||||
| chr12:122575769
|
T | G | 2 | a0001c0002t0001g0080a0001c0002t0001g0083 | 2 | NA18945.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.2487-31T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 28/63 | chr12 | 122575769 | ||||||
| chr12:122575922
|
C | CT | 24 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(21): Show | 24 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.2586+29dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/63 | INFO_REALIGN_3_PRIME | chr12 | 122575922 | |||||
| chr12:122576128
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2586+229C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/63 | chr12 | 122576128 | ||||||
| chr12:122576153
|
G | A | 1 | a0001c0034t0001g0229 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2586+254G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/63 | chr12 | 122576153 | ||||||
| chr12:122576204
|
C | T | 1 | a0001c0002t0001g0054 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2586+305C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/63 | chr12 | 122576204 | ||||||
| chr12:122576217
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0168 | 2 | HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2586+318G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/63 | chr12 | 122576217 | ||||||
| chr12:122576226
|
A | AT | 88 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0002t0001g0007others(85): Show | 88 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.2586+337dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/63 | INFO_REALIGN_3_PRIME | chr12 | 122576226 | |||||
| chr12:122576248
|
A | G | 2 | a0002c0009t0001g0263a0002c0009t0001g0264 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2586+349A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/63 | chr12 | 122576248 | ||||||
| chr12:122576408
|
C | T | 1 | a0001c0002t0001g0097 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2587-487C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/63 | chr12 | 122576408 | ||||||
| chr12:122576422
|
C | T | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG02602.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2587-473C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/63 | chr12 | 122576422 | ||||||
| chr12:122576554
|
G | C | 1 | a0001c0002t0001g0099 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2587-341G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/63 | chr12 | 122576554 | ||||||
| chr12:122576629
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2587-266C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/63 | chr12 | 122576629 | ||||||
| chr12:122576692
|
C | G | 2 | a0001c0002t0001g0056a0001c0002t0001g0057 | 2 | HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2587-203C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/63 | chr12 | 122576692 | ||||||
| chr12:122576758
|
C | T | 14 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.2587-137C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/63 | chr12 | 122576758 | ||||||
| chr12:122576797
|
T | C | 7 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2587-98T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/63 | chr12 | 122576797 | ||||||
| chr12:122576805
|
A | AT | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(85): Show | 90 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.2587-83dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/63 | INFO_REALIGN_3_PRIME | chr12 | 122576805 | |||||
| chr12:122576812
|
T | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2587-83T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/63 | chr12 | 122576812 | ||||||
| chr12:122576886
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2587-9C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 29/63 | chr12 | 122576886 | ||||||
| chr12:122577160
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2721+131C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 30/63 | chr12 | 122577160 | ||||||
| chr12:122577223
|
T | G | 1 | a0001c0001t0001g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2721+194T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 30/63 | chr12 | 122577223 | ||||||
| chr12:122577844
|
A | C | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02165.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.2841+53A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122577844 | ||||||
| chr12:122577876
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2841+85A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122577876 | ||||||
| chr12:122577942
|
A | G | 89 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0002t0001g0007others(86): Show | 89 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.2841+151A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122577942 | ||||||
| chr12:122578047
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(84): Show | 89 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(86): Show |
intron_variant | MODIFIER | c.2841+256C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122578047 | ||||||
| chr12:122578065
|
C | T | 1 | a0007c0013t0001g0203 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2841+274C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122578065 | ||||||
| chr12:122578075
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2841+284T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122578075 | ||||||
| chr12:122578114
|
A | G | 1 | a0001c0026t0001g0081 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2841+323A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122578114 | ||||||
| chr12:122578385
|
GCATGCAC others(3): Show |
G | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.2841+600_2841+609d others(12): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122578385 | |||||
| chr12:122578459
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0160 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2841+668G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122578459 | ||||||
| chr12:122578483
|
C | T | 1 | a0001c0002t0001g0109 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2841+692C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122578483 | ||||||
| chr12:122578486
|
G | C | 2 | a0003c0004t0001g0020a0003c0004t0001g0021 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2841+695G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122578486 | ||||||
| chr12:122578622
|
G | A | 1 | a0021c0036t0001g0013 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2841+831G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122578622 | ||||||
| chr12:122578655
|
A | G | 1 | a0001c0011t0001g0237 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2841+864A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122578655 | ||||||
| chr12:122578712
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2841+921A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122578712 | ||||||
| chr12:122578920
|
G | A | 164 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(161): Show | 165 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.2842-985G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122578920 | ||||||
| chr12:122578933
|
A | T | 1 | a0001c0001t0001g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2842-972A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122578933 | ||||||
| chr12:122578948
|
A | G | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.2842-957A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122578948 | ||||||
| chr12:122579025
|
CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0001g0219a0001c0001t0001g0238a0001c0001t0001g0239others(3): Show | 6 | HG00735.hp1 HG00735.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2842-832_2842-823d others(12): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0236a0001c0001t0001g0243a0002c0009t0001g0263 | 3 | NA18522.hp1 NA18940.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2842-834_2842-823d others(14): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(6): Show |
C | 9 | a0001c0001t0001g0199a0001c0001t0001g0211a0001c0001t0001g0214others(6): Show | 9 | HG01167.hp1 HG01496.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2842-835_2842-823d others(15): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(7): Show |
C | 13 | a0001c0001t0001g0130a0001c0001t0001g0215a0001c0001t0001g0217others(10): Show | 13 | HG00423.hp2 HG00738.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.2842-836_2842-823d others(16): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(8): Show |
C | 10 | a0001c0001t0001g0212a0001c0001t0001g0230a0001c0001t0001g0231others(7): Show | 10 | HG00280.hp1 HG00323.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.2842-837_2842-823d others(17): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0256 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2842-838_2842-823d others(18): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(10): Show |
C | 1 | a0022c0035t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2842-839_2842-823d others(19): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(11): Show |
C | 1 | a0021c0036t0001g0013 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2842-840_2842-823d others(20): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(13): Show |
C | 1 | a0002c0009t0001g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2842-842_2842-823d others(22): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(14): Show |
C | 2 | a0002c0009t0001g0201a0003c0004t0001g0028 | 2 | HG00280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2842-843_2842-823d others(23): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(15): Show |
C | 5 | a0001c0001t0001g0220a0001c0001t0001g0228a0001c0002t0001g0089others(2): Show | 5 | HG01255.hp1 HG01975.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.2842-844_2842-823d others(24): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(16): Show |
C | 3 | a0001c0002t0001g0091a0001c0002t0001g0101a0003c0004t0001g0025 | 3 | HG03942.hp1 NA18952.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.2842-845_2842-823d others(25): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(17): Show |
C | 12 | a0001c0001t0001g0208a0001c0001t0001g0266a0001c0002t0001g0050others(9): Show | 12 | HG00639.hp2 HG00738.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.2842-846_2842-823d others(26): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(18): Show |
C | 6 | a0001c0002t0001g0007a0001c0002t0001g0070a0001c0002t0001g0102others(3): Show | 6 | HG01515.hp1 HG03486.hp2 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.2842-847_2842-823d others(27): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(19): Show |
C | 27 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0002t0001g0038others(24): Show | 27 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.2842-848_2842-823d others(28): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(20): Show |
C | 64 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0002t0001g0009others(61): Show | 65 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2842-849_2842-823d others(29): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(21): Show |
C | 8 | a0001c0002t0001g0033a0001c0002t0001g0058a0001c0002t0001g0059others(5): Show | 8 | HG01099.hp2 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2842-850_2842-823d others(30): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(22): Show |
C | 10 | a0002c0003t0001g0272a0002c0003t0001g0275a0002c0003t0001g0277others(7): Show | 10 | HG01243.hp2 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2842-851_2842-823d others(31): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(23): Show |
C | 6 | a0002c0003t0001g0124a0002c0003t0001g0291a0002c0003t0001g0293others(3): Show | 6 | HG02723.hp2 HG03041.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.2842-852_2842-823d others(32): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(24): Show |
C | 2 | a0001c0001t0001g0006a0009c0014t0001g0003 | 3 | HG00597.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2842-853_2842-823d others(33): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(26): Show |
C | 7 | a0001c0001t0001g0153a0001c0001t0001g0176a0001c0001t0001g0177others(4): Show | 7 | HG01192.hp2 HG02071.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.2842-855_2842-823d others(35): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(27): Show |
C | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(76): Show | 81 | HG00438.hp1 HG01070.hp2 HG01074.hp2 others(78): Show |
intron_variant | MODIFIER | c.2842-856_2842-823d others(36): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(28): Show |
C | 6 | a0001c0001t0001g0129a0001c0001t0001g0178a0001c0001t0001g0205others(3): Show | 6 | HG00099.hp1 HG01081.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2842-857_2842-823d others(37): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(30): Show |
C | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2842-859_2842-823d others(39): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579025
|
CTTTTTTT others(33): Show |
C | 15 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2842-862_2842-823d others(42): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579025 | |||||
| chr12:122579096
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2842-809G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122579096 | ||||||
| chr12:122579116
|
G | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2842-789G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122579116 | ||||||
| chr12:122579126
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2842-779G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122579126 | ||||||
| chr12:122579213
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2842-692C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122579213 | ||||||
| chr12:122579221
|
C | T | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2842-684C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122579221 | ||||||
| chr12:122579292
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2842-613C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122579292 | ||||||
| chr12:122579310
|
T | C | 165 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(162): Show | 166 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.2842-595T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122579310 | ||||||
| chr12:122579360
|
G | A | 1 | a0001c0034t0001g0229 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2842-545G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122579360 | ||||||
| chr12:122579365
|
G | A | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2842-540G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122579365 | ||||||
| chr12:122579485
|
TC | T | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2842-418delC | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579485 | |||||
| chr12:122579510
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2842-395T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122579510 | ||||||
| chr12:122579577
|
CTTCTA | C | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.2842-323_2842-319d others(7): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | INFO_REALIGN_3_PRIME | chr12 | 122579577 | |||||
| chr12:122579582
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2842-323A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122579582 | ||||||
| chr12:122579635
|
G | A | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2842-270G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122579635 | ||||||
| chr12:122579799
|
A | T | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2842-106A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 31/63 | chr12 | 122579799 | ||||||
| chr12:122580171
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2914+194A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 32/63 | chr12 | 122580171 | ||||||
| chr12:122580678
|
T | C | 7 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.2982+8T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | chr12 | 122580678 | ||||||
| chr12:122580856
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2982+186G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | chr12 | 122580856 | ||||||
| chr12:122580888
|
C | T | 1 | a0002c0009t0001g0201 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2982+218C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | chr12 | 122580888 | ||||||
| chr12:122580928
|
C | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.2982+258C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | chr12 | 122580928 | ||||||
| chr12:122580952
|
C | T | 16 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(13): Show | 16 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.2982+282C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | chr12 | 122580952 | ||||||
| chr12:122581027
|
CA | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.2982+374delA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | INFO_REALIGN_3_PRIME | chr12 | 122581027 | |||||
| chr12:122581044
|
AG | A | 3 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0094 | 3 | HG02129.hp2 NA19000.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.2982+375delG | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | chr12 | 122581044 | ||||||
| chr12:122581088
|
TTCTCTCT others(3): Show |
T | 2 | a0002c0009t0001g0263a0002c0009t0001g0264 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2982+427_2982+436d others(12): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | INFO_REALIGN_3_PRIME | chr12 | 122581088 | |||||
| chr12:122581114
|
G | C | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2982+444G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | chr12 | 122581114 | ||||||
| chr12:122581198
|
A | AT | 92 | a0001c0001t0001g0011a0001c0001t0001g0240a0001c0001t0001g0260others(89): Show | 92 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.2982+545dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | INFO_REALIGN_3_PRIME | chr12 | 122581198 | |||||
| chr12:122581198
|
AT | A | 6 | a0001c0001t0001g0190a0001c0001t0001g0219a0001c0001t0001g0256others(3): Show | 6 | HG02895.hp1 HG03225.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.2982+545delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | INFO_REALIGN_3_PRIME | chr12 | 122581198 | |||||
| chr12:122581240
|
C | T | 1 | a0017c0020t0001g0310 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2982+570C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | chr12 | 122581240 | ||||||
| chr12:122581446
|
A | G | 89 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0002t0001g0007others(86): Show | 89 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.2982+776A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | chr12 | 122581446 | ||||||
| chr12:122581490
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2982+820C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | chr12 | 122581490 | ||||||
| chr12:122581732
|
C | A | 3 | a0003c0004t0001g0008a0003c0004t0001g0022a0003c0004t0001g0026 | 3 | HG02602.hp1 HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2983-973C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | chr12 | 122581732 | ||||||
| chr12:122581784
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2983-921C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | chr12 | 122581784 | ||||||
| chr12:122581789
|
G | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2983-916G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | chr12 | 122581789 | ||||||
| chr12:122581822
|
T | A | 2 | a0001c0002t0001g0054a0001c0002t0001g0055 | 2 | HG01256.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.2983-883T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | chr12 | 122581822 | ||||||
| chr12:122581957
|
A | C | 1 | a0001c0001t0001g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2983-748A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | chr12 | 122581957 | ||||||
| chr12:122581960
|
T | A | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2983-745T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | chr12 | 122581960 | ||||||
| chr12:122582138
|
C | T | 115 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(112): Show | 116 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.2983-567C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 33/63 | chr12 | 122582138 | ||||||
| chr12:122583040
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(84): Show | 89 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(86): Show |
intron_variant | MODIFIER | c.3263+55G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 34/63 | chr12 | 122583040 | ||||||
| chr12:122583087
|
G | A | 23 | a0001c0002t0001g0063a0001c0010t0001g0282a0001c0010t0001g0283others(20): Show | 23 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.3263+102G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 34/63 | chr12 | 122583087 | ||||||
| chr12:122583093
|
C | T | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3263+108C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 34/63 | chr12 | 122583093 | ||||||
| chr12:122583235
|
A | C | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG02258.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.3263+250A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 34/63 | chr12 | 122583235 | ||||||
| chr12:122583390
|
C | A | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.3263+405C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 34/63 | chr12 | 122583390 | ||||||
| chr12:122583403
|
T | C | 1 | a0001c0002t0001g0054 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3263+418T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 34/63 | chr12 | 122583403 | ||||||
| chr12:122583644
|
A | G | 1 | a0001c0011t0001g0237 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3264-634A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 34/63 | chr12 | 122583644 | ||||||
| chr12:122583852
|
G | A | 17 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(14): Show | 17 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.3264-426G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 34/63 | chr12 | 122583852 | ||||||
| chr12:122583968
|
T | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(86): Show | 91 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.3264-310T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 34/63 | chr12 | 122583968 | ||||||
| chr12:122584016
|
T | G | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3264-262T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 34/63 | chr12 | 122584016 | ||||||
| chr12:122584263
|
T | C | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3264-15T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 34/63 | chr12 | 122584263 | ||||||
| chr12:122584846
|
A | G | 1 | a0001c0002t0001g0051 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3437-47A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 35/63 | chr12 | 122584846 | ||||||
| chr12:122585175
|
T | C | 165 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(162): Show | 167 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.3534+185T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 36/63 | chr12 | 122585175 | ||||||
| chr12:122585212
|
A | T | 88 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0002t0001g0007others(85): Show | 88 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.3534+222A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 36/63 | chr12 | 122585212 | ||||||
| chr12:122585213
|
T | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0219 | 2 | HG03927.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.3534+223T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 36/63 | chr12 | 122585213 | ||||||
| chr12:122585291
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(86): Show | 91 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.3534+301C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 36/63 | chr12 | 122585291 | ||||||
| chr12:122585310
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(86): Show | 91 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.3534+320C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 36/63 | chr12 | 122585310 | ||||||
| chr12:122585336
|
C | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3535-300C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 36/63 | chr12 | 122585336 | ||||||
| chr12:122585491
|
T | C | 2 | a0003c0008t0001g0014a0003c0008t0001g0015 | 2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.3535-145T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 36/63 | chr12 | 122585491 | ||||||
| chr12:122585552
|
A | T | 8 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(5): Show | 9 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.3535-84A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 36/63 | chr12 | 122585552 | ||||||
| chr12:122585607
|
C | A | 1 | a0001c0002t0001g0107 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3535-29C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 36/63 | chr12 | 122585607 | ||||||
| chr12:122585860
|
C | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.3673+86C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/63 | chr12 | 122585860 | ||||||
| chr12:122585879
|
T | G | 11 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284others(8): Show | 12 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.3673+105T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/63 | chr12 | 122585879 | ||||||
| chr12:122585967
|
A | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3673+193A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/63 | chr12 | 122585967 | ||||||
| chr12:122586023
|
G | C | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3673+249G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/63 | chr12 | 122586023 | ||||||
| chr12:122586060
|
C | T | 1 | a0007c0013t0001g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3673+286C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/63 | chr12 | 122586060 | ||||||
| chr12:122586069
|
G | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(270): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.3673+295G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/63 | chr12 | 122586069 | ||||||
| chr12:122586071
|
GTTTGT | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(267): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.3673+321_3673+325d others(7): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/63 | INFO_REALIGN_3_PRIME | chr12 | 122586071 | |||||
| chr12:122586080
|
G | C | 124 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(121): Show | 126 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.3673+306G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/63 | chr12 | 122586080 | ||||||
| chr12:122586169
|
G | C | 1 | a0001c0034t0001g0229 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3673+395G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/63 | chr12 | 122586169 | ||||||
| chr12:122586193
|
G | A | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3673+419G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/63 | chr12 | 122586193 | ||||||
| chr12:122586378
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.3674-323G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/63 | chr12 | 122586378 | ||||||
| chr12:122586387
|
T | C | 14 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.3674-314T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/63 | chr12 | 122586387 | ||||||
| chr12:122586412
|
T | G | 3 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0094 | 3 | HG02129.hp2 NA19000.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.3674-289T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/63 | chr12 | 122586412 | ||||||
| chr12:122586473
|
T | A | 1 | a0001c0001t0001g0256 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3674-228T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/63 | chr12 | 122586473 | ||||||
| chr12:122586474
|
A | T | 1 | a0001c0001t0001g0256 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3674-227A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/63 | chr12 | 122586474 | ||||||
| chr12:122586524
|
T | C | 89 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0002t0001g0007others(86): Show | 89 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.3674-177T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/63 | chr12 | 122586524 | ||||||
| chr12:122586626
|
T | C | 1 | a0007c0013t0001g0203 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3674-75T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 37/63 | chr12 | 122586626 | ||||||
| chr12:122586806
|
A | ATTTTTTT others(38): Show |
1 | a0001c0002t0001g0032 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3730+52_3730+53ins others(45): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 38/63 | INFO_REALIGN_3_PRIME | chr12 | 122586806 | |||||
| chr12:122586810
|
A | T | 1 | a0001c0002t0001g0032 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3730+53A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 38/63 | chr12 | 122586810 | ||||||
| chr12:122586814
|
A | T | 1 | a0001c0002t0001g0032 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3730+57A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 38/63 | chr12 | 122586814 | ||||||
| chr12:122586818
|
A | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(236): Show | 243 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.3730+61A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 38/63 | chr12 | 122586818 | ||||||
| chr12:122586819
|
T | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(235): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.3730+62T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 38/63 | chr12 | 122586819 | ||||||
| chr12:122586819
|
T | TTTTA | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.3730+66_3730+69dup others(4): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 38/63 | INFO_REALIGN_3_PRIME | chr12 | 122586819 | |||||
| chr12:122586823
|
A | T | 1 | a0001c0002t0001g0032 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3730+66A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 38/63 | chr12 | 122586823 | ||||||
| chr12:122586836
|
A | G | 1 | a0001c0002t0001g0032 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3730+79A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 38/63 | chr12 | 122586836 | ||||||
| chr12:122586843
|
T | C | 1 | a0001c0002t0001g0032 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3730+86T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 38/63 | chr12 | 122586843 | ||||||
| chr12:122586851
|
T | C | 1 | a0001c0002t0001g0032 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3730+94T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 38/63 | chr12 | 122586851 | ||||||
| chr12:122586962
|
G | T | 3 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0094 | 3 | HG02129.hp2 NA19000.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.3730+205G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 38/63 | chr12 | 122586962 | ||||||
| chr12:122587048
|
G | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3730+291G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 38/63 | chr12 | 122587048 | ||||||
| chr12:122587300
|
T | C | 1 | a0001c0002t0001g0047 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3731-411T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 38/63 | chr12 | 122587300 | ||||||
| chr12:122587490
|
A | C | 1 | a0001c0001t0001g0260 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3731-221A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 38/63 | chr12 | 122587490 | ||||||
| chr12:122587933
|
CAG | C | 17 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(14): Show | 17 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.3894+62_3894+63del others(2): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 39/63 | INFO_REALIGN_3_PRIME | chr12 | 122587933 | |||||
| chr12:122587961
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3894+87A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 39/63 | chr12 | 122587961 | ||||||
| chr12:122588541
|
C | G | 1 | a0002c0003t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3895-171C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 39/63 | chr12 | 122588541 | ||||||
| chr12:122588962
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3999+146A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/63 | chr12 | 122588962 | ||||||
| chr12:122589471
|
G | GT | 30 | a0001c0001t0001g0220a0001c0001t0001g0222a0001c0001t0001g0226others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.3999+671dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/63 | INFO_REALIGN_3_PRIME | chr12 | 122589471 | |||||
| chr12:122589471
|
GT | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0111others(139): Show | 146 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(143): Show |
intron_variant | MODIFIER | c.3999+671delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/63 | INFO_REALIGN_3_PRIME | chr12 | 122589471 | |||||
| chr12:122589620
|
T | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.3999+804T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/63 | chr12 | 122589620 | ||||||
| chr12:122589621
|
T | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.3999+805T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/63 | chr12 | 122589621 | ||||||
| chr12:122589622
|
T | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.3999+806T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/63 | chr12 | 122589622 | ||||||
| chr12:122589701
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(86): Show | 91 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.3999+885G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/63 | chr12 | 122589701 | ||||||
| chr12:122589776
|
A | AT | 25 | a0001c0001t0001g0113a0001c0001t0001g0120a0001c0001t0001g0130others(22): Show | 25 | HG02056.hp2 HG02071.hp1 HG02129.hp1 others(22): Show |
intron_variant | MODIFIER | c.4000-806dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/63 | INFO_REALIGN_3_PRIME | chr12 | 122589776 | |||||
| chr12:122589776
|
A | ATT | 118 | a0001c0001t0001g0011a0001c0001t0001g0122a0001c0001t0001g0172others(115): Show | 120 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.4000-807_4000-806d others(4): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/63 | INFO_REALIGN_3_PRIME | chr12 | 122589776 | |||||
| chr12:122589776
|
A | ATTT | 21 | a0001c0002t0001g0012a0001c0002t0001g0046a0001c0002t0001g0058others(18): Show | 21 | HG00280.hp2 HG00639.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.4000-808_4000-806d others(5): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/63 | INFO_REALIGN_3_PRIME | chr12 | 122589776 | |||||
| chr12:122589776
|
A | ATTTT | 7 | a0001c0002t0001g0063a0001c0010t0001g0282a0001c0010t0001g0283others(4): Show | 7 | HG01106.hp1 HG02109.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.4000-809_4000-806d others(6): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/63 | INFO_REALIGN_3_PRIME | chr12 | 122589776 | |||||
| chr12:122589776
|
AT | A | 7 | a0001c0001t0001g0211a0001c0001t0001g0223a0001c0001t0001g0224others(4): Show | 7 | HG00323.hp1 HG01884.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.4000-806delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/63 | INFO_REALIGN_3_PRIME | chr12 | 122589776 | |||||
| chr12:122589940
|
C | T | 1 | a0001c0001t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4000-667C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/63 | chr12 | 122589940 | ||||||
| chr12:122590138
|
C | T | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.4000-469C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/63 | chr12 | 122590138 | ||||||
| chr12:122590343
|
C | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(255): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.4000-264C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/63 | chr12 | 122590343 | ||||||
| chr12:122590364
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4000-243G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/63 | chr12 | 122590364 | ||||||
| chr12:122590603
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115 | 3 | HG02055.hp2 HG02486.hp1 HG02559.hp2 |
splice_region_variant&intron_variant | LOW | c.4000-4G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 40/63 | chr12 | 122590603 | ||||||
| chr12:122591185
|
C | T | 1 | a0012c0022t0001g0043 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4129-152C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 41/63 | chr12 | 122591185 | ||||||
| chr12:122591186
|
G | A | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.4129-151G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 41/63 | chr12 | 122591186 | ||||||
| chr12:122591285
|
T | G | 2 | a0002c0009t0001g0201a0002c0009t0001g0202 | 2 | HG01109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4129-52T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 41/63 | chr12 | 122591285 | ||||||
| chr12:122591295
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4129-42T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 41/63 | chr12 | 122591295 | ||||||
| chr12:122591737
|
T | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4245+284T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122591737 | ||||||
| chr12:122591749
|
C | T | 10 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG01928.hp1 HG01981.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.4245+296C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122591749 | ||||||
| chr12:122591860
|
G | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4245+407G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122591860 | ||||||
| chr12:122591879
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4245+426C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122591879 | ||||||
| chr12:122591922
|
G | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4245+469G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122591922 | ||||||
| chr12:122592056
|
T | C | 22 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284others(19): Show | 22 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.4245+603T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122592056 | ||||||
| chr12:122592101
|
C | T | 29 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(26): Show | 30 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.4245+648C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122592101 | ||||||
| chr12:122592118
|
G | GCGGC | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.4245+675_4245+678d others(6): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | INFO_REALIGN_3_PRIME | chr12 | 122592118 | |||||
| chr12:122592220
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4245+767C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122592220 | ||||||
| chr12:122592231
|
C | A | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(253): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.4245+778C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122592231 | ||||||
| chr12:122592402
|
A | G | 1 | a0009c0014t0001g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4245+949A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122592402 | ||||||
| chr12:122592655
|
A | G | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4245+1202A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122592655 | ||||||
| chr12:122592777
|
A | G | 2 | a0010c0029t0001g0314a0010c0033t0001g0315 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4245+1324A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122592777 | ||||||
| chr12:122592803
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0111others(103): Show | 108 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(105): Show |
intron_variant | MODIFIER | c.4245+1350C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122592803 | ||||||
| chr12:122592905
|
G | C | 4 | a0001c0002t0001g0089a0001c0002t0001g0091a0001c0002t0001g0092others(1): Show | 4 | NA18952.hp2 NA18970.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.4246-1371G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122592905 | ||||||
| chr12:122592938
|
T | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(201): Show | 207 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.4246-1338T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122592938 | ||||||
| chr12:122593005
|
C | G | 1 | a0004c0005t0001g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4246-1271C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122593005 | ||||||
| chr12:122593046
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4246-1230C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122593046 | ||||||
| chr12:122593049
|
C | T | 2 | a0010c0029t0001g0314a0010c0033t0001g0315 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4246-1227C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122593049 | ||||||
| chr12:122593159
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4246-1117C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122593159 | ||||||
| chr12:122593171
|
G | T | 2 | a0021c0036t0001g0013a0022c0035t0001g0029 | 2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.4246-1105G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122593171 | ||||||
| chr12:122593252
|
T | G | 1 | a0001c0002t0001g0062 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.4246-1024T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122593252 | ||||||
| chr12:122593259
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.4246-1017T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122593259 | ||||||
| chr12:122593266
|
C | CT | 39 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(36): Show | 39 | HG00280.hp2 HG00639.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.4246-994dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | INFO_REALIGN_3_PRIME | chr12 | 122593266 | |||||
| chr12:122593335
|
C | G | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4246-941C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122593335 | ||||||
| chr12:122593357
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4246-919A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122593357 | ||||||
| chr12:122593404
|
C | T | 2 | a0003c0008t0002g0017a0003c0008t0002g0018 | 2 | HG01106.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.4246-872C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122593404 | ||||||
| chr12:122593496
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4246-780C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122593496 | ||||||
| chr12:122593836
|
C | T | 7 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.4246-440C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122593836 | ||||||
| chr12:122594036
|
A | G | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4246-240A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122594036 | ||||||
| chr12:122594170
|
C | A | 1 | a0001c0001t0001g0178 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4246-106C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122594170 | ||||||
| chr12:122594273
|
T | C | 1 | a0003c0004t0001g0019 | 1 | HG01975.hp1 | splice_region_variant&intron_variant | LOW | c.4246-3T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 42/63 | chr12 | 122594273 | ||||||
| chr12:122594473
|
T | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(211): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.4355+88T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122594473 | ||||||
| chr12:122594488
|
A | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.4355+103A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122594488 | ||||||
| chr12:122594612
|
A | C | 1 | a0001c0001t0001g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4355+227A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122594612 | ||||||
| chr12:122594633
|
A | G | 1 | a0017c0020t0001g0310 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4355+248A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122594633 | ||||||
| chr12:122594861
|
T | C | 1 | a0001c0001t0001g0303 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.4355+476T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122594861 | ||||||
| chr12:122594866
|
G | T | 8 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(5): Show | 9 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.4355+481G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122594866 | ||||||
| chr12:122594959
|
C | T | 4 | a0002c0003t0001g0124a0008c0012t0001g0005a0008c0012t0001g0125others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.4355+574C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122594959 | ||||||
| chr12:122594994
|
A | G | 21 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.4355+609A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122594994 | ||||||
| chr12:122595123
|
G | T | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.4355+738G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122595123 | ||||||
| chr12:122595156
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4355+771G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122595156 | ||||||
| chr12:122595219
|
C | A | 125 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(122): Show | 126 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.4355+834C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122595219 | ||||||
| chr12:122595537
|
G | A | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.4355+1152G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122595537 | ||||||
| chr12:122595540
|
A | G | 1 | a0001c0002t0001g0046 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4355+1155A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122595540 | ||||||
| chr12:122595632
|
C | T | 2 | a0004c0005t0001g0307a0004c0005t0001g0308 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4355+1247C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122595632 | ||||||
| chr12:122595660
|
T | A | 7 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.4355+1275T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122595660 | ||||||
| chr12:122595699
|
T | C | 1 | a0007c0013t0001g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4355+1314T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122595699 | ||||||
| chr12:122595759
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4355+1374A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122595759 | ||||||
| chr12:122595803
|
T | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4355+1418T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122595803 | ||||||
| chr12:122595978
|
G | C | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4355+1593G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122595978 | ||||||
| chr12:122596023
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4355+1638A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122596023 | ||||||
| chr12:122596079
|
C | CT | 126 | a0001c0001t0001g0011a0001c0001t0001g0121a0001c0001t0001g0122others(123): Show | 127 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.4356-1631dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | INFO_REALIGN_3_PRIME | chr12 | 122596079 | |||||
| chr12:122596079
|
C | CTT | 21 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(18): Show | 21 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.4356-1632_4356-163 others(6): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | INFO_REALIGN_3_PRIME | chr12 | 122596079 | |||||
| chr12:122596106
|
G | C | 1 | a0001c0002t0001g0054 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4356-1625G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122596106 | ||||||
| chr12:122596130
|
T | C | 14 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.4356-1601T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122596130 | ||||||
| chr12:122596246
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4356-1485T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122596246 | ||||||
| chr12:122596532
|
T | A | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4356-1199T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122596532 | ||||||
| chr12:122596610
|
G | T | 11 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0001g0157others(8): Show | 11 | HG01070.hp2 HG01928.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.4356-1121G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122596610 | ||||||
| chr12:122596662
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4356-1069G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122596662 | ||||||
| chr12:122596922
|
G | A | 1 | a0004c0005t0001g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4356-809G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122596922 | ||||||
| chr12:122597210
|
C | T | 35 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(32): Show | 36 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.4356-521C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122597210 | ||||||
| chr12:122597221
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4356-510C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122597221 | ||||||
| chr12:122597241
|
A | AT | 34 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0128others(31): Show | 34 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.4356-465dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | INFO_REALIGN_3_PRIME | chr12 | 122597241 | |||||
| chr12:122597241
|
A | ATTT | 14 | a0001c0001t0001g0258a0002c0003t0001g0272a0002c0003t0001g0273others(11): Show | 14 | HG01884.hp2 HG02257.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.4356-467_4356-465d others(5): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | INFO_REALIGN_3_PRIME | chr12 | 122597241 | |||||
| chr12:122597241
|
AT | A | 36 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(33): Show | 37 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.4356-465delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | INFO_REALIGN_3_PRIME | chr12 | 122597241 | |||||
| chr12:122597241
|
ATT | A | 6 | a0001c0001t0001g0116a0001c0001t0001g0209a0001c0001t0001g0210others(3): Show | 6 | HG02109.hp2 HG02683.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.4356-466_4356-465d others(4): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | INFO_REALIGN_3_PRIME | chr12 | 122597241 | |||||
| chr12:122597439
|
G | A | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.4356-292G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122597439 | ||||||
| chr12:122597464
|
G | A | 1 | a0001c0002t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4356-267G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122597464 | ||||||
| chr12:122597542
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4356-189C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122597542 | ||||||
| chr12:122597549
|
A | G | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.4356-182A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 43/63 | chr12 | 122597549 | ||||||
| chr12:122598219
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.4563+281A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122598219 | ||||||
| chr12:122598421
|
C | CT | 130 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(127): Show | 131 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.4563+500dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | INFO_REALIGN_3_PRIME | chr12 | 122598421 | |||||
| chr12:122598421
|
C | CTT | 18 | a0001c0001t0001g0199a0001c0002t0001g0100a0002c0009t0001g0202others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.4563+499_4563+500d others(4): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | INFO_REALIGN_3_PRIME | chr12 | 122598421 | |||||
| chr12:122598421
|
C | CTTT | 6 | a0001c0001t0001g0165a0002c0003t0001g0293a0002c0003t0001g0295others(3): Show | 6 | HG01099.hp1 HG01243.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.4563+498_4563+500d others(5): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | INFO_REALIGN_3_PRIME | chr12 | 122598421 | |||||
| chr12:122598421
|
C | CTTTT | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(87): Show | 92 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(89): Show |
intron_variant | MODIFIER | c.4563+497_4563+500d others(6): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | INFO_REALIGN_3_PRIME | chr12 | 122598421 | |||||
| chr12:122598421
|
C | CTTTTT | 14 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0161others(11): Show | 14 | HG01168.hp1 HG01175.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.4563+496_4563+500d others(7): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | INFO_REALIGN_3_PRIME | chr12 | 122598421 | |||||
| chr12:122598621
|
G | A | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(303): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.4563+683G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122598621 | ||||||
| chr12:122598875
|
A | G | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4563+937A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122598875 | ||||||
| chr12:122598915
|
T | A | 1 | a0001c0001t0001g0304 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4563+977T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122598915 | ||||||
| chr12:122598947
|
C | G | 1 | a0007c0013t0001g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4563+1009C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122598947 | ||||||
| chr12:122598961
|
T | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(250): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.4563+1023T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122598961 | ||||||
| chr12:122598965
|
A | G | 14 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.4563+1027A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122598965 | ||||||
| chr12:122599015
|
A | T | 3 | a0001c0002t0001g0106a0003c0008t0002g0017a0003c0008t0002g0018 | 3 | HG01106.hp1 HG01346.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.4563+1077A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122599015 | ||||||
| chr12:122599016
|
T | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0129a0001c0002t0001g0009others(3): Show | 6 | HG01081.hp1 HG02698.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.4563+1078T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122599016 | ||||||
| chr12:122599131
|
G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG02258.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.4563+1193G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122599131 | ||||||
| chr12:122599161
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4563+1223C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122599161 | ||||||
| chr12:122599209
|
G | A | 4 | a0001c0002t0001g0048a0001c0002t0001g0079a0001c0002t0003g0090others(1): Show | 4 | HG00099.hp2 HG01106.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.4563+1271G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122599209 | ||||||
| chr12:122599241
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4563+1303C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122599241 | ||||||
| chr12:122599363
|
A | ATT | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(247): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.4563+1436_4563+143 others(6): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | INFO_REALIGN_3_PRIME | chr12 | 122599363 | |||||
| chr12:122599363
|
A | T | 1 | a0002c0003t0001g0293 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4563+1425A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122599363 | ||||||
| chr12:122599640
|
T | C | 1 | a0004c0005t0001g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4563+1702T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122599640 | ||||||
| chr12:122599901
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4564-1635C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122599901 | ||||||
| chr12:122599927
|
G | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4564-1609G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122599927 | ||||||
| chr12:122599990
|
G | A | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.4564-1546G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122599990 | ||||||
| chr12:122600053
|
TAGAA | T | 25 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0035others(22): Show | 25 | HG00597.hp1 HG01433.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.4564-1474_4564-147 others(8): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | INFO_REALIGN_3_PRIME | chr12 | 122600053 | |||||
| chr12:122600115
|
TTTGAGAT others(14): Show |
T | 1 | a0001c0001t0001g0260 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.4564-1417_4564-139 others(25): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | INFO_REALIGN_3_PRIME | chr12 | 122600115 | |||||
| chr12:122600259
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(86): Show | 91 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.4564-1277C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122600259 | ||||||
| chr12:122600289
|
A | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.4564-1247A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122600289 | ||||||
| chr12:122600423
|
T | C | 30 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(27): Show | 31 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.4564-1113T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122600423 | ||||||
| chr12:122600510
|
CCA | C | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | NA18953.hp1 NA19056.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.4564-1023_4564-102 others(6): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | INFO_REALIGN_3_PRIME | chr12 | 122600510 | |||||
| chr12:122600552
|
C | T | 1 | a0001c0002t0001g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4564-984C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122600552 | ||||||
| chr12:122600558
|
G | C | 1 | a0001c0001t0001g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4564-978G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122600558 | ||||||
| chr12:122600671
|
C | CT | 13 | a0001c0002t0001g0095a0001c0026t0001g0081a0004c0005t0001g0004others(10): Show | 14 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.4564-853dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | INFO_REALIGN_3_PRIME | chr12 | 122600671 | |||||
| chr12:122600726
|
C | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG02258.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.4564-810C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122600726 | ||||||
| chr12:122600809
|
G | T | 1 | a0001c0001t0001g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4564-727G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122600809 | ||||||
| chr12:122601207
|
C | T | 87 | a0001c0002t0001g0007a0001c0002t0001g0009a0001c0002t0001g0010others(84): Show | 87 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.4564-329C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122601207 | ||||||
| chr12:122601240
|
G | A | 12 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(9): Show | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.4564-296G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 44/63 | chr12 | 122601240 | ||||||
| chr12:122601628
|
A | AT | 8 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(5): Show | 9 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.4653+4dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 45/63 | INFO_REALIGN_3_PRIME | chr12 | 122601628 | |||||
| chr12:122601756
|
T | A | 1 | a0001c0001t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4653+131T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 45/63 | chr12 | 122601756 | ||||||
| chr12:122602102
|
A | T | 1 | a0001c0001t0001g0211 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.4654-467A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 45/63 | chr12 | 122602102 | ||||||
| chr12:122602156
|
T | A | 1 | a0001c0001t0001g0211 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.4654-413T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 45/63 | chr12 | 122602156 | ||||||
| chr12:122602157
|
A | T | 1 | a0001c0001t0001g0211 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.4654-412A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 45/63 | chr12 | 122602157 | ||||||
| chr12:122602158
|
T | A | 1 | a0001c0001t0001g0211 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.4654-411T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 45/63 | chr12 | 122602158 | ||||||
| chr12:122602249
|
T | C | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.4654-320T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 45/63 | chr12 | 122602249 | ||||||
| chr12:122602315
|
G | T | 1 | a0001c0001t0001g0178 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4654-254G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 45/63 | chr12 | 122602315 | ||||||
| chr12:122602778
|
A | G | 8 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(5): Show | 9 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.4825+38A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 46/63 | chr12 | 122602778 | ||||||
| chr12:122602895
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(254): Show |
splice_region_variant&intron_variant | LOW | c.4884+8A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 47/63 | chr12 | 122602895 | ||||||
| chr12:122603272
|
T | TA | 21 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284others(18): Show | 21 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.5101+44dupA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | INFO_REALIGN_3_PRIME | chr12 | 122603272 | |||||
| chr12:122603272
|
T | TAA | 7 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(4): Show | 8 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.5101+43_5101+44dup others(2): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | INFO_REALIGN_3_PRIME | chr12 | 122603272 | |||||
| chr12:122603332
|
A | T | 8 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(5): Show | 9 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.5101+89A>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | chr12 | 122603332 | ||||||
| chr12:122603434
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5101+191C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | chr12 | 122603434 | ||||||
| chr12:122603570
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG01081.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.5101+327G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | chr12 | 122603570 | ||||||
| chr12:122603614
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5101+371C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | chr12 | 122603614 | ||||||
| chr12:122603639
|
C | T | 2 | a0010c0029t0001g0314a0010c0033t0001g0315 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5101+396C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | chr12 | 122603639 | ||||||
| chr12:122603646
|
T | C | 48 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284others(45): Show | 49 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.5101+403T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | chr12 | 122603646 | ||||||
| chr12:122603804
|
A | G | 87 | a0001c0001t0001g0011a0001c0002t0001g0007a0001c0002t0001g0009others(84): Show | 87 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.5101+561A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | chr12 | 122603804 | ||||||
| chr12:122603836
|
A | G | 1 | a0003c0008t0001g0014 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.5101+593A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | chr12 | 122603836 | ||||||
| chr12:122604162
|
G | A | 1 | a0002c0003t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5102-402G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | chr12 | 122604162 | ||||||
| chr12:122604168
|
C | CT | 17 | a0001c0001t0001g0175a0001c0001t0001g0188a0001c0001t0001g0192others(14): Show | 17 | HG00423.hp2 HG00735.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.5102-372dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | INFO_REALIGN_3_PRIME | chr12 | 122604168 | |||||
| chr12:122604168
|
C | G | 1 | a0007c0013t0001g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5102-396C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | chr12 | 122604168 | ||||||
| chr12:122604168
|
CT | C | 69 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(66): Show | 70 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(67): Show |
intron_variant | MODIFIER | c.5102-372delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | INFO_REALIGN_3_PRIME | chr12 | 122604168 | |||||
| chr12:122604191
|
T | A | 1 | a0002c0009t0001g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5102-373T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | chr12 | 122604191 | ||||||
| chr12:122604192
|
T | A | 8 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(5): Show | 9 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.5102-372T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | chr12 | 122604192 | ||||||
| chr12:122604209
|
G | A | 86 | a0001c0002t0001g0007a0001c0002t0001g0009a0001c0002t0001g0010others(83): Show | 86 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.5102-355G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | chr12 | 122604209 | ||||||
| chr12:122604344
|
T | C | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5102-220T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 48/63 | chr12 | 122604344 | ||||||
| chr12:122604662
|
G | A | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.5175+25G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 49/63 | chr12 | 122604662 | ||||||
| chr12:122604785
|
G | A | 8 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(5): Show | 9 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.5176-92G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 49/63 | chr12 | 122604785 | ||||||
| chr12:122604785
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.5176-92G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 49/63 | chr12 | 122604785 | ||||||
| chr12:122604788
|
G | C | 1 | a0001c0001t0001g0239 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5176-89G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 49/63 | chr12 | 122604788 | ||||||
| chr12:122605161
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.5386+74C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 50/63 | chr12 | 122605161 | ||||||
| chr12:122605199
|
A | ATATACT | 40 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284others(37): Show | 40 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.5387-102_5387-97du others(7): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 50/63 | INFO_REALIGN_3_PRIME | chr12 | 122605199 | |||||
| chr12:122605608
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.5496+193C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122605608 | ||||||
| chr12:122605690
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(80): Show | 85 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(82): Show |
intron_variant | MODIFIER | c.5496+275C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122605690 | ||||||
| chr12:122605734
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5496+319C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122605734 | ||||||
| chr12:122605833
|
T | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(267): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.5496+418T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122605833 | ||||||
| chr12:122605875
|
G | A | 1 | a0002c0009t0001g0264 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5496+460G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122605875 | ||||||
| chr12:122605971
|
T | C | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | NA18968.hp1 NA19009.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.5496+556T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122605971 | ||||||
| chr12:122606018
|
T | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(198): Show | 204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.5496+603T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122606018 | ||||||
| chr12:122606025
|
G | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(194): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.5496+610G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122606025 | ||||||
| chr12:122606222
|
C | CT | 29 | a0001c0001t0001g0135a0001c0001t0001g0149a0001c0001t0001g0181others(26): Show | 30 | HG01109.hp1 HG01109.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.5496+829dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | INFO_REALIGN_3_PRIME | chr12 | 122606222 | |||||
| chr12:122606222
|
CT | C | 18 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(15): Show | 18 | HG00609.hp2 HG01169.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.5496+829delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | INFO_REALIGN_3_PRIME | chr12 | 122606222 | |||||
| chr12:122606222
|
CTTTT | C | 19 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.5496+826_5496+829d others(6): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | INFO_REALIGN_3_PRIME | chr12 | 122606222 | |||||
| chr12:122606449
|
C | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.5496+1034C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122606449 | ||||||
| chr12:122606481
|
G | A | 3 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0094 | 3 | HG02129.hp2 NA19000.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.5496+1066G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122606481 | ||||||
| chr12:122606720
|
C | T | 1 | a0001c0002t0001g0048 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5496+1305C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122606720 | ||||||
| chr12:122606773
|
A | G | 2 | a0001c0002t0001g0040a0001c0002t0001g0041 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.5496+1358A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122606773 | ||||||
| chr12:122606781
|
C | T | 1 | a0001c0001t0001g0299 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.5496+1366C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122606781 | ||||||
| chr12:122606788
|
G | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5496+1373G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122606788 | ||||||
| chr12:122606894
|
C | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0160 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.5496+1479C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122606894 | ||||||
| chr12:122607209
|
G | A | 2 | a0003c0008t0002g0017a0003c0008t0002g0018 | 2 | HG01106.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.5496+1794G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122607209 | ||||||
| chr12:122607212
|
C | T | 85 | a0001c0002t0001g0007a0001c0002t0001g0009a0001c0002t0001g0010others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.5496+1797C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122607212 | ||||||
| chr12:122607254
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5496+1839G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122607254 | ||||||
| chr12:122607255
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5496+1840G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122607255 | ||||||
| chr12:122607363
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.5496+1948C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122607363 | ||||||
| chr12:122607591
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.5497-1793G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122607591 | ||||||
| chr12:122607750
|
C | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.5497-1634C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122607750 | ||||||
| chr12:122608046
|
C | CAG | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | NA18953.hp1 NA19056.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.5497-1337_5497-133 others(6): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | INFO_REALIGN_3_PRIME | chr12 | 122608046 | |||||
| chr12:122608048
|
C | T | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | NA18953.hp1 NA19056.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.5497-1336C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122608048 | ||||||
| chr12:122608049
|
C | A | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | NA18953.hp1 NA19056.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.5497-1335C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122608049 | ||||||
| chr12:122608667
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5497-717A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122608667 | ||||||
| chr12:122608674
|
C | G | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.5497-710C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122608674 | ||||||
| chr12:122608711
|
T | A | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5497-673T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122608711 | ||||||
| chr12:122608818
|
G | C | 4 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.5497-566G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122608818 | ||||||
| chr12:122608994
|
G | T | 123 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0114others(120): Show | 124 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.5497-390G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122608994 | ||||||
| chr12:122609016
|
G | A | 1 | a0001c0002t0001g0107 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5497-368G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122609016 | ||||||
| chr12:122609181
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(86): Show | 91 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.5497-203C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 51/63 | chr12 | 122609181 | ||||||
| chr12:122609810
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5543+380G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 52/63 | chr12 | 122609810 | ||||||
| chr12:122610017
|
G | A | 1 | a0001c0002t0001g0094 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.5543+587G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 52/63 | chr12 | 122610017 | ||||||
| chr12:122610044
|
C | G | 1 | a0001c0025t0001g0207 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.5543+614C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 52/63 | chr12 | 122610044 | ||||||
| chr12:122610173
|
G | C | 164 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(161): Show | 165 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.5544-649G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 52/63 | chr12 | 122610173 | ||||||
| chr12:122610235
|
C | T | 2 | a0002c0003t0001g0272a0002c0003t0001g0273 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.5544-587C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 52/63 | chr12 | 122610235 | ||||||
| chr12:122610284
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0255 | 2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.5544-538G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 52/63 | chr12 | 122610284 | ||||||
| chr12:122610291
|
A | G | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.5544-531A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 52/63 | chr12 | 122610291 | ||||||
| chr12:122610318
|
G | A | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.5544-504G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 52/63 | chr12 | 122610318 | ||||||
| chr12:122610379
|
T | C | 1 | a0007c0013t0001g0203 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5544-443T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 52/63 | chr12 | 122610379 | ||||||
| chr12:122610494
|
T | C | 88 | a0001c0001t0001g0260a0001c0002t0001g0007a0001c0002t0001g0009others(85): Show | 88 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.5544-328T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 52/63 | chr12 | 122610494 | ||||||
| chr12:122610500
|
G | A | 5 | a0006c0006t0001g0245a0006c0006t0001g0246a0006c0006t0001g0247others(2): Show | 5 | HG02109.hp1 HG02257.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.5544-322G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 52/63 | chr12 | 122610500 | ||||||
| chr12:122610788
|
T | TA | 14 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.5544-28dupA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 52/63 | INFO_REALIGN_3_PRIME | chr12 | 122610788 | |||||
| chr12:122611022
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5622+122A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122611022 | ||||||
| chr12:122611169
|
C | G | 1 | a0021c0036t0001g0013 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5622+269C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122611169 | ||||||
| chr12:122611509
|
A | G | 1 | a0011c0015t0001g0274 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5622+609A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122611509 | ||||||
| chr12:122611658
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.5622+758A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122611658 | ||||||
| chr12:122611748
|
C | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5622+848C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122611748 | ||||||
| chr12:122611917
|
A | AT | 47 | a0001c0001t0001g0153a0001c0010t0001g0282a0001c0010t0001g0283others(44): Show | 47 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.5622+1029dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | INFO_REALIGN_3_PRIME | chr12 | 122611917 | |||||
| chr12:122611929
|
T | C | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5622+1029T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122611929 | ||||||
| chr12:122611965
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.5622+1065C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122611965 | ||||||
| chr12:122612067
|
T | G | 26 | a0001c0001t0001g0306a0002c0009t0001g0201a0002c0009t0001g0202others(23): Show | 26 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.5623-1045T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122612067 | ||||||
| chr12:122612071
|
GT | G | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.5623-1029delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | INFO_REALIGN_3_PRIME | chr12 | 122612071 | |||||
| chr12:122612091
|
A | G | 1 | a0001c0001t0001g0211 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.5623-1021A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122612091 | ||||||
| chr12:122612318
|
G | A | 3 | a0008c0012t0001g0005a0008c0012t0001g0125a0008c0012t0001g0126 | 3 | HG01884.hp2 HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.5623-794G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122612318 | ||||||
| chr12:122612397
|
G | GTTTTCT | 4 | a0001c0001t0001g0306a0001c0002t0001g0055a0001c0002t0001g0056others(1): Show | 4 | HG01943.hp1 HG03831.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.5623-692_5623-687d others(8): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | INFO_REALIGN_3_PRIME | chr12 | 122612397 | |||||
| chr12:122612397
|
GTTTTCT | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(86): Show | 91 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.5623-692_5623-687d others(8): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | INFO_REALIGN_3_PRIME | chr12 | 122612397 | |||||
| chr12:122612476
|
G | A | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.5623-636G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122612476 | ||||||
| chr12:122612477
|
T | A | 1 | a0001c0001t0001g0006 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.5623-635T>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122612477 | ||||||
| chr12:122612480
|
C | T | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5623-632C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122612480 | ||||||
| chr12:122612483
|
G | A | 1 | a0001c0002t0001g0061 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.5623-629G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122612483 | ||||||
| chr12:122612505
|
C | T | 4 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.5623-607C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122612505 | ||||||
| chr12:122612600
|
G | C | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0288 | 3 | HG01081.hp1 HG01993.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.5623-512G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122612600 | ||||||
| chr12:122612665
|
G | A | 1 | a0020c0037t0001g0292 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5623-447G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122612665 | ||||||
| chr12:122612789
|
C | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5623-323C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122612789 | ||||||
| chr12:122612981
|
C | A | 114 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(111): Show | 115 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.5623-131C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122612981 | ||||||
| chr12:122612981
|
C | T | 1 | a0002c0003t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5623-131C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122612981 | ||||||
| chr12:122613103
|
G | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5623-9G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 53/63 | chr12 | 122613103 | ||||||
| chr12:122613383
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5741+153G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 54/63 | chr12 | 122613383 | ||||||
| chr12:122613489
|
T | C | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5742-137T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 54/63 | chr12 | 122613489 | ||||||
| chr12:122613885
|
G | T | 1 | a0001c0011t0001g0218 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.5877+124G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 55/63 | chr12 | 122613885 | ||||||
| chr12:122614311
|
T | C | 90 | a0001c0001t0001g0011a0001c0001t0001g0132a0001c0001t0001g0260others(87): Show | 90 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.5877+550T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 55/63 | chr12 | 122614311 | ||||||
| chr12:122614346
|
C | G | 2 | a0003c0004t0001g0019a0003c0004t0001g0028 | 2 | HG00280.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.5877+585C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 55/63 | chr12 | 122614346 | ||||||
| chr12:122614359
|
G | A | 1 | a0001c0002t0001g0261 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.5877+598G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 55/63 | chr12 | 122614359 | ||||||
| chr12:122614527
|
T | C | 1 | a0001c0002t0001g0088 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.5878-464T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 55/63 | chr12 | 122614527 | ||||||
| chr12:122614692
|
C | T | 1 | a0010c0029t0001g0314 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5878-299C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 55/63 | chr12 | 122614692 | ||||||
| chr12:122614719
|
A | G | 2 | a0001c0001t0001g0183a0001c0023t0001g0184 | 2 | NA18982.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.5878-272A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 55/63 | chr12 | 122614719 | ||||||
| chr12:122615150
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.5973+64C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 56/63 | chr12 | 122615150 | ||||||
| chr12:122615171
|
A | G | 11 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0035others(8): Show | 11 | HG01433.hp2 HG01496.hp2 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.5973+85A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 56/63 | chr12 | 122615171 | ||||||
| chr12:122615352
|
T | C | 2 | a0002c0003t0001g0272a0002c0003t0001g0273 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.5974-118T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 56/63 | chr12 | 122615352 | ||||||
| chr12:122615597
|
A | C | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.6030+71A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | chr12 | 122615597 | ||||||
| chr12:122615641
|
G | A | 2 | a0001c0002t0001g0054a0001c0002t0001g0055 | 2 | HG01256.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.6030+115G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | chr12 | 122615641 | ||||||
| chr12:122615735
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(86): Show | 91 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.6030+209C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | chr12 | 122615735 | ||||||
| chr12:122615736
|
G | A | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.6030+210G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | chr12 | 122615736 | ||||||
| chr12:122615746
|
C | G | 7 | a0004c0005t0001g0004a0004c0005t0001g0309a0004c0005t0001g0311others(4): Show | 8 | HG01891.hp1 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.6030+220C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | chr12 | 122615746 | ||||||
| chr12:122615850
|
C | T | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0111others(248): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.6030+324C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | chr12 | 122615850 | ||||||
| chr12:122616266
|
CT | C | 5 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0236others(2): Show | 6 | HG02683.hp2 HG02895.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.6030+754delT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | INFO_REALIGN_3_PRIME | chr12 | 122616266 | |||||
| chr12:122616413
|
C | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0271 | 2 | HG00099.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.6030+887C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | chr12 | 122616413 | ||||||
| chr12:122616482
|
C | T | 5 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(2): Show | 5 | HG02055.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.6030+956C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | chr12 | 122616482 | ||||||
| chr12:122616561
|
G | A | 1 | a0002c0003t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.6030+1035G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | chr12 | 122616561 | ||||||
| chr12:122616601
|
A | C | 1 | a0001c0001t0001g0152 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.6030+1075A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | chr12 | 122616601 | ||||||
| chr12:122616749
|
C | T | 4 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(1): Show | 4 | HG01109.hp1 HG02145.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.6030+1223C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | chr12 | 122616749 | ||||||
| chr12:122616805
|
G | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.6030+1279G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | chr12 | 122616805 | ||||||
| chr12:122617100
|
T | C | 1 | a0009c0014t0001g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.6031-1243T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | chr12 | 122617100 | ||||||
| chr12:122617126
|
G | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0111others(248): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.6031-1217G>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | chr12 | 122617126 | ||||||
| chr12:122617535
|
C | G | 7 | a0002c0009t0001g0201a0002c0009t0001g0202a0002c0009t0001g0263others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.6031-808C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | chr12 | 122617535 | ||||||
| chr12:122617597
|
A | C | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.6031-746A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | chr12 | 122617597 | ||||||
| chr12:122617964
|
T | C | 1 | a0022c0035t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6031-379T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 57/63 | chr12 | 122617964 | ||||||
| chr12:122618421
|
G | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.6085+24G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 58/63 | chr12 | 122618421 | ||||||
| chr12:122618461
|
G | GT | 103 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(100): Show | 103 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.6086-14dupT | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 58/63 | INFO_REALIGN_3_PRIME | chr12 | 122618461 | |||||
| chr12:122618468
|
TG | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.6086-13delG | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 58/63 | chr12 | 122618468 | ||||||
| chr12:122618469
|
G | T | 159 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(156): Show | 160 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.6086-13G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 58/63 | chr12 | 122618469 | ||||||
| chr12:122618653
|
C | T | 1 | a0001c0002t0001g0067 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.6149+108C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 59/63 | chr12 | 122618653 | ||||||
| chr12:122618935
|
A | G | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.6149+390A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 59/63 | chr12 | 122618935 | ||||||
| chr12:122619026
|
GTTTTGTT | G | 19 | a0001c0001t0001g0306a0003c0004t0001g0008a0003c0004t0001g0016others(16): Show | 19 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.6149+506_6149+512d others(9): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 59/63 | INFO_REALIGN_3_PRIME | chr12 | 122619026 | |||||
| chr12:122619080
|
C | T | 1 | a0009c0014t0001g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.6149+535C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 59/63 | chr12 | 122619080 | ||||||
| chr12:122619164
|
T | C | 1 | a0022c0035t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6149+619T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 59/63 | chr12 | 122619164 | ||||||
| chr12:122619346
|
A | G | 88 | a0001c0001t0001g0011a0001c0002t0001g0007a0001c0002t0001g0009others(85): Show | 88 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.6149+801A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 59/63 | chr12 | 122619346 | ||||||
| chr12:122619361
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.6149+816A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 59/63 | chr12 | 122619361 | ||||||
| chr12:122619400
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.6149+855C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 59/63 | chr12 | 122619400 | ||||||
| chr12:122619434
|
A | G | 1 | a0001c0002t0001g0107 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.6149+889A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 59/63 | chr12 | 122619434 | ||||||
| chr12:122619573
|
C | T | 1 | a0004c0005t0001g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6150-906C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 59/63 | chr12 | 122619573 | ||||||
| chr12:122619664
|
G | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.6150-815G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 59/63 | chr12 | 122619664 | ||||||
| chr12:122619750
|
AC | A | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.6150-728delC | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 59/63 | chr12 | 122619750 | ||||||
| chr12:122620037
|
C | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG02258.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.6150-442C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 59/63 | chr12 | 122620037 | ||||||
| chr12:122620140
|
G | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(88): Show | 93 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(90): Show |
intron_variant | MODIFIER | c.6150-339G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 59/63 | chr12 | 122620140 | ||||||
| chr12:122620168
|
CA | C | 70 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(67): Show | 71 | HG00280.hp2 HG00639.hp2 HG01099.hp2 others(68): Show |
intron_variant | MODIFIER | c.6150-293delA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 59/63 | INFO_REALIGN_3_PRIME | chr12 | 122620168 | |||||
| chr12:122620644
|
A | G | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.6279+36A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 60/63 | chr12 | 122620644 | ||||||
| chr12:122620735
|
A | G | 1 | a0001c0001t0001g0299 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.6279+127A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 60/63 | chr12 | 122620735 | ||||||
| chr12:122620748
|
G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG02258.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.6279+140G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 60/63 | chr12 | 122620748 | ||||||
| chr12:122620829
|
T | C | 2 | a0001c0002t0001g0044a0001c0002t0001g0045 | 2 | HG02071.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.6279+221T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 60/63 | chr12 | 122620829 | ||||||
| chr12:122620958
|
A | AGAT | 3 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0001t0001g0267 | 3 | NA18964.hp1 NA19001.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.6279+352_6279+354d others(5): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 60/63 | INFO_REALIGN_3_PRIME | chr12 | 122620958 | |||||
| chr12:122621197
|
T | C | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.6279+589T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 60/63 | chr12 | 122621197 | ||||||
| chr12:122621510
|
T | C | 2 | a0002c0009t0001g0263a0002c0009t0001g0264 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.6280-371T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 60/63 | chr12 | 122621510 | ||||||
| chr12:122621554
|
C | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0307a0004c0005t0001g0308others(8): Show | 12 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.6280-327C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 60/63 | chr12 | 122621554 | ||||||
| chr12:122621581
|
G | A | 1 | a0003c0008t0001g0015 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6280-300G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 60/63 | chr12 | 122621581 | ||||||
| chr12:122621627
|
G | A | 2 | a0001c0001t0001g0183a0001c0023t0001g0184 | 2 | NA18982.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.6280-254G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 60/63 | chr12 | 122621627 | ||||||
| chr12:122621828
|
G | T | 28 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(25): Show | 29 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.6280-53G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 60/63 | chr12 | 122621828 | ||||||
| chr12:122622015
|
C | A | 1 | a0004c0005t0001g0312 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.6369+45C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 61/63 | chr12 | 122622015 | ||||||
| chr12:122622346
|
G | A | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.6370-116G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 61/63 | chr12 | 122622346 | ||||||
| chr12:122622364
|
G | A | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.6370-98G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 61/63 | chr12 | 122622364 | ||||||
| chr12:122622618
|
T | TA | 7 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284others(4): Show | 8 | HG02109.hp2 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.6515+24dupA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 62/63 | INFO_REALIGN_3_PRIME | chr12 | 122622618 | |||||
| chr12:122622618
|
TA | T | 8 | a0001c0001t0001g0252a0001c0002t0001g0098a0002c0003t0001g0272others(5): Show | 8 | HG00323.hp1 HG02647.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.6515+24delA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 62/63 | INFO_REALIGN_3_PRIME | chr12 | 122622618 | |||||
| chr12:122622948
|
CA | C | 11 | a0001c0002t0001g0054a0001c0002t0001g0055a0001c0002t0001g0056others(8): Show | 11 | HG01109.hp1 HG01256.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.6515+354delA | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 62/63 | INFO_REALIGN_3_PRIME | chr12 | 122622948 | |||||
| chr12:122623346
|
G | A | 17 | a0002c0003t0001g0124a0002c0003t0001g0272a0002c0003t0001g0273others(14): Show | 17 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.6515+739G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 62/63 | chr12 | 122623346 | ||||||
| chr12:122623649
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.6516-949T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 62/63 | chr12 | 122623649 | ||||||
| chr12:122623727
|
G | A | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG02602.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.6516-871G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 62/63 | chr12 | 122623727 | ||||||
| chr12:122623809
|
G | A | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.6516-789G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 62/63 | chr12 | 122623809 | ||||||
| chr12:122624007
|
G | T | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6516-591G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 62/63 | chr12 | 122624007 | ||||||
| chr12:122624016
|
C | T | 86 | a0001c0002t0001g0007a0001c0002t0001g0009a0001c0002t0001g0010others(83): Show | 86 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.6516-582C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 62/63 | chr12 | 122624016 | ||||||
| chr12:122624228
|
G | T | 1 | a0021c0036t0001g0013 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.6516-370G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 62/63 | chr12 | 122624228 | ||||||
| chr12:122624261
|
T | TTTTTC | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(86): Show | 91 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.6516-317_6516-313d others(7): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 62/63 | INFO_REALIGN_3_PRIME | chr12 | 122624261 | |||||
| chr12:122624261
|
T | TTTTTCTT others(3): Show |
2 | a0001c0001t0001g0189a0001c0001t0001g0193 | 2 | HG02056.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.6516-322_6516-313d others(12): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 62/63 | INFO_REALIGN_3_PRIME | chr12 | 122624261 | |||||
| chr12:122624261
|
TTTTTCTT others(3): Show |
T | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.6516-322_6516-313d others(12): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 62/63 | INFO_REALIGN_3_PRIME | chr12 | 122624261 | |||||
| chr12:122624443
|
T | C | 86 | a0001c0002t0001g0007a0001c0002t0001g0009a0001c0002t0001g0010others(83): Show | 86 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.6516-155T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 62/63 | chr12 | 122624443 | ||||||
| chr12:122624457
|
A | C | 8 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0172others(5): Show | 8 | NA18940.hp1 NA18941.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.6516-141A>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 62/63 | chr12 | 122624457 | ||||||
| chr12:122624542
|
G | A | 1 | a0007c0013t0001g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6516-56G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 62/63 | chr12 | 122624542 | ||||||
| chr12:122625043
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.6606+355G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625043 | ||||||
| chr12:122625074
|
T | C | 4 | a0002c0003t0001g0124a0008c0012t0001g0005a0008c0012t0001g0125others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.6606+386T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625074 | ||||||
| chr12:122625126
|
T | C | 29 | a0001c0001t0001g0306a0001c0010t0001g0282a0001c0010t0001g0283others(26): Show | 29 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.6606+438T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625126 | ||||||
| chr12:122625219
|
A | G | 2 | a0001c0002t0001g0007a0001c0002t0001g0053 | 2 | NA18954.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.6606+531A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625219 | ||||||
| chr12:122625264
|
G | A | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6606+576G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625264 | ||||||
| chr12:122625286
|
C | G | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0288 | 3 | HG01081.hp1 HG01993.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.6606+598C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625286 | ||||||
| chr12:122625357
|
C | G | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG02602.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.6606+669C>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625357 | ||||||
| chr12:122625427
|
CATG | C | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115 | 3 | HG02055.hp2 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.6606+740_6606+742d others(5): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625427 | ||||||
| chr12:122625471
|
G | T | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.6607-734G>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625471 | ||||||
| chr12:122625589
|
C | A | 1 | a0001c0002t0001g0096 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.6607-616C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625589 | ||||||
| chr12:122625593
|
A | AC | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.6607-612_6607-611i others(3): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625593 | ||||||
| chr12:122625602
|
C | A | 7 | a0001c0002t0001g0034a0001c0002t0001g0050a0001c0002t0001g0084others(4): Show | 7 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.6607-603C>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625602 | ||||||
| chr12:122625683
|
T | C | 2 | a0001c0002t0001g0054a0001c0002t0001g0055 | 2 | HG01256.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.6607-522T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625683 | ||||||
| chr12:122625818
|
T | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0111others(209): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.6607-387T>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625818 | ||||||
| chr12:122625846
|
G | A | 18 | a0003c0004t0001g0008a0003c0004t0001g0016a0003c0004t0001g0019others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.6607-359G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625846 | ||||||
| chr12:122625854
|
T | C | 3 | a0001c0010t0001g0282a0001c0010t0001g0283a0001c0010t0001g0284 | 3 | HG02109.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.6607-351T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625854 | ||||||
| chr12:122625857
|
G | A | 1 | a0001c0001t0001g0262 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.6607-348G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625857 | ||||||
| chr12:122625875
|
A | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(248): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.6607-330A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625875 | ||||||
| chr12:122625906
|
G | A | 86 | a0001c0002t0001g0007a0001c0002t0001g0009a0001c0002t0001g0010others(83): Show | 86 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.6607-299G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625906 | ||||||
| chr12:122625942
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.6607-263C>T | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122625942 | ||||||
| chr12:122626038
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(86): Show | 91 | HG00099.hp1 HG00438.hp1 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.6607-167G>A | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122626038 | ||||||
| chr12:122626107
|
T | C | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0111others(249): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.6607-98T>C | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122626107 | ||||||
| chr12:122626136
|
A | G | 1 | a0004c0005t0001g0309 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6607-69A>G | KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 63/63 | chr12 | 122626136 |